IP Library Patent Application 17263663
Patent Application
App. No. 17/263,663

THERAPEUTIC COMPOSITION AND RELATED METHODS

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Patent No.
US None
App. No.
17/263,663
Abstract

A composition. The composition includes a compound of Formula (I) HOCH 2 —(═CHOH═) n —CH2NR 1 R 2 (I) wherein R 1 and R 2 are independently selected from the group consisting of a hydrogen atom, an alkyl group, C(O)R 3 , and SO 2 R 4 , wherein at least one of R 1 and R 2 is C(O)R 3 or SO 2 R 4 , R 3 and R 4 are selected from the group consisting of an alkyl group having seven carbon atoms, an alkyl group having eight carbon atoms, and an alkyl group having nine carbon atoms, and n is an integer from about 2 to about wherein a concentration of the compound of Formula (I) is more than its critical micelle concentration; and an antimicrobial agent selected from the group consisting of a biguanide antimicrobial agent and a polymeric, cationic, non-micelle forming antimicrobial material; wherein a concentration of the antimicrobial agent is no more than 5 wt %.

Claims (36)

1 . A composition, comprising:

a compound of Formula (I)

HOCH 2 —(═CHOH═) n —CH2NR 1 R 2   (I)

wherein R 1 and R 2 are independently selected from the group consisting of a hydrogen atom, an alkyl group, C(O)R 3 , and SO 2 R 4 ;

wherein at least one of R 1 and R 2 is C(O)R 3 or SO 2 R 4 , R 3 and R 4 are selected from the group consisting of an alkyl group having seven carbon atoms, an alkyl group having eight carbon atoms, and an alkyl group having nine carbon atoms, and n is an integer from about 2 to about 5;

wherein a concentration of the compound of Formula (I) is more than its critical micelle concentration; and

an antimicrobial agent selected from the group consisting of a biguanide antimicrobial agent and a polymeric, cationic, non-micelle forming antimicrobial material;

wherein a concentration of the antimicrobial agent is no more than 5 wt %.

2 . The composition of claim 1 , wherein the concentration of the compound of Formula (I) is more than 120% of its critical micelle concentration .

3 . The composition of claim 1 , wherein the concentration of the compound of Formula (I) is more than 150% of its critical micelle concentration.

4 . The composition of claim 1 , wherein the concentration of the compound of Formula (I) is more than 180% of its critical micelle concentration.

5 . A composition, comprising:

a compound of Formula (I)

HOCH 2 —(═CHOH═) n —CH2NR 1 R 2   (I)

wherein R 1 and R 2 are independently selected from the group consisting of a hydrogen atom, an alkyl group, C(O)R 3 , and SO 2 R 4 ,

wherein at least one of R 1 and R 2 is C(O)R 3 or SO 2 R 4 , R 3 and R 4 are selected from the group consisting of an alkyl group having seven carbon atoms, an alkyl group having eight carbon atoms, and an alkyl group having nine carbon atoms, and n is an integer from about 2 to about 5;

wherein a concentration of the compound of Formula (I) is more than 0.2 wt %; and

an antimicrobial agent selected from the group consisting of a biguanide antimicrobial agent and a polymeric, cationic, non-micelle forming antimicrobial material;

wherein a concentration of the antimicrobial agent is no more than 5 wt %.

6 . The composition of claim 5 , wherein the concentration of the compound of Formula (I) is more than 0.6 wt %.

7 . The composition of claim 5 , wherein the concentration of the compound of Formula (I) is more than 1.8 wt %.

8 . The composition of claim 1 , wherein the concentration of the antimicrobial agent is no more than 4 wt %.

9 . The composition of claim 1 , wherein the concentration of the antimicrobial agent is no more than 3 wt %.

10 . The composition of claim 1 , further comprising a glucamine compound.

11 . The composition of claim 10 , wherein the glucamine compound is selected from the group of D-glucamine, N-methyl-D-glucamine, N-Ethyl-D-Glucamine, N-Propyl-Glucamine, N-Butyl-D-Glucamine, N-octyl-D-glucamine, and combinations thereof.

12 . The composition of claim 1 , further comprising a glucosamine compound.

13 . The composition of claim 12 , wherein the glucosamine compound is selected from the group of D-Glucosamine Hydrochloride, D-Glucosamine Sulfate, D-Glucosamine Phosphate, D-Glucosamine gluconate and combinations thereof.

14 . The composition of claim 1 , further comprising a pharmaceutically acceptable carrier or solvent selected from the group consisting of water, alcohol, glycerol, polyethylene glycol, triethanolamine, methoxypropanol, isopropanol, ethyl acetate, polypropylene glycol and a combination thereof.

15 . The composition of claim 1 , wherein the compound of Formula (I) is MEGA-8, MEGA-9, or MEGA-10.

16 . The composition of claim 1 , further comprising a binder.

17 . The composition of any one of claim 16 , wherein the binder is natural polysaccharides and derivatives selected from murein, pectins, hyaluronate, chondroitin-4-sulfate, dermatan sulfate, keratan sulfate, heparin, heparan sulfate, hydroxyethyl cellulose, hydroxypropyl cellulose, guar gum, and combinations thereof.

18 . The composition of claim 1 , further comprising sugar-alcohol humectant including xylitol, sorbitol, mannitol and erythritol.

19 . The composition of claim 1 , wherein the composition is in a form selected from the group consisting of a solution, a dispersion, a suspension, an emulsion, a solid, a paste, a foam, a gel, a spray, a wipe, a mitt and a brush.

20 . A method, comprising:

providing the composition of claim 1 ; and

applying the composition to a surface of a subject or a medical device.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2024
From: 3M INNOVATIVE PROPERTIES COMPANY
To: SOLVENTUM INTELLECTUAL PROPERTIES COMPANY
Reel/Frame 066431/0915 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 27, 2021
From: KOHLER RIEDI, PETRA L.; BARAN, JIMMIE R., JR.; YANG, JIE; PARTHASARATHY, RANJANI V.
To: 3M INNOVATIVE PROPERTIES COMPANY
Reel/Frame 055046/0459 →