IP Library Granted Patent US 10,391,202
Granted Patent B2
US 10,391,202 · App. 16/186,451 · Granted Aug 27, 2019

Hyaluronic acid-based gels including lidocaine

Inventor: Pierre F. Lebreton (Annecy, FR)
Assignee: Allergan Industrie SAS
A61L27/52A61K8/42A61K8/735A61K9/0021A61K9/06A61K31/167A61K31/728A61K47/36A61L27/20A61L27/54A61Q19/08A61L2300/402A61L2300/602A61L2400/06
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Quick Facts
Patent No.
US 10,391,202
App. No.
16/186,451
Granted
Aug 27, 2019
Kind
B2
Abstract

Disclosed herein are soft tissue fillers, for example, dermal and subdermal fillers, based on hyaluronic acids and pharmaceutically acceptable salts thereof. In one aspect, hyaluronic acid-based compositions described herein include a therapeutically effective amount of at least one anesthetic agent, for example, lidocaine. The present hyaluronic acid-based compositions including lidocaine have an enhanced stability, relative to conventional compositions including lidocaine, for example when subjected to sterilization techniques or when stored for long periods of time. Methods and processes of preparing such hyaluronic acid-based compositions are also provided.

Claims (59)

1. A stable, sterile soft tissue filler comprising:

a hyaluronic acid (HA) component comprising HA crosslinked with 1,4-butanediol diglycidyl ether (BDDE), and uncrosslinked HA, wherein the HA component comprises greater than about 10% uncrosslinked HA by volume; and

lidocaine at a concentration of about 0.3% by weight of the soft tissue filler combined with the HA component;

wherein the stable, sterile soft tissue filler is made by a process comprising:

providing the HA component;

adjusting the pH of the HA component to an adjusted pH above about 7.2;

adding a solution containing lidocaine to the HA component having the adjusted pH to obtain a soft tissue filler; and

heat sterilizing the soft tissue filler to obtain a stable, sterile soft tissue filler.

2. The soft tissue filler of claim 1 , wherein the HA component comprises at least about 15% uncrosslinked HA by volume.

3. The soft tissue filler of claim 1 , wherein the HA component comprises at least about 20% uncrosslinked HA by volume.

4. The soft tissue filler of claim 1 , wherein the HA component comprises particles of crosslinked HA in a relatively fluidic medium of uncrosslinked HA.

5. The soft tissue filler of claim 1 , wherein the adjusting the pH comprises adjusting the pH above about 7.5.

6. The soft tissue filler of claim 1 , wherein the step of providing a HA component comprises providing dry uncrosslinked NaHA material and hydrating the dry uncrosslinked NaHA material in an alkaline solution to obtain an alkaline, NaHA gel.

7. The soft tissue filler of claim 6 , wherein the alkaline NaHA gel has a pH greater than about 8.0.

8. The soft tissue filler of claim 6 , wherein the alkaline NaHA gel has a pH greater than about 10.0.

9. A stable, sterile soft tissue filler comprising:

a hyaluronic acid (HA) component comprising HA crosslinked with 1,4-butanediol diglycidyl ether (BDDE), and uncrosslinked HA; and

lidocaine at a concentration of about 0.3% by weight of the soft tissue filler combined with the crosslinked HA component;

wherein the soft tissue filler is stable after heat sterilization at between about 120° C. and about 130° C.;

wherein the soft tissue filler has a pH of about 7; and

wherein the stable, sterile soft tissue filler is made by a process comprising:

providing the HA component crosslinked with BDDE;

adding a solution containing lidocaine to the HA component crosslinked with BDDE to obtain a soft tissue filler; and

heat sterilizing the soft tissue filler to obtain a stable, sterile soft tissue filler.

10. The soft tissue filler of claim 9 , wherein the HA component comprises at least about 15% uncrosslinked HA by volume.

11. The soft tissue filler of claim 9 , wherein the HA component comprises at least about 20% uncrosslinked HA by volume.

12. The soft tissue filler of claim 9 , wherein the HA component comprises particles of crosslinked HA in a relatively fluidic medium of uncrosslinked HA.

13. The soft tissue filler of claim 9 , wherein the process further comprises adjusting the pH of the HA component to an adjusted pH above about 7.5.

14. The soft tissue filler of claim 9 , wherein the step of providing a HA component crosslinked with BDDE comprises the steps of providing dry uncrosslinked NaHA material and hydrating the dry uncrosslinked NaHA material in an alkaline solution to obtain an alkaline, uncrosslinked NaHA gel.

