• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    reinforced absorbable synthetic matrix for hemostatic applications. The present invention relates to a reinforced absorbable hemostat comprising at least one hemostatic agent in a single layer of nonwoven synthetic fabric having a compressed fiber staple blend of a polyglycolide / polylactpide copolymer and a polydioxanone.
    公开号:BR112012029293B1
    申请号:R112012029293-5
    申请日:2011-05-16
    公开日:2019-04-24
    发明作者:Olajompo Moloye-Olabisi；Dhanuraj S. Shetty；Robert W. Van Holten；Degang Zhong
    申请人:Ethicon, Inc；
    IPC主号:
    专利说明:

    SYNTHETIC MOSTATIC AND ITS MANUFACTURING METHOD.
    FIELD OF THE INVENTION
    The present invention relates to a bioabsorbable hemostat device that is useful as a construct for use in medical devices.
    BACKGROUND OF THE INVENTION
    Bleeding control is essential in surgical procedures to optimize results and to shorten the duration of surgery in the operating room. Various hemostatic materials, including material with oxidized cellulosic base, have been used as a dressing in a variety of surgical procedures, including neurosurgery, abdominal surgery, cardiovascular surgery, chest surgery, head and neck surgery, pelvic surgery and skin tissue procedure and subcutaneous.
    It is generally accepted to use multiple layer cloths in connection with medical procedures. For example, multilayered cloths are used as all-purpose surgical pads, wound dressings, surgical nets, including hernia repair nets, adhesion prevention nets and tissue reinforcement nets, defect closure devices and hemostats.
    US patent No. 5,593,441 granted to Lichtenstein et al. describes a composite prosthesis preferably that has a polypropylene mesh blade that allows for growing tissue mesh, such as Marlex®. This reference shows that other surgical materials that are suitable for tissue reinforcement and defect closure can be used, including absorbable nets such as polyglactin 910 (Vicryl®). The composite prosthesis of Lichtenstein et al. it also has an adhesion barrier, preferably a sheet of silicone elastomer. This reference generally suggests that oxidized regenerated cellulose such as the Interceed® (TC7) absorbable adhesion barrier (commercially available from Ethicon, Inc., in Somerville, NJ, USA) may be used as the
    Petition 870180071844, of 16/08/2018, p. 6/12
    2/12 adhesion barrier to produce a composite prosthesis that is effective in the short term.
    US patent No. 5,686,090 issued to Schilder et al. describes the use of a fleece in combination with an absorbable or non-absorbable film to prevent erroneous growth in adjacent tissue and to reduce adhesions. Schilder et al. they generally show that polypropylene, polyester, polyglactin, polydioxanone or polyglecaprone 25 can be used as the fleece material or film material. Published patent application US 2006/00084930, granted to Dhanaraj et al., Describes an absorbable and reinforced multilayered cloth that can be used in medical devices specifically for tissue handling applications. The matrix first comprises preparing a repair site for implantation and then arranging the reinforced, multi-layered cloth in place. The first absorbable non-woven cloth comprises fibers comprising polymers of aliphatic polyester, copolymers or blends thereof; while the second mesh cloth or absorbable fabric comprises oxidized regenerated cellulose fibers. Although the cells are inoculated into the PLGA 9010 component of the matrix before migrating through the nonwoven matrix and coming into contact with the ORC component. The ORC component typically breaks down in about two weeks and the degradation components create an acidic environment that may not be useful for cell proliferation or viability. The present invention relates to the fact that having a fully absorbable synthetic matrix that does not create such an environment that is not conducive to cell viability
    US patent No. 4,626,253 issued to Broadnax et al., Describes a device that refers to a surgical hemostat (SURGICEL) for bleeding control, and more particularly, to an oxidized cellulose mesh fabric that has superior handling and hemostatic properties. US Patent No. 7,666,803 issued to Shetty et al .. describes the method for making the absorbent and reinforced multilayered cloth that can be used as a hemostat. The matrix first comprises preparing a repair site for implantation and then arranging the cloth in bed3 / 12 of the multiple absorbable and reinforced in place. The first absorbable non-woven cloth comprises fibers comprising polymers of aliphatic polyester, copolymers or blends thereof; while the second mesh cloth or absorbable fabric comprises oxidized regenerated cellulose fibers. The method also describes the appropriate densities and thicknesses that can be used to manufacture the matrix in this particular invention. However, in certain applications where both hemostasis function and increased mechanical properties are required for a long period of time, the aforementioned matrix will not satisfy both requirements primarily because of its weaker mechanical properties.
