dental device and method for dental and / or gum treatment

专利摘要:
TOOTH WHITENING DEVICES AND SYSTEMS A device and system are provided to assist teeth whitening. The device includes a mold suitable for dental treatment, the tray including one or more layers of dental coverings suitable for forming a treatment cavity having a vacuum, and the layers of dental coverings include a layer on the teeth. upper teeth and / or a layer on the lower teeth; and one or more treatment supply layers where the treatment supply layer has one or more flow channels in fluid communication with the treatment cavity such that the treatment supply layer can supply and / or remove one or more fluids treatment cavity.
公开号:BR112014005672B1
申请号:R112014005672-2
申请日:2012-09-11
公开日:2021-01-12
发明作者:Daniel Sanders；Ben Zion Spector
申请人:Mavrik Dental Systems Ltd.；
IPC主号:

专利说明:

[0001] [001] The device and method of the present invention relate to dental treatments and more specifically, to teeth whitening treatments. Background of the invention
[0002] [002] There is a wide variation in the shade scale of the teeth. It is commonly found a wide variation within the same individual of the different teeth in the mouth, due to a variety of natural factors. Often, in the same individual, for example, the natural hue of the upper and lower canines is more "yellowish" than the upper and lower central and lateral incisors and it is more common to find that the upper (jaw) teeth are generally "whiter" than the lower teeth (mandibular). It is also often common to find that the anterior teeth are generally "whiter" than the posterior teeth. The known dental bleaching treatments that will be described below do not appear to take into account any of these significant variations in the baseline color shades (pre-treatment) that are normally present in the same patient prior to treatment. This means that, whatever the whitening result obtained using the various whitening techniques currently in use, they cannot, in general, be standardized for the needs of a given patient based on the baseline shade values, differing from the teeth that the patient had before treatment. It is, therefore, extremely unlikely to obtain a completely uniform final bleaching result using the current systems in use.
[0003] [003] There are numerous over-the-counter "whitening" products such as toothpaste, whitening tapes and mouthwashes. These will not be discussed further.
[0004] [004] The standard professional dental treatment to whiten teeth is to provide the user through the dental office with some form of dental mold (produced to order from dental molds taken from each patient and produced to fit each patient) and mild concentrations of a bleaching agent for self-application at home. These treatments are commonly referred to as the "household" bleaching method.
[0005] [005] The anatomical area posterior to the terminal teeth on the right and left sides of any of the upper and lower jaws is referred to as the retromolar cushion. The dental impression device is typically manufactured to cover these terminal teeth and its terminal edges are the retrromolar cushions. There is significant variation between patients regarding the size of their teeth and the shape of their dental arches. Regarding the manufacture of a mold to adequately cover all the teeth contained within any given arch, the variable width and length of the dental arch must be considered.
[0006] [006] The user is instructed to completely fill the mold with the mild chemical whitening agent (gel) and place the mold on the teeth for up to several hours each day during the course of a minimum of one to two weeks. The custom dental mold covers all teeth in the upper or lower jaw. This means that the user can whiten both the front and back teeth with this treatment method using a mold for the upper teeth and a mold for the lower teeth. This teeth whitening technique is referred to as a "compression" technique, since the whitening agent is mainly contained during treatment inside the closed mold and not left exposed to the atmosphere.
[0007] [007] It has been demonstrated that the use of a compression technique with bleaching agents enhances bleaching as this encourages oxygen ions released by the bleaching agent (the primary means for whitening teeth) to migrate towards the interior of the enamel structure teeth instead of being released into the surrounding air (Miara and Miara, 2003).
[0008] [008] It has been shown that saliva, natural in the oral cavity, contains a peroxidase enzyme that naturally breaks down and neutralizes hydrogen peroxide (Tenovuo and Pruitt, 1984). Using professional custom-made whitening molds that adapt to teeth, more closely than standard counter whitening molds, reduces the amount of saliva that can seep into the molds and come into contact with the active hydrogen peroxide that has been placed on the teeth. molds. This reduces the amount of deactivation or decomposition by the active gel and then saliva. enhances the chemical whitening effect of this professional whitening treatment compared to "normal" over-the-counter whitening molds (which are not well adapted to the teeth and therefore allow a significant amount of saliva to leak into the molds).
[0009] [009] The custom "whitening" dental mold (s) apparatus (s) of the "domestic" treatment method mentioned above requires two office visits. During the first visit to the office, impressions of the dental arches are taken, from which "whitening" molds are made of rigid or semi-rigid thin plastic fitted to measure. These external mold limiting surfaces can be closely contoured to the teeth or produced significantly larger than the teeth. The "home" treatment method above requires that the user devotes considerable time (as mentioned above) to achieve a moderate degree of teeth whitening and, due to the excessive exposure time of teeth and gums to whitening agents, can often make teeth become sensitive, as well as irritate or chemically burn the gums and oral mucosal tissues of the mouth. Many patients find the effort required to achieve a sufficient "whiter teeth" result to be very painful and there is often a high rate of non-compliance, resulting in a poor final whitening result.
[0010] [0010] These obvious disadvantages of the professional "domestic" whitening treatment method have in recent years given rise to professional dental treatments referred to in the dental fields as "in-office" or "powerful whitening" treatment. This treatment method involves applying in the dental office, using and under the supervision of a professional dental team, more highly concentrated (and more caustic) formulations of various chemical teeth whitening agents that were previously used for "home" whitening treatments. This "powerful" teeth whitening technique typically takes around an hour of treatment time. To protect the gingival tissues from these highly concentrated bleaching agents, a "painted dam" or protective coating (a layer of material applied to a strip on the gum line that is placed in a stepped shape to contour the gum line) is applied by hand (very time consuming) and hardened with a standard dental UV light. Additionally, any uncomfortable lip and cheek retractor device is inserted into the mouth along with cotton rolls (and gauze as necessary) to try to protect the rest of the oral tissues from the mouth from these highly concentrated and caustic bleaching agents.
[0011] [0011] These precautions are necessary, since the contact of these highly concentrated chemical bleaching agents used in "powerful" bleaching with the soft tissues mentioned above the mouth will, in a few seconds, cause significant chemical burning and pain to the patient. Typically, three applications of the bleaching agent (for approximately 20 minutes each) limited to the buccal (front) surfaces of only the front teeth are made, with the previous application being washed and sucked from the teeth and replaced by the next application. The lingual (internal) surfaces of these anterior and posterior teeth in their entirety are not "bleached" using this technique. The "powerful" bleaching technique does not use a mold device of any kind. The bleaching agent is applied in an open "uncompressed" manner on the outer buccal surfaces of the limited teeth to be treated and does not have the bleaching advantages of the compression effect of the bleaching gel using molds as previously described (domestic bleaching technique) .
[0012] [0012] During the past two decades, there has also been a change in treatments "in the office" or "powerful whitening" to use "light-activated" bleaching agents compared to older bleaching agents that did not require light activation to enhance a chemical oxidation reaction (bleach). These new light-activated bleaching agents are chemically formulated to oxidize when exposed to an intense concentrated light source that acts as a catalyst to enhance the chemical oxidation of these bleaching agents.
[0013] [0013] There is much controversy in the dental fields regarding the use of light activation of bleaching gels to reinforce the chemical whitening effect of these gels. It has been postulated that it is actually the heat generated by the light and not any specific wavelength of the light that actually increases the chemical activity and, therefore, the bleaching activity of these bleaching gels.
[0014] [0014] The light-emitting devices currently used in the dental field can, in general, only reach the anterior portion of the mouth and only after the lips and cheeks have been retracted using devices, as described above. This is due to the limited natural elasticity of the lips and muscles around the mouth that limit the number of teeth that can be comfortably and safely retracted and exposed to the light source and highly concentrated "powerful" bleaching chemicals while still protecting soft tissues. of the oral cavity of these highly caustic bleaching agents.
[0015] [0015] As mentioned above, these limitations typically result in "powerful whitening" treatments of, at most, the 10 upper front teeth and 10 lower front teeth, (from the upper and lower central and lateral incisors, canines and first and second bicuspids) ) for a maximum treatment of 20 teeth (there are typically 28-32 teeth in the human mouth). Due to the limitations already mentioned, it is common practice to find that only the 8 upper teeth and 8 lower teeth are whitened "strongly" for a total of 16 (only 50%) of the teeth frequently present in the patient's mouth, a distinct disadvantage of this technique of teeth whitening.
[0016] [0016] An additional limitation of the treatment area is that in general the lights used in "powerful" whitening can be positioned by the operator in the patient's mouth to mainly illuminate the buccal surfaces (front and external) of the anterior teeth while only dimly illuminating the teeth. lingual surfaces (posterior or internal) of these frontal teeth. It is also extremely difficult for the dentist to apply the "painted barrier" protective coating to the gum line of the lingual "internal" surfaces of the anterior teeth and it is almost impossible for the dentist to isolate the tongue, which is very active with current insulation devices and materials. available in the dental field. This means that these sensitive oral tissues are extremely difficult to isolate from the caustic chemical burning of highly concentrated "powerful" bleaching agents.
[0017] [0017] The above explains why the whitening of the internal (lingual) surfaces of the anterior teeth is rarely done in this technique and the posterior teeth are never whitened altogether with this technique. In addition, the "powerful" whitening of only the buccal (external) surfaces of the anterior teeth adversely affects the outcome of the overall final whitening, since the natural enamel layers of the teeth (found naturally on both the external and internal surfaces of all teeth). teeth) are naturally somewhat translucent. This allows the "darker" shade of the internal (lingual) untreated surfaces of the teeth to "show off" for the frontal surfaces. This naturally occurring optical effect can "knock down" or decrease the overall final whitening effect of these teeth when using the current "powerful" whitening treatment method.
[0018] [0018] The advantages of the "in-office" or "powerful" bleaching treatment method compared to "domestic" treatment include: a. Enable faster teeth whitening compared to "home" treatment due to the use of highly concentrated whitening agents. This significantly reduces the overall treatment time; B. As it is done "in the office", there are fewer problems of non-compliance with the patient since he is often faced with the longer "home" treatment; and c. The shorter treatment time tends to minimize irritation or sensitivity of the teeth, since the teeth are exposed to these agents for a shorter period of time, although some users experience sensitivity of the teeth due to the more concentrated potency of the chemical oxidizing agents used in this treatment method and the often found unwanted leakage of small amounts of highly concentrated bleaching agents, in addition to the protective barriers placed by the dentist on oral tissues during the "powerful" bleaching treatment.
[0019] [0019] The disadvantages of the "in-office" treatment method compared to "domestic" treatment include: a. As noted above, only the front teeth can be comfortably whitened with the "in-office" method, compared to the "domestic" treatment that allows the bleaching of both the front and posterior teeth; B. As mentioned above, the most highly concentrated formulations of oxidizing bleaching agents are more caustic to the hard tissue (tooth) and soft tissue (gums, oral mucosa, tongue) of the mouth and therefore require the application of gingival and mucosal barriers oral applied by hand by professional dental assistants under the supervision of a dentist or by the dentist himself on the gingival tissues and oral mucosa of the areas to be treated to protect them from these highly concentrated bleaching chemicals. This is a time-consuming procedure that often needs to be reapplied during treatment to adequately protect the soft tissues of the mouth from these highly concentrated bleaching agents. Even with all this isolation effort, as mentioned above, it is typical to find some leakage and burning of the patient's oral tissues resulting in temporary pain and discomfort for the patient; ç. Due to the inaccessibility of the posterior teeth and the difficulty (due to the cheeks and tongue) of the posterior areas of the mouth, these whitening treatments are invariably restricted or limited (due to the extreme difficulty in protecting the oral soft tissues surrounding the posterior teeth) to the anterior segments of the mouth; d. It mainly whitens the frontal (buccal) surfaces of the anterior teeth and is only rarely used to lighten the internal (lingual) surfaces of the anterior teeth; and. It is common to see a more pronounced "recovery" effect (loss of whitening results) after treatment with this treatment method "in the office" compared to the "domestic" treatment method. This is due to the short duration of the treatment (compared to a much longer treatment time of the "domestic" treatment method) and the resulting rehydration of the teeth after treatment (the "powerful" whitening process tends to temporarily dehydrate the teeth. which temporarily increases the result of the initial bleaching). This means that the typical final "bleaching" result using the "powerful" bleaching technique is significantly weaker than the final "bleaching" result that can be obtained when the patient is highly obedient and using the bleaching technique " household "correctly. Summary of the invention
[0020] [0020] According to a configuration of the present invention, a device, method and system is provided to assist teeth whitening. The device may include a nozzle suitable for applying dental treatment, the nozzle including one or more layers of dental cap material suitable for forming a treatment cavity having a vacuum, the dental cap layers including a layer on the teeth upper teeth and / or a layer on the lower teeth; and one or more treatment supply layers wherein the treatment supply layer has one or more flow channels in fluid communication with the treatment cavity such that the treatment supply layer can supply and / or remove one or more treatment fluids to or from the treatment cavity.
[0021] [0021] In some configurations, the dental vacuum cap is formed using a continuous or selectively sustainable sealing mechanism that includes a sealing edge formed of a compressible material in conjunction with one or more sealing plugs connectable to the (s) posterior opening (s) of the dental cap layer, the sealing mechanism sufficiently sealing the treatment cavity.
[0022] [0022] In some configurations, the sealing mechanism is adapted to prevent saliva from entering the treatment cavity and is adapted to prevent treatment material from leaving the treatment cavity.
[0023] [0023] In some configurations, the treatment supply layer includes one or more heaters to heat a treatment material, to heat at least a portion of the treatment cavity; or both.
[0024] [0024] In some configurations, the device includes an integrated cable in the treatment supply layer suitable for: inserting one or more layers of dental covers over the upper and / or lower teeth, to adjust the position of the one or more layers of dental covers, to remove layers of dental covers after a dental treatment is completed, or any combination thereof.
