IP Library Granted Patent US 10,485,896
Granted Patent B2
US 10,485,896 · App. 16/186,448 · Granted Nov 26, 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 10,485,896
App. No.
16/186,448
Granted
Nov 26, 2019
Kind
B2
Abstract

Disclosed herein are cohesive 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 and cohesivity, 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 (56)

1. A dermal filler comprising:

hyaluronic acid (HA) crosslinked with 1,4 butanediol diglycidyl ether (BDDE), and

lidocaine;

wherein the lidocaine is freely released in vivo;

wherein the dermal filler is sterile; and

wherein the dermal filler is made by a process comprising:

crosslinking HA with BDDE to obtain a crosslinked HA composition;

adding lidocaine to the crosslinked HA composition; and

heat sterilizing the crosslinked HA composition with added lidocaine to obtain a sterile dermal filler.

2. The dermal filler of claim 1 , wherein the process further comprises adjusting the pH of the crosslinked HA composition to obtain an alkaline crosslinked HA composition.

3. The dermal filler of claim 2 , wherein the pH adjustment is performed before adding the lidocaine.

4. The dermal filler of claim 2 , wherein the pH adjustment comprises adjusting the pH to about 7.5 to about 8.0.

5. The dermal filler of claim 2 , wherein the pH adjustment comprises adjusting the pH to above about 7.5.

6. The dermal filler of claim 1 , wherein the adding the lidocaine comprises adding a solution containing lidocaine HCl.

7. The dermal filler of claim 1 , wherein the process further comprises passing the crosslinked HA composition through a sieve before adding the lidocaine.

8. The dermal filler of claim 7 , wherein the process further comprises adding free HA gel to the crosslinked HA composition after the crosslinked HA composition has been passed through the sieve.

9. The dermal filler of claim 7 , wherein the crosslinked HA composition, after being passed through the sieve, comprises particles of crosslinked HA having an average particle size of at least about 200 μm.

10. The dermal filler of claim 7 , wherein the crosslinked HA composition, after being passed through the sieve, comprises particles of crosslinked HA having an average particle size of at least about 250 μm.

11. The dermal filler of claim 7 , wherein the crosslinked HA composition, after being passed through the sieve, comprises particles of crosslinked HA having an average particle size of less than about 200 μm.

12. The dermal filler of claim 1 , wherein the process further comprises homogenizing the crosslinked HA composition before adding the lidocaine.

13. The dermal filler of claim 1 , wherein the dermal filler has a lidocaine concentration of between about 0.1% and about 5.0% w/w.

14. The dermal filler of claim 1 , wherein the dermal filler has a HA concentration between about 20 mg/mL and about 30 mg/mL.

15. The dermal filler of claim 1 , having a lidocaine concentration of 0.3% w/w and a HA concentration between about 20 mg/mL and about 30 mg/mL.

16. A dermal filler composition comprising:

a composition comprising hyaluronic acid (HA) crosslinked with 1,4 butanediol diglycidyl ether (BDDE), wherein the HA is not crosslinked to a non-HA biopolymer, and lidocaine;

wherein the dermal filler is made by a process comprising:

crosslinking HA with BDDE to obtain a crosslinked HA;

adding lidocaine to the crosslinked HA; and

heat sterilizing the crosslinked HA with added lidocaine to obtain a sterile dermal filler.

17. The dermal filler of claim 16 , wherein the process further comprises adjusting the pH of the crosslinked HA to obtain an alkaline crosslinked HA.

18. The dermal filler of claim 17 , wherein the adjusting the pH is performed before adding the lidocaine.

19. The dermal filler of claim 16 , wherein adding the lidocaine comprises adding a solution containing lidocaine HCl.

20. The dermal filler of claim 16 , wherein the crosslinked HA comprises particles of crosslinked HA having an average particle size of at least about 200 μm.

21. The dermal filler of claim 16 , wherein the crosslinked HA comprises particles of crosslinked HA having an average particle size of less than about 200 μm.

22. The dermal filler of claim 16 , wherein the dermal filler has a lidocaine concentration of between about 0.1% and about 5.0% w/w.

23. The dermal filler of claim 16 , wherein the dermal filler has a HA concentration of between about 20 mg/mL and about 30 mg/mL.

24. A dermal filler composition comprising:

a hyaluronic acid (HA) crosslinked with 1,4 butanediol diglycidyl ether (BDDE), and about 0.3% lidocaine by weight, wherein the lidocaine is freely released in vivo and wherein the composition is sterile;

wherein the composition is made by a process comprising:

crosslinking HA with BDDE to obtain a crosslinked HA;

adding a free HA gel to the crosslinked HA;

adding a solution of lidocaine HCl to the crosslinked HA; and

autoclaving the crosslinked HA having free HA gel and lidocaine HCl added thereto, to obtain a sterile dermal filler composition.

25. A dermal filler product comprising:

a dermal filler composition comprising a hyaluronic acid (HA) crosslinked with 1,4 butanediol diglycidyl ether (BDDE), and between about 0.1% to about 5.0% lidocaine by weight, wherein the HA is not crosslinked to a non-HA biopolymer, and wherein the composition is sterile;

a syringe containing the sterile composition;

wherein the product is made by a process comprising:

crosslinking HA with BDDE to obtain a crosslinked HA;

adding lidocaine to the crosslinked HA to obtain a crosslinked HA containing lidocaine; and

packaging the crosslinked HA containing lidocaine in a syringe; and

autoclaving the syringe containing the crosslinked HA containing lidocaine to obtain a dermal filler product.

26. The dermal filler product of claim 25 , wherein the sterile composition contained in the syringe has a volume between about 0.8 mL and about 2.5 mL.

27. The dermal filler product of claim 25 , wherein the sterile composition has a HA concentration of about 20 mg/mL to about 30 mg/mL.

28. The dermal filler product of claim 25 , wherein the sterile composition is stable at ambient temperature for at least about 6 months.

29. The dermal filler product of claim 25 , wherein the sterile composition comprises particles of crosslinked HA having an average particle size of at least about 200 μm.

30. The dermal filler product of claim 25 , wherein the sterile composition comprises particles of crosslinked HA having an average particle size of less than about 200 μm.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 6, 2019
From: LEBRETON, PIERRE F.
To: ALLERGAN INDUSTRIE, SAS
Reel/Frame 049979/0787 →
Continuity (9)
Continuation 15443080 · Feb 27, 2017
Continuation 14754504 · Jun 29, 2015
Continuation 14242752 · Apr 1, 2014
Continuation 13419079 · Mar 13, 2012
Continuation 12393884 · Feb 26, 2009
Provisional Application 61085956 · Aug 4, 2008
Provisional Application 61087934 · Aug 11, 2008
Provisional Application 61096278 · Sep 11, 2008
Related Publication 20190076579A1 · Mar 14, 2019