    US published patent application No. 2008/0033333 granted to MacPhee et al. describes the use of DEXON (woven matrix of polyglycolic acid) as a reinforcement material for fibrinogen and thrombin. US patent No. 6,762,336 describes the use of polymers or copolymers based on glycolic acid or lactic acid (VICRYL) as a layer to support the sandwiched layers of fibrinogen and thrombin. Similarly, fibrin sealing surgical pads that have been described as developed by the American Red Cross are described in several articles, such as The Potential Utility of Fibrin Sealant Dressing in Repairing of Vascular Injury in Swine, Bijan Kheirabadi et al .., Journal of Trauma Injury, Infection and Critical Care, January 2007, pages 94 to 103 and Comparison of 10 Different Hemostatic Dressings iri an Aortic Injury, Jill Sondeen et al .., Journal of Trauma, Injury, Infection and Critical Care, February 2003 , pages 280 to 285.
    SUMMARY OF THE INVENTION
    The present invention is directed to a reinforced absorbable hemostat comprising a single layer of synthetic non-woven cloth. The absorbable non-woven cloth comprises fibers comprising aliphatic polyester polymers, copolymers, or blends thereof. Aliphatic polyesters are typically synthesized in a monomer ring opening polymerization including, but not limited to, lactic acid, lactide
    4/12 (mixtures including L-, D-, meso and D, L), glycolic acid, glycolide, epsiloncaprolactone, p-dioxanone (1,4-dioxan-2-one), and trimethylene carbonate (1,3 -dioxan-2-one). In one embodiment, the synthetic non-woven cloth essentially consists of a blend of a polyglycolide / polylactide and polydioxanone copolymer. The present invention is additionally intended for a hemostatic cloth which comprises at least one hemostatic agent in a non-woven layer of a first absorbable cloth which comprises a polyglycolide / polylactide copolymer and a second absorbable cloth which comprises polydioxanone, in which both cloths are clamp-shaped.
    The first absorbable cloth may consist essentially of a glycolide / lactide copolymer in a 90/10 mol / mol composition. The first absorbable cloth may be in the form of a clamp that is about 1.91 to 6.35 cm (0.75 to 2.5 inches) long. The second absorbable cloth may be in the form of a clamp that is 1.91 to 6.35 cm long (0.75 to 2.5 inches). One or both of the same clips can be crimped, chemically or mechanically. The weight ratio between the first cloth clips and the second cloth clips can be around 70:30. The mixture of staple materials can be compacted to a thickness of about 1.5 mm and a density of about 100 mg / cc.
    In one embodiment, the hemostatic device is substantially free of any oxidized polysaccharide material. In one embodiment, the hemostatic agent comprises thrombin. In another embodiment, the hemostatic agent in the hemostatic device comprises thrombin and fibrinogen.
    The present invention is also directed to a method for using the hemostatic cloth described above as a medical device. The medical device described above preferably provides hemostasis when applied to a tissue or wound that needs hemostasis. More particularly, the device can control and alleviate mild to moderate bleeding within an effective period of time from about 1 to about
    5/12 of 10 minutes.
    The present invention is also directed to a method for making a hemostatic cloth described above which comprises the steps of suspending thrombin and fibrinogen in a perfluorinated hydrocarbon to form a suspension and applying the suspension to the absorbable non-woven cloth. Thrombin activity in the hemostatic cloth can be in the range of about 20 to 500 IU / cm2, and the fibrinogen in the dressing can be in the range of about 2 to 15 mg / cm2. The method may additionally include the step of sterilizing the hemostatic cloth, such as by radiation.
    DETAILED DESCRIPTION
    The reinforced absorbable cloth is a non-woven material comprising at least two synthetic polymer fibers and one or more hemostatic agents. The cloth preferably does not include material amounts of cellulosic or oxidized polysaccharides as a separate layer or combined as part of the nonwoven layer. Examples of cellulosic or oxidized polysaccharides that were previously used in hemostatic devices include oxidized cellulose and the neutralized derivatives thereof. For example, cellulose can be oxidized carboxylic or oxidized aldehyde cellulose. Regenerated cellulose and a detailed description of how to manufacture oxidized regenerated cellulose are presented in US Patent No. 3,364,200, in US Patent No. 5,180,398, and in US Patent No. 4,626,253, the contents of which are incorporated into reference title in its entirety in this document. Although such cellulosic-derived materials have been shown to improve hemostasis, the present invention has certain advantages, particularly when used in combination with the particulate form or with lyophilized hemostatic agents, such as thrombin and fibrinogen.