[0025] [0025] In some configurations, the device includes a power line to supply an electrical current to the treatment supply layer and one or more tubes to supply and / or extract one or more treatment materials to the treatment supply layer , the cable includes the power line; or both.
[0026] [0026] In some configurations, the layer of dental cover covers the edges of the gum.
[0027] [0027] In some configurations, the device includes two layers of dental covers to cover the upper teeth and the lower teeth; at least one treatment supply layer interposed between the two layers of dental caps to allow the upper and lower teeth to be treated simultaneously; the device including one or more breathing holes in the treatment supply layer suitable for providing an air passage in and out of the mouth during dental treatment.
[0028] [0028] In some configurations, the cable includes one or more inlet flow tubes to flow one or more treatment materials into the treatment supply layer (s); and one or more outflow tubes to flow one or more treatment materials out of the treatment supply layer (s).
[0029] [0029] In some configurations, the nozzle may include: one or more supply holes to drain a treatment material from the treatment supply layer to the treatment cavity and one or more drain holes to drain a treatment material from the cavity treatment for the treatment supply layer; and the treatment supply layer includes one or more supply channels for transporting treatment material from an inlet flow tube to the treatment cavity and one or more drainage channels for transporting treatment material from one or more drain holes for an outlet flow tube.
[0030] [0030] In some configurations, the dental cap layer includes a compressible cavity connector suitable for sealing the cavity to prevent material flow out of the back sides of the vacuum forming layer.
[0031] [0031] In some configurations, the device includes one or any combination of the following design characteristics: the layer of dental cover incorporates a cut, rolled apron design to conform to the edges of the gum; the treatment supply layer includes one or more individually controllable heating zones; the dental treatment layer is between the upper and lower dental layers and is shaped to mirror an angle of geometric axis of articulation to facilitate the natural movement of the jaw.
[0032] [0032] In some configurations, the vacuum described above is formed via the treatment supply layer, reducing the pressure in the dental treatment cavity below ambient pressure.
[0033] [0033] In some configurations, the device may include a pumping system, to pump one or more treatment materials into the nozzle; a multiposition flow control module; and a control unit to automate dental treatment.
[0034] [0034] In some configurations, the device includes a mouth protection component for additional protection against treatment materials.
[0035] [0035] In some configurations, the device includes a mouth protection component that includes a layer of gum treatment on its internal surfaces to supply one or more therapeutic materials for the gums.
[0036] [0036] According to some configurations, a mouthguard is provided, which can include a drape with a flexible surgical arch shape designed to substantially conform to the anatomy of the gingival edge, and having pre-configured cut-out holes for personalized insertion on the teeth that act to provide a dry field.
[0037] [0037] In some configurations, mouth protection includes a layer of treatment material on one or more surfaces, the treatment material being suitable for neutralizing treatment materials.
[0038] [0038] In still further configurations, a method is provided to perform dental treatments, including positioning a mouthpiece including one or more layers of dental covers on upper and / or lower teeth; applying vacuum to the dental cap layer such that a sealed treatment cavity having a pressure below ambient pressure is formed around the teeth; and draining one or more treatment materials into the sealed treatment cavity.
[0039] [0039] In some configurations, the process includes any or any combination of the following steps: preparing a pump module to connect to a nozzle designed for a teeth whitening treatment; configure treatment settings on a control device attached to the pump module; apply a flow control module to cause a vacuum between the mouthpiece and the anatomy of the patient's gingival edge; apply a flow control module to automatically manage the supply of materials according to the aforementioned treatment definitions, and / or use a flow control module to remove treatment materials from the nozzle.
[0040] [0040] In some configurations, the method includes a step to apply flow control to change flow patterns during a treatment, to optimize the conformity to a treatment plan.
[0041] [0041] In some configurations, the method includes a step to monitor treatment to track compliance to a treatment plan.
[0042] [0042] In some configurations, the method includes a step to monitor the treatment to identify problems during a treatment.
[0043] [0043] In some configurations, the treatment supply layer includes a plurality of zones including a first zone and a second zone, the process including providing different treatment materials for the first zone and the second zone.
[0044] [0044] In some configurations, the treatment materials differ with respect to the temperature of the materials, with respect to the concentration of the materials, or both.
[0045] [0045] The treatment device, according to some configurations, can be a stock item that can be supplied in various sizes of materials and that is reusable or a disposable item that can include a single dental arch nozzle or double dental arches with breathing tubes incorporated in the device body that allow the patient to breathe through the mouth when the double dental arch nozzle is inserted in the oral cavity. The mouthpiece device has flexible side walls with a unique design circumferential deformable apron that adapts to the upper and lower alveolar edges of the mouth. Each well formed by the arch contains at its distal end (right and left sides) a posterior seal connector. The connector is made of a highly deformable material that, when bitten strongly, conforms to the anatomy of the crown segment of the tooth that is biting it. The connectors in conjunction with the deformable circumferential apron designed only from the edge wells allow the mouthpiece device to adapt intimately to the edges of the upper and lower gingival alveoli and to the most distal teeth (right and left side) creating a continuous or selectively sustainable intimate seal the nozzle with these structures.
[0046] [0046] The nozzle device also incorporates in its intermediate layer, multiple flow channels with outlets and inlets and multiple heating elements in several different arrangements along its various surfaces whose temperatures can be controlled, individually, by a microprocessor unit contained inside a control unit. In some configurations, these heating elements may be printed circuit resistors. Metal pins can be connected to these pins and the pin heads can come into contact with the treatment cavity, thus effectively transferring the heat generated by the resistors to the treatment cavity and the treatment material contained within it. The microprocessor unit can control electricity, time duration, alarms, sensors, individual or multiple heat emitting elements, pumps, motors and other controls. Several different types and sizes of separate custom-made or stock protective / mouthguard elements can be inserted into the mouth before inserting the mouthpiece and used in conjunction with the device.
[0047] [0047] A pump component can be used to create a vacuum within the nozzle device. Different concentrations of chemical bleaching agents can be preheated to a specific temperature controlled in a disposable heating chamber and then released in a controlled manner via the aforementioned disposable pump and a set of disposable flexible tubing connected to the nozzle device. Pressure sensors are integrated into the system to monitor the volume and flow rate of the gel and the integrity of the mouthpiece vacuum seal. The bleaching gel agents can similarly be removed from the device in a manner controlled by said system. Similarly, fresh water can be supplied to and removed from the nozzle device to wash or rinse any remaining gel residue from the teeth and the inner surfaces of the nozzle.
[0048] [0048] To achieve the above, a rotary multi-position flow control valve driven by a motor incorporated in the pump and controlled by the microprocessor of the control unit allows: 1. The creation of continuous or selectively sustained vacuum in the nozzle 2. The supply for the nozzle and removal of the whitening gel nozzle 3. A steady or pulsating "closed loop" dynamic flow of the gel into the nozzle 4. Supply and removal of water from the nozzle to wash or rinse any residual gel from both the surfaces of the the internal surfaces of the nozzle.
[0049] [0049] An optional tooth shade combination sensor unit for recording pre and post treatment tooth shade values can be incorporated into the control unit. In addition, a removable belt with a sensor that is connected to the control unit and that measures certain vital signs (such as the pulse rate) of the patient can be connected to the patient to monitor the patient's comfort level throughout the treatment .
[0050] [0050] According to various aspects of the invention, the device for providing dental treatment may include a gingival sealing portion to cover the gingiva; a distal tooth sealing portion, where the gum sealing portion and the distal tooth sealing portion define a gap between at least a portion of the device and the tooth on which they lie; and at least a portion of fluid conduit for passing fluid into or out of the treatment cavity; being that in a placement in a patient's mouth over a plurality of teeth the gingival sealing portion contacts and deforms against a patient's gum to form intimate contact with the gingiva and the tooth sealing portion deforms against the distally located to substantially define a seal on the distal tooth, such that a fluid can be introduced, removed, or both from the treatment cavity while maintaining a seal with the deformable components of gingival sealing and tooth sealing. Brief description of the drawings
[0051] - A Fig. 1a é uma vista de topo de um exemplo de um dispositivo do bocal 1, de acordo com algumas configurações, onde está representada uma camada formadora de vácuo com formato de arco dental, construída de material flexível com bordas compressíveis projetadas para formar uma cavidade de tratamento sobre os dentes superiores ou inferiores e bordas da gengiva; - A Fig. 1b é uma vista inferior de um exemplo de um dispositivo do bocal 1, de acordo com algumas configurações; - A Fig. 1c é uma vista adicional de um exemplo de um dispositivo do bocal 1, de acordo com algumas configurações; - A Fig. 2a é uma vista frontal de um exemplo de um dispositivo do bocal 1, de acordo com algumas configurações; - A Fig. 2b é uma vista lateral de um exemplo de um bocal 1, de acordo com algumas configurações; - A Fig. 2c é uma vista de topo de um exemplo de uma camada intermediária, de acordo com algumas configurações; - A Fig. 2d é uma vista inferior de um exemplo de uma camada intermediária 4, de acordo com algumas configurações; - A Fig. 3 é uma vista de topo em detalhe de um exemplo de um segmento anterior da camada intermediária, de acordo com algumas configurações; - A Fig. 4a é uma vista frontal (labial) de um exemplo de uma camada intermediária, de acordo com algumas configurações; - A Fig. 4b é uma vista interna (lingual) da Fig. 4a, de acordo com algumas configurações; - A Fig. 4c é uma vista frontal (labial) de um exemplo das placas e camadas do dispositivo, de acordo com algumas configurações; - A Fig. 5a é uma vista frontal (bucal) explodida de pilha vertical de uma possível configuração de componentes que compreendem o bocal de arco dental duplo, de acordo com algumas configurações; - A Fig. 5b é uma vista posterior (lingual) explodida de pilha vertical da Fig. 5a onde estão representados os componentes que compreendem o bocal de arco dental duplo, de acordo com algumas configurações; - A Fig. 6a é uma vista interna (lingual) de um exemplo de um dispositivo do bocal, de acordo com algumas configurações; - A Fig. 6b ilustra uma vista da Fig. 6a onde uma fatia vertical de seção transversal distal do dispositivo do bocal foi tomada, de acordo com algumas configurações; - A Fig. 6c representa a Fig. 6b onde os conectores distais superior 7 e inferior 8 foram removidos, de acordo com algumas configurações; - A Fig. 6d é uma vista interna (lingual) da camada intermediária, de acordo com algumas configurações; - A Fig. 6e é uma vista frontal angulada do dispositivo do bocal, de acordo com algumas configurações; - A Fig. 7 é uma vista interna em detalhe (lingual) de um exemplo de um bocal, de acordo com algumas configurações; - A Fig. 8a é uma vista frontal (labial) de um exemplo de um bocal, de acordo com algumas configurações; - A Fig. 8b é uma vista lateral interna em detalhe (faceando a superfície do bocal), de acordo com algumas configurações; - A Fig. 8c é uma vista externa em detalhe (faceando para longe da superfície do bocal 1 não representado) do conector de engate rápido, de acordo com algumas configurações; - A Fig. 9a é uma vista angulada de um lado de um exemplo de um conjunto de mecanismo de bomba, de acordo com algumas configurações; - A Fig. 9b é uma vista angulada do lado oposto da Fig. 9a, de acordo com algumas configurações; - A Fig. 9c é uma vista de topo do conjunto de mecanismo de bomba, de acordo com algumas configurações; - A Fig. 9d é uma vista frontal do conjunto de bomba, de acordo com algumas configurações; - A Fig. 10 é uma vista de topo/frontal de uma configuração possível da unidade de controle, de acordo com algumas configurações; - A Fig. 11 é uma vista de topo/posterior da caixa de controle 50 e unidade de carregador do conjunto de bateria 52, de acordo com algumas configurações; - A Fig. 12a é uma vista de superfície externa (por baixo) de uma configuração possível da proteção bucal superior, de acordo com algumas configurações; - A Fig. 12b é uma vista (de topo) da superfície interna da Fig. 12a, de acordo com algumas configurações; - A Fig. 12c é uma vista (de topo) da superfície externa de uma configuração possível da proteção bucal inferior, de acordo com algumas configurações; - A Fig. 12d é uma vista (inferior) interna da Fig. 12c, de acordo com algumas configurações; - A Fig. 13a é uma vista frontal empilhada verticalmente da proteção bucal superior 59 e da proteção bucal inferior 60, de acordo com algumas configurações; - A Fig. 13b é uma vista frontal da mandíbula superior, de acordo com algumas configurações; - A Fig. 13c é uma vista frontal de um exemplo de um dispositivo do bocal 1 inserido dentro das mandíbulas superior 24 e inferior 25 respectivamente, de acordo com algumas configurações; e - A Fig. 14 é um diagrama de fluxo descrevendo um exemplo de um processo para proceder a um tratamento de branqueamento de dentes usando um bocal e componentes associados como descrito aqui, de acordo com algumas configurações. [0051] The principles and operation of the system, apparatus and method, according to the present invention, can be better understood with reference to the drawings and the following description, it being understood that these drawings are provided for illustrative purposes only and do not mean to be limiting, where: - Fig. 1a is a top view of an example of a nozzle device 1, according to some configurations, where a dental arc-shaped vacuum forming layer is constructed, constructed of flexible material with compressible edges designed to form a treatment cavity on the upper or lower teeth and gingival edges; - Fig. 1b is a bottom view of an example of a nozzle device 1, according to some configurations; - Fig. 1c is an additional view of an example of a nozzle device 1, according to some configurations; Fig. 2a is a front view of an example of a nozzle device 1, according to some configurations; - Fig. 2b is a side view of an example of a nozzle 1, according to some configurations; - Fig. 2c is a top view of an example of an intermediate layer, according to some configurations; - Fig. 2d is a bottom view of an example of an intermediate layer 4, according to some configurations; - Fig. 3 is a top view in detail of an example of an anterior segment of the middle layer, according to some configurations; - Fig. 4a is a frontal view (lip) of an example of an intermediate layer, according to some configurations; - Fig. 4b is an internal (lingual) view of Fig. 4a, according to some configurations; - Fig. 4c is a front view (lip) of an example of the device's plates and layers, according to some configurations; - Fig. 5a is an exploded frontal (buccal) view of a vertical stack of a possible configuration of components comprising the double dental arch nozzle, according to some configurations; - Fig. 5b is an exploded rear (lingual) view of the vertical stack of Fig. 5a showing the components that comprise the double dental arch