US2019343988A1PendingUtilityA1
Acellular tissue matrix compositions for tissue repair
Est. expiryJul 10, 2027(~1 yrs left)· nominal 20-yr term from priority
A61P 43/00A61L 2420/02A61L 27/3633A61L 31/005A61L 27/16A61L 27/362A61L 27/36A61L 27/18A61L 2400/18C08L 89/06
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Claims
Abstract
The invention provides tissue repair compositions and methods of making the tissue repair compositions. Also featured are methods of treatment using the tissue repair compositions and articles of manufacture that include the tissue repair compositions.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of treatment, comprising:
selecting a biocompatible mesh composition, comprising:
a polypropylene sheet substrate; and
a biocompatible coating surrounding the sheet substrate, wherein the coating comprises a dried group of particulate acellular tissue matrix (ATM) particles, wherein the ATM particles comprise acid-swollen intact ATM that retains biological functions provided by undenatured collagenous proteins and non-collagenous molecules;
selecting an anatomical site; and implanting the mesh composition at the anatomical site.
2 . The method of claim 1 , wherein the anatomical site comprises a hernia site.
3 . The method of claim 1 , wherein the anatomical site comprises an abdominal wall defect.
4 . The method of claim 1 , wherein the ATM comprises dermal ATM.
5 . The method of claim 1 , wherein the ATM comprises ATM derived from at least one of fascia, pericardial tissue, dura, umbilical cord tissue, placental tissue, cardiac valve tissue, ligament tissue, tendon tissue, arterial tissue, venous tissue, neural connective tissue, urinary bladder tissue, ureter tissue, and intestinal tissue.
6 . The method of claim 1 , wherein the ATM is derived from human tissue.
7 . The method of claim 1 , wherein the ATM is derived from non-human mammalian tissue.
8 . The method of claim 7 , wherein the non-human mammalian tissue is porcine.
9 . The method of claim 7 , wherein the tissue is from a non-human mammal that is genetically engineered to lack expression of α-1,3-galactosyl epitopes.
10 . The method of claim 9 , wherein the non-human mammal lacks a functional α-1,3-galactosyltransferase gene.
11 . The method of claim 1 , wherein the polypropylene sheet is a mesh.
12 . The method of claim 11 , wherein the polypropylene sheet comprises polypropylene monofilament.Cited by (0)
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