    The first absorbable non-woven cloth comprises fibers comprising polymers of aliphatic polyester, copolymers, or blends thereof. Aliphatic polyesters are typically synthesized in a ring opening polymerization of monomers including, but not limited to, lactic acid, lactide (mixtures including L-, D-, meso and D, L), acid
    6/12 glycolic, glycolide, epsilon-caprolactone, p-dioxanone (1,4-dioxan-2-one), and trimethylene carbonate (1,3-dioxan-2-one). In one embodiment, the first polymeric fiber material consists essentially of a blend of glycolide and lactide copolymer, such as a poly (glycolide-collactide) copolymer (PGLA, 90/10 in mol / mol) and polydioxanone (PDO). The two materials are processed in a single layer of non-woven fiber material and are preferably combined in a weight ratio of about 80:20 to about 60:40, more preferably about 70:30 PGLA and PDO . The weight ratio between PLGA and PDO in the non-woven blend can be from 10:90 to 90:10, with the most preference in the 70:30 range.
    In one embodiment, poly (glycolide-co-lactide) (PGLA, 90/10 mol / mol) is fused by spinning on a polymeric fiber. A multiple filament PGLA yarn is consolidated, crimped and cut into staples that are 0.25 to 7.62 cm (0.1 to 3.0 inches) in length, preferably between 1.91 to 6.35 cm (from 0.75 to 2.5 inches). PDO is fused by spinning in polymeric fiber. A PDO multiple filament yarn is consolidated, crimped and cut into staples that are 0.25 to 7.62 cm (0.1 to 3.0 inches) in length, preferably between 1.91 to 6.35 cm (from 0.75 to 2.5 inches). The mixture of these staple materials essentially consists of PGLA / PDO with a weight ratio of 70/30 was carded to create a non-woven mat and then compacted to a thickness of about 0.25 to 2.5 mm, preferably from 1.25 to 1.75 mm and at a density of 50 to 200 mg / cc, preferably from 75 to 125 mg / cc.
    One method for making the cloth described in this document is through the following process. Absorbable polymer fibers, which have a size of g / km per fiber (denier per fiber) of about 0.11 to 0.44 (from 1 to 4), can be consolidated at about 8.89 to 13, 3 g / km (from 80 to 120 deniers) of multiple filament yarn and then at about 88.9 to 133 g / km (from 800 to 1200 deniers) of yarn, thermally crimped and then cut into a staple that has a length between about 1.91 to 6.35 cm (0.75 and 2.5 inches). The clamp can be fed into a carding machine arranged dry in a multiple ball applicator one or more times
    7/12 and carded in a uniform non-woven blanket, while humidity is controlled between about 20 to 60% at an ambient temperature of 15 to 24 ° C. For example, the uniform non-woven mat can be manufactured using a single-cylinder top ball spike card, which has a main cylinder covered by alternating ball applicators and peeling rollers, where the mat is removed from the surface of the cylinder through a defibrator ball apiicator and deposited on a collecting roller. The reinforced absorbable cloth can then be washed by washing in an appropriate solvent and drying under moderate conditions for 10 to 30 minutes.
    The cloth is washed using suitable solvents to dissolve any spin finish. Solvents include, but are not limited to, isopropyl alcohol, hexane, ethyl acetate and methylene chloride. The cloth is then dried in a condition to provide sufficient drying while minimizing shrinkage.
    The hemostat described in this document provides and maintains effective hemostasis when applied to a wound that needs hemostasis. Effective hemostasis, for use in the present invention, is the ability to control and / or alleviate mild to moderate bleeding in an effective time, as recognized by those skilled in the hemostasis technique. Additional indications of effective haemostasis may be provided by governmental and similar regulatory standards. Examples of mild to moderate bleeding include, without limitation, bleeding due to resection of the spleen, resection of the liver, blunt liver trauma and blunt splenic trauma.
    The nonwoven substrate described above can include one or more hemostatic agents. Hemostatic agents, for the purposes of the present patent application, are agents that have a hemostatic effect, more preferably, delay, prevent and eventually stop bleeding at the injury site. One method to produce a hemostatic effect at the site of an injury is to introduce one or more agents found in the blood clotting cascade process that can react with each other or with other agents naturally present in the body. Thrombin
    8/12 was used to produce a hemostatic effect, while in another modality, thrombin and fibrinogen are used together to produce the desired hemostatic effect. Additional components, such as calcium, can also be provided to further accentuate the hemostatic effect.