nozzle, according to some configurations; - Fig. 6a is an internal (lingual) view of an example of a mouthpiece device, according to some configurations; - Fig. 6b shows a view of Fig. 6a where a vertical slice of distal cross section of the nozzle device has been taken, according to some configurations; - Fig. 6c represents Fig. 6b where the upper 7 and lower 8 distal connectors have been removed, according to some configurations; - Fig. 6d is an internal (lingual) view of the middle layer, according to some configurations; - Fig. 6e is an angled front view of the nozzle device, according to some configurations; - Fig. 7 is an internal view in detail (lingual) of an example of a nozzle, according to some configurations; - Fig. 8a is a frontal view (lip) of an example of a mouthpiece, according to some configurations; - Fig. 8b is an internal side view in detail (facing the nozzle surface), according to some configurations; - Fig. 8c is an external view in detail (facing away from the surface of the nozzle 1 not shown) of the quick connector, according to some configurations; - Fig. 9a is an angled view on one side of an example of a pump mechanism assembly, according to some configurations; - Fig. 9b is an angled view on the opposite side of Fig. 9a, according to some configurations; - Fig. 9c is a top view of the pump mechanism assembly, according to some configurations; - Fig. 9d is a front view of the pump set, according to some configurations; - Fig. 10 is a top / front view of a possible configuration of the control unit, according to some configurations; - Fig. 11 is a top / rear view of the control box 50 and the battery pack charger unit 52, according to some configurations; - Fig. 12a is an external surface view (below) of a possible configuration of the upper mouthguard, according to some configurations; - Fig. 12b is a (top) view of the inner surface of Fig. 12a, according to some configurations; - Fig. 12c is a (top) view of the external surface of a possible configuration of the lower mouthguard, according to some configurations; - Fig. 12d is an internal (bottom) view of Fig. 12c, according to some configurations; - Fig. 13a is a vertically stacked front view of the upper mouthguard 59 and the lower mouthguard 60, according to some configurations; - Fig. 13b is a frontal view of the upper jaw, according to some configurations; Fig. 13c is a front view of an example of a nozzle device 1 inserted into the upper and lower jaws 25 respectively, according to some configurations; and - Fig. 14 is a flow diagram describing an example of a process for proceeding with a teeth whitening treatment using a nozzle and associated components as described here, according to some configurations.
[0052] [0052] It will be appreciated that for simplicity and clarity of illustration, the elements shown in the drawings were not necessarily drawn to scale. For example, the dimensions of some of the elements may be exaggerated in relation to other elements for clarity. In addition, certain amounts of elements have been represented, according to specific configurations, however, other configurations can be provided with fewer or more elements, such as holes, pins, heating elements, tubes etc. In addition, where deemed appropriate, reference numerals may be repeated between the drawings to indicate corresponding or similar elements throughout all serial views. Detailed description of the invention
[0053] [0053] The following description is presented to allow someone of ordinary experience in the art to produce and use the invention as provided in the context of a particular application and its requirements. Several modifications to the described configurations will be apparent to those with experience in the art and the general principles defined here can be applied to other configurations. Therefore, the present invention is not intended to be limited to the particular configurations shown and described, but the broader scope consistent with the new principles and features disclosed herein should be agreed upon. In other cases, well-known methods, procedures and components have not been described in detail so as not to obscure the present invention.
[0054] [0054] Preferred dental treatments employ one or more chemicals, such as peroxides that lighten teeth by one or more chemical reactions. Configurations of the present invention allow to increase and efficiency and effectiveness of dental treatments, using vacuum to create a sealed cavity or treatment zone where treatment materials can be optimally applied and also prevented from escaping out of the sealed treatment cavity. Non-limiting configurations of the invention include a dental treatment device, method and system, such as for teeth whitening.
[0055] [0055] The configurations of the present invention incorporate features that take into account any or any combination of the advantages and disadvantages listed above for the two treatment methods described (such as powerful in the office and bleaching by custom household mold) and materials currently in use in the dental field. The configurations of the present invention include a dental treatment nozzle which can include a single or double dental arch. The nozzle can be used to provide a bleaching treatment. The nozzle may include one or more layers of dental caps to cover the upper teeth and / or the lower teeth. A layer of dental cover is preferably an arch, such as a dental arch, configured to fit over the lower teeth or the upper teeth. For example, the nozzle may include an upper tooth layer and a lower dental layer layer (e.g., the mouthpiece may include double dental arches). The dental cap layer may have a dental arch well that covers the teeth. A particularly preferred nozzle includes two layers of dental caps, each having a dental arch well, where the two layers of dental caps are joined together to create a unique device. It will be appreciated that, according to the teachings here, two layers of dental caps joined together can be joined via one or more additional layers, such as one or more layers of treatment supply.
[0056] [0056] The mouthpiece, according to some configurations of the present invention, allows the use of generic or stock nozzles in patients, such that the variable widths and lengths of the patient's complete dental arches can be handled, without the need to manufacture a personalized mouthpiece for each patient. When using such stock nozzles, the configurations of the present invention allow the maintenance of a continuous seal of the nozzle for the given dental arch on which it is placed. The distal connectors are highly deformable such that when the patient is instructed to bite the mouthpiece, the connectors will readily deform around the coronal segments of the terminal teeth. This intimate fitting of the improved mouthpiece of the present invention to any given dental arch is independent of the length and width of the dental arch to which it must be attached and independent of the position of the right or left terminal teeth of any given dental arch to their respective spaces retromolar.
[0057] [0057] The device, the dental treatment nozzle (eg the whitening nozzle), or both can be reusable or disposable after a single use. The nozzle can be made of several generic or stock sizes (eg small, medium, large and extra-large) or can be customized for both upper and lower teeth. The nozzle may include one or more heating elements to heat a dental treatment fluid (e.g., a dental treatment fluid suitable for chemically whitening teeth), to heat an area of the dental cap layer or both. For example, the dental treatment nozzle can have a plurality of zones, each heated by a different thermal element. Each zone can be heated to the same temperature such that the teeth receive the same dental treatment. In various aspects of the invention, two or more zones are heated to different predetermined temperatures such that the teeth receive different treatments. The use of different predetermined temperatures can beneficially result in teeth having a more uniform color (eg between different teeth or between different regions of the same tooth).
[0058] [0058] The device can be used in a system including one or more control units, such as a control unit including a microprocessor. The control unit can be an external control unit. The control unit can control the temperature of one or more heating elements (eg, so that multiple zones have a predetermined temperature that can be the same or different). The control unit can control a nozzle having double dental arches each having a dental arch such that simultaneous whitening of both upper and lower teeth is controlled.
[0059] [0059] An arch of the dental nozzle (eg, each arch of a double-arch nozzle) preferably has a layer of dental cap with an arc-shaped well or other design suitable to form a treatment cavity that may contain one or more dental treatment fluids. For example, the arch-shaped well may contain a dental fluid that includes a predetermined concentration of an active ingredient. The active ingredient can be any chemical that is suitable for whitening teeth in situ. A particularly preferred active ingredient includes one or more peroxides. The two layers of dental covers of a double-arched mouthpiece can have wells that contain the same concentration of active ingredient or different concentrations. A single well can have multiple zones or regions with different concentrations of an active ingredient. It will be appreciated that the nozzle, according to the teachings here, can be used to provide large differences in concentrations of a bleaching agent. The difference in concentrations of the active ingredient (eg the bleaching agent, which can be a peroxide, such as hydrogen peroxide) between two layers of dental layers and / or between two zones or regions can be about 0% or more , about 5% or more, about 15% or more, or about 25% or more. It will be appreciated that even greater variations in concentrations of the active ingredient can be about 35% or more. The active ingredient can be activated or have a reactivity that is otherwise accelerated or enhanced (eg catalyzed or otherwise) by heat. The treatment fluid (eg the treatment fluid including an active ingredient) can be delivered via a pumping system (eg an automatic pumping system), via vacuum, or both, into well sections the nozzle. Preferably, while in the well, the treatment fluid substantially covers the portions of the natural crowns of the teeth (eg the tooth undergoing treatment). Alternatively, while in the well, the treatment fluid substantially covers that portion of the gum tissue surrounding the crown portions of the teeth (eg the gums subject to treatment).
[0060] [0060] The sealed compartment (i.e., sealed treatment cavity) around the teeth formed by the well of the dental cap layer can be used to supply one or more treatment materials for the crown portions of a plurality of teeth. For example, a sequence of two or more different treatment fluids can be passed through the sealed compartment. Without limitation, treatment fluids can include one or more preparation fluids, one or more active treatment fluids (eg one or more bleaching treatment fluids), one or more neutralizing fluids, one or more washing fluids , or any combination thereof. Preferably, the treatment fluids include one or more bleaching treatment fluids and one or more washing fluids. The whitening treatment fluid can include any active and / or non-active ingredients known to whiten teeth. Without limitation, the bleaching treatment fluid may include any or any combination of characteristics of the fluid compositions described in U.S. Patent Nos. 7,189,385 (see, e.g., column 1, row 2 through column 18 row 40); 6,770,266 (see eg column 2, row 9 to column 6, row 35), 6,746,679 (see eg column 1, row 13 to column 11, row 18); 5,668,934 (see, for example, column 1, row 33 through column 16, row 10); 7,601,002 (see eg column 1, row 11 through column 16, row 8); US Patent Application Publications No. 2008/0063612 (see, eg, paragraphs 11 to 165); 2005/0214720 (see, for example, paragraphs 10 to 102); and 2004/0185013 (see, eg, paragraphs 3 to 150); each incorporated here by reference. Any of the treatment fluids can be a liquid that flows under gravitational forces, or a gel that does not flow under gravitational forces. The treatment fluid can preferably be pumped and / or flow under vacuum. Preferably, any treatment fluid that may be harmful to soft tissue in the oral cavity (eg gums or other soft tissues) is in the form of a sufficiently high viscosity fluid or gel such that the fluid does not flow out of the sealed compartment surrounding the teeth being treated. For example, such a treatment fluid can have a viscosity of about 0.1 Pa.s or more, about 1.0 Pa.s or more, about 10.0 Pa.s or more, about 100 Pa. s or more, or about 1000 Pa.s or more.
[0061] [0061] One or more of the treatment fluids can be heated to reduce viscosity, to increase reactivity or both. For example, increasing the temperature of the treatment fluid, such as a bleaching agent (hereinafter referred to as gel, although high viscosity fluids can be used according to the teachings here) can increase the rate of peroxide decomposition to create radicals free of oxygen from the gel and therefore can increase the resulting whitening effect on tooth enamel surfaces. Of course, other treatment materials can be used, including water, salt, gases, chemicals and / or biological solutions for drugs or other materials, compounds etc. Each well (eg, arc-shaped well) of the dental cap layer may contain one or more inlet holes (eg one or more inlet holes on each of the right and left sides of the arch) for the provision of treatment materials into each well, as well as outlet holes (ie drainage) (eg, before or after) to remove treatment materials from each dental arch well. The device may include multiple heat emitting elements arranged and controlled in such a way that the control unit (eg the microprocessor control unit) independently controls the temperature of each heat emitting element in order to create " separately controlled bleaching zones and / or a predetermined custom bleaching pattern. The temperature control is preferably selected based on one or more characteristics of the patient (eg the initial color and / or the initial color variation).
[0062] [0062] The components, devices, systems and methods according to the teachings here can advantageously be used in accelerated dental treatments, such as an accelerated whitening treatment. By employing treatment fluids (eg, a bleaching fluid, such as a bleaching gel) having a high temperature, having a high concentration of active ingredient (such as peroxide), or both, the bleaching rate can be increased such that treatment is accelerated. It will be appreciated that bleaching treatment can be achieved without the need for photodynamic therapy. An accelerated dental treatment can be performed by heating the dental treatment fluid. Although treatment at room temperature can be employed, some or all of the treatment fluid is heated to a temperature of about 27 ° C or more, more preferably about 30 ° C or more, even preferably about 34 ° C or more , even more preferably about 38 ° C or more, even more preferably about 42 ° C or more and most preferably about 46 ° C or more. Of course, higher or lower temperatures can be used as needed. The treatment fluid in the treatment zones (i.e., in the sealed cavity formed by the dental cap layer) may have a generally uniform temperature or may have varying temperatures. A temperature differential can be advantageously employed between two zones such that the two zones have different treatment rates. For example, two zones within a sealed cavity may have a sufficiently different temperature such that the ratio of the bleaching rate in the first zone to the bleaching rate in the second zone is about 1.1 or greater, preferably about 1.3 or greater, more preferably about 2 or greater, and most preferably about 4 or greater. Of course, different bleaching rates can be used as needed. It will be appreciated that similar increases in treatment rates can be achieved by using a higher concentration of active ingredient in the treatment fluid in one or more (eg, all) of the treatment zones.
[0063] [0063] The devices and systems according to the teachings here can be used in a process that includes a step to measure color characteristics (that is, baseline) of a natural pretreatment of a patient's different teeth. A treatment for the patient can be determined based on tooth color, based on tooth color variation, or both. According to the teachings here, the devices, systems and methods of the present invention can be advantageously employed in patients having variability in the natural pretreatment shade (reference base) value of the different teeth to reduce this variation. In various aspects of the present invention, the ability to achieve a more uniform final whitening (i.e., resulting color) is achieved by controlling the temperature and, therefore, the oxidizing activity of a whitening gel in a plurality of areas of the mouthpiece ( such as various areas of the dental cap layer). The control of the various zones can effect a varied color change (eg, whitening intensity) of different teeth, different tooth surfaces, or both. The heating elements can be positioned at various locations on the nozzle to allow separate and differential heating of the different tooth surfaces located in each zone. For example, the placement of one or more heating elements can be selected based on the measured color and / or color variation. One or more of these characteristics can be used to achieve a more uniform esthetic final whitening result.
