• 专利附录
  • 专利说明
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    • 专利摘要:
    The invention relates to an encapsulation chamber for secretory cells, comprising a closed envelope made in a semi-permeable membrane, said membrane comprising at least one layer of porous biocompatible polymer, and a non-woven biocompatible polymer layer.
    公开号:FR3014316A1
    申请号:FR1362342
    申请日:2013-12-10
    公开日:2015-06-12
    发明作者:Aoun Richard Bou；Severine Sigrist；Stefan Sproll
    申请人:DEFYMED；
    IPC主号:
    专利说明:

    [0001] The invention relates to the field of implantable bioartificial organs and in particular being in the form of encapsulation chambers of cells secreting a substance of interest. The membranes for the manufacture of such encapsulation chambers and bioartificial organs are also objects of the invention.
    [0002] The treatment of diseases requiring a continuous supply to the body of substances of therapeutic interest has made it necessary to develop devices that can be implanted in a patient and are able to release these substances effectively sometimes for long periods of time. time.
    [0003] To meet this need, bioartificial organs have been developed which contain cells producing one or more substances of therapeutic interest. The cells contained in a bioartificial organ are confined in internal spaces, or encapsulation chambers, delimited by at least one semipermeable membrane. Such a membrane is said to be "semi-permeable" when it allows the diffusion of the substances of therapeutic interest out of the encapsulation chamber to the target cells in the body of the patient, while being impervious to the antibodies and cells of the patient. immune system of the patient, thus preventing them from directly attacking the cells producing the substance or substances of therapeutic interest.
    [0004] A bioartificial member is understood as a device, in particular intended to be implanted in a patient, comprising at least one encapsulation chamber consisting of at least one semipermeable membrane; said encapsulation chamber is intended to contain secretory cells of one or more substance (s) of therapeutic interest.
    [0005] These substances of therapeutic interest are any substance intended to have a beneficial effect in the patient. It can therefore be a neurotransmitter, a hormone, a growth factor, a coagulation factor or a cytokine. In particular, these substances may be, without limitation, insulin, glucagon, growth hormone, coagulation factor IX, coagulation cofactor VIII, or calcitonin.
    [0006] Examples of devices (bioartificial organs, semi-permeable membranes, encapsulation chambers) are known in the prior art. It is thus possible to cite the application WO 02/060409 which describes a membrane consisting of a biocompatible film of porous polycarbonate modified on the surface by the creation of polar sites and covered by a layer of at least one hydrophilic polymer, and its use for the manufacture of bioartificial organs. Application WO 2012/017337 discloses a functionalized semipermeable membrane composed of a porous biocompatible support previously treated to increase the surface energy and comprising at least two layers each comprising a hydrophilic polymer and at least one biologically active molecule, and its use especially for the manufacture of a bioartificial organ. The application WO 2012/010767 describes a pouch for forming an implantable artificial organ, which comprises a closed envelope and made in a semi-permeable membrane. This pocket further comprises a web contained in the envelope, the web having on its surface protuberances to maintain a space for cells between the web and the envelope. However, there is a need to provide surgeons with 20 new bioartificial organs, which in particular have interesting biomechanical characteristics, that is to say a good resistance after implantation. Indeed, the bioartificial organs are intended to be implanted, generally in the intraperitoneal cavity or in the extraperitoneal space and are likely to undergo tensile or shear forces depending on the movements of the patient receiving. In addition, these bioartificial organs must be able to contain a large number of cells, in order to be able to have a prolonged physiological effect after implantation in the patient. It is therefore necessary to design organs of sufficiently large size to do this, but which then have the disadvantage of risk of tearing after implantation due to the movements of the patient (this problem being less important for micro-organs containing only a small number of cells). Increasing the thickness of the membranes to improve the mechanical strength can not be a solution because the diffusion of the molecules of interest is then greatly reduced as the thickness of the membrane increases.
    [0007] It is therefore necessary to develop new semipermeable membranes with improved mechanical properties for the production of bioartificial organs. The selective permeability properties must be at least 5 preserved. In a first embodiment, the invention thus relates to a chamber for encapsulating secretory cells producing at least one substance of therapeutic interest, comprising a closed envelope and made in a semi-permeable membrane, delimiting a space capable of to contain the secretory cells producing at least one substance of therapeutic interest, characterized in that said membrane comprises at least one layer of porous biocompatible polymer, and a biocompatible nonwoven polymer layer. It is recalled that the term "biocompatible" refers to a material which is well tolerated by a living organism and which does not cause a rejection reaction, toxic reaction, injury or harmful effect on the biological functions of the organism. this last. This does not exclude the possibility of an inflammatory reaction due to the insertion of the material into the body or of an immune reaction in the case of a biocompatible organ comprising exogenous cells: this immune reaction is then not not due to the organ as such, but rather to its content (secretion of chemochines by exogenous cells). As seen above, the semipermeable membrane has a cutoff threshold, the molecules having a mass greater than this cutoff threshold can not cross the membrane, while molecules having a mass below this cutoff threshold can pass through the membrane. The determination of the cut-off threshold is carried out by a person skilled in the art, depending on the characteristics of the molecules that he wishes to stop or allow to penetrate. In a preferred embodiment, and in order to allow the passage of small molecules such as insulin, glucagon or glucose and to stop the effector molecules of the immune system (such as cytokines), this cut-off is between 100 kDa and 500 kDa, most preferably between 100 kDa and 150 kDa. The internal diameter of the pores of the semi-porous polymer makes it possible to obtain the desired cutoff threshold. Thus, in a particular case, the internal diameter of the pores present on the porous biocompatible polymer layer is between 5 and 100 nm, and most preferably between 5 and 50 nm. Nonwoven Polymer It is recalled that a nonwoven polymer (nonwoven) is such that its fibers are maintained randomly. It is thus a sheet made of fibers oriented in a particular direction or at random, linked by friction and / or cohesion and / or adhesion. The fibers are thus arranged statistically, that is to say deposited at random.
    [0008] Nonwoven polymers can be made using any type of polymeric fibers. Polyesters may be mentioned: PET (polyethylene terephthalate), PBT (polybutylene terephthalate), PVC (polyvinyl chloride), PP (polypropylene), PE (polyethylene) or mixtures thereof. of these polymers. Polyamides or polycarbonates can also be used to make nonwoven polymers. In a preferred manner, the nonwoven polymer is chosen from polycarbonate (PC), polyester, polyethylenimine, polypropylene (PP), polyethylene terephthalate (PET) and polyvinyl chloride. ) (PVC), polyamide, and polyethylene (PE). Blends of these polymers can also be used for making the nonwoven polymer. Polyethylene terephthalate (PET) is particularly preferred. Generally, this nonwoven polymer is obtained by the melt blown method. Its composition is an entanglement of microfibers that have been "meltblown". This method of obtaining is particularly suitable for polymers which can be melt-spun, in particular polypropylene, polyethylene terephthalate, polyamides or polyethylene. This method generates nonwovens of greater mechanical strength. In a particular embodiment, said membrane comprises two layers of porous biocompatible polymers, on either side of the biocompatible nonwoven polymer layer. Thus, this layer of biocompatible nonwoven polymer is located, positioned, or located between these two layers of porous biocompatible polymers.