    In one embodiment, the bioabsorbable non-woven cloth retains solid thrombin and / or solid fibrinogen in particulate powder without separation and with minimal loss of dust from its surface due in part to the means for adding the agent (s) hemostatic (s) and the non-woven nature of the substrate. In a preferred method for applying thrombin and / or fibrinogen to the matrix, one or more solutions containing biological products are lyophilized separately. The lyophilized materials are then crushed into powders with the use of a superfine mill, ball mill or a cooled blade mill. The powders are weighed and suspended together in a carrier fluid in which the proteins are not soluble. A preferred carrier fluid is a perfluorinated hydrocarbon, including but not limited to HFE-7000, HFE-7100, HFE-7300 and PF-5060 (commercially available from 3M Minnesota). Any other carrier fluid in which proteins do not dissolve can be used, such as alcohols, ethers or other organic fluids. The suspension is carefully mixed and applied to the absorbable non-woven cloth using conventional means such as wet or dry electrostatic spray, dip coating, painting, or spraying, while maintaining an ambient temperature of about 15 to 24 ° C and relative humidity of about 10 to 60%, preferably not more than 30%. The single-layer dressing is then dried at room temperature and packed in a suitable moisture barrier container. The dressing containing thrombin and / or fibrinogen contains no more than 25% moisture, preferably no more than 15% moisture, and most preferably no more than 5% moisture.
    Thrombin and / or fibrinogen can be derived from animals, humans, or can be recombinant. Thrombin activity in the dressing can be in the range of about 20 to 500 IU / cm 2 , preferably from about 20 to 200 IU / cm 2 and most preferably about 50 to 200
    9/12
    UI / cm 2 . The fibrinogen activity in the dressing can be in the range of about 2 to 15 mg / cm 2 , preferably about 3 to 12 mg / cm 2 and most preferably about 5 to 10 mg / cm 2 . The amount of thrombin and / or fibrinogen powder is preferably applied to the non-woven cloth in an amount sufficient to cover its surface so that no area is visibly devoid of dressing. The dust can settle mostly on top of the non-woven cloth or, more preferably, it penetrates the non-woven cloth.
    As a surgical dressing, the dressing described in this document can be used as an aid to primary wound closure devices, such as arterial closure devices, staples and sutures, to seal potential leaks of gases, liquids, or solids as well as to provide hemostasis. For example, the dressing can be used to seal tissue air or organ and tissue fluids, including but not limited to, bile, lymph, cerebrospinal fluids, gastrointestinal fluids, interstitial fluids and urine.
    The hemostat described in this document has additional medical applications and can be used for a variety of clinical functions including, but not limited to, matrix / substrate, that is, fibrinogen / thrombin coating, tissue reinforcement and support, that is, for vascular or gastrointestinal anastomoses, approximation, that is, to connect anastomoses that are difficult to perform (that is, in tension) and release of tension. The hemostat matrix can additionally promote and possibly improve the natural tissue healing process in all of the above events. This dressing can be used internally in various types of surgery, including, but not limited to, cardiovascular, peripheral vascular, cardio-thoracic, gynecological, neurological and general surgeries. The hemostat can also be used to attach medical devices (for example, stitches, clips and film) to fabrics, from fabric to fabric or medical device to medical device.
    Example 1 A single PGLA / PDO matrix layer
    Poly (glycolide-co-lactide) (PGLA, 90/10 mol / mol) is melted
    10/12 by spinning in polymeric fiber. A multiple filament yarn is consolidated, crimped and cut in PGLA staple material having a length of 5.08 cm (2.0 inches). Polydioxanone (PDO) is fused by spinning in the polymeric fiber. A single filament yarn is consolidated, crimped and cut into PDO staple material that is 5.08 cm (2.0 inches) long. The mixture of PGLA / PDO staple materials is combined in a 70/30 weight ratio and is carded to create a non-woven mat and then compacted to a thickness of about 1.5 mm and a density of about 100 mg / cc.