[0064] [0064] The use of a controller capable of separately controlling multiple nozzle treatment zones (eg, bleaching "zones") or otherwise performing bleaching patterns within each of the nozzle cap layers can allow a dentist to customize the whitening process based on the individual needs of the patient. The controller can allow a dentist to provide personalized treatment in an automated manner.
[0065] [0065] The layer (s) of dental cover (s) preferably has a circumferential edge formed of a material sufficiently soft and arranged such that the edge will compress and deform to fit tightly. against the sides of the edges of the alveoli of the gums of the upper and lower jaws. The edges can therefore create a sealed cavity (eg, formed from the well of the dental cap layer) with the crown of the teeth contained within the cavity.
[0066] [0066] The improved nozzle of the present invention can incorporate one or more air breathing holes. Preferably, the breathing holes are designed to penetrate through a nozzle treatment supply layer without compromising the ability of this treatment supply layer to flow one or more treatment materials into the wells (eg shaped wells) of the dental cap layers, without compromising the ability of this treatment supply layer to drain one or more treatment fluids from the dental cap layer or both. For example, the breathing holes can be integrated within a treatment supply layer in a way that allows one or more treatment fluids to flow into and out of the mouthpiece.
[0067] [0067] The sealing edges, preferably made of a soft deformable material, can have a unique structural shape, such as a shape that forms a highly deformable apron or circular hook design that acts to seal the mouthpiece device (e.g. the dental cap layer) of the present invention to the alveolar edges of the gingiva. The sealing can preferably be partially or totally performed by a patient biting the mouthpiece. The sealing edges can effectively seal the well of the dental cap layer, such that the treatment materials (i.e., treatment fluids) supplied to the mouthpiece are prevented from leaking into the oral cavity. Sealing can be carried out partially or completely by applying vacuum. For example, when a vacuum is applied, the sealing edges can be sucked against the side walls of the gingival edges. A treatment fluid that is pumped into a sealed well of a dental cap layer, preferably comes into contact with the respective teeth on the front surface, on the top surface, on the rear surface or any combination thereof. More preferably, the treatment fluid contacts the teeth on the front and rear surfaces. Even more preferably, the treatment fluid comes into contact with the teeth on all exposed surfaces. The sealing effect of the highly deformable apron and / or sealing edge can be realized or reinforced by the treatment system's ability to remove (eg, suck out) the air inside the nozzle using an external pump to achieve a seal vacuum the mouthpiece with the alveolar edges of the upper and / or lower gums of the upper and / or lower jaws.
[0068] [0068] Due to the fact that there is great variation in the length of dental arches between individuals, it may be difficult or even impossible to effectively use a generic stock dental arch to seal the most posterior region of the well of the dental cap layer. For example, it may be difficult or impossible to effectively seal the areas corresponding to the right and / or left terminal tooth in any given dental arch. Without a sufficient seal in these areas, the treatment fluid may undesirably leak out of one or more sides (i.e., the right side, the left side or both) from one or both of the upper and lower arc wells through of these large unsealed openings. Such unsealed openings (ie, unsealed regions) can also prevent the creation and / or maintenance of a vacuum seal from dental wells without providing some means to isolate these open areas. The formation of a vacuum seal between a layer of dental cover and a retromolar space can face obstacles such as having to select or prepare a layer of dental cover of sufficient length and possible contact of the soft tissue of the retromolar space with a fluid of treatment. To overcome these obstacles, the vacuum seal on the posterior portion of the dental cap layer is preferably made with a molar on each side of the dental arch. While this may limit the ability to provide dental treatment to one or more molars, the benefits mentioned above generally outweigh this concern. However, the need to form a sufficient seal (eg, to maintain a vacuum) can present particular challenges when sealing on a molar. Surprisingly enough seal was achieved using a single distal connector insert. To prevent such leakage of the treatment material and to allow the ability to create and maintain a continuous or selectively sustained vacuum in the nozzle, various teachings of the present invention may incorporate one or more distal connector inserts (i.e., distal sealing connectors. The term "selectively sustained vacuum" can refer to the ability of a user or practitioner to determine how long to maintain the vacuum, to initiate and release vacuums multiple times in a treatment etc. Preferably, distal connector inserts are employed with both ends of each layer of dental cover The distal connector inserts can be designed and / or positioned to connect only within the rear left and right ends of the wells of the dental layer. Preferably, the distal connector inserts effectively seal these openings. , the distal connector inserts can seal the openings when the patient bites his mouth l.
[0069] [0069] The distal connector inserts are preferably produced from a material that is sufficiently deformable, such that an insert intimately contours the variable anatomy of the tooth of one or more of the posterior teeth, such as the right and left terminal teeth (p .ex., despite the variability between different individuals regarding the length of their dental arches). The distal connector insert can be produced from a polymeric material. The preferred polymeric materials for the distal connector insert are elastomeric such that after being distorted the distal connector insert usually returns to its original shape. The distal connector insert can be produced from an elastomeric material. The elastomeric material has a crystallinity of about 0%, however, elastomeric materials, having a higher crystallinity, can be used (eg, about 0.5% or greater). Preferred elastomeric materials have a crystallinity of about 15% or less, about 10% or less, or about 5% or less. The distal connector insert can be produced from a foamed material. Preferred foamed materials have a closed cell foam structure. Typically, elastomeric materials have a glass transition temperature of about 10 ° C or less, about -10 ° C or less, or about -40 ° C or less. The elastomeric material preferably has a sufficiently low hardness such that the distal connector insert can be deformed to conform to the surface of a molar. The elastomeric material preferably has a Shore A hardness of about 60 or less, more preferably about 50 or less, even more preferably about 40 or less and most preferably about 30 or less. The elastomeric material of the distal connector insert may have a sufficiently high hardness such that the insert does not shear during storage and use. For example, Shore A hardness can be about 2 or greater, about 5 or greater, or about 8 or greater. The elastomeric material is preferably cured sufficiently that the material does not flow. The elastomeric material can be formed from any polymer, such as a polymer including a carbon backbone or a polymer including a silicon backbone. By way of example, the elastomeric material of the distal connector insert may include a silicone rubber, such as an RTV silicone rubber capable of curing at room temperature, or an HTV silicone rubber capable of curing at one or more temperatures high. The elastomeric material can avoid the need to remove residual material after providing dental treatment, as required when using wax or other moldable materials. As such, the distal connector insert can function without the need for a moldable material. The elastomeric material can be a generally solid material (i.e., having a void content of about 10% by volume or less, about 5% by volume or less, or about 1% by volume or less). Such material can be essentially free of, or totally free of voids. Suitable elastomeric materials can be a cellular material, such as a material having an open cell foam structure, a closed cell foam structure, or both.
[0070] [0070] The distal connector insert preferably has sufficient width, such that it is able to form a seal along the upper surface of a molar going from the posterior part of the tooth to the front of the tooth. The distal connector insert is preferably of sufficient length that it will generally seal at least one molar in an individual, regardless of the length of the individual's dental arch. A long distal connector insert can also allow a seal to form in individuals who have undergone molar extraction. The length of the distal connector insert is preferably about 2 mm or more, more preferably about 4 mm or more, even more preferably about 6 mm or more, even more preferably about 8 mm or more and most preferably about 10 mm or more. It will be appreciated that the distal connector insert can be interchangeable such that a distal connector insert of sufficient length and / or width can be selected to provide optimal sealing based on one or more characteristics of the patient's dental arch (such as its length).
[0071] [0071] Each dental arch nozzle device includes one or more layers of treatment supply. The treatment supply layer can provide one or more treatment fluids for a dental cap layer, can provide heat for a dental cap layer, or both. If the nozzle includes two layers of dental cap, each layer of dental cap can have a separate treatment supply layer or a single treatment supply layer can be used for both layers of dental cap. For example, a single treatment supply layer can be positioned between two layers of dental caps. The treatment supply layer can contain embedded channels or flow tubes capable of draining one or more treatment fluids. The flow channels or tubes of the treatment supply layer preferably run through all of these nozzle layers. The treatment supply layer preferably has one or more (e.g., two or more) inlet holes to provide fluid for a well (e.g., sealed cavity) of a dental cap layer. The treatment supply layer preferably has one or more (e.g., two or more) outlet holes for removing fluid from a well (e.g., sealed cavity) of a dental cap layer. It will be appreciated that the flow directions can be changed such that an outlet hole can function as an inlet hole, such that an inlet hole can function as an outlet hole or both. A treatment supply layer that serves the upper and lower dental cap layers may have (1) one or more holes (eg inlet and outlet holes) in the treatment supply layer floor to provide fluid communication with the cavity or well of the dental cap layer of the lower teeth; and (2) one or more holes (eg inlet and outlet holes) in the roof of the treatment supply layer to provide fluid communication with the dental cap layer over the upper teeth. These flow channels or tubes preferably transport and substantially uniformly distribute one or more treatment fluids to the dental cap layer. The treatment fluid can be any treatment fluid known in the art, as described herein. For example, the treatment fluid can include a bleaching material (such as a gel material), water, air, medicinal materials, therapeutic materials, cleaning materials, washing materials or any combination thereof. The treatment supply layer can deliver any or any combination of treatment fluids into the wells (eg dental arch wells) of the dental cap layer. As such, the treatment supply layer can effectively bathe one or more (eg, all) tooth surfaces in the well and covered by the dental cap layer (s) with the whitening gel or other treatment materials. . Preferably, the channels or tubes are capable of supplying and / or removing a plurality of treatment fluids, such as water or air.
[0072] [0072] The components, devices, systems and process, according to the teachings here, can be used in a dental treatment to provide a treatment for one or more teeth, to provide a treatment for the gums or both. These components, devices, systems and processes can find application in teeth whitening; antibiotic treatment, antimicrobial treatment, fluoride treatment or any combination thereof. It will be appreciated that other applications in the field of dentistry may find use of the features in accordance with the teachings here. Dental treatment can be a generally short treatment, such as for about 10 minutes or less, or it can be a generally long treatment, such as for more than 10 minutes, preferably 20 minutes or more, more preferably about 30 minutes or more . It will be appreciated that the duration of dental treatment will typically be about 3 hours or less, more preferably about 2 hours or less, and most preferably about 1 hour or less. Dental treatments lasting more than 3 hours are also provided (for example, from about 3 hours to about 8 hours, such as during the hours of night sleep). Vacuum can be applied to the cap layer for a substantial portion (eg, at least 50% of the duration, at least 70% of the duration, at least 80% of the duration, or at least 90% of the duration) of the time of treatment. The dental cap component, surprisingly, is able to maintain vacuum for such long durations even when the dental cap component is a generic stock cover (that is, a non-custom-made cover).
[0073] [0073] As mentioned above, according to some configurations, a dental treatment system may include a pumping component to pump one or more treatment fluids. For example, the pumping component can be in fluid communication with a nozzle according to the teachings here. Preferably, the pumping component is in fluid communication with the nozzle treatment supply layer. The system can include a control unit to control the pumping component. A pumping component can be incorporated into the housing of an external control unit or it can be a separate element. The pumping component may incorporate a heating chamber to preheat the treatment fluid to one or more predetermined temperatures. For example, a control unit including a microprocessor can monitor and / or control the temperature of a treatment fluid. Temperature control, preferably, employs a feedback loop. Using temperature control, the temperature of a treatment fluid being supplied to the nozzle can be controlled. A heating chamber can advantageously allow a practitioner to use a bleaching fluid (eg a bleaching gel) immediately from storage and thus eliminate the need for a step to thaw the bleaching fluid, a step to heat the bleaching fluid, a step to prepare the whitening fluid for use in a dental treatment or any combination thereof. As such, dental treatment processes according to the teachings here can be free of combination or all of the steps mentioned above.
[0074] [0074] The treatment supply system may include one or more control valves, and preferably one or more multiposition flow control valves. The multiposition flow control valve is preferably in fluid communication with the pumping component. For example, the control valve can be incorporated into the pumping unit. However, a control valve can be positioned outside the pumping unit. The control valve can be operated manually or it can be operated automatically. For example, the control valve can be driven by a motor, can be controlled by a controller or both. The multiposition valve can rotate to different positions, with each valve position allowing different routes of flow of treatment materials through the system's flexible piping. The valve can be rotated by being engaged by a motor drive shaft that is controlled by the microprocessor unit or by other means. For example, the microprocessor can control the rotational position of the valve and thus allow, depending on the position of the valve, different flow patterns. Examples of flow patterns that can be achieved using a control valve include: 1. Providing a fluid connection between a vacuum line and the nozzle to remove air from the nozzle, to create a vacuum seal from the nozzle with the gingival edges or both; 2. Provide a fluid connection between a treatment fluid and the nozzle to supply the treatment fluid to a sealed cavity (eg a cavity formed by a layer of dental cap); 3. Remove a treatment fluid from the nozzle; 4. Create a "closed circuit" flow of a treatment fluid inside the nozzle (eg, where the flow is a dynamic turbulent flow or one of a convection type); 5. Provide a fluid connection between a washing fluid (such as water, or an aqueous solution) and the nozzle for supplying the washing fluid and removing the washing fluid from the nozzle (eg, for washing or rinse a treatment fluid from the surfaces of the teeth and the inner surfaces of the mouthpiece); and providing a fluid connection between a neutralizing fluid and the nozzle for supplying a neutralizing fluid to the nozzle to neutralize a treatment fluid. One or any combination of the steps mentioned above can be controlled by a single control valve, or by a plurality of control valves.
