US2021077658A1PendingUtilityA1

Heat stable hyaluronic acid compositions for dermatological use

69
Assignee: ALLERGAN IND SASPriority: Jan 13, 2010Filed: Oct 6, 2020Published: Mar 18, 2021
Est. expiryJan 13, 2030(~3.5 yrs left)· nominal 20-yr term from priority
A61K 8/735A61K 8/42A61L 27/20A61P 17/04A61Q 19/00A61L 27/54A61Q 19/08A61P 9/00A61L 2300/232A61P 39/06A61K 8/415A61L 27/00A61L 2300/204A61L 2300/402A61P 7/04A61K 8/73A61P 17/00A61P 29/00
69
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Claims

Abstract

The disclosure provides hyaluronic acid (HA) gel formulations and methods for treating the appearance of the skin. The formulations contain hyaluronic acid and at least one additional ingredient. Methods for treating lines, wrinkles, fibroblast depletions, and scars with the disclosed composition are provided as well.

Claims

exact text as granted — not AI-modified
1 - 20 . (canceled) 
     
     
         21 . A method of improving the appearance of fine lines, wrinkles, fibroblast depletions, or scars of a patient, the method comprising administering a local injection of a steam sterilized dermal filler composition to the patient, wherein the appearance of the fine lines, wrinkles, fibroblast depletions, or scars is diminished by the injection, the dermal filler composition comprising crosslinked hyaluronic acid (HA), ascorbyl-2-glucoside and an anesthetic agent, wherein the dermal filler composition is steam-sterilization stable. 
     
     
         22 . The method of  claim 21 , wherein the hyaluronic acid is crosslinked with 1,4-butanediol diglycidyl ether. 
     
     
         23 . The method of  claim 21 , wherein the anesthetic agent is lidocaine. 
     
     
         24 . The method of  claim 23 , wherein the lidocaine is present in an amount of about 0.001% w/w to about 10% w/w. 
     
     
         25 . The method of  claim 23 , wherein the lidocaine is present in an amount of about 0.001% w/w to about 5% w/w. 
     
     
         26 . The method of  claim 23 , wherein the lidocaine is present in an amount of about 0.001% w/w to about 3% w/w. 
     
     
         27 . The method of  claim 23 , wherein the lidocaine is present in an amount of 0.3% w/w. 
     
     
         28 . The method of  claim 21 , wherein the crosslinked HA is present in an amount of about 1 mg/mL to about 40 mg/mL. 
     
     
         29 . The method of  claim 28 , wherein the crosslinked HA is present in an amount of about 10 mg/mL to about 40 mg/mL. 
     
     
         30 . The method of  claim 28 , wherein the crosslinked HA is present in an amount of about 20 mg/mL to about 30 mg/mL. 
     
     
         31 . The method of  claim 28 , wherein the crosslinked HA is present in an amount of about 20 mg/mL to about 25 mg/mL. 
     
     
         32 . The method of  claim 21 , wherein the ascorbyl-2-glucoside is present in an amount of about 0.001% w/w to about 10% w/w. 
     
     
         33 . The method of  claim 32 , wherein the ascorbyl-2-glucoside is present in an amount of about 0.1% w/w to about 3.0% w/w. 
     
     
         34 . The method of  claim 32 , wherein the ascorbyl-2-glucoside is present in an amount of 1% w/w. 
     
     
         35 . The method of  claim 32 , wherein the ascorbyl-2-glucoside is present in an amount of 2% w/w. 
     
     
         36 . The method of  claim 32 , wherein the ascorbyl-2-glucoside is present in an amount of 0.6% w/w. 
     
     
         37 . The method of  claim 21 , wherein the steam-sterilization stability of the dermal filler composition is determined by subjecting the dermal filler composition to a steam sterilization treatment at between about 120° C. and about 135° C. for between about 1 minute and about 5 minutes, with substantial retention after the treatment of one or more of the dermal filler characteristics of being clear, homogenous or cohesive. 
     
     
         38 . The method of  claim 37 , wherein the HA is crosslinked with 1,4-butanediol diglycidyl ether, and the anesthetic agent is lidocaine. 
     
     
         39 . The method of  claim 38 , wherein the crosslinked HA is present in an amount of about 10 mg/mL to about 40 mg/mL. 
     
     
         40 . The method of  claim 39 , wherein the ascorbyl-2-glucoside is present in an amount of about 0.1% w/w/to about 3.0% w/w, and the lidocaine is present in an amount of about 0.3% w/w to about 3% w/w.

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