    Example 2
    A mild to moderate bleeding model is created by making a 15 mm long and 3 mm deep incision in a pig spleen. A PGLA / PDO matrix as described in example 1 is then applied to the surgical site and a buffer is applied for two minutes. Hemostasis is checked for 30 seconds after the two-minute buffer. If bleeding with free flow is not observed within 30 seconds, the time for haemostasis is observed. If bleeding with free flow is observed, a buffer of 30 seconds is applied again until the hemostasis is reached or until the test period reaches ten minutes, which is defined as a failure in the hemostasis. All three test samples achieved hemostasis in 3.14 ± 1.26 minutes (table 1).
    Table 1. Hemostasis of the PGLA / PDO matrix in a Bacchus model
    Sample No. 1 2 3 Average Standard deviation Hemostasis (min) 2.00 2.92 4.50 3.14 1.26
    Example 3
    The mechanical property of the reinforced cloth is characterized in an in vitro test. The PGLA / PDO material matrix described in example 1 is cut into strips (approximately 0.95 cm (3/8 inch) wide by 5.08 cm (2 inches) long). The tensile strength of the cloth is then assessed in dry and wet conditions using an Instron tension analyzer. In wet conditions, the strips are arranged in
    11/12 um in a conical tube containing STF buffer at a pH of 7.4 to 37 ° C. The tensile strength of the strips is then measured for 120 minutes, 4 days, 7 days, 11 days, and 14 days. The tensile strength values of PGLA / PDO materials, as described in example 1, are shown in Table 2. Table 2. PGLA / PDO tensile strength in dry and wet conditions
    Dry 120 minutes 4 days 7 days 11 days 14 days Tensile strength (New-ton / cm) 63.2 ± 10.7 58.6 ± 4.8 50.3 ± 3.7 35.3 ± 6.7 17.5 ± 4.9 11.0 + 2.0
    Example 4
    A hemostatic device that combines the PGLA / PDO material matrix and one or more hemostatic agents can be prepared by coating fibrinogen and thrombin in an example 1 PGLA / PDO material matrix for the management of severe bleeding. Such a combination product is constructed by coating porcine fibrinogen and thrombin on the PGLA / PDO matrix as described in example 1. The PGLA / PDO matrix is cut to 5 x 10 cm and sterilized by gamma irradiation (from 25 to 35 kGy). A variable amount of fibrinogen and porcine thrombin (see table 3) is mixed thoroughly with approximately 6.5 ml of HFE-7000. The slurry is poured into a 5.5 x 10.5 cm tray and the PGLA / PDO matrix is immersed in the tray. The coated hemostatic devices are air-dried for approximately 30 minutes. Environmental conditions are maintained at 24C and with 45% RH throughout the process. The dressing is vacuum dried and packed in a plastic bag with nitrogen gas. The packaged dressing is sterilized again using an electronic bundle (8 to 12.5 kGy). The effectiveness of the dressing is tested in a severe bleeding model (porcine partial nephrectomy model). The results are shown in table 3.
    Table 3. PGLA / PDO hemostasis time with different levels of fibrinogen and thrombin
    Sample identification Matrix Fibrinogen (mg / cm 2 ) Thrombin (IU / cm 2 ) Hemostasis(min) THE PGLA / PDO 0 0 9.5 + 4.0 B PGLA / PDO 0 100 6.5 ± 5.2
    12/12
    Sample identification Matrix Fibrinogen (mg / cm 2 ) Thrombin (IU / cm 2 ) Hemostasis(min) Ç PGLA / PDO 9 0 6.1 ± 2.2 D PGLA / PDO 5 20 3.8 ± 1.6 AND PGLA / PDO 5 50 £ 3.0 F PGLA / PDO 5 100 3.8 ± 1.5 G PGLA / PDO 9 20 6.1 ± 0.1 H PGLA / PDO 9 50 6.2 ± 0.1 I PGLA / PDO 9 100 6.2 ± 2.6
    Example 5
    Poly (glycolide-co-lactide) (PGLA, 90/10 in mol / mol) is melted by spinning in the polymeric fiber. A multiple filament yarn is consolidated, crimped and cut in PGLA staple material that is 5.08 cm (2.0 inches) long. PGLA staple materials are carded to create a non-woven blanket and compacted to a thickness of about 2.3 mm and a density of about 59 mg / cc. A mild to moderate bleeding model is created by making a 15 mm long and 3 mm deep incision in a pig spleen. The PGLA matrix is applied to a surgical site and a tampon is applied for two minutes. Hemostasis is checked for 30 seconds after the two-minute buffer. If bleeding with free flow is not observed within 30 seconds, the time for haemostasis is observed. If bleeding with free flow is observed, a buffer of 30 seconds is applied again until the hemostasis is reached or until the test period reaches ten minutes, which is defined as a failure in the hemostasis. Two samples were tested and both reached hemostasis (5.5 and 4.75 minutes).