[0075] [0075] The closed loop flow mode allows the treatment fluid to circulate in the nozzle device of the present invention. This flow can be continuous or sporadic (eg pulsed or intermittent). For example, when whitening fluid is flowing in a turbulent manner into the sealed cavity formed by the dental cap layer, such that the amount of chemically active treatment fluid that contacts the enamel surfaces of the teeth is greatly increased compared to the case where the Treatment fluid is supplied into the nozzle and held statically in place during the bleaching treatment. This convection-type flow of the treatment fluid around the enamel surfaces of the teeth increases the whitening potential of a fixed volume of treatment fluid that is supplied to the mouthpiece. This is exactly analogous to the higher thermal flow when heating food in a convection oven. For example, by draining treatment fluid contained in the nozzle device around the teeth in a turbulent manner (just like hot air flows in a convection oven), the system significantly increases the volume of chemically active bleaching fluid delivered to the nozzle, which can come into contact with all enamel surfaces of the teeth. The increased volume of chemically active whitening fluid in contact with all tooth enamel surfaces results in significantly increased fluid whitening effect on all these tooth enamel surfaces.
[0076] [0076] In another configuration, sporadically draining a treatment fluid, such as a bleaching fluid (eg gel) into the nozzle device, allows the fluid to remain stationary in a particular area or zone of the mold for a specified period of time during treatment between time periods of active fluid flow. It will be appreciated that according to the teachings here all or selected portions of the treatment fluid, such as the static bleaching fluid in an area or zone, can be heated by the individual heating element (s) for a specific temperature in that zone or area of the mold during this period of static fluid time. This can advantageously allow differential bleaching activity in each zone or area for each of these static time periods and thus allow differential or "custom" bleaching of the teeth located in each zone or area of the nozzle device.
[0077] [0077] As mentioned above, the treatment fluid flow can employ a pump component, such as a microprocessor-controlled pump component, in a sporadic or pulsating manner for a given time interval. This can allow alternating static or convection flow of the treatment materials (around the teeth) for defined periods of time in the nozzle device.
[0078] [0078] Systems and methods can employ one or more pressure sensors to measure pressure in a tube, to measure pressure in a sealed cavity, to measure pressure in a nozzle layer (eg the supply layer) treatment, and / or the dental cap layer) or any combination thereof. The pressure sensor (s) can be incorporated into the control unit. The pressure sensor (s) can monitor, for example, the degree of vacuum in the nozzle, one or more flow rates, the total amount of treatment materials supplied inside, or alternatively removed from the nozzle device by the pump or any combination thereof. A sensor can also monitor the flow rate of a treatment fluid during a "closed loop" treatment cycle.
[0079] [0079] By maintaining a vacuum seal of the dental cap layer of the dental mouthpiece with the alveolar edges, the peroxidase enzyme naturally found in saliva is, substantially or even totally, prevented from migrating into or otherwise penetrating the sealed cavity. This new vacuum sealing feature of the present invention can effectively protect chemically active treatment fluids, such as whitening gel, from being chemically deactivated by the peroxidase of salivary enzymes. Since the chemical oxidizing potential of the treatment fluid is never substantially compromised by saliva, the bleaching result of the present invention is intensified.
[0080] [0080] It will be further appreciated that a pumping component can allow continuous flow of a treatment fluid into and out of the nozzle throughout the treatment. As such, fresh fluid having full chemical activity can be supplied and applied to some or all of the tooth enamel surfaces contained within the dental cap layer throughout the treatment. When used in a whitening treatment, this significantly increases the whitening result that can be obtained within a defined period of time of the present invention compared to the static supply of treatment materials, as is the case in known tooth whitening procedures.
[0081] [0081] According to some configurations, flexible tubes can be connected to the pumping component from the fresh and used treatment fluid containers and a separate set of flexible tubes connected to the pumping component which in turn also connect to tubes inlet and outlet flow integrated in front of the nozzle. These inlet and outlet flow tubes can additionally be integrated into an integral cable design of the nozzle device. Such a pump, which can come in contact with the fluid having been in the sealed cavity, can be a disposable pump such that aseptic conditions are maintained. The pump can incorporate a locking and unlocking feature to allow quick connection and detachment of the pump, optionally disposable, to engage a motor or motors embedded within the control unit. Alternatively, a pump that pushes the treatment fluid, such as a peristaltic pump, can be used. Once it pushes treatment fluids that are contained within the tubing, it can be reusable, as it does not come into contact with the active treatment materials.
[0082] [0082] The set of tubes, from the pump set to the nozzle device, can be attached via a gripping device or small brace to the patient's clothing, patient's dental apron or some element of a dental chair or other point of fixation such that any drag they create in the nozzle is reduced or eliminated, such that the tubes are skillfully organized or both. The tubes and a power cable can additionally be connected to a quick connector that fits inside the integrated cable of the nozzle device of the present invention.
[0083] [0083] Another aspect of the invention is directed to a separate disposable gingival protective component. The gum protective component can be used with a dental treatment fluid. The gum protective component can be used in a process to treat teeth with one or more fluids to whiten teeth. The protective gingival component can provide a sufficient barrier to the gums such that highly active treatment fluids can be employed. The gingiva protective component can be designed for insertion on the alveolar edge (s) of the gingiva (s) of the upper jaw, the lower jaw or both. The protective gingival component is preferably inserted into the oral cavity prior to insertion of the mouthpiece into the oral cavity. For example, gum protectors / guards can act to isolate both the maxillary and mandibular gum tissues from highly concentrated hydrogen peroxide bleaching gels, which will be supplied into the mouthpiece (s) of the mouthpiece device or other potentially hazardous treatment materials. The gingiva protective component can sufficiently protect the gums from peroxide having a concentration of about 15% or greater, about 25% or greater, about 35% or greater, or about 45% or greater.
[0084] [0084] The gingiva protective component can be provided as a set including a plurality of gingiva protective components of different sizes. The gingival protective component can be sufficiently malleable, such that only a few generic gingival protective components of different sizes are required to treat most patients. For example, the set may include gingival components having about 2 or more different generic stock sizes, preferably about 3 or more different sizes and more preferably about 4 or more different sizes. The number of different generic stock sizes is preferably about 10 or less.
[0085] [0085] The separate and disposable gingiva protector (ie, gingiva protective component or mouth protection component) in one of its configurations can be comprised of two distinct layers that can be firmly adhered to each other. As an example, the main body of the gum protector can be made of a stretchable polymeric material. Preferred polymeric materials have an elongation at break of about 100% or greater, more preferably about 200% or greater, and most preferably about 300% or greater. Preferred polymeric materials have a sufficiently low stress strain such that the material recovers its initial shape after being stretched. For example, the strain under stress (measured at room temperature, 10 minutes after stretching the material by 200%) can be about 10% or less, preferably 7% or less, more preferably 5% or less and most preferably about 3% or less. The polymeric material can have a carbon-containing main chain or a silicon-containing main chain. The polymeric material can be an elastomer. Examples of elastomers that can be used include silicone elastomers, natural rubber / latex materials, polyisoprene, styrene butadiene rubber, SEBS rubbers or any combination thereof. The gingival protective component may have a coating or chemical layer that has been applied and attached to one or more of its surfaces. For example, a layer can be applied to the inner (proximal) surfaces of the gingival protective component, such that the layer is in contact with the gum tissues.
[0086] [0086] The silicone and / or rubber body of the protector / mouthguard can be shaped to mirror the horse's hoof shape and the edge shape of the alveolar edges of the gums of the upper and lower jaws in order to adapt well closely to these oral structures.
[0087] [0087] The body of the protective / mouthguard component can be further modified to allow multiple cutouts of varying diameters and varying spacing between them (fully cut out or perforated for selective removal) along the section of said protection that mirrors the location of the lines of central edges of the alveolar edges and the teeth of the upper and lower jaws. These cutouts can mirror or conform in their shape to the staggered shape / shape of the gum line (interdental papilla) of the teeth to be treated.
[0088] [0088] The inner lining of the protective / mouthguard component as noted above, may contain various chemical compounds such as a sugar-based gel or self-adhesive spray coating whose purpose is to provide a chemical neutralization of the active treatment materials, for example whitening gel based on peroxide and thus act as a chemical barrier to additionally protect gum tissues from treatment materials. As mentioned above, the mouth guard / protection can provide an effective barrier to protect gum tissues from even very high concentrations of treatment materials, such as, for example, 35% or higher hydrogen peroxide bleaching gels.
[0089] [0089] The optional disposable protective / mouthguard component described above can provide a tight yet flexible fitting barrier for the gums and alveolar gingival edges that can be placed over the teeth and gums to be treated. When positioned in a dental arch in the mouth, the crowns of the teeth may protrude out of the protective gum component while covering the gums. This fitted barrier (the disposable protective / mouthguard component) is additionally shaped so as to also allow a good fit and seal of the deformable well edges of the single or double dental arch nozzle device for both gum protectors / protections upper and lower. This allows a good seal of the treatment fluid that is supplied to the mouthpiece device and prevents the mouthpiece device treatment materials from leaking into the oral cavity (although the mouth guard protects the gums).
[0090] [0090] When the gingival protective component is used with a dental treatment layer, the seal of the space around a row of teeth can be further reinforced by the unique deformable flap apron design and edge of the mouthpiece layer of the mouthpiece . This seal, in conjunction with the unique distal sealing connectors, can enhance the pump's ability to suck air from the nozzle and create an effective vacuum seal of the dental cap layer with the outer sidewall surfaces of the placed gingiva components previously. It will be appreciated that an upper and lower gum protective component can be employed to protect each of the upper and lower jaw gums.
[0091] [0091] This configuration and the relationship of these components to each other in the oral cavity effectively and surely isolate the various concentrations of bleaching agents, applied to the teeth, from the soft tissues (gums, tongue, cheeks, palate, oral mucosa) and, therefore, , can protect these soft tissues from the caustic effects of even more highly concentrated formulations of these chemical agents during the improved bleaching treatment of the present invention.
[0092] [0092] The configurations of the protective / protective component of the disposable gingiva allow adaptation by the dental assistant of its shape to adapt the internal edges of the multiple cutouts to the stepped gum line. Varying the thickness of the cross-section of the protector / mouthguard allows it to maintain its shape (thicker areas) as well as allows thinner (slanted) edges for the cutouts and strips of dental floss areas of the protector / mouthguard.
[0093] [0093] This varied thickness design of the gingival protector / shield allows the operator to bend inward (using a hand held dental tool) the thinnest edges of the cutouts into the natural gingival groove space (usually three millimeters deep in healthy gingival tissue) that exists between the gums and the teeth as well as flossing the proximal spaces in the teeth of the protector / mouthguard strips area and thus can provide a more effective adaptation of the protective / mouthguard component to gum tissues and a better seal between them.
[0094] [0094] As mentioned above, other configurations of the disposable gum protector may also include an inner lining that is self-adhesive lining when placed in contact with the gingival tissues. These coatings may include various medications or chemical compounds for the therapeutic release of these various medications or compounds into the gum tissues. Additional configurations of the disposable mouth guard / protection have broader dental and medical applications whenever what is known in the dental field as a "dry field" is required or advantageous for a given medical / dental procedure. The mentioned gum protector / shield can be used in many dental procedures as a replacement for what is commonly known in the dental field as a rubber dam.
[0095] [0095] Additionally, the disposable protective / mouthguard component is not integrated into the device and can be provided in various stock sizes to match a given stock dimension nozzle device and thus provide, without the need to customize the nozzle or mouth guard / protection for each patient, effective isolation of gums and other soft tissues from the mouth of even highly concentrated formulations of treatment materials without the need to manually apply a hardened foam material as is common use in the powerful bleaching procedures administered professionally.
[0096] [0096] As mentioned above, the mouth guard / protection can be a component that is itself a stock item manufactured in various stock sizes or alternatively it can be manufactured as a device tailored to each patient using molding techniques and matrix known in the field.
[0097] [0097] The single or double dental arch nozzle device may also incorporate an external thermal barrier layer. This layer can act to protect the patient from the heat generated by the multiple heating elements activated during the bleaching treatment method of the present invention.
[0098] [0098] According to some configurations, an optional tooth shade combination sensor unit can be incorporated into the control unit, which can be used to record pre and / or post treatment tooth shade values.
[0099] [0099] It is well known in the medical field that pulse rates can be used to monitor a subject's levels of pain / discomfort. An optional adjustable strap can be placed on the patient such as a chest strap that is attached to the control unit and incorporates a sensor to monitor certain user vital signs, such as the patient's pulse rate, throughout the bleaching treatment and in this way monitor the patient's comfort levels throughout the treatment.
