IP Library Granted Patent US 10,993,441
Granted Patent B2
US 10,993,441 · App. 16/591,785 · Granted May 4, 2021

Antimicrobial coatings comprising organosilane homopolymers

Inventors: Gavri Grossman (Dallas, TX); Jie Fang (Carrollton, TX); Parham Asgari (Arlington, TX); Maha El-Sayed (Fremont, CA); Craig Grossman (Point Roberts, WA); Daniel Moros (New York, NY)
Assignee: ALLIED BIOSCIENCE, INC.
A01N55/00A01N25/02A01N33/08A01N59/16A61L2/00B05D1/02B05D1/04B05D7/14B05D7/544C08G77/26C09D5/14C09D179/02C09D183/08C23C26/00C07F7/081C08K3/22C08K2003/2241C09D183/00C09D183/06
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Quick Facts
Patent No.
US 10,993,441
App. No.
16/591,785
Granted
May 4, 2021
Kind
B2
Abstract

Aqueous antimicrobial coating compositions are disclosed comprising at least one organosilane homopolymer, present as a distribution of polymer chain lengths, and optionally at least one amine. A method of preparing an antimicrobial coating comprises coating a surface with the aqueous antimicrobial coating composition and allowing the composition to dry into a film that exhibits residual antimicrobial efficacy against microorganisms even after mechanical abrasion of the coating. The organosilane homopolymer may comprise only 3-aminopropylsilanetriol homopolymer, mixtures of 3-aminopropylsilanetriol homopolymer, 3-chloropropylsilanetriol homopolymer and 3-(trihydroxysilyl)propyl dimethyloctadecyl ammonium chloride homopolymer, or any one of various unique organosilane homopolymers having multiple amine functionality.

Claims (37)

1. An aqueous antimicrobial coating composition comprising:

an organosilane homopolymer having the polymeric structure:

wherein n≥2;

an organosilane homopolymer having the polymeric structure:

wherein n≥2;

an organosilane homopolymer having the polymeric structure:

wherein n≥2; and

triethanolamine.

2. The aqueous antimicrobial coating composition of claim 1 , wherein the organosilane homopolymers are present in the aqueous antimicrobial coating in total at from about 0.01 wt. % to about 15 wt. %, based on the total weight of the composition.

3. The aqueous antimicrobial coating composition of claim 1 , further comprising from about 0.01 wt. % to about 5.0 wt. % of at least one amine, based on the total weight of the composition, wherein the at least one amine has the structure R 9 R 10 R 11 N, wherein R 9 , R 10 , and R 11 are independently H, alkyl, substituted alkyl, aryl, substituted aryl or cyclic, having a molecular weight of less than about 200 g/mole and a pKa of from about 7 to about 12.

4. The aqueous antimicrobial coating composition of claim 1 , wherein triethanolamine is present in the aqueous antimicrobial coating composition at from about 0.01 wt. % to about 1.0 wt. %, based on the total weight of the composition.

5. The aqueous antimicrobial coating composition of claim 1 , wherein the only organosilane homopolymers present in the aqueous antimicrobial coating composition are 3-aminopropylsilanetriol homopolymer, having a chain length distribution of n=2 to about 30; 3-chloropropylsilanetriol homopolymer, having a chain length distribution of n≥2; and 3-(trihydroxysilyl)propyl dimethyloctadecyl ammonium chloride homopolymer having a chain length distribution of n≥2.

6. The aqueous antimicrobial coating composition of claim 1 , wherein the triethanolamine is present at from about 0.01 wt. % to about 5.0 wt. %, based on the total weight of the composition.

7. A method of preparing an antimicrobial coating on a surface, the method comprising:

(a) disposing on the surface an aqueous antimicrobial coating composition comprising:

an organosilane homopolymer having the polymeric structure:

wherein n≥2;

an organosilane homopolymer having the polymeric structure:

wherein n≥2;

an organosilane homopolymer having the polymeric structure:

wherein n≥2; and

triethanolamine;

and

(b) allowing the aqueous antimicrobial coating composition thus disposed on the surface to dry.