    [0009] Such an embodiment makes it possible to optimize the resistance of the device. Indeed, this layer of nonwoven can be considered to behave like a "sponge", which gives it the ability to absorb shocks and to deform, thus increasing the rigidity of the membrane in situ, but what can be troublesome in the presence of cells, which may tend to form aggregates around this nonwoven. Locating the nonwoven layer between two porous layers of biocompatible polymers thus makes it possible to avoid cell aggregation while providing additional protection / resistance to the device, and having no effect on the molecular diffusion of the biological substances.
    [0010] The porous and nonwoven biopolymers need not be identical. Likewise, in the presence of two layers of porous biopolymers, these may be of the same polymer or of different polymers.
    [0011] Porous Biocompatible Polymer The porous biocompatible polymer is comprised of a polymer known in the art. Thus, it can be chosen from polycarbonate (PC), polyester, polyethylenimine, polypropylene (PP), polyethylene terephthalate (PET), polyvinyl chloride (PVC), polyamide, and polyethylene (PE).
    [0012] In a particular embodiment, at least one layer or both layers, as the case may be, are made of poly (ethylene terephthalate) (PET). Pore formation is performed by any method known in the art. In particular, it is possible to use the method of electron bombardment or heavy ion bombardment (this second technique is described in particular in US Patent 4,956,219). In the case of heavy ion bombardment, the density of heavy ions bombarded at the surface of the biocompatible substrate determines the pore density while the chemical erosion treatment time determines the pore size. The membranes are thus prepared using the "track30 etching" method, known in the art and described in particular in patents US Pat. No. 4,956, 219, DE19536033 or CH701975. This technology consists of the irradiation of a polymer film by means of heavy energy ions leading to the formation of linear latent traces characterized by a local degradation of this polymer; these traces are then revealed in the form of pores by selective etching.
    [0013] The membrane is irradiated by a heavy ion beam. Heavy ions pass through the entire thickness of the polymer film. By passing through the polymer, heavy ions destroy or cut the polymer chains and thus form a clean, straight opening through the material. The final alignment of the pores is determined by the angle of the beam with respect to the polymer film during the irradiation process. The beam can thus be perpendicular to the polymer film or at any other angle. In the next step, the film is passed through an etching bath and the openings become pore after contact with alkaline solutions such as sodium hydroxide or potassium hydroxide. Unlike the rest of the film, these openings made by the ions allow the passage of the alkaline solution, which fills them and allows the etching of the pores by removing the material (polymer) around these openings. The pore size is controlled by the concentration of the alkaline solution, the contact time and the temperature of the solution. If polyester or polycarbonate is used, the resulting membrane is hydrophilic and can either be used as it is or treated by surface treatment processes (plasma, spray or coating). The preparation of the membranes according to this "track etching" technology 20 is more precisely described in patents US 4, 956, 219 and CH701975. This technology allows the production of porous polymer membranes characterized in particular by a flat surface and a narrow cutoff threshold. The advantage of using membranes obtained by this technology is the high accuracy of pore size, number of pores, and pore shapes. The pores are preferably cylindrical, but this technology can also make it possible to obtain pores of other shapes such as conical shapes. Preferably, the pores are aligned, and have an angle of between 10 ° and 45 °, relative to the vertical but may also have angles> 45 ° or <10 °. These angles are obtained by the orientation of the ion beam during the bombardment of the membrane. This technology is applicable to various materials such as polycarbonate (PC), polyester (PET), or polyimide (PI). Polyamide, polyvinylidene fluoride, polyacrylate, or polyolefins can also be used.
    [0014] This method makes it easy to obtain pores with a controlled size of between 0.02 μm and 15 μm, a pore density of between 103 pores / cm 2 and 10 10 pores / cm 2 and membranes with a thickness of between 5 μm and 80 μm. .
    [0015] In a preferred embodiment, at least one of the porous biocompatible polymer layers of the membrane is rendered hydrophilic. The hydrophilicity property can be achieved by creating polar sites on the surface of this porous biocompatible polymer layer. This modification of the surface can be carried out by physical means (such as the creation of charged polar sites on the surface, in particular by plasma surface treatment, by corona discharge or else by electromagnetic discharge at atmospheric pressure or under vacuum) or chemical (One can consider an alkaline treatment especially with soda).
    [0016] Preferably, the porous biocompatible polymer layer is treated with a radio frequency plasma of argon or air. It can be treated at an emission power of the plasma reactor of between 3 and 10 watts per liter of reactor capacity, lasting between about 1 and 20 minutes. The treatment can also be performed by a microwave plasma, at the same power, but for 5 seconds to 20 minutes. Preferably, the plasma treatment is carried out under vacuum. The applications WO 02/060409 and WO 2012/017337 describe in particular the plasma surface treatment for introducing polar sites onto the porous biocompatible polymer.
    [0017] After at least one layer of porous biocompatible biopolymer has been rendered hydrophilic, it is possible to cover it with at least one layer of hydrophilic polymer, or even with two layers of different hydrophilic polymers. An active molecule may optionally be contained in at least one hydrophilic polymer layer. Applications WO 02/060409 and WO 2012/017337 also describe the addition of at least one hydrophilic polymer to the surface of a porous biocompatible polymer treated to be rendered hydrophilic, in particular by adding polar sites. Hydrophilic Polymer Constitutes a hydrophilic polymer within the meaning of the invention, a polymer or a mixture of polymers, which, after application to a porous biocompatible polymer film has an angle value of less than 40 °, preferably less than 30 ° after measurement according to the test of the "sessile drop" described in Example 2 of WO 02/060409. It should be noted that the angle value according to the "sessile drop" test may vary depending on the treatment of the polymer. Thus, it is possible to observe contact angles of less than 20 ° (of the order of 16-17 °) for the biocompatible biopolymer, when two plasma treatments are carried out, this increasing angle (generally less than 30 °) when the the hydrophilic polymer (in particular HPMC) is deposited after the two plasma treatments. If a mixture of hydrophilic polymers is used, which also contains a biologically active molecule (in particular an HPMC mixture, ethylcellulose + heparin), the angle may be greater than 30 ° but remains less than 40 °. Preferably, the hydrophilic polymer is soluble in water. Indeed, because of the implantation of the bio-artificial organ in the body of a host organism, the use of organic solvents is excluded because their total elimination is difficult, and their presence, even in small quantities, n is not compatible with therapeutic or surgical use in humans or animals. Preferably, the hydrophilic polymer material is chosen from the following hydrophilic polymers: celluloses and their derivatives, such as ethylcellulose (EC), hydroxypropyl methylcellulose (HPMC), or carboxymethylcellulose (CMC); polyacrylamides and their copolymers - polyvinylpyrrolidone (PVP) and its copolymers, polyvinylalcohols; copolymers of vinyl acetate, such as a copolymer of polyvinyl acetate and of polyvinyl alcohol; polyethylene glycols - propylene glycols; hydrophilic poly (meth) acrylates, - polysaccharides, - chitosans.