    权利要求:
    Claims (16)
    [1]
    1. Synthetic hemostatic cloth, characterized by the fact that it comprises at least one hemostatic agent in a simple non-woven layer of a first absorbable cloth that comprises a copolymer of
    5 polyglycolide / polylactide and a second absorbable cloth comprising polydioxanone, both cloths being in the form of a staple and said synthetic hemostatic cloth is free of any cellulosic or oxidized polysaccharide material.
    [2]
    2. Synthetic hemostatic cloth according to claim 1, 10 characterized by the fact that the first absorbable cloth consists of a glycolide / lactide copolymer in a composition of 90/10 in mol / mol.
    [3]
    3. Synthetic hemostatic cloth according to claim 2, characterized by the fact that the first absorbable cloth comprises a clamp that has a length of 1.91 to 6.35 cm (from 0.75 to 2.5
    15 inches).
    [4]
    4. Synthetic hemostatic cloth, according to claim 1, characterized by the fact that the hemostatic agent comprises thrombin.
    [5]
    5. Synthetic hemostatic cloth, according to claim 1, characterized by the fact that the clamp is crimped.
    20
    [6]
    6. Synthetic hemostatic cloth according to claim 4, characterized in that the second absorbable cloth comprises a clip having a length of 1.91 to 6.35 cm (from 0.75 to 2.5 inches).
    [7]
    7. Synthetic hemostatic cloth according to claim 6,
    25 characterized by the fact that the clamp is crimped.
    [8]
    8. Synthetic hemostatic cloth, according to claim 4, characterized by the fact that the hemostatic agent additionally comprises fibrinogen.
    [9]
    9. Synthetic hemostatic cloth according to claim 1, 30 characterized by the fact that the weight ratio between the first cloth clamps and the second cloth clamps is 70:30.
    [10]
    10. Synthetic hemostatic cloth according to claim 9,
    Petition 870190004694, of 16/01/2019, p. 4/9
    2/2 characterized by the fact that the mixture of the staples is compacted to a thickness of 0.25 to 2.5 mm.
    [11]
    11. Synthetic hemostatic cloth, according to claim 10, characterized by the fact that the mixture of the staples is compacted to a density of 50 to 200 mg / cc.
    [12]
    12. Synthetic hemostatic cloth, according to claim 1, characterized by the fact that it has a tensile strength (Newton / cm) of:
    The. 63 in dry condition;
    B. 59 in wet condition for 120 minutes;
    ç. 50 in wet condition for 4 days;
    d. 35 in wet condition for 7 days;
    and. 18 in wet condition for 11 days;
    f. 11 in wet condition for 14 days.
    [13]
    13. Method for making a synthetic hemostatic cloth as defined in claim 1, characterized by the fact that it comprises the steps of:
    The. suspend thrombin and fibrinogen in a perfluorinated hydrocarbon to form a suspension; and
    B. apply the suspension to the absorbable non-woven cloth.
    [14]
    14. Method, according to claim 13, characterized by the fact that thrombin activity in the synthetic hemostatic cloth is in the range of 20 to 500 IU / cm 2 , and the fibrinogen in the dressing is in the range of 2 to 15 mg / cm 2 .
    [15]
    15. Method, according to claim 14, characterized by the fact that it additionally comprises the step of sterilizing the synthetic hemostatic cloth.
    [16]