8. The method of claim 7 , wherein the aqueous antimicrobial coating composition further comprises from about 0.01 wt. % to about 5.0 wt. % of at least one amine, based on the total weight of the aqueous antimicrobial coating composition, wherein the at least one amine has the structure R 9 R 10 R 11 N, wherein R 9 , R 10 , and R 11 are independently H, alkyl, substituted alkyl, aryl, substituted aryl or cyclic, having a molecular weight of less than about 200 g/mole and a pKa of from about 7 to about 12.

9. The method of claim 7 , wherein triethanolamine is present in the aqueous antimicrobial coating composition at from about 0.01 wt. % to about 1.0 wt. %, based on the total weight of the aqueous antimicrobial coating composition.

10. The method of claim 7 , wherein the only organosilane homopolymers present in the aqueous antimicrobial coating composition are 3-aminopropylsilanetriol homopolymer, having a chain length distribution of n=2 to about 30; 3-chloropropylsilanetriol homopolymer, having a chain length distribution of n≥2; and 3-(trihydroxysilyl)propyl dimethyloctadecyl ammonium chloride homopolymer having a chain length distribution of n≥2.

11. The method of claim 7 , wherein the aqueous antimicrobial coating composition comprises from about 0.01 wt. % to about 5.0 wt. % of triethanolamine, based on the total weight of the composition.

12. The aqueous antimicrobial coating composition of claim 1 consisting essentially of:

a total of from about 0.01 wt. % to about 15 wt. % of a mixture of 3-aminopropylsilanetriol homopolymer having a chain length distribution of n=3 to about 30, 3-chloropropylsilanetriol homopolymer having a chain length distribution of n≥2, 3-(trihydroxysilyl)propyl dimethyloctadecyl ammonium chloride homopolymer having a chain length distribution of n≥2;

from about 0.01 wt. % to about 5.0 wt. % triethanolamine; and

water.

13. The method of claim 7 , wherein the organosilane homopolymers are present in the aqueous antimicrobial coating in total at from about 0.01 wt. % to about 15 wt. %, based on the total weight of the composition.

14. The method of claim 7 , wherein the aqueous antimicrobial coating composition consists essentially of:

a total of from about 0.01 wt. % to about 15 wt. % of a mixture of 3-aminopropylsilanetriol homopolymer having a chain length distribution of n=3 to about 30, 3-chloropropylsilanetriol homopolymer having a chain length distribution of n≥2, 3-(trihydroxysilyl)propyl dimethyloctadecyl ammonium chloride homopolymer having a chain length distribution of n≥2;

from about 0.01 wt. % to about 5.0 wt. % triethanolamine; and

water.

Assignments (4)
CHANGE OF NAME Recorded May 27, 2022
From: ALLIED BIOSCIENCE, INC.
To: SRFC BIO, INC.
Reel/Frame 060205/0169 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 12, 2020
From: MOROS, DANIEL
To: ALLIED BIOSCIENCE, INC.
Reel/Frame 052637/0695 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 22, 2019
From: GROSSMAN, CRAIG
To: ALLIED BIOSCIENCE, INC.
Reel/Frame 051087/0113 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 3, 2019
From: GROSSMAN, GAVRI; FANG, JIE; ASGARI, PARHAM; EL-SAYED, MAHA
To: ALLIED BIOSCIENCE, INC.
Reel/Frame 050615/0485 →
Continuity (6)
Continuation In Part 15718997 · Sep 28, 2017
Division 15041974 · Feb 11, 2016
Continuation In Part 14932840 · Nov 4, 2015
Provisional Application 62114998 · Feb 11, 2015
Provisional Application 62075020 · Nov 4, 2014
Related Publication 20200068897A1 · Mar 5, 2020
Cited By (1)
US 12,516,199