[0100] [00100] Another aspect of the invention is directed to a set that includes a plurality of nozzles such as a plurality of nozzles according to the teachings here. The set preferably includes generic stock nozzles (i.e., not made to measure) and includes nozzles having different sizes. The set may include nozzles having different widths to match mouths having different widths of the dental arch (e.g., as measured between corresponding left and right molars). The set may include nozzles having different lengths of arches. It will be appreciated, according to the teachings here, that the use of distal sealing connectors can reduce or eliminate the need for nozzles having different lengths. By employing a set of generic stock nozzles, the need to tailor a nozzle (eg using a dental impression) can be eliminated. The set may include pre-assembled nozzles or may include layers of generic stock dental caps, such as layers of dental caps according to the teachings here. The set may include layers of dental caps suitable for the lower dental arches, suitable for the upper dental arches or both. The set preferably includes layers of dental caps having different widths for use on individuals having dental arches of different widths. The set can include one or more treatment supply layers, such as a treatment supply layer according to the teachings here. The treatment supply layer may be suitable for connection with one or two layers of dental caps. The need for dental cap layers having different lengths can be reduced or eliminated by using distal sealing connectors in the appropriate cap layer to seal the posterior ends of the dental arch. Preferred sets include nozzles and / or layers of dental caps having two or more different generic stock sizes, more preferably three or more different generic stock sizes and most preferably four or more different generic stock sizes. The number of different sizes can be generally large, but preferably it is about 20 or greater, more preferably about 10 or less and most preferably about 6 or less. Treatment method
[0101] [00101] A method for performing dental treatment is provided here, according to some configurations, which may include one or more of the following steps: positioning a mouthpiece including one or more layers of dental covers on the upper and / or lower teeth ; and applying vacuum to the dental cap layer such that a sealed treatment cavity having a pressure below ambient pressure is formed around the teeth; and draining one or more treatment materials into the sealed treatment cavity.
[0102] [00102] In an additional configuration, a method for performing a teeth whitening treatment is provided, where one or more of the following steps can be performed: configuring a procedure to whiten custom teeth simultaneously; prepare a pump module to connect with a nozzle designed for a teeth whitening treatment; configure treatment settings on a control device attached to the pump module; position the mouthpiece in a patient's mouth; apply a flow control to cause a vacuum between the mouthpiece and the anatomy of the patient's gingival rim; apply flow control to automatically manage the supply of materials according to treatment definitions; and use flow control to remove treatment materials from the nozzle. Of course, other steps or combinations of steps can be used. For example, before a treatment, the reference shades of the respective teeth can be measured, to allow personalized treatment of the respective teeth. In addition, dental impressions can be taken to allow the construction of a patient-specific mouthpiece. In some cases, a mouth guard can be used in addition to the mouthpiece, which can be a custom-made or stock type of protection. In additional cases, the treatment materials can be preheated before treatment and / or can be heated as necessary during treatments.
[0103] [00103] Reference is now made to the respective figures, which describe elements or aspects of multiple configurations of the present invention. The drawings are provided for illustrative purposes only and are not intended to be limiting.
[0104] [00104] Fig. 1a is a top view of an example of a nozzle device 1, where a covering layer conforming to the dental arch is shown, sometimes referred to here as a vacuum forming layer, constructed of flexible material with compressible edges designed to form a treatment cavity on the upper and lower teeth and gingival edges, hereinafter referred to as the upper or lower dental arch well 2. In other words, the negative space contained between the curved walls of the well forms what is referred to here as the treatment cavity. The dental arch well 2 may include, for example, deformable edges 2a, the upper well floor 2c, the upper labial frenulum cutout 2b of the outer wall of the edge 2 and upper distal deformable seal connectors 7 with its pin holes 7a. Also shown is a portion of an intermediate arc-shaped layer for supplying and removing treatment materials tailored to and from the vacuum-forming layer, referred to herein as the intermediate layer or the treatment supply layer. The intermediate layer can support, for example, an integrated cable 9, thermal transfer pin heads 17, 17a, the arc well material supply holes 13, the material drain depression hole 14a, one or more connectors electrical devices or any combination thereof. The electrical connector can be a printed circuit board (s) 15. The cable 9 can be designed to facilitate the positioning of the mouthpiece in the mouth of the patients, the supply of materials for the mouthpiece, the extraction of treatment materials from the mouthpiece and the power supply to the nozzle etc. For example, the cable may have one or more characteristics that facilitate its handling, such as a thumb depression 9a.
[0105] [00105] Fig. 1b is a bottom view of an example of a nozzle device 1 showing distal seal connectors 8 and their pin holes 8a, the supply holes for arc well treatment material 13a, the bore of drainage depression 14a, a vacuum forming layer with the shape of a lower dental arch, hereinafter referred to as the lower dental arch well 3 with its deformable edges 3a, the lower floor well 3c, the lower labial frenulum cutout 3b , the distal sealing wall 3d of the lower arc well 3, the distal sealing wall 2d of the upper arc well 2 and the printed circuit board (s) 15.
[0106] [00106] Fig. 1c is a view of an example of a nozzle device 1 in which the vacuum forming layer with the shape of an upper dental arch, or dental arch well 2, with material supply holes 13, hole is represented drain depression 14a, drain channel hole 19a, arc well pin holes 16a and arc well thermal transfer pin holes 17b.
[0107] [00107] Fig. 2a is a front view of an example of a nozzle device 1 showing the upper dental arch well 2, the lower dental arch well 3, the intermediate layer 4, the inlet flow tube 10, the outlet flow tube 11 and the air breathing holes 12.
[0108] [00108] Fig. 2b is a side view of an example of a nozzle 1 showing the integrated cable 9, the upper dental arch well 2, the lower dental arch well 3, and the intermediate layer 4. In some configurations, the intermediate arc layer is shaped to mirror an angle of geometric axis of articulation to facilitate the natural movement of the jaw when the upper and lower vacuum forming layers are being used. Such angled articulation axis design of the nozzle 1 is adapted to directly relate to the relationship between the lower axis and the upper mandible. The angle of the design of the nozzle hinge geometric axis design (e.g. the angle between the two vacuum forming layers) is preferably one that is comfortable for a patient to maintain during dental treatment. Preferably, the angle is about 0.5 ° or greater, preferably about 1 ° or greater, and most preferably about 2 ° or greater. Preferably, the angle is about 20 ° or less, more preferably about 15 ° or less, even more preferably about 10 ° or less and most preferably about 7 ° or less. It will be appreciated that a larger angle can be advantageously employed to allow larger breathing holes, to provide more flexibility in the design of the intermediate layer or both.
[0109] [00109] Fig. 2c is a top view of an example of an intermediate layer 4 where the channel floor of upper treatment material of intermediate layer 4a with its flow channel side walls 4b is represented, the inlet holes treatment material 13, heating elements 18, heat transfer pins 17, connector pins 16, printed circuit board (s) 15 and inlet flow tube 10 and flow stream tube output 11 integrated in cable 9.
[0110] [00110] Fig. 2d is a bottom view of an example of an intermediate layer 4, its flow channel side walls 4b and lower treatment material channel floor 4c. Also shown is the drainage channel 19 and its drainage or outlet flow 20 that connects to the outlet flow tube 11, the treatment material inlet holes 13, the connector pins 16 and the breathing holes of air 12.
[0111] [00111] Fig. 3 is a top view in detail of an example of an anterior segment of the intermediate layer 4 where the drain hole 19 and the drain tube 20 that connect to the outlet flow tube 11 are shown, the heads 17a and pin ends 17b of the heat transfer pins and heating elements 18. The heating elements are preferably inserted into or otherwise connected with the printed circuit board 15. The connection between the heating element 18 and the printed circuit board can also be represented as air breathing holes 12. The connection between the heating elements 18 and the printed circuit board 15 can be below the channel floor such that the connection is isolated from any fluid flowing through of the channel.
[0112] [00112] Fig. 4a is a front view (lip) of an example of an intermediate layer 4, of the upper intermediate layer cover plate 5, of the lower intermediate layer cover plate 6, of the air breathing holes 12 and inlet flow tube 10 and outlet flow tube 11.
[0113] [00113] Fig. 4b is an internal (lingual) view of Fig. 4a showing an example of the internal aspects of the air breather holes 12, of the upper cover plate of intermediate layer 5, with its pin holes. connector 5b and its thermal transfer pin holes 5a as well as the drain hole depression well 14. Also shown are the connector pins 16 that hold the upper cover plate 5 and lower cover plate 6 in the intermediate layer 4, treatment material inlet holes 13 that allow treatment material to flow from treatment material flow channels 4a and 4c into intermediate layer 4 for upper dental arch 2 and lower 3 wells (not shown) ). Also shown are the air breathing holes 12 that pass through the body of the intermediate layer 4.
[0114] [00114] Fig. 4c is a front view (labial) of an example of the top cover plate 5 and the bottom cover plate 6 with the intermediate layer missing and the structural connections of the thermal transfer pins 17 between the cover plate the upper cover 5, the lower cover plate 6 and the printed circuit board 15. Also shown are the connector pin holes 5b of the upper cover plate 5 and the drain hole depression well 14 of the upper cover plate 5.
[0115] [00115] Fig. 5a is a frontal (buccal) view exploded in a vertical stack of a possible configuration of components comprising the double dental arch nozzle 1 of the present invention where the upper flexible dental arch well 2, the well lower flexible dental arch 3, intermediate layer 4, lower cover 5, upper cover 6, upper distal connector sealers 7 and lower distal connector sealers 8. Also shown are thermal transfer pins 17 and a ( s) printed circuit board (s) 15.
[0116] [00116] Fig. 5b is a posterior (lingual) view of the exploded vertical stack of Fig. 5a where the components comprising the double dental arch nozzle 1 of the present invention are represented, where the flexible dental arch well is represented. upper 2, the lower flexible dental arch well 3, the intermediate layer 4, the lower cover 5, the upper cover 6, the upper distal connector sealers 7 and the lower distal connector sealers 8. The transfer pins are also shown Thermal 17. Printed circuit board 15 is not shown in this illustration.
[0117] [00117] Fig. 6a is an internal (lingual) view of an example of a nozzle device 1 showing the upper dental arch well 2, the lower dental arch well 3, the upper distal connectors 7 and the connectors distal distances 8 as well as the air breathing holes 12.
[0118] [00118] Fig. 6b illustrates a view of Fig. 6a where a vertical slice of distal cross section of the nozzle device 1 has been taken, in order to remove the distal sealing walls 2d and 3d of the upper and lower dental arch wells respectively, in order to reveal the cross-sectional structure of the apron or rolled-up cross-sectional design 21 of the edge 2a of the upper well of dental arch 2 and lower well of dental arch 3. Additionally, the shape of the cross section of the connectors distal upper 7 and lower 8 and their structural relationship with wells upper 2 and lower 3 respectively are revealed.
[0119] [00119] Fig. 6c represents Fig. 6b where the upper 7 and lower 8 distal connectors have been removed to better reveal the structural shape of the highly deformable outer coiled apron 21 and inner coiled apron 21a of the top edge 2a and bottom edge 3a of the dental arch wells.
[0120] [00120] Fig. 6d is an internal (lingual) view of the intermediate layer 4 with the top 5 and bottom 6 cover plate attached to which the top 7 and bottom 8 distal connector sealers were attached respectively. Also shown is the drain hole well 14 in the upper cover plate 5, the pin connectors 16 inserted through the upper cover plate holes 5a and the upper cover plate hole 5b that accommodates the thermal transfer pin heads 17a (not shown). Additionally, the illustration represents the air breathing holes 12.
[0121] [00121] Fig. 6e is an angled front view of the nozzle device 1 where the nozzle is represented in an arrangement of three configurations with the leftmost configuration representing the inlet flow tube 10 and outflow tube 11 , the intermediate configuration represents the connection of the quick coupler 22, which integrates the hole 22a which aligns with the inlet flow tube 10, hole 22b which aligns with the outlet flow tube 11 and hole 22c which aligns printed circuit board 15 (not shown). Also shown in the rightmost configuration are the cable / tube bundle 23 which is inserted into the quick coupler 22 and which includes an outflow tube 23b, an inlet tube 23a and a power cable 23c.
[0122] [00122] Fig. 7 is an internal (lingual) detail view of an example of a nozzle 1 showing the upper arch well 2 with highly deformable external apron 21 and internal apron 21a of its compressible edge 2a, the well lower arch 3 with its highly deformable outer apron 21 and inner apron 21a from its compressible edge 3a, the intermediate layer 4 with its air-breathing holes 12, and the connector pins 16 that secure the upper arch 2 and lower 3 wells to the middle layer 4.
[0123] [00123] Fig. 8a is a frontal view (labial) of an example of a nozzle 1 where the upper arc 2 and lower arc 3 wells are represented in a transparent flexible material in order to reveal their coverage, respectively, of the maxillary teeth 28 and maxillary alveolar gingiva edges 26 of the upper jaw 24, and mandibular teeth 27 and mandibular alveolar gingival edges 26a of the lower jaw 25. Also shown is the intermediate layer 4 of the nozzle device 1 and the inlet flow tube 10 and outlet flow tube 11 from the nozzle device 1.
[0124] [00124] Fig. 8b is a detail of the internal side (facing the surface of the nozzle 1 not shown) of the quick coupler 22 where internal aspects of the holes 22a and 22b and the printed circuit board connectors 22d are represented.
[0125] [00125] Fig. 8c is an external view in detail (facing away from the surface of the nozzle 1 not shown) of the quick connector 22, where the external aspects of the holes 22a, 22b, 22c and the depression for the thumb are represented 22e on the upper surface of the coupler 22.
[0126] [00126] Fig. 9a is an angled view on one side of an example of a pump mechanism assembly 30 where the flow control valve assembly 32 inserted within the control valve assembly structure 39 is shown. flow control valve motor 33, gear set 34 inserted into gear set structure 42, flexible pump membrane 36 inserted into hole 38 of flow control valve set 32 and piston 41, connected to the coupler drive shaft 40. An example of a treatment material dispenser is represented, for example, the fresh gel tube 32b, which connects to a fresh gel container 46 (not shown) and the pump motor 31 inserted into the pump mechanism assembly floor 43.
[0127] [00127] Fig. 9b is an angled view from the opposite side of Fig. 9a showing the outlet flow tube 32a, a treatment material tube 32b, the pump connector tubes 32c and 32d, the flow chamber preheating 29 with its treatment material tube 29a, the thermal transfer block 44 with its heating elements 45, the disposal tube 32f and the washing tube 32g and the pump motor 31.
[0128] [00128] Fig. 9c is a top view of the pump mechanism assembly 30 showing a transparent view of the flow control valve assembly 32 which reveals the multiposition flow control valve 35 with its multiple holes 35a inside of the flow control valve assembly 32. Also shown is the preheat chamber 29 with its treatment material tube 29a connected to the multiposition flow control valve 35, the gear set 34, the control valve motor flow rate 33 and the multiple position 37 holes on the top surface of the drive shaft coupler 40.
[0129] [00129] Fig. 9d is a front view of the flow control valve assembly 32. The flow control valve assembly 32 includes an outlet flow tube 32a and a treatment material tube 32b. The flow control valve assembly 32 includes pump connector tubes 32c and 32d. The flow control valve assembly includes a preheat chamber flow connection 32e for connection to the preheat chamber 29 (not shown). The flow control valve assembly 32 additionally includes a discharge tube 32f and a wash tube 32g.