    [0018] As the hydrophilic polymer, both a polymeric material consisting of one of the hydrophilic polymers as defined above and a mixture of several of the above hydrophilic polymers, generally a mixture of two or more three of the hydrophilic polymers above. Preferably, the hydrophilic polymer is chosen from cellulose compounds, in particular HPMC, EC, TEC or CMC, polyvinylpyrrolidones, polyvinylalcohols, or polyacrylates such as poly (hydroxyethyl acrylate) ("HEMA") or copolymers of Acrylic acid The hydrophilic polymer may also be composed of a mixture of two or more hydrophilic polymers mentioned above, in particular a mixture of HPMC and CMC, or HPMC and EC Celluloses and cellulose derivatives are preferred. In particular, hydroxypropyl methylcellulose (HPMC) Membrane lamination For greater mechanical stability, the porous biocompatible polymer membrane is reinforced using a nonwoven membrane The combination of a nonwoven polymer and the membrane porous biocompatible polymer is preferably carried out by lamination, by methods known in the art, such as thermal lamination, with or without the presence of adhesives, preferably without adhesive. Thus, membrane reinforcement can be improved by means of an alternating multilayer system of woven or non-woven polymer layers and biocompatible porous polymers. However, any degradation of the diffusion properties should be avoided. In particular, the mechanical stability can be increased by combining a thin functional membrane with a high pore density with a thick protective membrane with a low pore density. There is no limitation to the number of polymer layers that can be used to make the membrane. Active Molecule As indicated above, the hydrophilic polymer deposited on the porous biocompatible polymer layer may optionally contain an active molecule.
    [0019] This "active molecule" is mixed with the hydrophilic polymer. It is intended to be released into the medium surrounding the semipermeable membrane in particular in order to reduce the inflammation due to the implantation of the bioartificial organ, and / or to induce a positive response (especially the increase in vascularization) of the tissue or tissues of the recipient patient of the bioartificial organ. Thus, the active molecule is chosen from anti-inflammatory agents, anti-infective agents, anesthetics, growth factors, stimulating agents angiogenesis and / or inducing vascularization, wound-inducing agents, agents immunosuppressive agents, anti-thrombotic agents including antiplatelet agents and anticoagulants, angiotensin-converting enzyme (ACE) inhibitors, or insulin secretory stimulating molecules (IGF, glucagon- like peptide 1 (GLP-1) or its derivatives, incretin mimetics). Among the anti-inflammatory agents, non-steroidal anti-inflammatory drugs (NSAIDs) such as acetaminophen, aminosalicylic acid, aspirin, celecoxib, choline magnesium trisalicylate, decafenac, diflunisal, etodolac, flurbiprofen, ibuprofen, indomethacin, interleukin IL-10, IL-6 mutein, anti-IL-6, NO synthase inhibitors (eg, LNAME or L-NMDA), interferon, ketoprofen, ketorolac, leflunomide, mefenamic acid, mycophenolic acid, mizoribine, nabumetone, naproxen, oxaprozin, piroxicam, rofecoxib, salsalate, sulindac, and tolmetin and corticosteroids such as cortisone, hydrocortisone, methylprednisolone, prednisone, prednisolone, betamethasone, betamethasone dipropionate, betamethasone valerate, beclomethasone dipropionate, budesonide, dexamethasone sodium phosphate, flunisolide, the propi fluticasone onate, paclitaxel, tacrolimus, tranilast, tnamcinolone acetonide, fluocinolone acetonide, fluocinonide, desonide, deoximetasone, fluocinolone, triamcinolone, triamcinolone, clobetasol propionate, and dexamethasone. Ibuprofen is particularly suitable and preferred. It is preferred to use antithrombotic agents such as antiaggregants (acetylsalicylic acid, clopidogrel, ticlopidine, dipyridamole, abciximab, eptifibatide and tirofiban), anticoagulants (heparin, bivalirudin, dabigatran, lepirudin, fondaparinux, rivaroxaban, epoprostenol, warfarin, phenprocoumon, protein C, drotrecogin alfa, antithrombin, pentosan) and thrombolytics (alteplase, urokinase, tenecteplase and reteplase). Particularly preferred is the use of heparin. In another embodiment, ibuprofen is used.
    [0020] In addition, it is possible to use a molecule to induce vascularization of tissues surrounding the bioartificial organ, including PDGF (Platelet derived growth factor), BMP (bone morphogenetic protein), VEGF (growth factor of vascular endothelium), VPF (vascular permeability factor), EGF (Epidermal Growth Factor), TGF (Transformation Growth Factor), FGF (Fibroblast Growth Factor). IGF-1 and IGF-2, a neurotropic factor (NGF), can also be used. In a particular embodiment, a cell growth factor that promotes vascularization by the induction of angiogenesis such as basic fibroblast growth factor (bFGF), vascular endothelial growth factor (VEGF) is selected. ), platelet-derived endothelial cell growth factor (PDGF A or B), bone morphogenetic protein (BMP 2 or 4), or hepatocyte growth factor (HGF). For the preparation of the hydrophilic polymer layer and the biologically active molecule, the hydrophilic polymer or hydrophilic polymer blend is dissolved in water. The addition of the hydrophilic polymer optionally containing an active molecule to the porous biocompatible polymer layer is carried out according to the methods described in WO 02/060409 and WO 2012/017337. In another embodiment, two layers each comprising a hydrophilic polymer and at least one biologically active molecule, as described in WO 2012/017337, may be added to the surface of the porous biocompatible polymer. Physical Characteristics of the Biocompatible Membrane In the preferred embodiment, the membrane according to the invention comprises two layers of porous biocompatible polymer, each covered by at least one hydrophilic polymer, which surround the nonwoven layer. Pore Diameter and Density As discussed above, the pores are introduced into each of the porous biocompatible polymer layers by methods known in the art. It is preferred when at least the layer (if single) or one of the two porous biocompatible polymer layers has a pore density greater than 106 pores / cm 2, preferably greater than 107 pores / cm 2. This pore density is generally less than 10 11 pores / cm 2, preferably less than 10 10 pores / cm 2. Membranes having a pore density preferably greater than 106 pores / cm 2, more preferably greater than 107 pores / cm 2, are therefore used. This density is preferably less than 10 11 pores / cm 2, or even less than 10 10 pores / cm 2. This density is therefore between 106 pores / cm 2 and 10 11 pores / cm 2. A density greater than 109, and less than 1010 pores / cm 2 is perfectly suitable. As seen above, the pores of the porous biocompatible polymer layers have an inner diameter such that they allow the semi-permeability of the membrane. Thus, at least one of the two layers (or the only layer, if any) of porous biocompatible polymer has pores having an internal diameter greater than 5, and less than 100 nm, and preferably greater than 10 nm, and Less than 50 nm, more preferably less than 40 nm. The density of the pores is then advantageously greater than 2.109 and less than 4.1010 pores / cm 2. When the membrane has two layers of porous biocompatible polymers, the inside diameter of the pores of one of the layers is preferentially as above. The inner diameter of the pores of the second layer may be larger, the cutting effect at the desired size being given by the pore diameter of the first layer. Thus, the inner diameter of the pores of the second layer may be greater than 100 and less than 2000 nm, preferably greater than 200 nm. These pores preferably have an inside diameter of less than 1000 nm. An inner pore diameter greater than 400 and less than 600 nm, or approximately 500 nm is perfectly suitable. The pore density is then advantageously greater than 5 × 10 6 and less than 5 × 10 7 pores / cm 2. When the membrane comprises two layers of porous biocompatible polymer, which surround the nonwoven layer, it is preferred when the encapsulation chamber is such that the layer for which the pore diameter is the lowest is located within the chamber (in contact with the secretory cells producing at least one substance of therapeutic interest) and the layer for which the pore diameter is the largest is located outside (in contact with the body of the patient). Membrane Thickness In a preferred embodiment, the total thickness of the membrane (comprising the nonwoven polymer layer and the one or more porous polymer layers) is greater than 45 μm. It is generally, and preferably, less than 200 μm, but may also be greater than this size; it is possible in particular to envisage thicknesses up to 300 μm, or even beyond. Preferably, it is greater than 50 μm. It is also preferentially less than 150 μm. This membrane thus generally has a thickness of between 45 and 200 μm. When the membrane has two layers of porous biocompatible polymers, they may have the same thickness or have different thicknesses.
