Polymeric treatment compositions
US-10588923-B2 · Mar 17, 2020 · US
US12376863B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12376863-B2 |
| Application number | US-202418587736-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 26, 2024 |
| Priority date | Aug 26, 2016 |
| Publication date | Aug 5, 2025 |
| Grant date | Aug 5, 2025 |
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Described herein are compositions comprising, a polymer, a non-physiological solution; and a visualization agent; wherein the polymer is soluble in the non-physiological solution and insoluble at physiological conditions. Methods of preparing the compositions are disclosed as well as methods of using these compositions to treat vascular conditions.
Opening claim text (preview).
We claim: 1. A method of treating a vascular condition comprising: administering a composition by injection into a vessel; wherein the vessel is at physiological conditions; wherein the composition includes a biocompatible polymer, a solvent, and a visualization agent; wherein the biocompatible polymer is soluble in the solvent and insoluble at physiological conditions; and wherein the composition has a viscosity less than or equal to 15 centistokes. 2. The method of claim 1 , wherein the visualization agent is integrated into or associated with the biocompatible polymer. 3. The method of claim 2 , wherein the visualization agent is triiodophenol-lactide-glycolide (TIP). 4. The method of claim 1 , wherein physiological conditions include contact with a physiological fluid including blood, urine, saliva, mucous, vaginal fluid, seminal fluid, cerebral spinal fluid, sweat, plasma, bile, stomach acid, intestinal fluids, or a combination thereof. 5. The method of claim 4 , wherein the physiological fluid has a pH of about 7.0. 6. The method of claim 4 , wherein the physiological fluid has a pH of between about 7.0 and about 7.8. 7. The method of claim 1 , wherein the solvent is a water miscible organic solvent. 8. The method of claim 1 , wherein the biocompatible polymer comprises an amine and the amine includes an amino group which is about 90% positively charged at pH 5 and about 10% positively charged at pH 7. 9. The method of claim 1 , wherein the biocompatible polymer includes hydroxyethylmethacrylate (HEMA), lactide, glycolide, polyvinyl pyridine (PVP), 1-vinylimidazole, aminoethyl methacrylate (AEMA), 4-vinylpyridine, alkylalkylacrylate, alkylacrylate, acrylate, styrene, polyvinyl alcohol (PVA), acrylamide, ethylene glycol, or combinations thereof. 10. The method of claim 1 , wherein the biocompatible polymer includes about 60% w/w HEMA and the visualization agent includes about 40% w/w TIP. 11. The method of claim 1 , wherein the biocompatible polymer includes about 15% w/w HEMA and the visualization agent includes about 85% w/w TIP. 12. The method of claim 1 , wherein the solvent is water or a co-solvent of water and dimethyl sulfoxide (DMSO). 13. The method of claim 1 , further comprising aminopropylmethacrylamide. 14. The method of claim 13 , wherein the composition has a viscosity of less than about 14 centistokes. 15. The method of claim 1 , wherein the composition has a viscosity of less than about 14 centistokes. 16. The method of claim 1 , wherein the biocompatible polymer, together with the visualization agent, forms a cohesive precipitate when insoluble at physiological conditions, and wherein the cohesive precipitate is more cohesive than a precipitate formed from an embolic composition comprising N-butyl-2-cyanoacrylate. 17. The method of claim 1 , wherein the biocompatible polymer is formed from hydroxyethylmethacrylate monomers and aromatic amine monomers. 18. The method of claim 1 , wherein: the biocompatible polymer comprises HEMA; the solvent comprises a co-solvent of water and DMSO; and the visualization agent comprises TIP. 19. The method of claim 1 , wherein the composition has a viscosity of less than about 13 centistokes. 20. The composition of claim 1 , wherein the composition has a viscosity of less than about 12 centistokes.
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