Hydrogels comprising cell adhesive peptides and methods of use thereof
US-2024376438-A1 · Nov 14, 2024 · US
US9662422B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9662422-B2 |
| Application number | US-201414535033-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 6, 2014 |
| Priority date | Sep 6, 2011 |
| Publication date | May 30, 2017 |
| Grant date | May 30, 2017 |
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Hydrogels comprising a macromolecular matrix and water may be used to augment soft tissue of a human being, promote or support cell or tissue viability or proliferation, create space in tissue, and for other purposes. A macromolecular matrix may comprise a hyaluronic acid component crosslinked to a collagen component.
Opening claim text (preview).
What is claimed is: 1. A method of treating a soft tissue defect in a subject, the method comprising injecting a dermal filler composition into the subject's skin; wherein the composition comprises: (i) a hydrogel comprising: (a) water; and (b) a crosslinked macromolecular matrix comprising hyaluronic acid crosslinked to collagen via a plurality of crosslink units, wherein at least a portion of the crosslink units comprise an amide bond, and wherein the crosslinked macromolecular matrix has a weight ratio of the hyaluronic acid to the collagen of 1:1 to 7:1; wherein said hydrogel has a hyaluronic acid concentration of 6 mg/mL to 21 mg/mL, a collagen concentration of 3 mg/mL to 12 mg/mL, and a storage modulus value of between 850 Pa and 5,000 Pa; and (ii) a cellular component comprising cells obtained from adipose tissue; wherein the composition has a fat:hydrogel weight ratio of 1:1 to 5:1; and wherein the injection results in an increase in soft tissue volume and an increase in the volume retention, thereby treating the defect. 2. The method of claim 1 , wherein the hyaluronic acid is crosslinked to the collagen using a coupling agent, and wherein the coupling agent is not part of the crosslink unit. 3. The method of claim 1 , wherein the crosslinked macromolecular matrix has a weight ratio of the hyaluronic acid to the collagen of 1:1 to 2:1. 4. The method of claim 1 , wherein the hydrogel has a collagen concentration of greater than or equal to 6 mq/mL. 5. The method of claim 1 , wherein the hydrogel has a hyaluronic acid concentration of at least 9 mg/mL. 6. The method of claim 1 , wherein the hydrogel has a storage modulus value of between 1,000 Pa and 4,000 Pa. 7. The method of claim 1 , wherein the cellular component comprises adipocytes, adipose-derived stem cells, stromal vascular fraction cells, or a combination thereof. 8. The method of claim 1 , wherein the adipose tissue is human adipose tissue. 9. The method of claim 8 , wherein the adipose tissue is a lipoaspirate. 10. The method of claim 1 , wherein the adipose tissue comprises stem cells, progenitor cells, precursor cells or a combination thereof. 11. The method of claim 1 , wherein the hyaluronic acid is crosslinked to the collagen using hyaluronic acid having a molecular weight of 1,000,000 to 5,000,000 daltons. 12. The method of claim 1 , wherein the defect is a wrinkle. 13. The method of claim 1 , wherein the increase in the volume retention is a fat graft volume retention. 14. The method of claim 1 , wherein the hydrogel has a collagen concentration of 6 mg/mL, 8 mg/mL or 12 mg/mL. 15. The method of claim 1 , wherein the hydrogel has a hyaluronic acid concentration of 12 mg/mL and a collagen concentration of 6 mg/mL; a hyaluronic acid concentration of 12 mg/mL and a collagen concentration of 12 mg/mL; or a hyaluronic acid concentration of 16 mg/mL and a collagen concentration of 8 mg/mL. 16. The method of claim 1 , wherein the hyaluronic acid is crosslinked to the collagen using hyaluronic acid having a molecular weight of 1,000,000 daltons to 3,000,000 daltons. 17. The method of claim 1 , wherein the hydrogel has a hyaluronic acid concentration of at least 9 mg/mL and a collagen concentration of greater than or equal to 6 mg/mL. 18. The method of claim 1 , wherein the composition is injected intradermally. 19. The method of claim 1 , wherein the composition is injected subcutaneously.
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