    [0021] The nonwoven polymer layer generally has a thickness greater than 40 μm, preferably greater than 60 μm, more preferably greater than 80 μm. This layer has a thickness generally less than 250 μm and preferably less than 150 μm. Thus, the thickness of the nonwoven polymer layer is often between 40 μm and 150 μm.
    [0022] When the membrane has only one layer of biocompatible polymer, it then has a thickness greater than 5 .mu.m. This layer is less than 200 μm, preferably less than 100 μm, but is preferably less than 50 μm.
    [0023] When the membrane has two layers of porous biocompatible polymer, and they have different thicknesses, the thickness of the first layer is then greater than 5 .mu.m. It is also preferably less than 200 μm, but preferably less than 40 μm; a thickness less than 15 μm (and preferably greater than 5 μm) is perfectly suitable.
    [0024] This thickness is preferably the thickness of the layer having pores of the smallest inner diameter, if the inner diameter of the pores is different for the two layers. The thickness of the second layer is generally greater than 25 μm. It is preferably less than 200 μm, preferably less than 100 μm, more preferably less than 50 μm; a thickness of between 30 and 50 μm is perfectly suitable. The thickness of each hydrophilic polymer layer optionally present on one or both layers of porous biocompatible polymers is negligible, relative to the total thickness of the membrane. It is indeed preferably less than 500 nm, and generally between 25 and 250 nm. In a preferred embodiment, the membrane has two layers of porous biocompatible polymers on either side of a nonwoven polymer layer. In this embodiment, a porous biocompatible polymer layer has pores with an inside diameter of greater than 100 nm, preferably greater than 200 nm, more preferably greater than 400, and less than 1000 nm, more preferably less than 600 nm, preferably at a density of about 5 × 10 7 pores / cm 2. It is then advantageous for this layer to have a thickness of between 25 and 200 μm (see above). The other layer of porous biocompatible polymer has pores with an internal diameter greater than 5 nm, preferably greater than 10 nm (and generally less than 100 nm, preferably less than 50 nm, preferably less than 40 nm). preferably at a density of the order greater than 2 × 10 9 pores / cm 2. This density is also preferably less than 7.109 pores / cm 2. It is advantageous if it is the layer of thickness between 5 and 200 μm (preferably 5 to 15 μm). The invention also relates to a chamber for encapsulating secretory cells producing at least one substance of therapeutic interest, comprising a closed envelope and made in a membrane according to the invention, delimiting a space likely to contain the secretory cells producing at least one substance of therapeutic interest. This encapsulation chamber may also be called "pocket" and can form a bioartificial implantable organ in the patient. In a particular embodiment, this encapsulation chamber 5 also comprises a biocompatible sheet contained in said envelope, said sheet preferably comprising, on its surface, protuberances. These protuberances are advantageous for maintaining a space for the cells between the sheet and the envelope, but also for distributing the cells homogeneously and flatly, thereby maximizing the exchange surface. This sheet is preferably made of silicone. Such an embodiment is described in application WO 2012/010767. Thus, in a preferred embodiment, the envelope is formed of two membranes heat sealed together. The method described in WO 2012/010767 or a method of ultrasonic heat sealing, known in the art can be used. The method of forming the envelope is simple and allows to enclose the sheet in the envelope. In a preferred embodiment, the encapsulation chamber is circular. Such a form has several advantages: - absence of "corners" or protrusions that are likely to create cellular or inflammatory clusters during implantation - ease of manufacture of the encapsulation chamber (no need to orient the two In a particular embodiment, the diameter of the encapsulation chamber 25 is greater than 3 cm, preferably greater than 5 cm, or 8 cm. It is generally less than 20 cm, is preferably less than 15 cm, or 14 cm. A diameter between 8 and 14 cm is perfectly acceptable. When the chamber is not round, its largest dimension is generally greater than 3 cm, preferably greater than 5 cm, or 8 cm. It is generally less than 20 cm, is preferably less than 15 cm, or 14 cm. As seen above, the encapsulation chamber preferably makes it possible to manufacture a "macro" organ when it introduces the secretory cells producing at least one substance of therapeutic interest, that is to say that it allows said cells to secrete this substance for a long time (greater than 3 months, preferably greater than 6 months) at levels of physiological interest (that is to say, to meet the need of the patient). It is therefore appropriate that the encapsulation chamber can receive a large number of cells.
    [0025] It is generally believed that the preferred internal volume of the encapsulation chamber should be greater than 15 ml, preferably greater than 20 ml, more preferably greater than 25 ml, and up to 50 ml, for use in the man. For use in other animals, the volume will be different (about 1 ml in the rat, for example).
