Antimicrobial polymers formed by bulk polyaddition

Patent metadata

Field	Value
Publication number	US-2016374335-A1
Application number	US-201514749764-A
Country	US
Kind code	A1
Filing date	Jun 25, 2015
Priority date	Jun 25, 2015
Publication date	Dec 29, 2016
Grant date	—

Abstract

Cationic antimicrobial polymers have been synthesized by a bulk addition polymerization of a nucleophilic agent comprising two tertiary amines and an electrophilic agent that comprises two leaving groups and an aromatic ring between the leaving groups. The reaction solvent for the polymerization is chosen to allow precipitation of the cationic polymer at the polymerization temperature, thereby limiting molecular weight. Quaternization and polymerization occur concurrently. The cationic polymers can be highly active against Gram-negative and Gram-positive microbes, and/or fungi. The cationic polymers can also be non-hemolytic and non-cytotoxic at the effective concentration against the microbes.

First claim

1 . A cationic polymer comprising:
i) a cationic repeat unit of formula (C-1):

wherein
atomic centers nitrogen 1 and carbon 2 of formula (C-1) are labeled,
each X′ is an independent negative-charged counterion, and
each R′ is an independent monovalent radical selected from the group consisting of methyl, ethyl and propyl, and

ii) a second cationic repeat unit of formula (C-3):

wherein
atomic centers nitrogen 1 and carbon 2 of formula (C-3) are labeled,
each X′ is an independent negative-charged counterion,

each R″ is an independent monovalent radical selected from the group consisting of methyl, ethyl and propyl;
wherein the cationic repeat units of formula (C-1) and formula (C-3) are covalently linked.

2 . The cationic polymer of claim 1 , wherein each X′ of formulas (C-1) and (C-3) is an independent anion selected from the group consisting of chloride, bromide, and iodide.

3 . The cationic polymer of claim 1 , wherein the cationic polymer is toxic to a microbe selected from the group consisting of Gram-positive microbes, Gram-negative microbes, fungi, and combinations thereof.

4 . The cationic polymer of claim 1 , wherein each R′ is ethyl.

5 . The cationic polymer of claim 1 , wherein the cationic polymer has a number average molecular weight of about 1,000 to about 10,000.

6 . The cationic polymer of claim 1 , wherein each R′ is methyl.

7 . The cationic polymer of claim 1 , wherein each X′ of formulas (C-1) and (C-3) is a chloride ion.

8 . The cationic polymer of claim 1 , wherein each R′ is propyl.

9 . The cationic polymer of claim 1 , wherein the cationic polymer is a random copolymer.

10 . The cationic polymer of claim 1 , wherein the cationic polymer comprises the cationic repeat units of formulas (C-1) and (C-3) in a (C-1):(C-3) molar ratio of 90:10 to 10:90.

11 . The cationic polymer of claim 1 , wherein each R″ is methyl.

12 . An antimicrobial composition, comprising the cationic polymer of claim 1 and a second component.

13 . The antimicrobial composition of claim 12 , wherein the composition is an aqueous mixture of the cationic polymer.

14 . The antimicrobial composition of claim 12 , wherein the antimicrobial composition is selected from the group consisting of laundry detergents, cosmetics, soaps, hand washes, lotions, and contact lens disinfectants.

15 . The antimicrobial composition of claim 12 , wherein the cationic polymer is a random copolymer of (C-1) and (C-3).

16 . A method of killing a microbe, comprising contacting the microbe with the cationic polymer of claim 1 .

17 . The method claim 16 , wherein the cationic polymer is a random copolymer of (C-1) and (C-3).

18 . A cationic polymer comprising a cationic repeat unit of formula (C-5):

wherein
each R′ is an independent monovalent radical selected from the group consisting of methyl, ethyl and propyl, and
each X′ is an independent negative-charged counterion.

19 . The cationic polymer of claim 18 , wherein the cationic polymer is a homopolymer.

20 . The cationic polymer of claim 18 , wherein the cationic polymer is a random copolymer comprising a second cationic repeat unit of formula (C-7):

wherein
atomic centers nitrogen 1 and carbon 2 are labeled,
each X′ is an independent negative-charged counterion,
each R″ is an independent monovalent radical selected from the group consisting of methyl, ethyl and propyl.

21 . An antimicrobial composition, comprising the cationic polymer of claim 18 and a second component.

22 . The antimicrobial composition of claim 21 , wherein the cationic polymer is a random copolymer comprising a second cationic repeat unit of formula (C-7):

wherein
atomic centers nitrogen 1 and carbon 2 are labeled,
each X′ is an independent negative-charged counterion,
each R″ is an independent monovalent radical selected from the group consisting of methyl, ethyl and propyl.

23 . The cationic polymer of claim 22 , wherein the cationic polymer comprises the cationic repeat units of formulas (C-5) and (C-7) in a (C-5):(C-7) molar ratio of 90:10 to 50:50.

24 . A method of killing a microbe, comprising contacting the microbe with the cationic polymer of claim 18 .

25 . A method of forming the cationic polymer of claim 1 , comprising:
forming a reaction mixture comprising i) a solvent, ii) an electrophilic agent of structure

wherein each Y′ is an independent leaving group selected from the group consisting of chloride, bromide, iodide, mesylate, and tosylate, and each Y′ is capable of undergoing a nucleophilic substitution reaction with a tertiary amine to form a positive-charged quaternary amine, iii) a first nucleophilic agent comprising two nitrogens of two tertiary amine groups, wherein the two nitrogens of the first nucleophilic agent are linked by an ethane-1,2-diyl group (*—CH 2 CH 2 —*), and iv) a second nucleophilic agent comprising two nitrogens of two tertiary amine groups, wherein the two nitrogens of the second nucleophilic agent are linked by a benzene-1,4-diyl group:

and
heating the reaction mixture at an elevated temperature with agitation, thereby forming the cationic polymer by addition polymerization of the electrophilic agent, the first nucleophilic agent, and the second nucleophilic agent, wherein the cationic polymer is not soluble in the solvent at the elevated temperature.

26 . A cationic polymer, comprising a cationic repeat unit of formula (C-3):

wherein
atomic centers nitrogen 1 and carbon 2 are labeled,
each X′ is an independent negative-charged counterion,
each R″ is an independent monovalent radical selected from the group consisting of methyl, ethyl and propyl.

27 . The cationic polymer of claim 26 , wherein the cationic polymer is a homopolymer.

28 . The cationic polymer of claim 26 , wherein the cationic polymer is a random copolymer comprising a second cationic repeat unit of formula (C-5):

wherein
each R′ is an independent monovalent radical selected from the group consisting of methyl, ethyl and propyl, and
each X′ is an independent negative-charged counterion.

29 . An antimicrobial composition, comprising the cationic polymer of claim 26 and a second component.

30 . A cationic polymer, comprising a cationic repeat unit of formula (C-7):

Assignees

• IBM
• Agency Science Tech & Res

Inventors

• Chan Julian M W
• Hedrick James L
• Ono Robert J
• Teo Jye Yng
• Yang Yi Yan
• Zhang Mu San

Classifications

• A01N33/12 Primary

  Quaternary ammonium compounds · CPC title

• C08G73/024

  Polyamines containing oxygen in the form of ether bonds in the main chain · CPC title

• C08G73/0206

  Polyalkylene(poly)amines · CPC title

• C08G73/0213

  Preparatory process · CPC title

• C08G73/02

  Polyamines · CPC title