[0130] [00130] Fig. 10 is a top / front view of a possible configuration of the control unit 50 where the interactive screen 49, the interface buttons 50a, the emergency stop button 50b, the speaker 50c , the optionally rechargeable battery pack or power supply 48, a gel container bench 47 (not shown in the drawing) to which the gel container 46 is attached, the inlet flow tube (to the nozzle device 1) 23a and the outlet flow tube 23b and the power cable 56 with its quick coupling armature connected 51 with its clip 51a to organize the inlet flow tubes 23a and outflow 23b.
[0131] [00131] Fig. 11 is a top / rear view of the control box 50 and the battery pack charger unit 52. Also shown are the inlet flow 23a and outflow 23b tubes, the water container fresh 55 and waste water container 53 with its weight pressure sensor 54 on the floor of the water container compartment 57 of the control unit 50. Also shown are the power cable 56, the battery pack 48, the connector battery charger 52a and treatment material container 46.
[0132] [00132] Fig. 12a is a view of the outer surface (bottom) of a possible configuration of the upper mouthguard 59 where the outer floor 59d is represented with its multiple tooth holes 59a of varying diameters and spacings, the outer side walls 59b and the upper lip frenulum cleft 59c.
[0133] [00133] Fig. 12b is a view of the inner (upper) surface of Fig. 12a showing the internal aspects of the tooth holes 59a, the inner side wall 59c and the inner floor 59f which, in some configurations, can be coated with a neutralizing layer of treatment material 61.
[0134] [00134] Fig. 12c is a view of the outer (upper) surface of a possible configuration of the lower mouthguard 60 where the outer floor 60d is represented with its multiple tooth holes 60a of varying diameters and spacing and the outer side walls 60b .
[0135] [00135] Fig. 12d is an internal view (bottom) of Fig. 12c showing the internal aspects of the tooth holes 60a and the internal side walls 60e and internal floor 60f that can be coated with a neutralizing layer of treatment 61. The cleft lower lip frenulum 60c is also shown.
[0136] [00136] Fig. 13a is a vertically stacked view of the upper mouthguard 59 and the lower mouthguard 60.
[0137] [00137] Fig. 13b is a front view of the upper jaw 24, which depicts a transparent version of the upper mouthguard that was pulled over the maxillary teeth 28 and is seated on the upper alveolar gingival edges 26 and the lower jaw 25 with a transparent version of the lower mouthguard 60 which has been pulled over the mandibular teeth 27 and is seated on the lower alveolar gingival edges 26a.
[0138] [00138] Fig. 13c is a front view of an example of a nozzle device 1 inserted between the upper jaws 24 and lower 25, respectively, and where the upper arc well 2 and lower arc well 3 of the nozzle are represented. 1. Also shown are the upper mouthguard 59 and lower mouthguard 60 on which the nozzle 1 rests. Additionally, the illustration represents the nozzle cable 9 to which the quick coupler 22 with its cable bundle / is connected / 23 tubes attached to it.
[0139] [00139] Fig. 14 is a flow diagram describing an example of a process for proceeding with a teeth whitening treatment using a nozzle and associated components as described here, according to some configurations. In step 14a, at the initial visit the dentist assistant or the dentist team determines and documents the current (reference) shades of the teeth to be whitened. This can be accomplished using the optional shade guide comparator device which can be provided with the control unit or an alternate shade guide comparator. If necessary, in step 14B initial dental impressions of the arch or arches to be treated can be taken and stone dental models of the arches are produced as is well known in the field. These models can then be used to manufacture a custom-made disposable gum protector as described above. Alternatively, various gingival protectors / protections with stock sizes can be used in conjunction with matching stock sizes from the mouthpiece device without the need to take dental impressions or fabricate dental stone models. In step 14C, the customized or stock nozzle is provided, assembled and selected based on the good fit to the patient's mouth.
[0140] [00140] In the treatment visit, in step 14D, the system must be calibrated and treatment materials prepared. For example, a fresh gel container can be connected to the disposable pump set that has been inserted into the control unit and fresh water can be filled into the refillable fresh water container. In step 14E disposable gum guards / guards can be applied and fitted to the gums or alveolar gingival edges of the upper and lower jaws and adapted to the teeth to provide a sealed barrier between the teeth and the soft tissues immediately surrounding the teeth. If a milder concentration of treatment material is to be used then gum guards / guards may not be required. In step 14F, the relevant tubes are connected to the treatment material container and the pump mechanism. The disposable tubing is now also connected to the mouthpiece device and can include armor, clip or other connecting elements to keep the tubes in a specific orientation and position in relation to the mouthpiece device and the patient. In step 14G the control unit is energized and the treatment settings configured and may include, for example, configuring a personalized treatment plan or session for a patient, according to their particular whitening needs or expectations, comfort zone and health conditions.
[0141] [00141] In step 14H, the treatment material (s) can be preheated in the heating chamber of the pump mechanism. In step 14I the mouthpiece is inserted into the mouth and the patient can be instructed to close and bite the mouthpiece, etc. In step 14J the control unit can apply flow control to cause a vacuum around the alveolar edges. For example, the control unit can activate the engine which then turns the flow control valve to the vacuum position to activate the pump to suck out the air contained between the nozzle and the alveolar edges of the upper and lower jaws. on which he rests. This negative pressure inside the mouthpiece creates a vacuum seal of the mouthpiece with these edges as the soft flexible thin edges or apron of the edges of the mouthpiece are sucked strongly against and conform to the gums covering the buccal and lingual plates of the alveolar edges of the jaws. Superior and inferior. This vacuum seal can be monitored by a pressure sensor throughout the treatment. In some configurations, if the vacuum seal is compromised, the control unit can alert the user to the loss of vacuum integrity.
[0142] [00142] In step 14K, the control unit can apply flow control to allow the release of treatment materials. For example, the control unit can activate the engine which then turns the flow control valve to the treatment material release position and then also activates the pump component to deliver a selected amount of treatment material that has been preheated to a temperature defined by the heating element contained in the control unit which is in contact with a heating component of the pump component optionally at a controlled rate for the nozzle device. In some configurations, several other changes can be made during treatment, such as heating treatment materials inside the nozzle or otherwise managing timing, materials, temperatures, lighting, etc. in the treatment environment.
[0143] [00143] In step 14L the control unit continues to monitor treatment definitions throughout the treatment. For example, the control unit can monitor the various pre-configured settings for flow rates, temperature of the individual heating elements in the mouth, material compositions, exposure intervals, etc. For example, the pump component can pump preheated bleaching gel into the inner well (s) of the nozzle device and the flow rate and the total amount of gel dispensed and delivered can be controlled by pressure sensor (s) or other sensors located throughout the system and the microprocessor controller of the control unit. In some cases, for example, the microprocessor can additionally control the various temperature results of each of the multiple heating elements in the nozzle, during the treatment process.
[0144] [00144] In some configurations, a pressure sensor can be incorporated in the pump mechanism to monitor the internal pressure inside the nozzle device during the entire treatment. In one example, increasing the pressure inside the mouthpiece means degrading the integrity of the vacuum seal and increases the potential risk that treatment materials will leak out of the mouthpiece and into the patient's mouth or, alternatively, allow saliva to enter the mouthpiece. Both possibilities are undesirable.
[0145] [00145] Chemically active treatment materials, such as bleaching agents, can release, for example, oxygen during their oxidation / bleaching reaction. This release of free oxygen from a gel can increase the internal pressure inside the nozzle device. In some configurations, if the internal pressure (monitored by the pressure sensor and the microprocessor) reaches a critically high value, the patient may be instructed to bite harder on the mouthpiece and the system will automatically begin to evacuate the treatment materials contained within the mouthpiece. nozzle and pump water to brush your teeth or alternatively pump in new treatment material. Alternatively, removing super-active treatment material present in the nozzle with fresh treatment material (s) can help to reduce the internal pressure inside the nozzle and thus allow you to continue treatment without the need to brush your teeth.
[0146] [00146] In step 14M, the microprocessor can activate flow controls to vary flow patterns, as may be necessary. For example, the motor can be activated to rotate the flow control valve to the position that allows a "closed loop" flow of treatment materials already supplied into the nozzle to circulate within the complete upper and lower arc-shaped wells the nozzle, in a steady flow pattern or in a sporadic pulsating manner. In some applications, the flow direction within the nozzle can be switched as well, creating an additional dynamically turbulent flow of treatment materials similar to the convection flow of a gas or liquid. In some configurations, additional treatment modalities can be applied during treatment as necessary, either by manual action by a helper or assistant and / or via programming of the control unit. For example, several fresh gel applications may be required for each bleaching treatment on the same patient since the amount of gel material used to fill the nozzle device to a specific level within each well has a limited chemical reaction potential to release the free radical of oxygen and thus whiten the teeth.
[0147] [00147] In additional configurations, the microprocessor of the control unit can be prepared to monitor substantially in real time the duration of the treatment time and / or temperature settings for each zone or area of the mouthpiece device, the patient's situation, etc. optionally throughout the treatment. In some configurations, a screen embedded in the control unit displays this data to the user or practitioner throughout the bleaching procedure. In some configurations alerts can be generated as needed, to warn a practitioner of any problems, dangers, complications etc. For example, the control unit can alert the operator via buzzer sounds, voice activation messages, and / or illuminated indicators when each gel application treatment is complete or warn about gel volumes, gel temperatures, and values vacuum pressure etc. in the nozzle that are not desirable.
[0148] [00148] At the end of treatment, in step 14N, the control unit can apply flow control to remove treatment materials and / or wash treatment materials. For example, to facilitate the removal of spent bleaching gel (chemically less active or inactive) from the nozzle device well (s), the microprocessor can activate the motor, which then turns the flow control valve to the position that allows the system's pump mechanism (which was also activated by the microprocessor) or a separate suction device common in a dental operation that has been connected to the mold device, (such as can be used in case of catastrophic failure of the pump or control system, or both) to substantially remove spent or remaining gel material from the nozzle device. Alternatively, spent chemically inactive treatment materials can simply be replaced by pumping new treatment materials into the nozzle. In some configurations, to remove any residual spent bleaching gel from the tooth surfaces and the inner surfaces of the mouthpiece, fresh water can be pumped into the treatment area, for example, from a removable container of fresh water included and connected to the pump and flow control valve unit. The water can be supplied by these to the inside of the nozzle via the same flexible tubing and can be used to wash or rinse the waste treatment materials out to a separate disposal container. In one example, a sensor such as a simple weight sensor or another type of sensor can be incorporated below or adjacent to the water disposal container to monitor the amount of water used in each wash / rinse cycle.
[0149] [00149] In step 14O, the flow control valve can be activated to release the vacuum seal from the mouthpiece and the alveolar edges of the gums and teeth, for example, by pumping air into the mouthpiece.
[0150] [00150] In step 14P, the mouthpiece and gum guards (if used) are removed from the patient's mouth and the optional shade comparator device can be used to record the bleaching results obtained.
[0151] [00151] The characteristics described above of the system allow easy and quick removal of the treatment material and the nozzle device such that when removing the device from the patient's nozzle, there is little of the treatment material spent both on the nozzle device itself and on the enamel surfaces of the treated teeth. This simplifies the operator's task of removing any partially or completely worn treatment material from the patient's mouth. In some applications, the controlled removal of spent treatment materials can be automated by the control unit at the end of a defined period of time or initiated manually by the operator by pressing a button that activates the removal / suction of treatment material at any time during treatment.
[0152] [00152] Alternatively, as mentioned above, spent treatment materials can be quickly removed (sucked) via the evacuation system of the standard dental operation unit.
[0153] [00153] In some configurations, various applications (of a volume of gel required to fill the mouthpiece) of fresh treatment materials can be applied and removed until the operator and the patient are satisfied with the whitening results obtained. Of course, any combination of the steps above can be applied. In addition, other steps or series of steps can be used.
[0154] [00154] In the respective configurations of the present invention, the design elements described above allow the rapid, intense and controlled bleaching of a dental arch or arches of both anterior and posterior teeth simultaneously and the whitening of both external (buccal), internal surfaces ( lingual) and occlusal (upper / bite) teeth both anterior and posterior. These configurations additionally allow to effectively protect the patient's soft tissues from the caustic effects of the various concentrations of whitening agents applied to the teeth, while optionally maintaining and monitoring in real time the safety, progress and / or comfort of the patient throughout the treatment.
[0155] [00155] According to some configurations, the design of the dental arch nozzle, of the present invention, allows a new bleaching technique by "compression" (based on its new vacuum seal integrity of the mouthpiece in the mouth) that enhances the effect of oxidation (whitener) forcing oxygen ions into the enamel surfaces of the teeth. As mentioned above, this compression technique also protects the bleaching gel from any deactivation by the salivary peroxidase enzyme and therefore further enhances the bleaching effect of a given amount of gel supplied into the mouthpiece device of the present invention.
[0156] [00156] It should be noted that for simplicity and clarity of illustration, the elements shown in the drawings were not necessarily drawn to scale. For example, the dimensions of some of the elements may be exaggerated in relation to other elements for clarity. In addition, where deemed appropriate, reference numerals may be repeated between the drawings to indicate corresponding or similar elements throughout the various views.
[0157] [00157] The principles and operation of the device, and method according to the present invention can be better understood with reference to the drawings, and the following description, it being understood that these drawings are provided for illustrative purposes only and are not intended to be limiting, where:
[0158] [00158] The previous description of the configurations of the invention was presented for the purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise form disclosed. It should be appreciated by people experienced in the technique that many modifications, variations, substitutions, changes and equivalents are possible in light of the above teachings. It should, therefore, be understood that the appended claims are not intended to cover all such modifications and changes as they fall within the true spirit of the invention.

