US2014010709A1PendingUtilityA1
Implantation Compositions for Use in Tissue Augmentation
Est. expiryFeb 6, 2026(expired)· nominal 20-yr term from priority
A61L 2/04A61L 27/20C08L 1/286A61K 47/38A61L 27/50A61K 47/10A61K 47/02A61L 2430/34A61L 2400/06A61F 2/20A61K 31/167A61L 27/54A61L 2430/00A61L 2103/05A61L 2/0023
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Abstract
A composition of matter and method for preparation of a tissue augmentation material. A polysaccharide gel composition is prepared with rheological properties selected for a particular selected application. The method includes preparing a polymeric polysaccharide in a buffer to create a polymer solution or gel suspending properties in the gel and selecting a rheology profile for the desired tissue region.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of preparing a tissue implant comprising:
(i) preparing an aqueous carboxymethylcellulose composition comprising between 2.3 wt. % and 2.9 wt. % carboxymethylcellulose; and (ii) sterilizing the composition of step (i) by autoclaving for about 3 minutes to about 12 minutes to prepare said tissue implant.
2 . The method of claim 1 , wherein the carboxymethylcellulose composition is in 25 mM to 100 mM phosphate buffer.
3 . The method of claim 2 , wherein the phosphate buffer has a pH from 7.2 to 8.0.
4 . The method of claim 3 , wherein the water content of the tissue implant is between 57.9% and 70.3%.
5 . The method of claim 1 , wherein the tissue implant is a midfacial tissue implant.
6 . A method of preparing a tissue implant comprising:
(i) preparing an aqueous carboxymethylcellulose composition comprising between 2.3 wt. % and 2.9 wt. % carboxymethylcellulose; (ii) adding calcium hydroxyapatite between 5 wt. % and 65 wt. % to form a composition; and (iii) sterilizing the composition of step (ii) by autoclaving for about 3 minutes to about 12 minutes to prepare said tissue implant.
7 . The method of claim 6 , wherein the carboxymethylcellulose composition is in 25 mM to 100 mM phosphate buffer.
8 . The method of claim 7 , wherein the phosphate buffer has a pH from 7.2 to 8.0.
9 . The method of claim 8 , wherein the water content of the tissue implant is between 57.9% and 70.3%.
10 . The method of claim 6 , wherein the tissue implant is a midfacial tissue implant.
11 . The method of claim 6 , wherein the calcium hydroxyapatite is added between 10 wt. % and 50 wt. %.
12 . The method of claim 6 , wherein the calcium hydroxyapatite is added between 30 wt. % and 45 wt. %.Join the waitlist — get patent alerts
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