US2012209381A1PendingUtilityA1
Bioerodible matrix for tissue involvement
Est. expiryMar 27, 2029(~2.7 yrs left)· nominal 20-yr term from priority
A61L 27/3886A61L 27/56A61L 27/3834A61L 27/3804A61L 2430/04A61L 27/18A61L 2420/06A61F 2/12A61L 27/34A61L 27/58A61L 27/3604A61P 17/00
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Claims
Abstract
Disclosed herein are polyurethane polymer matrices with a porosity of from about 20 microns to about 90 microns that are useful in promoting closure and protection of incision sites; supporting the lower pole position of breast implants; and providing a partial or complete covering of breast implants to provide a beneficial interface with host tissue and to reduce the potential for malpositioning or capsular contracture. The disclosed matrices can be seeded with mammalian cells.
Claims
exact text as granted — not AI-modified1 . A method of augmenting or reconstructing a breast of a patient, the method comprising:
implanting a matrix in a breast of a patient, the matrix comprising a biodegradable polymer material admixed with an active cell population formed from processed lipoaspirate.
2 . The method of claim 1 wherein the polymer material is a hydrogel.
3 . The method of claim 2 wherein the hydrogel is selected from the group of hydrogels consisting of alginate, coral, agarose, fibrin, collagen, cartilage, hydroxyapatite, calcium phosphate, polylactic acid (PLA), polyglycolic acid (PGA) polylacticglycolic acid (PLGA), chitosan, and polyethylene glycol-based polymers.
4 . The method of claim 3 wherein the hydrogel is a polyethylene glycol-based polymer.
5 . The method of claim 4 wherein the polyethylene glycol-based polymer is one of a polyethylene glycol diacrylate, polyethylene glycol dimethacrylate or a mixture thereof.
6 . The method of claim 3 wherein the hydrogel comprises collagen.
7 . The method of claim 1 wherein the active cell population comprises adipose tissue.
8 . The method of claim 1 wherein the active cell population consists essentially of adipose tissue.
9 . The method of claim 1 wherein the matrix is implanted so as to support a lower pole position of a breast implant.
10 . The method of claim 1 wherein the matrix is structured to promote tissue ingrowth.
11 . An implantable composition useful for augmenting or reconstructing a breast of a patient, the composition comprising a matrix comprising a biodegradable polymer material admixed with an active cell population formed from processed lipoaspirate.
12 . The composition of claim 11 wherein the polymer material is a hydrogel.
13 . The composition of claim 12 wherein the hydrogel is selected from the group of hydrogels consisting of alginate, coral, agarose, fibrin, collagen, cartilage, hydroxyapatite, calcium phosphate, polylactic acid (PLA), polyglycolic acid (PGA) polylacticglycolic acid (PLGA), chitosan, and polyethylene glycol-based polymers.
14 . The composition of claim 13 wherein the hydrogel is a polyethylene glycol-based polymer.
15 . The composition of claim 14 wherein the polyethylene glycol-based polymer is one of a polyethylene glycol diacrylate, polyethylene glycol dimethacrylate or a mixture thereof.
16 . The composition of claim 13 wherein the hydrogel comprises collagen.
17 . The composition of claim 11 wherein the active cell population consists essentially of adipose tissue.
18 . The composition of claim 11 wherein the matrix is structured to support a lower pole position of a breast implant.
19 . The composition of claim 11 wherein the matrix is structured to promote tissue ingrowth.Cited by (0)
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