US2015050251A1PendingUtilityA1
Cosmetic Preparations
Est. expiryJan 18, 2026(expired)· nominal 20-yr term from priority
C12N 5/0629A61K 35/12C12N 2502/02A61K 35/50C12N 5/0605A61P 17/02C12N 2501/11
66
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Claims
Abstract
The invention is directed to methods for the treatment of wounds. Such methods utilize novel compositions, including but not limited to amnion-derived multipotent cells (herein referred to as AMP cells), conditioned media derived therefrom (herein referred to as amnion-derived cellular cytokine suspension or ACCS), cell lysates derived therefrom, cell products derived therefrom, each alone or in combination.
Claims
exact text as granted — not AI-modified1 - 17 . (canceled)
18 . A cosmetic preparation consisting of:
a) conditioned medium, wherein the conditioned medium is made by a method comprising the steps of
i) obtaining a placenta and isolating an amnion from the placenta,
ii) enzymatically releasing amnion-derived epithelial cells from the amnion,
iii) collecting the released amnion-derived epithelial cells, and
iv) culturing the collected amnion-derived epithelial cells of step (c) in basal culture medium that is supplemented with human serum albumin and recombinant human EGF; and
b) a gelling agent.
19 . The cosmetic preparation of claim 18 wherein the gelling agent is selected from the group consisting of xanthan, guar gum, starches, alginates, crosslinked polymeric gelling agents and partially neutralized 2-acrylamido-2-methylpropanesulfonic acid polymers.
20 . The cosmetic preparation of claim 18 wherein the basal medium is IMDM.
21 . The cosmetic preparation of claim 18 wherein the IMDM is supplemented with 0.5% human serum albumin.
22 . The cosmetic preparation of claim 18 wherein the recombinant human EGF is at a concentration of 10 ng/mL of culture medium.
23 . The cosmetic preparation of claim 18 wherein the substantially purified population of cultured amnion-derived epithelial cells, the basal medium, and all medium supplements are free of xeno-contamination.Cited by (0)
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