Methods of manufacture of immunocompatible chorionic membrane products
US-11638725-B2 · May 2, 2023 · US
US12558377B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12558377-B2 |
| Application number | US-202217969461-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 19, 2022 |
| Priority date | Feb 18, 2010 |
| Publication date | Feb 24, 2026 |
| Grant date | Feb 24, 2026 |
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Provided herein is a placental product comprising an immunocompatible chorionic membrane. Such placental products can be cryopreserved and contain viable therapeutic cells after thawing. The placental product of the present invention is useful in treating a patient with a tissue injury (e.g. wound or burn) by applying the placental product to the injury. Similar application is useful with ligament and tendon repair and for engraftment procedures such as bone engraftment.
Opening claim text (preview).
The invention claimed is: 1 . A method of treating a skin wound, the method comprising topically applying to the skin wound a placental product comprising a chorionic membrane, wherein the chorionic membrane is substantially free of trophoblasts, and wherein the chorionic membrane comprises: one or more matrix metalloproteases (MMPs) comprising MMP-9 and TIMP-1, wherein a ratio of MMP-9 to TIMP-1 is from about 7-10 to 1; and viable cells native to the chorionic membrane, wherein at least 70% of the cells native to the chorionic membrane are viable, and wherein the viable cells comprise mesenchymal stem cells (MSCs) and fibroblasts wherein the placental product is cryopreserved, and wherein the method further comprises thawing the placental product prior to applying the placental product to the skin wound. 2 . The method of claim 1 , wherein the skin wound is selected from a chronic wound, an ulcer, a diabetic ulcer, a foot ulcer, a diabetic foot ulcer, a venous ulcer, a venous leg ulcer, a leg ulcer, a pressure ulcer, a burn, a thermal burn, a chemical burn, a partial thickness burn, or a full thickness burn. 3 . The method of claim 1 , wherein the skin wound is selected from a laceration, a scrape, an incision, a puncture, a wound caused by a projectile, an epidermal wound, a dermal wound, a surgical wound, an acute wound, a congenital wound, a toxic epidermal necrolysis, an epidermolysis bullosa, or a pyoderma gangrenosum. 4 . The method of claim 1 , wherein less than 5% of cells of the chorionic membrane are CD14+ macrophages. 5 . The method of claim 1 , wherein the chorionic membrane comprises one or more therapeutic factors native to the chorionic membrane. 6 . The method of claim 1 , wherein the chorionic membrane comprises extracellular matrix native to the chorionic membrane. 7 . The method of claim 1 , wherein the chorionic membrane is immunocompatible. 8 . The method of claim 1 , wherein the placental product further comprises a cryopreservation medium. 9 . The method of claim 1 , wherein the placental product further comprises an amniotic membrane wherein the amniotic membrane comprises a layer of amniotic epithelial cells.
Basic fibroblast growth factor (bFGF, FGF-2) · CPC title
Cells from extra-embryonic tissues, e.g. placenta, amnion, yolk sac, Wharton's jelly · CPC title
from animals; from humans {(A61K38/553, A61K38/556 take precedence)} · CPC title
Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin, cold insoluble globulin [CIG] · CPC title
Transforming growth factor [TGF] · CPC title
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