    [0026] Such encapsulation chambers must be able to contain a large number of cells. In the treatment of diabetes, the equivalent of 500 000 islets of Langerhans should be encapsulated at least, preferably the equivalent of more than 700 000 islets, and possibly up to the equivalent of one million islets of Langerhans. Knowing that an island contains, on average of the order of 1000 cells, this gives an estimate of the number of cells that can contain the encapsulation chamber according to the invention. The number of cells will obviously vary depending on the type of cells that it is desired to encapsulate and implant in the patient.
    [0027] In a preferred embodiment, the membrane forming the encapsulation chamber comprises two layers of biocompatible polymers porous on both sides of the nonwoven polymer. In this embodiment, it is preferred that at least the inner layer (located inside the chamber after formation of the chamber) is the layer whose ports ensure the semi-permeable nature of the membrane (cutoff threshold ), that is to say which has pores with an internal diameter greater than 5 nm (and generally less than 100 nm) or other dimensions mentioned above. the layer external to the envelope (in contact with the tissues and cells of the patient) may have pores of greater internal diameter, in particular greater than 100 nm, but preferably less than 2000 nm, or the other dimensions mentioned above. . In one embodiment, and as described in WO 2012/010767, the encapsulation chamber may comprise at least one connector (in particular fixed on the envelope and / or the sheet), which makes it possible to establish a communication between outside and inside the envelope. By connecting these connectors to flexible hoses, this makes it possible to fill and empty the chamber. The invention thus relates to a bioartificial member comprising at least one encapsulation chamber according to the invention. Such a bioartificial organ also advantageously has the pipes connected to the connectors and making it possible to fill and empty the bioartificial organ, making it possible to renew the contents of the bioartificial organ when it is implanted in a patient, without carrying out an explantation.
    [0028] This bioartificial organ may contain various cell types. Cells encapsulated in the bioartificial organ The cells present in the bioartificial organ produce at least one biologically active substance of interest. They may in particular be insulin-secreting cells or islets of Langerhans, which produce insulin, when the encapsulation chamber is intended for the manufacture of a bioartificial pancreas. The cells may also be liver cells when the encapsulation chamber is for the manufacture of a bioartificial liver. In a particular embodiment, the cells are transfected or transformed with at least one nucleic acid allowing the expression of a biologically active substance of interest. Among the biologically active substances of interest are, for example, insulin, cytokines, peptide hormones, growth hormone, coagulation factors VIII and IX and calcitonin. Generally, a "biologically active substance" is a substance that is released or secreted by the cell that produces it and exerts its effect on a target cell or a target molecule in the host organism, such as a neurotransmitter. a hormone, a growth factor, a clotting factor or a cytokine. A wide variety of cells can be used, including immortalized cell lines such as primary cultures of dividing cells or pluripotent stem cells.
    [0029] The cells may be, for example, myoblasts, which are precursor cells of muscle cells derived from mesoderm stem cell populations, and which can easily be transformed by a nucleic acid allowing the expression of the biologically active substance of interest.
    [0030] Those skilled in the art may advantageously refer for example to WO 94/02129, WO 93/03768 and WO 90/15863. Preferably, the cells contained in an encapsulation chamber according to the invention are included in a matrix, such as a type IV or fibrin collagen matrix, if appropriate in combination with laminin, of the entactin and heparan sulfate. The cells contained in an encapsulation chamber according to the invention may, in general, be included in a matrix composed of any product or combination of products allowing the immobilization of these cells in a viable form. Cells producing at least one biologically active substance of interest may also be encapsulated in an alginate matrix. Manufacture of an Encapsulation Chamber The encapsulation chamber is made by any method known in the art. The teaching of WO 2012/010767 is preferably used, which should be regarded as an integral part of the present application. The invention thus relates to a method of manufacturing an encapsulation chamber according to the invention comprising a heat-sealing step of two membranes according to the invention (or even of a folded membrane), so as to form a pocket for receiving cells producing at least one biologically active substance of interest. In a particular embodiment, as seen above, the encapsulation chamber contains a sheet, as well as one or more connectors. The method of manufacturing such a pouch is described in WO 2012/010767. The reader is referred to WO 2012/010767 for further explanation of the method of manufacturing the encapsulation chamber. DESCRIPTION OF THE FIGURES FIG. 1: Permeability of membranes according to the invention made of polyethylene terephthalate (PET) or polycarbonate (PC), treated or not treated with heparin, EC and H PMC, with glucose (A) ), insulin (B) and IgG (C) under static conditions.
    [0031] Figure 2: Insulin secretion of pancreatic islet cells stimulated with glucose through a membrane according to the invention in PET treated or untreated with heparin, EC and HPMC. A start of insulin diffusion is observed from 4 hours and a permeability which appears to be improved at 24 hours by the surface treatment.
    [0032] FIG. 3: snapshots of sections prepared 30 days after the implantation of membranes according to the invention made of polyethylene terephthalate (PET) or polycarbonate (PC) treated or not with heparin, EC and HPMC. Surface treatment reduces fibrosis and cellular infiltration (black arrows) and increases vascularization (*) for both types of membranes.
    [0033] Figure 4: Appearance of bioartificial organs after 15 days of implantation in pigs. One of the devices is composed of single layer PC membranes and the other of multilayer PET membranes. The device with PC membranes has large tears. The device with multilayered PET membranes does not present, in turn, any macroscopic damage. The latter were thus analyzed by scanning electron microscopy which showed no microcracks. EXAMPLES Example 1 Manufacture of Semi-Permeable Membranes The membranes are manufactured in such a way that two porous PET (polyethylene terephthalate) layers have been prepared from biocompatible PET films by the "track-etching" process. followed by lamination with the nonwoven PET layer of density between 30 and 60 g / m2 (located between the two porous biocompatible PET layers). Thermal lamination is carried out without the use of adhesives. One of the porous PET layers has a pore density of between 2.109 and 7.109 pores / cm 2 with an internal pore diameter of 10 to 30 nm. The thickness of this membrane is between 8 and 12 μm. The other porous PET layer has a pore density of between 107 and 5 × 10 7 pores / cm 2 with an internal pore diameter of between 400 and 600 nm. The thickness of this membrane is between 30 and 50 μm. The total thickness of the membrane is less than 200 μm. EXAMPLE 2 Surface Treatment of the Membranes The membranes prepared according to Example 1 were surface-treated according to the protocol of Example 1 of WO 2012/017337. The membranes are functionalized with a first layer of Heparin mixed with a solution of Ethyl Cellulose (EC) then covered with a layer of hydroxypropyl methylcellulose (HPMC).
