IP Library › Granted Patent US 10,543,182
Granted Patent B2
US 10,543,182 · App. 16/137,332 · Granted Jan 28, 2020

Compositions, methods and devices for forming gel implants from injected liquids

Inventor: Chandrashekhar P. Pathak (Phoenix, AZ)
Assignee: Pathak Holdings LLC
A61K31/155A61K9/0021A61K9/0024A61K9/0048A61K9/1641A61K9/1647A61K9/1658A61K31/337A61K31/37A61K31/496A61K31/573A61K31/7036A61K31/727A61K41/0028A61K47/34A61L27/50A61L27/54A61M37/0015A61L2400/06A61M5/3015A61M37/0076A61M2037/0023A61M2205/3606A61M2205/3653C12Y304/21068C12Y304/24069
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,543,182
App. No.
16/137,332
Granted
Jan 28, 2020
Kind
B2
Abstract

A method of forming a gel implant in tissue can include: providing an injectable composition configured for thermoreversible gel formation at about 37° C.; injecting the injectable composition into the tissue at the rate of about 10-12000 injections per minute; and forming a thermoreversible gel at about 37° C. from the injected injectable composition so as to form the gel implant. The injecting can be at an amount of 1.0E-02 ml to 1.0E-16 ml per needle per injection. The injecting can form an implant with area greater than or equal to 5 mm 2 . The injecting can be at a depth of 10 microns to 5 mm. The injectable composition can include a visualization agent, drug or other agent.

Claims (29)

1. A method of forming a gel implant in a tissue, the method comprising:

providing an injectable composition configured for thermoreversible gel formation at about 37° C.;

injecting the injectable composition into the tissue at the rate of about 10-12000 injections per minute; and

forming a thermoreversible gel at about 37° C. from the injected injectable composition so as to form the gel implant.

2. The method according to claim 1 , wherein injectable composition comprises a biostable or biodegradable polymer dissolved in an aqueous solution.

3. The method according to claim 2 , wherein the biostable or biodegradable polymer shows a thermoreversible property in the aqueous solution and is selected from a group consisting of polymers or copolymers of: pluronics; poly ethyleneoxides; polypropylene oxides; reverse pluronics; polyacrylamides; gelatins; cellulose derivatives; polylactones, polylactic acids; polyglycolic acids; polylactice-co-glycolides; polyhydroxy acids; and combinations thereof.

4. The method according to claim 2 , wherein a concentration of the biostable or biodegradable polymer in the aqueous solution ranges from about 2% to about 45%.

5. The method according to claim 1 , comprising forming a shape of the gel implant to be a straight line, crossed line, rectangular, triangular, pentagonal, hexagonal, circular disk, circular ring, solid square, or irregular shape.

6. The method according to claim 1 , comprising forming the gel implant to have a size greater than or equal to about 5 mm 2 .

7. The method according to claim 1 , wherein the injectable composition and formed gel implant include a visualization agent.

8. The method according to claim 7 , wherein the visualization agent is a coloring composition, a fluorescent composition, a radio opaque contrast agent, or an NMR contrast agent.

9. The method of claim 1 , comprising injecting the injectable composition into the tissue at a depth of about 10 microns to about 5 mm.

10. The method of claim 1 , wherein the injectable composition comprises a drug.

11. The method of claim 10 , wherein drug is dissolved, suspended or emulsified in the injectable composition before injecting.

12. The method of claim 2 , wherein drug is present at a concentration from about 1% to about 40% relative to polymer weight in the injectable composition or formed implant.

13. The method of claim 10 , wherein the drug selected from the agents comprising: antiinfectives; antibiotics; antiviral agents; antifungal agents; antibacterial agents; antipruritics; anticancer agents; antipsychotics; cholesterol- or lipid-reducing agents; cell cycle inhibitors; anticancer agents; antiparkinsonism drugs; HMG-CoA inhibitors; antirestenosis agents; antiinflammatory agents; antiasthmatic agents; anthelmintic; immunosuppressives; muscle relaxants; antidiuretic agents; vasodilators; nitric oxide; nitric oxide-releasing compounds; beta-blockers; hormones; antidepressants; decongestants; calcium channel blockers; growth factors, bone growth factors or bone morphogenic proteins; wound healing agents; analgesics and analgesic combinations; local anesthetic agents; antihistamines; sedatives; angiogenesis-promoting agents; angiogenesis-inhibiting agents; or tranquilizers.

14. The method of claim 1 , wherein the tissue is a live tissue.

15. The method of claim 1 , wherein the tissue is a bioprosthesis tissue.

16. A method of forming an implant in a tissue, the method comprising:

providing an injectable composition configured for thermoreversible gel formation at about 37° C.;

injecting the injectable composition into the tissue at the rate of about 10-12000 injections per minute and/or at an amount of 1.0E-02 ml to 1.0E-16 ml per needle per injection; and

forming a thermoreversible gel at about 37° C. from the injected injectable composition so as to form the gel implant.

17. The method according to claim 16 , wherein the injectable composition includes a polymer is selected from a group consisting of polymers or copolymers of: pluronics; poly ethyleneoxides; polypropylene oxides; reverse pluronics; polyacrylamides; gelatins; cellulose derivatives; polylactones, polylactic acids; polyglycolic acids; polylactice-co-glycolides; polyhydroxy acids; and combinations thereof.

18. The method according to claim 16 , wherein the injectable composition and formed gel implant include a visualization agent.

19. The method of claim 1 , wherein the injectable composition comprises a drug.

20. A method of forming an implant in a tissue, the method comprising:

providing an injectable composition configured for thermoreversible gel formation at about 37° C.;

injecting the injectable composition into the tissue at an amount of 1.0E-02 ml to 1.0E-16 ml per injection; and

forming a thermoreversible gel at about 37° C. from the injected injectable composition so as to form the gel implant.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 20, 2018
From: PATHAK, CHANDRASHEKHAR P.
To: PATHAK HOLDINGS LLC
Reel/Frame 046932/0253 →
Continuity (9)
Continuation 15704792 · Sep 14, 2017
Continuation 15099456 · Apr 14, 2016
Continuation In Part 14736007 · Jun 10, 2015
Division 14209827 · Mar 13, 2014
Provisional Application 61946825 · Mar 2, 2014
Provisional Application 61934795 · Feb 2, 2014
Provisional Application 61820449 · May 7, 2013
Provisional Application 61786215 · Mar 14, 2013
Related Publication 20190022035A1 · Jan 24, 2019
Cited By (1)
US 12,629,345