Tumor suppression using human placental perfusate and human placenta-derived intermediate natural killer cells
US-9216200-B2 · Dec 22, 2015 · US
US2021093675A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2021093675-A1 |
| Application number | US-202017106916-A |
| Country | US |
| Kind code | A1 |
| Filing date | Nov 30, 2020 |
| Priority date | May 18, 2018 |
| Publication date | Apr 1, 2021 |
| Grant date | — |
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The present disclosure provides methods of treating defects such as wrinkles or scars via a subdermal injection of placental tissue components. It also provides placental tissue compositions maintained within the barrel of a syringe, which may be for use in treating such defects.
Opening claim text (preview).
What is claimed is: 1 . A method of treating a defect in a patient by injecting a composition comprising placental tissue components at the site of the defect. 2 . The method of claim 1 , wherein the placental tissue components are particles, said particles comprising placental disc and at least one of amniotic membrane, chorionic membrane, and umbilical cord. 3 . The method of claim 2 , wherein the particles comprise placental disc and amniotic membrane. 4 . The method of claim 2 , wherein the particles comprise placental disc and chorionic membrane. 5 . The method of claim 2 , wherein the particles comprise placental disc, amniotic membrane, and chorionic membrane. 6 . The method of claim 2 , wherein the particles comprise placental disc and umbilical cord. 7 . The method of claim 2 , wherein the particles comprise placental disc, amniotic membrane, chorionic membrane, and umbilical cord. 8 . The method of claim 2 , wherein the particles are rehydrated. 9 . The method of claim 2 , wherein the placental tissue components are or were previously dehydrated by lyophilization. 10 . The method of claim 2 , wherein the particles are micronized. 11 . The method of claim 9 , wherein the particles are 50-150 μm. 12 . The method of claim 10 , wherein the particles are 70-150 μm. 13 . The method of any one of claims 1 - 11 , wherein the defect is selected from the group consisting of scars and wrinkles. 14 . The method of any one of claims 1 - 7 , wherein the placental tissue components comprise about 1-20% dehydrated amniotic membrane and/or chorionic membrane particles if present, about 1-30% dehydrated umbilical cord particles if present, and about 50-98% dehydrated placental disc particles, by weight. 15 . The method of any one of claims 1 - 7 , wherein the placental tissue components comprise about 11-30% non-placental disc components. 16 . The method of any one of claims 1 - 15 , wherein the composition is injected by a method selected from the group consisting of subdermal, intradermal, and dermal. 17 . The method of any one of claims 1 - 16 , wherein the method is not repeated at the site of the treated defect until at least six months after the prior injection. 18 . A placental tissue composition maintained within the barrel of a syringe. 19 . The composition of claim 18 , said placental tissue composition comprising particles of placental disc and at least one of amniotic membrane, chorionic membrane, and umbilical cord. 20 . The composition of claim 19 , wherein the particles comprise placental disc and amniotic membrane. 21 . The composition of claim 19 , wherein the particles comprise placental disc and chorionic membrane. 22 . The composition of claim 19 , wherein the particles comprise placental disc, amniotic membrane, and chorionic membrane. 23 . The composition of claim 19 , wherein the particles comprise placental disc and umbilical cord. 24 . The composition of claim 19 , wherein the particles comprise placental disc, amniotic membrane, chorionic membrane, and umbilical cord. 25 . The composition of claim 19 , wherein the particles are rehydrated. 26 . The composition of claim 19 , wherein the placental tissue components are or were previously dehydrated by lyophilization. 27 . The composition of claim 19 , wherein said particles are micronized. 28 . The composition of claim 27 , wherein said micronized dehydrated particles are 50-150 μm. 29 . The composition of claim 28 , wherein said micronized dehydrated particles are 70-150 μm. 30 . The composition of any one of claims 17 - 29 , wherein the placental tissue components comprise about 1-20% dehydrated amniotic membrane and/or chorionic membrane particles if present, about 1-30% dehydrated umbilical cord particles if present, and about 50-98% dehydrated placental disc particles, by weight. 31 . The composition of any one of claims 17 - 29 , wherein the placental tissue components comprise about 11-30% non-placental disc components 32 . The composition of any one of claims 17 - 31 , for use in treating a scar or a wrinkle.
Anti-ageing preparations · CPC title
for treating wounds, ulcers, burns, scars, keloids, or the like · CPC title
Reproductive organs; Embryos, Eggs · CPC title
lyophilised {, i.e. freeze-dried, solutions or dispersions (lyophilised products with subsequent particle size reduction A61K9/14; granules or pellets made by lyphilisation A61K9/1682; solid oral dosage forms made by lyophilisation A61K9/2095; lyophilisation additives A61K47/00)} · CPC title
Umbilical cord; Umbilical cord blood; Umbilical stem cells · CPC title
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