US2023256137A1PendingUtilityA1
Encapsulation of pancreatic cells derived from human pluripotent stem cells
Est. expiryNov 14, 2028(~2.3 yrs left)· nominal 20-yr term from priority
A01N 1/125A61L 27/3804A61K 35/39C12N 5/0676A61L 27/14A61L 27/54A01N 1/0221A61K 38/28A61M 5/00A61F 2/022A61L 27/50A61L 27/56C12N 5/0678A61M 31/002A61M 31/00A61K 2035/126C12N 2501/115C12N 2501/117C12N 2501/119C12N 2501/16C12N 2501/19C12N 2501/385C12N 2501/41C12N 2501/415C12N 2506/02A61L 2300/64A61P 5/50A61P 3/10A61L 2300/62A61L 2300/252A61M 2202/07A61M 2205/04
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Claims
Abstract
The present invention relates to methods for encapsulating pancreatic progenitors in a biocompatible semi-permeable encapsulating device. The present invention also relates to production of human insulin in a mammal in response to glucose stimulation.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A perforated semi-permeable device comprising
human pancreatic endocrine cells within a semi-permeable membrane comprising a synthetic material, wherein the synthetic material is polysulfone (PST), nano-fiber mats, polyimide, tetrafluoroethylene/polytetrafluoroethylene (PTFE), expanded polytetrafluoroethylene (ePTFE), polyacrylonitrile, polyethersulfone, acrylic resin, cellulose acetate, cellulose nitrate, polyamide, or hydroxylpropyl methyl cellulose (HPMC); a cell encapsulation chamber; and at least one seal that is within the cell encapsulation chamber, wherein the at least one seal within the cell encapsulation chamber does not increase the surface area of the cell encapsulation chamber relative to the absence of the at least one seal.
2 . The device of claim 1 , wherein the device is implanted into a mammalian host.
3 . The device of claim 2 , wherein the mammalian host is immuno-suppressed.
4 . The device of claim 1 , wherein the device comprises more than one cell encapsulation chamber.
5 . The device of claim 1 , wherein the device is refillable.
6 . The device of claim 1 , wherein the device is vascularized on the exterior and interior of the device.
7 . The device of claim 1 , wherein the synthetic material is PTFE.
8 . The device of claim 1 , wherein the synthetic material is ePTFE.
9 . A perforated semi-permeable device comprising
a human PDX1-positive pancreatic endoderm cell populations within a semi-permeable membrane consisting of a synthetic material, wherein the synthetic material is polysulfone (PSF), nano-fiber mats, polyimide, tetrafluoroethylene/polytetrafluoroethylene (PTFE), expanded polytetrafluoroethylene (ePTFE), polyacrylonitrile, polyethersulfone, acrylic resin, cellulose acetate, cellulose nitrate, polyamide, or hydroxylpropyl methyl cellulose (HPMC); a cell encapsulation chamber; and at least one seal that is within the cell encapsulation chamber, wherein the at least one seal within the cell encapsulation chamber does not increase the surface area of the cell encapsulation chamber relative to the absence of the at least one seal.
10 . The device of claim 9 , wherein the device is implanted into a mammalian host.
11 . The device of claim 10 , wherein the mammalian host is immuno-suppressed.
12 . The device of claim 9 , wherein the device comprises more than one cell encapsulation chamber.
13 . The device of claim 9 , wherein the device is refillable.
14 . The device of claim 9 , wherein the device is vascularized on the exterior and interior of the device.
15 . The device of claim 9 , wherein the synthetic material is PTFE.
16 . The device of claim 9 , wherein the synthetic material is ePTFE.
17 . A perforated semi-permeable device comprising
a human pancreatic endocrine cell population within a semi-permeable membrane consisting of expanded polytetrafluoroethylene (ePTFE); a cell encapsulation chamber; and at least one seal that is within the cell encapsulation chamber, wherein the at least one seal within the cell encapsulation chamber does not increase the surface area of the cell encapsulation chamber relative to the absence of the at least one seal.
18 . The device of claim 17 , wherein the device comprises more than one cell encapsulation chamber.
19 . The device of claim 17 , wherein the device is refillable.
20 . The device of claim 17 , wherein the device is vascularized on the exterior and interior of the device.Cited by (0)
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