    [0034] EXAMPLE 3 Characterization of the Membrane Permeability Insulin glucose and immunoglobulin (IgG) permeability tests of the previously prepared membranes were carried out according to the following protocol: Equipment Diffusion chamber consisting of a top compartment and a a low compartment separated by the membrane whose permeability is to be tested (the seal between the two compartments is ensured by a seal), glucose (Fischer Scientifc, Illkirch, France, ref: G / 0500/53), NaCl, IgG (Sigma, Lyon, France, ref: 19640), Insulin (Sigma, ref: 19278), distilled water. Preparation of solutions - Physiological serum For 1 L: Dissolve 9 g of NaCl in 1 L of distilled water. - Glucose (4 g / L) For 1 L: dissolve 4g of Glucose in 1 L of saline. - IgG (5.75 μg / mL) For 60 mL: dilute 34.5 μL of IgG stock solution (10 mg / mL) in 59.966 mL of saline. - Insulin (10 μg / mL) For 60 mL: dilute 60 μL stock solution of insulin (10 mg / mL) in 59.960 mL of saline. Protocol 3 ml of saline are introduced into the lower compartment of the diffusion chamber, the membrane whose permeability is to be tested is positioned on the physiological saline avoiding the presence of air bubbles. 3 ml of glucose solution are introduced into the upper compartment, then the diffusion chamber is closed with parafilm and incubated at 37 ° C. At the end of the incubation time, 1 ml of the solution in the upper compartment of the diffusion chamber is removed after gentle homogenization. The membrane is then removed and 1 ml of the solution of the lower compartment is removed after homogenization.
    [0035] The enzymatic determination of glucose is carried out using the Glucose RTU® kit (BioMérieux, Craponne, France ref: 61,269). The insulin and IgG assay is performed using the Bicinchonic acid (BCA) method using the Quantipro BCA Assay kit (Sigma, ref: QPBCA-1KT). The results are expressed as percentage permeability, calculated as follows: Permeability (in%) = (Ccompartment low / Compartment high + Compartment low) X 100 C: concentration of glucose, IgG or insulin. At equilibrium, the concentrations in the top compartment and the bottom compartment are identical, which corresponds to a maximum permeability of 50%.
    [0036] Results The results are presented in FIG. 1. Polyethylene terephthalate (PET) multilayer membranes according to the invention (example 1) were tested, as well as membranes of the prior art as described in WO 02/060409 or WO 2012/017337, made of polycarbonate and having a heparin layer mixed with EC and a HPMC layer. Slower diffusion of insulin and glucose is observed with PET membranes. Without being bound by this theory, it is possible that it is due to the presence of the multilayers that compose them.
    [0037] PET membranes are completely impervious to IgG. EXAMPLE 4 Implantation Assays for Semipermeable Membranes The membranes are implanted in the peritoneal cavity of healthy Wistar rats, according to the protocol described in Example 3 of WO 2012/01733.
    [0038] However, the sampling protocol has been modified and the samples are taken as follows: Tissue samples Solutions used - 2.5% glutaraldehyde prepared in a fume hood from glutaraldehyde 25% (Sigma, ref: G5882 - 10x10 mL ) diluted tenth in ultrapure water - PBS (Reference: GIBCO - 14190-094). Pre-filled pot with 4% paraformaldehyde (Labonord, ref: PFFOR0060AF59001) The membranes tested are the PET membranes according to the invention (multilayers) and the PC membranes of the prior art, having undergone or not a surface treatment for Heparin, EC and HPMC are deposited. The results are shown in Figure 3: it is observed that the surface treatment with heparin reduces fibrosis and cellular infiltration (black arrows). and increases vascularization (*) for both types of membrane. Example 5 Islet glucose stimulation test across the membrane a) Isolation of pancreatic islets from rats Animals used The animals used are male Wistar rats of 250-300 g (Janvier laboratory, Genes St. Ile, France). The rats are housed in standard collective cages at a temperature of 23 ± 1 ° C, a humidity of 55 ± 3% and with a cycle of 12 hours of light and 12 hours in the dark. Food SAFE-A04 (Villemoisson-sur-Orge, France) and water are available ad libitum. Animal experiments are carried out in compliance with the European Directive 2010/63 / EU. Pancreas removal The animal is anesthetized with a mixture of Imalgene 1000® (Active ingredient: Ketamine, Centravet ref: IMA004) supplemented with 2.7mL of Rompun® (Active ingredient: Xylazine 2%, Centravet ref: ROM001) injected intraperitoneally at a dose of 100 μL / 100 g body weight. After verifying the absence of reflexes of the animal, it is placed in the supine position. A laparotomy is then performed and the bile duct is ligated at its duodenal mouth. It is then catheterized at the level of its hepatic mouth and the animal is sacrificed by exsanguination. Through the inserted catheter, 10 ml of collagenase type XI (Sigma, ref: C7657) at 1 mg / ml at 4 ° C. are then injected into the pancreas.
    [0039] The pancreas is then removed and placed in a 50 mL Falcon tube containing 3.75 mL of sterile "infusion solution". This solution consists of 500 mL HBSS (Hanks Balanced Salt Solution, LONZA, ref: BE10-5277F), 2.1mL 8.4% Sodium Bicarbonate, 1.175mL 1M Calcium Chloride and 12.5mL of HEPES 1M. To limit the action of the enzyme during the sampling, the tubes containing the pancreas are kept in the ice. Digestion As soon as the pancreas is removed, the tube is placed for 10 minutes in a water bath at 37 ° C. It is then stirred strongly for a few seconds so that the tissue is well dissociated. It is then completed with a cold wash solution. The washing solution is composed of M199 (Sigma, ref: M0393-50L) supplemented with 0.35 g / l of sodium bicarbonate (Sigma, ref: S5761), of 10% of fetal calf serum (SVF, Lonza, ref DE14-801F) and 1% Anti-Mycotic Antibiotic (AB / AM, Fisher, ref: W3473M).