    16. Method, according to claim 15, characterized by the fact that the wound dressing is sterilized by radiation.
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    同族专利:
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    CN102892439A|2013-01-23|
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    WO2011146359A1|2011-11-24|
    CA2799916A1|2011-11-24|
    US20120315316A1|2012-12-13|
    ES2659173T3|2018-03-14|
    CN106215217A|2016-12-14|
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    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US3364200A|1960-03-28|1968-01-16|Johnson & Johnson|Oxidized cellulose product and method for preparing the same|
    US4440789A|1982-11-16|1984-04-03|Ethicon, Inc.|Synthetic absorbable hemostatic composition|
    US4626253A|1984-10-05|1986-12-02|Johnson & Johnson Products, Inc.|Surgical hemostat comprising oxidized cellulose|
    US4741337A|1985-07-17|1988-05-03|Ethicon, Inc.|Surgical fastener made from glycolide-rich polymer blends|
    CN1035803C|1990-07-24|1997-09-10|中国化工进出口总公司|Soluble hemostyptic fabric|
    US5180398A|1990-12-20|1993-01-19|Johnson & Johnson Medical, Inc.|Cellulose oxidation by a perfluorinated hydrocarbon solution of nitrogen dioxide|
    WO1993017635A1|1992-03-04|1993-09-16|C.R. Bard, Inc.|Composite prosthesis and method for limiting the incidence of postoperative adhesions|
    CA2114282A1|1993-01-28|1994-07-29|Lothar Schilder|Multi-layered implant|
    US5393594A|1993-10-06|1995-02-28|United States Surgical Corporation|Absorbable non-woven fabric|
    US6762336B1|1998-01-19|2004-07-13|The American National Red Cross|Hemostatic sandwich bandage|
    US6733774B2|2001-01-25|2004-05-11|Nycomed Pharma As|Carrier with solid fibrinogen and solid thrombin|
    US7824701B2|2002-10-18|2010-11-02|Ethicon, Inc.|Biocompatible scaffold for ligament or tendon repair|
    JP4769578B2|2003-01-20|2011-09-07|一般財団法人化学及血清療法研究所|Hemostasis material|
    RU2005134239A|2003-04-04|2006-05-10|Тиссьюмед Лимитед |COMPOSITIONS OF FABRIC ADHESIVES|
    US9358318B2|2004-10-20|2016-06-07|Ethicon, Inc.|Method of making a reinforced absorbable multilayered hemostatic wound dressing|
    DK1809342T3|2004-10-20|2015-08-17|Ethicon Inc|absorbable hemostat|
    CA2584717C|2004-10-20|2013-12-17|Ethicon, Inc.|A reinforced absorbable multilayered fabric for use in medical devices and method of manufacture|
    CN101084021B|2004-10-20|2011-05-04|伊西康公司|Reinforced absorbable multilayered hemostatic wound dressing and its manufacture method and uses|
    EP2018190A1|2006-04-10|2009-01-28|Ethicon, Inc|A reinforced absorbable multilayered hemostatic wound dressing and method of making|
    BRPI0621587A2|2006-04-10|2011-12-13|Ethicon Inc|reinforced and absorbable multilayer fabric for use in medical devices and manufacturing method|
    NZ574653A|2006-08-04|2012-11-30|Stb Lifesaving Technologies Inc|Solid dressing for treating wounded tissue|
    US20080095830A1|2006-10-20|2008-04-24|Van Holten Robert W|Method for making a dressing|
    US20090004253A1|2007-06-29|2009-01-01|Brown Laura J|Composite device for the repair or regeneration of tissue|
    JP2010069031A|2008-09-19|2010-04-02|Chemo Sero Therapeut Res Inst|Sheet-like fibrin glue adhesive|
    US8758447B2|2009-06-30|2014-06-24|Ethicon, Inc.|Device and method for repair of urological structures|BR112012032169B1|2010-06-17|2020-04-14|Univ Washington|system to produce a structure that includes radially aligned fibers and fiber structure to repair an empty space in biological tissue|
    WO2013172472A1|2012-05-14|2013-11-21|帝人株式会社|Sheet molding and hemostatic material|
    DK2851085T3|2012-05-14|2019-09-09|Teijin Ltd|PROTEIN COMPOSITION STERILIZED BY RADIATION|
    US9259435B2|2012-08-31|2016-02-16|W. L. Gore & Associates, Inc.|Reactive oxidative species generating materials and methods of use|
    US20140065090A1|2012-08-31|2014-03-06|W. L. Gore & Associates, Inc.|Reactive Oxidative Species Generating Materials and Methods of Use|
    AU2015268656B2|2012-08-31|2016-11-03|W. L. Gore & Associates, Inc.|Reactive oxidative species generating materials and methods of use|