15. The soft tissue filler of claim 14 , wherein the alkaline uncrosslinked NaHA gel has a pH greater than about 8.0.

16. The soft tissue filler of claim 14 , wherein the alkaline uncrosslinked NaHA gel has a pH greater than about 10.0.

17. A sterile, stable injectable soft tissue filler composition comprising:

a mixture of soluble form hyaluronic acid (HA), crosslinked HA, and lidocaine in an amount effective to mitigate pain upon injection of the composition, the crosslinked HA being crosslinked with 1,4-butanediol diglycidyl ether (BDDE);

the composition having a HA concentration of between about 20 mg/ml and about 30 mg/ml;

wherein the sterile, stable injectable soft tissue filler composition is made by a process comprising:

providing the soluble form HA and crosslinked HA;

adjusting the pH of the soluble form HA and crosslinked HA;

adding a solution containing lidocaine to the soluble form HA and crosslinked HA having the adjusted pH to obtain a HA-based injectable soft tissue filler composition; and

heat sterilizing the HA-based injectable soft tissue filler composition to obtain the sterile, stable injectable soft tissue filler composition.

18. The soft tissue filler composition of claim 17 , wherein the soluble form HA and crosslinked HA comprises at least about 15% soluble form HA by volume.

19. The soft tissue filler composition of claim 17 , wherein the soluble form HA and crosslinked HA comprises at least about 20% soluble form HA by volume.

20. The soft tissue filler composition of claim 17 , wherein the soluble form HA and crosslinked HA comprises particles of crosslinked HA in a relatively fluidic medium of the soluble form HA.

21. The soft tissue filler composition of claim 17 , wherein the adjusting the pH comprises adjusting the pH above about 7.5.

22. The soft tissue filler composition of claim 17 , wherein the step of providing the soluble form HA and crosslinked HA comprises the steps of providing dry uncrosslinked NaHA material and hydrating the dry uncrosslinked NaHA material in an alkaline solution to obtain an alkaline uncrosslinked NaHA gel.

23. The soft tissue filler composition of claim 22 , wherein the alkaline uncrosslinked NaHA gel has a pH greater than about 8.0.

24. The soft tissue filler composition of claim 22 , wherein the alkaline uncrosslinked NaHA gel has a pH greater than about 10.0.

25. A sterile, stable injectable soft tissue filler composition comprising:

a mixture of soluble form hyaluronic acid (HA), crosslinked HA, and lidocaine in an amount effective to mitigate pain upon injection of the composition, the crosslinked HA being crosslinked with 1,4-butanediol diglycidyl ether (BDDE); and

the lidocaine of the mixture being present in a concentration of about 0.3% by weight of the composition;

wherein the sterile, stable injectable soft tissue filler composition is made by a process comprising:

providing the soluble form HA and crosslinked HA;

adjusting the pH of the soluble form HA and crosslinked HA to an adjusted pH above about 7.2;

adding a solution containing lidocaine to the soluble form HA and crosslinked HA having the adjusted pH to obtain a HA-based injectable soft tissue filler composition; and

heat sterilizing the HA-based injectable soft tissue filler composition to obtain the sterile, stable injectable soft tissue filler composition.

26. The soft tissue filler composition of claim 25 , wherein the soluble form HA is present in an amount of about 10% to about 20% by volume.

27. The soft tissue filler composition of claim 25 , wherein the adjusted pH is above about 7.5.

28. The soft tissue filler composition of claim 25 , wherein the step of providing the HA crosslinked with BDDE comprises the steps of providing dry uncrosslinked NaHA material and hydrating the dry uncrosslinked NaHA material in an alkaline solution to obtain an alkaline, uncrosslinked NaHA gel.

29. The soft tissue filler composition of claim 28 , wherein the alkaline uncrosslinked NaHA gel has a pH greater than about 8.0.

30. The soft tissue filler composition of claim 28 , wherein the alkaline uncrosslinked NaHA gel has a pH greater than about 10.0.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 24, 2019
From: LEBRETON, PIERRE F.
To: ALLERGAN INDUSTRIE, SAS
Reel/Frame 049848/0740 →
Continuity (7)
Continuation 15173850 · Jun 6, 2016
Continuation 13891052 · May 9, 2013
Continuation 12393768 · Feb 26, 2009
Provisional Application 61085956 · Aug 4, 2008
Provisional Application 61087934 · Aug 11, 2008
Provisional Application 61096278 · Sep 11, 2008
Related Publication 20190076580A1 · Mar 14, 2019