IP Library Granted Patent US 10,098,961
Granted Patent B2
US 10,098,961 · App. 13/983,448 · Granted Oct 16, 2018

Hyaluronic acid composition

Inventors: Åsa Wiebensjö (Uppsala, SE); Katarina Edsman (Uppsala, SE)
Assignee: Q-MED AB
A61K47/4823A61K8/42A61K8/602A61K8/676A61K8/735A61K31/167A61K31/245A61K31/375A61K31/445A61K31/728A61K45/06A61K47/24A61L27/20A61L27/54A61L31/042A61L31/16A61Q7/00A61Q19/004A61Q19/007A61Q19/08A61K9/0019A61K47/22A61K47/36A61K2800/91A61L2300/402A61L2400/06A61L2400/16
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Quick Facts
Patent No.
US 10,098,961
App. No.
13/983,448
Granted
Oct 16, 2018
Kind
B2
Abstract

An injectable hyaluronic acid composition including a hyaluronic acid; a local anesthetic selected from the group of amide and ester type local anesthetics or a combination thereof; and an ascorbic acid derivative in an amount which prevents or reduces the effect on the viscosity and/or elastic modulus G′ of the composition caused by the local anesthetic upon sterilization by heat. Further, the medical and non-medical, such as cosmetic, use of such a composition, and a method of manufacturing such a composition.

Claims (18)

1. A method for preventing or reducing the effect of a local anesthetic on the viscosity and/or elastic modulus G′ of an injectable hyaluronic acid composition due to sterilization by heat, said method comprising adding to the composition an ascorbic acid derivative selected from the group consisting of ascorbyl phosphates, ascorbyl sulfates and ascorbyl glycosides,

wherein said injectable hyaluronic acid composition further comprises

a hyaluronic acid gel and

a therapeutically relevant concentration of a local anesthetic selected from the group consisting of amide and ester type local anesthetics or a combination thereof, and

wherein the ascorbic acid derivative is added to the composition to a concentration in the range of 0.01 to 5 mg/ml,

wherein the hyaluronic acid gel is crosslinked by modification with a chemical crosslinking agent and wherein a degree of modification of the hyaluronic acid gel is less than 2 mol %,

wherein the hyaluronic acid composition does not exhibit increased stability compared to the same composition without an ascorbic acid derivative,

wherein said local anesthetic is lidocaine.

2. The method according to claim 1 , wherein said ascorbic acid derivative is selected from the group consisting of ascorbyl phosphates and ascorbyl glycosides, or a combination thereof.

3. The method according to claim 1 , wherein the concentration of said ascorbic acid derivative is in the range of 0.01 to 0.5 mg/ml.

4. The method according to claim 2 , wherein said ascorbic acid derivative is selected from the group consisting of sodium ascorbyl phosphate (SAP) and magnesium ascorbyl phosphate (MAP) and the concentration of said sodium ascorbyl phosphate (SAP) or magnesium ascorbyl phosphate (MAP) is in the range of 0.01 to 1 mg/ml.

5. The method according to claim 2 , wherein said ascorbic acid derivative is ascorbyl glucoside and the concentration of said ascorbyl glucoside is in the range of 0.01 to 1 mg/ml.

6. A method of manufacturing a sterilized hyaluronic acid composition comprising:

a) mixing a hyaluronic acid gel, a therapeutically relevant concentration of a local anesthetic selected from the group consisting of amide and ester type local anesthetics or a combination thereof, and an ascorbic acid derivative selected from the group consisting of ascorbyl phosphates, ascorbyl sulfates and ascorbyl glycosides, in an amount which prevents or reduces the effect on the viscosity and/or elastic modulus G′ of the composition caused by the local anesthetic upon sterilization by heat, wherein the concentration of said ascorbic acid derivative in the composition is in the range of 0.01 to 5 mg/ml, and

b) subjecting the mixture to sterilization by autoclaving at a F 0 -value ≥4,

wherein the hyaluronic acid gel is crosslinked by modification with a chemical crosslinking agent and wherein a degree of modification of the hyaluronic acid gel is less than 2 mol %,

wherein the hyaluronic acid composition does not exhibit increased stability compared to the same composition without an ascorbic acid derivative, and

wherein said local anesthetic is lidocaine.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 14, 2023
From: Q-MED AB
To: NESTLÉ SKIN HEALTH S.A.
Reel/Frame 062694/0694 →
CHANGE OF NAME Recorded Feb 14, 2023
From: NESTLÉ SKIN HEALTH S.A.
To: GALDERMA HOLDING SA
Reel/Frame 062696/0065 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 6, 2013
From: WIEBENSJO, ASA; EDSMAN, KATARINA
To: Q-MED AB
Reel/Frame 031153/0162 →
Priority Claims (1)
EP 11153232 · Feb 3, 2011 · regional
Continuity (1)
Related Publication 20140039061A1 · Feb 6, 2014
Cited By (1)
US 12,414,917