    [0040] The contents of the tube are filtered on inserts (Corning Netwells inserts, Sigma, ref: CLS3480) and the filtrate is transferred into a 200mL Corning type tube which is centrifuged for 1 minute at 1200 rpm at 4 ° C. The supernatant is then removed and the pellet resuspended with cold wash solution and transferred to a 50mL Falcon tube. After centrifuging for 1 minute at 1200 rpm at 4 ° C, a maximum of supernatant is removed before proceeding to the purification step. Purification Purification of the islets is carried out using a discontinuous Ficoll gradient (Fisher, ref: BP525-500) which is composed of 3 different solutions of different density prepared in the laboratory: 1,108 (Ficoll 1): 1,108, 1,096 (Ficoll 2): 1.096 and 1.069 (Ficoll 3): 1.069. The cell pellet is resuspended in 12 ml of Ficoll 1 and 10 ml of Ficoll 2 and then of Ficoll 3 are added delicately on top. Finally 5 ml of PBS (Fisher, ref: 20012-019) are deposited on the Ficoll 3. The whole is centrifuged for 4 minutes at 400 rpm at 4 ° C. and then for 12 minutes at 2000 rpm at 4 ° C. vs. In order not to disturb the gradients, the braking and acceleration speeds of the centrifuge are set to a minimum. The islets are recovered at the interphase between Ficoll 2 and Ficoll 3, and then washed three times in a cold wash solution in order to remove all traces of Ficoll. Culture The islets are cultured in M199 medium (Gibco, ref: 22340-020) containing 10% FCS (Lonza, ref: DE14-801F) and 1% ABAM (Fisher, ref: W3473M) in flasks of 25cm2 untreated (Dutscher, ref: 690195), for 24 hours at 37 ° C and in a humid atmosphere at 5% CO2. b) Stimulation test Ten rat islands are placed in inserts (sort of cylinders) at one end of which is fixed the PET membrane. This membrane is oriented in such a way that the nanoporous membrane (having pores of internal diameter between 10 and 50 nm and selective for molecules up to 150 kDa) is inside the insert, in contact with the islands of rat, the layer having the pore diameter of between 400 and 600 nm being oriented towards the outside of the insert. The insert contains 400 μl of Krebs solution at 10% FCS and 2.5 mM glucose. The inserts thus filled are placed in 24-well plate wells containing 1 ml Krebs Krebs solution containing 10% FCS and 25 mM glucose. The 24-well plate is then incubated at 37 ° C and media samples in the well are taken at 1 h, 2 h, 4 h, 6 h, 8 h and 24 h. Insulin is then assayed in the samples by the ELISA method (Mercodia, ref: 125001). The islets are also removed and placed in 50 μl of lysis buffer (ThermoScientific, ref: 78501), supplemented with a protease inhibitor (ThermoScientific, ref: 78441), in order to extract the total proteins. The extraction is carried out by placing the tubes on ice for 30 min by regularly vortexing the samples. The total protein content of the islets is determined by a Bradford assay and serves to normalize insulin secretion between the different islet cultures. EXAMPLE 7 Implantation and explantation of MAILPAN® in pigs An encapsulation chamber (MAILPAN®, for MAcro-encapsulation of PANcreative ILots) is prepared according to the method described in WO 2012/010767. Two semipermeable membranes are welded to each other.
    [0041] This encapsulation chamber has an inner layer, as well as connectors. Anesthesia Premedication is systematic prior to any anesthesia and consists of intramuscular administration of a combination of a butyrophenone azaperone (Stresnil *) 2 mg / kg and ketamine (Imalgene *) 10 mg / kg. The general anesthesia is performed according to the protocol described below: - The animals are brought premedicated to the operating room and installed on operating table in lateral decubitus. 15 - A peripheral vein is catheterized (G 22) on one ear and its permeability ensured by rinsing with 0.9% NaCl solution. Induction is carried out by intravenous injection of a hypnotic (thiopental 5 mg / kg or propofol 4 mg / kg) and a curarizing agent (pancuronium 0.1 mg / kg). It is immediately followed by orotracheal intubation (Portex Blue Line 20, low pressure balloon, 6 gauge for a subject of 25 to 35 kg) and pulmonary ventilation using a semi-closed circular system connected to a respirator operating in controlled pressure mode. The ventilation (Fi02 = 0.5 FiN2O = 0.5) is adjusted to maintain ETCO2 between 35 and 45 mmHG. The respirator is a state-of-the-art human device (GE Avance *, Aisys * or 25 Aespire *) with current flow, pressure and volume controls. - The maintenance of the anesthesia is ensured in the inhalation mode by isoflurane (inspired fraction = 2 vol%) with a flow of fresh gas of 2 L / min of a mixture 02 / N20 50% / 50% serving as a carrier gas. If necessary, the administration of subsequent doses of pancuronium ensures optimum myorelaxation under the guise of deep inhalation anesthesia (MAC of isoflurane in pure O2 = 1.15 vol% and MAC of N20 = 110 vol %). Implantation of MAILPAN® After anesthesia of the animal, the abdomen of the sleeping animals is sanitized with 70% ethanol and then with Betadine (taking care not to generate hypothermia) and is shaved using a scalpel blade at the level of the abdomen. A longitudinal incision of about 10 to 15 centimeters from the cutaneous and muscular planes to the peritoneum is made in the middle of the open area. After a median laparotomy, the prototype is implanted after being filled with physiological saline extra-peritoneal and fixed to the wall with yarn (Vicryl 2/0). The two MAILPAN catheters (one used for filling and the other for emptying the islets in the MAILPAN, in a period subsequent to implantation) are connected to two injection chambers placed subcutaneously before ligation. peritoneum by sinusoidal movement, using 4-0 suture. At the end of the surgery, the wounds are infiltrated with Naropein, and fentanyl will be administered in IV before waking the animal. Granular fentanyl is administered peroperatively with the food ration, at a rate of 2 mg / kg. Explanation of MAILPAN® MAILPAN devices are explanted at 15 days and 60 days post-transplantation under general anesthesia to evaluate the mechanical strength of MAILPAN, its sterility and its biocompatibility (vascularization at the surface, absence of inflammation, absence fibrosis and inflammation on the surrounding tissues). Thus tissue samples surrounding the MAILPAN are made at each explantation of the device for subsequent histological tests. Pigs are sacrificed after each explantation by intravenous injection of KCI. The tissue samples are taken under the same conditions as for the rat (see Example 5: same solutions for tissues and membranes, same analyzes carried out). Example 8: Membrane analyzes by scanning electron microscopy After sampling, the membranes are rinsed in ultrapure water and fixed for 24 to 48 h at 4 ° C in glutaraldehyde (Sigma, ref: G5882) diluted to 2.5%. The fixed membranes are then rinsed for 10 minutes in ultrapure water.
    [0042] The samples are then dehydrated by successive baths of ethanol: two 10-minute baths in 50% ethanol, a 25-minute bath in 70% ethanol and then a 10-minute bath of water. 95% ethanol and finally two 10-minute baths in 100% ethanol. In order to completely eliminate traces of water that may still be present in the samples, a 2-minute incubation is carried out in Hexamethyl disilaxane (HMDS) (Sigma, ref: 440191). After drying in the open air, the samples are then glued flat on pads (Deltamicroscopies, ref: 75220), using conductive carbon glue 10 (Deltamicroscopies, ref: 76510). Once the glue has solidified, the samples are metallized by depositing a thin layer of gold-palladium and then carbon. The observation is carried out on a scanning electron microscope (SEM) with a field effect (Hitachi S800) (in vitro imaging platform of the Neurochemistry Center of Strasbourg) at a voltage of 5 KV, which makes it possible to obtain a good resolution without damaging the samples. Results It is observed that the device made with PC membranes has wide tears (Figure 4). On the other hand, the device made with the multilayer PET membranes does not present, in turn, any macroscopic damage. The latter were thus analyzed by scanning electron microscopy which showed no microcracks (Figure 4).
    [0043] It thus appears that the membranes according to the invention allow diffusion similar to that observed for the membranes of the prior art and have the property of semi-permeability (blocking IgG, and other proteins of the immune system). These membranes have a much better resistance when they are used in a bioartificial organ implanted in vivo.