权利要求:
Claims (15)
[0001]
Dental device for dental treatment, characterized by comprising a mouthpiece (1) suitable for implementing dental and / or gum treatment, in which the mouthpiece (1) includes: (i) one or more layers of dental cap material suitable to form a vacuum-sealed treatment cavity (2, 3), wherein the dental cap layers include a layer on the surrounding upper teeth and / or gums and / or a layer on the lower teeth and / or surrounding gums, and where the dental cap vacuum is formed using a continuous sealing mechanism that includes a sealing edge (2a, 3a) formed of compressible material together with at least one plug seal (7, 8) connectable to a rear opening (s) of each layer of toothpaste in which the sealing edge (2a, 3a) and at least one sealing plug (7, 8) seal the treatment cavity (2, 3) to allow pressure reduction in the dental treatment cavity (2, 3) below ambient pressure and provide a fluid seal to selectively prevent the flow of material into and out of the cavity dental (2, 3) while the vacuum is applied; (ii) an intermediate treatment supply layer (4) wherein the treatment supply layer has one or more flow channels (4a, 4c) in fluid communication with the treatment cavity (2, 3) to provide one or more more material fluids for the cavity and the intermediate layer (4) includes one or more material removal element (s), wherein the material removal element has one or more flow channels (4a, 4c) in fluid communication with the cavity (2, 3) to remove one or more treatment fluids from the treatment cavity (2, 3).
[0002]
Dental device according to claim 1, characterized in that each of the sealing plugs (7, 8) is made of a material sufficiently deformable so that the sealing plug (7, 8) intimately outlines the dental anatomy of one or more rear teeth, thus, the sealing plug is of sufficient length and / or width to provide optimal sealing based on one or more characteristics of the patient's dental arch and / or different dimensions of terminal teeth.
[0003]
Device according to claim 1, characterized in that the intermediate layer (4) includes a plurality of zones, each of which is configured to be heated by a heating element (18) and, optionally, a control unit (50 ) to independently control the temperature of the heating elements, so that several zones have the same or different predetermined temperature.
[0004]
Dental device according to claim 1, characterized in that it includes an integrated cable (9) in the intermediate layer (4), the cable is suitable for inserting one or more layers of dental cover over the surrounding teeth and / or gums and / or lower teeth and / or surrounding gums, to adjust the position of one or more layers of the dental cap, to remove the layers of the dental cap after a dental treatment is completed, or any combination thereof; wherein the integrated cable (9) includes one or more inlet tubes (10) to flow one or more materials to the supply elements and one or more outlet tubes (11) to flow one or more materials out of the supply elements material removal.
[0005]
Dental device according to claim 1, characterized in that it includes two layers of dental cover to cover the surrounding upper teeth and / or gums and the surrounding lower teeth and / or gums, respectively, at least one material that provides elements between the two layers of the dental cap to simultaneously apply the materials to the surrounding upper teeth and / or gums and the surrounding lower teeth and / or gums where the device includes one or more breathing holes (12) suitable for providing an air passage into the mouth during dental treatment.
[0006]
Dental device according to claim 1, characterized in that the nozzle (1) includes: one or more supply holes for draining a treatment material from the treatment supply layer to the treatment cavity (2, 3), and a or more drainage channels (19) for draining a treatment material from the treatment cavity (2, 3) to the material removal elements; and wherein the intermediate layer (4) includes one or more delivery channels for transporting a treatment material from an inlet flow tube (10) to the treatment cavity (2, 3) and one or more delivery channels. drainage (19) to transport a treatment material from one or more drainage channels (19) to an outlet flow tube (11).
[0007]
Dental device according to claim 1, characterized in that the device is shaped to mirror an angle of geometric axis of articulation in relation to the maxillary axis to facilitate the natural movement of the jaw, when the device is used.
[0008]
Dental device according to claim 1, characterized by further comprising: (i) a pumping system (30) for pumping one or more treatment materials into the nozzle (1); (ii) a multiposition flow control module (32); and (iii) a control unit (50) to automate the treatment of teeth and / or gums.
[0009]
Dental device according to claim 1, characterized in that it includes a mouth protection component (59, 60) for additional protection against treatment materials.
[0010]
Device according to claim 9, characterized in that the mouth protection component (59, 60) includes a gum treatment layer on its internal surfaces for supplying one or more materials to the gums.
[0011]
Dental device according to claim 9, characterized in that the mouth protection component (59, 60) comprises a flexible apron with an arc shape designed to substantially conform to the anatomy of the gingival edge, and having pre-cut holes configured with different diameters for personalized insertion of the mouth protection component (59, 60) on the erupted teeth, so that the erupted teeth penetrate through the pre-configured cut-out holes that act to provide a dry field.
[0012]
Dental device according to claim 9, characterized in that the mouth protection component (59, 60) includes a layer of treatment material on one or more surfaces, in which the layer of treatment material is suitable for neutralizing the treatment materials teeth whitening.
[0013]
Method of treatment of teeth and / or gums according to claims 1 to 12, characterized in that it comprises: (i) positioning a mouthpiece (1) including one or more layers of dental cover and a sealing edge (2a, 3a) formed of compressible material with at least one sealing plug (7, 8) on the upper teeth and / or gums surrounding and / or lower and / or surrounding gums; (ii) applying vacuum to the dental cap layer such that a sealed treatment cavity (2, 3) having a pressure below ambient pressure is formed around the teeth and / or gums; (iii) draining one or more treatment materials into the sealed treatment cavity (2, 3); (iv) draining one or more treatment materials out of the sealed treatment cavity (2, 3).
[0014]
Method according to claim 13, characterized in that it includes any or any combination of the following steps: (i) prepare a pump module (30) to connect to a nozzle (1) designed for an application plan; (ii) configure treatment settings on a control device (50) coupled to the pump module (30); (iii) applying flow control to cause a vacuum between the mouthpiece (1) and the anatomy of the patient's gingival edge; (iv) apply flow control to automatically manage the supply of one or more materials according to the aforementioned treatment definitions and / or use a flow control module (32) to remove treatment materials from said nozzle (1 ).
[0015]
Method according to claim 13, characterized in that the method includes any or any combination of the following steps: (i) a step of controlling the temperature and / or concentration of the materials in the sealed cavity (2, 3); (ii) a flow control application step to change flow patterns during an application, to optimize compliance with a treatment plan; (iii) an application monitoring step to track compliance with a treatment plan; (iv) an application monitoring step to identify problems during a treatment.

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法律状态:
2019-07-16| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|

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2020-03-10| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|

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2020-11-10| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|

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2021-01-12| B16A| Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 11/09/2012, OBSERVADAS AS CONDICOES LEGAIS. |

优先权:

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申请号 | 申请日 | 专利标题

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US201161533303P| true| 2011-09-12|2011-09-12|

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US61/533,303|2011-09-12|

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US201261596238P| true| 2012-02-08|2012-02-08|

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US61/596,238|2012-02-08|

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PCT/US2012/054652|WO2013039906A1|2011-09-12|2012-09-11|Devices, systems and methods for the whitening of teeth|

---