    JP6295258B2|2012-09-21|2018-03-14|ワシントン・ユニバーシティＷａｓｈｉｎｇｔｏｎ Ｕｎｉｖｅｒｓｉｔｙ|Medical patch with spatially arranged fibers|
    KR101878774B1|2015-04-15|2018-07-17|주식회사 삼양바이오팜|Multifunctional hemostatic material and method for preparing the same|
    US10188389B2|2015-08-31|2019-01-29|Ethicon Llc|Adjunct material for delivery to colon tissue|
    US10349938B2|2015-08-31|2019-07-16|Ethicon Llc|Surgical adjuncts with medicants affected by activator materials|
    US10279086B2|2015-08-31|2019-05-07|Ethicon Llc|Composite adjunct materials for delivering medicants|
    US10076329B2|2015-08-31|2018-09-18|Ethicon Llc|Adjunct material to promote tissue growth in a colon|
    US10285692B2|2015-08-31|2019-05-14|Ethicon Llc|Adjuncts for surgical devices including agonists and antagonists|
    US9937283B2|2015-08-31|2018-04-10|Ethicon Endo-Surgery, Llc|Adjunct material to provide drug elution from vessels|
    US10463366B2|2015-08-31|2019-11-05|Ethicon Llc|Adjunct materials for delivery to liver tissue|
    US10188390B2|2015-08-31|2019-01-29|Ethicon Llc|Adjunct material to provide heterogeneous drug elution|
    US10172973B2|2015-08-31|2019-01-08|Ethicon Llc|Surgical adjuncts and medicants for promoting lung function|
    US10130738B2|2015-08-31|2018-11-20|Ethicon Llc|Adjunct material to promote tissue growth|
    US10499913B2|2015-08-31|2019-12-10|Ethicon Llc|Tubular surgical constructs including adjunct material|
    US10194936B2|2015-08-31|2019-02-05|Ethicon Endo-Surgery, Llc|Adjunct material for delivery to stomach tissue|
    US10086116B2|2015-08-31|2018-10-02|Ethicon Llc|Adjunct material to provide controlled drug release|
    US10213520B2|2015-08-31|2019-02-26|Ethicon Llc|Surgical adjuncts having medicants controllably releasable therefrom|
    US10245034B2|2015-08-31|2019-04-02|Ethicon Llc|Inducing tissue adhesions using surgical adjuncts and medicants|
    US10076324B2|2015-08-31|2018-09-18|Ethicon Llc|Adjunct material to provide controlled drug elution|
    US11020116B2|2015-08-31|2021-06-01|Ethicon Llc|Surgical adjuncts with medicants affected by activators|
    US10569071B2|2015-08-31|2020-02-25|Ethicon Llc|Medicant eluting adjuncts and methods of using medicant eluting adjuncts|
    US10111661B2|2015-08-31|2018-10-30|Ethicon Llc|Matrix metalloproteinase inhibiting adjuncts for surgical devices|
    AU2016348312B2|2015-11-06|2020-09-10|Ethicon, Inc.|Compacted hemostatic cellulosic aggregates|
    EP3426207A1|2016-03-08|2019-01-16|Urgo Recherche Innovation et Développement|Dressing in the form of a self-adhesive tape|
    US10632228B2|2016-05-12|2020-04-28|Acera Surgical, Inc.|Tissue substitute materials and methods for tissue repair|
    CA3024193A1|2016-05-12|2017-11-16|Acera Surgical, Inc.|Tissue substitute materials and methods for tissue repair|
    CN107754005B|2016-08-15|2021-06-15|广州倍绣生物技术有限公司|Hemostatic compositions and methods of making same|
    US11254061B2|2017-01-06|2022-02-22|Ethicon, Inc.|Scaffolds for implanting absorbable hemostats in field conditions|
    US20210379237A1|2020-06-08|2021-12-09|Ethicon, Inc.|Napped Coated Wound Dressing|
    US20210393245A1|2020-06-10|2021-12-23|Ethicon, Inc.|Two component sealing systems including synthetic matrices and biosynthetic adhesives for sealing resected surfaces of organs to control bleeding, fluid leaks and air leaks|
    法律状态:
    2018-04-10| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
    2018-07-10| B06T| Formal requirements before examination [chapter 6.20 patent gazette]|
    2018-10-23| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]|
    2019-02-19| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|
    2019-04-24| 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 16/05/2011, OBSERVADAS AS CONDICOES LEGAIS. (CO) 20 (VINTE) ANOS CONTADOS A PARTIR DE 16/05/2011, OBSERVADAS AS CONDICOES LEGAIS |
    优先权:
    申请号 | 申请日 | 专利标题
    US12/781,103|2010-05-17|
    US12/781,103|US8273369B2|2010-05-17|2010-05-17|Reinforced absorbable synthetic matrix for hemostatic applications|
    PCT/US2011/036590|WO2011146359A1|2010-05-17|2011-05-16|Reinforced absorbable synthetic matrix for hemostatic applications|
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