    权利要求:
    Claims (17)
    [0001]
    REVENDICATIONS1. Chamber for encapsulating secretory cells producing at least one substance of therapeutic interest, comprising a closed envelope and made in a semi-permeable membrane, delimiting a space capable of containing the secretory cells producing at least one substance of therapeutic interest, characterized in that said membrane comprises at least one porous biocompatible polymer layer, and a biocompatible nonwoven polymer layer.
    [0002]
    2. encapsulation chamber according to claim 1, characterized in that said membrane comprises a layer of biocompatible nonwoven polymer located between two layers of porous biocompatible polymers.
    [0003]
    3. encapsulation chamber according to claim 1 or 2, characterized in that said nonwoven polymer is selected from polycarbonate (PC), polyester, polyethylenimine, polypropylene (PP), polyethylene terephthalate (PET), polyvinyl chloride (PVC), polyamide, and polyethylene (PE).
    [0004]
    4. encapsulation chamber according to one of claims 1 to 3, characterized in that said porous biocompatible polymer of at least one layer is selected from polycarbonate (PC), polyester, polyethylenimine, polypropylene (PP) , polyethylene terephthalate (PET), polyvinyl chloride (PVC), polyamide, and polyethylene (PE).
    [0005]
    5. encapsulation chamber according to one of claims 1 to 4, characterized in that at least one or both layers of porous biocompatible polymer are rendered hydrophilic by physical or chemical surface modification, and covered by at least one hydrophilic polymer.
    [0006]
    6. encapsulation chamber according to one of claims 1 to 5, characterized in that the porous biocompatible polymer layer or one of two layers of porous biocompatible polymers has a pore density of between 106 pores / cm2 and 1011 pores / cm2.35
    [0007]
    7. encapsulation chamber according to one of claims 1 to 6, characterized in that the total thickness of the membrane is between 45 pm and 200 pm.
    [0008]
    8. encapsulation chamber according to one of claims 1 to 7, characterized in that, when said membrane has a single layer of porous biocompatible polymer, the layer has a thickness between 5 pm and 100 pm, and when said membrane has two layers of porous biocompatible polymer, the thickness of one of the biocompatible polymer layers is between 5 and 40 μm, and the thickness of the other layer of biocompatible polymer is between 25 and 100 μm.
    [0009]
    9. encapsulation chamber according to one of claims 1 to 8, characterized in that when said membrane has a single layer of porous biocompatible polymer, the internal diameter of the pores present on the biocompatible polymer layer is between 5 and 100 nm, and most preferably between 5 and 50 nm, and in that when said membrane has two layers of porous biocompatible polymer, the internal diameter of the pores present on one of the biocompatible polymer layers is between 5 and 100 nm, the internal diameter of the pores present on the other layer of biocompatible polymer is between 100 and 2000 nm, preferably between 200 and 1000 nm.
    [0010]
    10. Encapsulation chamber according to one of claims 5 to 9, characterized in that at least one layer containing a hydrophilic polymer contains at least one biologically active molecule.
    [0011]
    11. encapsulation chamber according to one of claims 1 to 10, also comprising a biocompatible sheet contained in said envelope, said web optionally having protrusions on its surface.
    [0012]
    12. Encapsulation chamber according to one of claims 1 to 11, characterized in that said membrane comprises two layers of biocompatible polymers, the outer layer to the casing having pores with an internal diameter of between 100 and 2000 nm, and the inner layer of the casing having pores with an internal diameter of between 5 and 100 nm.
    [0013]
    13. Encapsulation chamber according to one of claims 1 to 12, characterized in that it comprises at least one connector for establishing a communication between the outside and inside of the envelope.
    [0014]
    14. Encapsulation chamber according to one of claims 1 to 13, characterized in that it is circular and has a diameter of between 3 cm and 20 cm.
    [0015]
    15. A bioartificial organ characterized in that it comprises at least one encapsulation chamber according to one of claims 1 to 13, wherein there are present secretory cells producing at least one substance of therapeutic interest.
    [0016]
    16. Bioartificial organ according to claim 14, characterized in that it is a bioartificial pancreas containing insulin-secreting cells or islets of Langerhans.
    [0017]
    17. Process for obtaining an encapsulation chamber according to one of claims 1 to 15, comprising a step of heat sealing of one or two membranes comprising at least one layer of porous biocompatible polymer, and a layer of polymer. biocompatible nonwoven, so as to form a closed pocket for receiving the secretory cells producing at least one substance of therapeutic interest.
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    同族专利:
    公开号 | 公开日
    CN105813630A|2016-07-27|
    CN105813630B|2019-11-08|
    EP3079658B1|2020-02-05|
    JP6424226B2|2018-11-14|
    JP2017502008A|2017-01-19|
    US20160310541A1|2016-10-27|
    EP3079658A1|2016-10-19|
    CA2932048A1|2015-06-18|
    US10022404B2|2018-07-17|
    US20180311282A1|2018-11-01|
    DK3079658T3|2020-04-27|
    AU2014363694B2|2020-03-05|
    AU2014363694A1|2016-06-16|
    US10668106B2|2020-06-02|
    WO2015086550A1|2015-06-18|
    ES2778044T3|2020-08-07|
    FR3014316B1|2017-01-20|
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    法律状态:
    2015-11-23| PLFP| Fee payment|Year of fee payment: 3 |
    2016-08-19| CA| Change of address|Effective date: 20160720 |
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    2021-11-18| PLFP| Fee payment|Year of fee payment: 9 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1362342A|FR3014316B1|2013-12-10|2013-12-10|BIOARTIFICIAL ORGAN|FR1362342A| FR3014316B1|2013-12-10|2013-12-10|BIOARTIFICIAL ORGAN|
    ES14809630T| ES2778044T3|2013-12-10|2014-12-09|A chamber to encapsulate secretory cells|
    US15/103,108| US10022404B2|2013-12-10|2014-12-09|Chamber for encapsulating secreting cells|
    PCT/EP2014/076955| WO2015086550A1|2013-12-10|2014-12-09|A chamber for encapsulating secreting cells|
    JP2016539148A| JP6424226B2|2013-12-10|2014-12-09|Chamber for encapsulating secretory cells|
    CA2932048A| CA2932048A1|2013-12-10|2014-12-09|A chamber for encapsulating secreting cells|
    CN201480066624.1A| CN105813630B|2013-12-10|2014-12-09|For encapsulating the chamber of secretory cell|
    AU2014363694A| AU2014363694B2|2013-12-10|2014-12-09|A chamber for encapsulating secreting cells|
    DK14809630.8T| DK3079658T3|2013-12-10|2014-12-09|ROOMS TO ENCOURAGE SECURING CELLS|
    EP14809630.8A| EP3079658B1|2013-12-10|2014-12-09|A chamber for encapsulating secreting cells|
    US16/031,040| US10668106B2|2013-12-10|2018-07-10|Chamber for encapsulating secreting cells|
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