IP Library Granted Patent US 10,136,639
Granted Patent B2
US 10,136,639 · App. 15/034,375 · Granted Nov 27, 2018

Polycationic amphiphiles as antimicrobial agents

Inventors: William Wuest (Wallingford, PA); Kevin Patrick Minbiole (Media, PA)
Assignees: Villanova University; Temple University of the Commonwealth System of Higher Education
A01N33/12A01N25/08A61K31/132Y02A50/473
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Quick Facts
Patent No.
US 10,136,639
App. No.
15/034,375
Granted
Nov 27, 2018
Kind
B2
Abstract

The present disclosure provides an antimicrobial composition including a polycationic amphiphile compound, and the method of making and the method of using such a compound or composition. The compound having the formula (I) or (II) R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 10 , or R 11 is H or a C 1-12 alkyl unsubstituted or optionally substituted with a functional group such as —OH, —OR′, —NH 2 , —NHR′, —NR′ 2 , —N—C(O)R′, —N—C(O)CR′═CR′, —SH, —SR′, —O—C(O)R′, —C(O)R′, —CF 3 , —OCF 3 , halogen, benzyl, o-vinylbenzyl, m-vinylbenzyl, p-vinylbenzyl, phenyl, allyl, and substituted allyl. R 7 , R 8 or R 9 is a C 1-12 alkyl unsubstituted or optionally substituted with a functional group such as —OH, —OR′, —NH 2 , —NHR′, —NR′ 2 , —SH, —SR′, —O—C(O)R′, —C(O)R′, —CF 3 , and —OCF 3 . R′ is H or a C 1-4 alkyl. X or Y is a halogen, m and n are integers in the range from 1 to 25.

Claims (51)

1. An antimicrobial composition comprising a compound having the formula

wherein:

R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 10 , or R 11 is H or a C 1-12 alkyl unsubstituted or optionally substituted with a functional group selected from the group consisting of —NH 2 , —NHR′, —NR′ 2 , —N—C(O)R′, —N—C(O)CR′═CR′, —SH, —SR′, —O—C(O)R′, —C(O)R′, —CF 3 , —OCF 3 , halogen, benzyl, o-vinylbenzyl, m-vinylbenzyl, p-vinylbenzyl, phenyl, allyl, and substituted allyl;

R 7 , R 8 or R 9 is a C 3-12 alkyl unsubstituted or optionally substituted with a functional group selected from the group consisting of —NH 2 , —NHR′, —NR′ 2 , —SH, —SR′, —O—C(O)R′, —C(O)R′, —CF 3 , and —OCF 3 ;

R′ is H or a C 1-4 alkyl;

X or Y is a halogen; and

m and n are integers in the range of from 5 to 25.

2. The antimicrobial composition of claim 1 , wherein

R 7 , R 8 or R 9 is a C 3-5 alkyl unsubstituted or optionally substituted.

3. The antimicrobial composition of claim 1 , wherein

R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 10 , or R 11 is H or a C 1-4 alkyl.

4. The antimicrobial composition of claim 1 , wherein

at least one of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 10 , or R 11 is a C 1-12 alkyl substituted with a functional group selected from the group consisting of —SH, allyl, and substituted allyl.

5. The antimicrobial composition of claim 1 , wherein

X or Y is chlorine or bromine.

6. The antimicrobial composition of claim 1 , wherein

m and n are integers in the range from 10 to 16.

7. The antimicrobial composition of claim 1 , wherein

at least one of m and n is 12.

8. The antimicrobial composition of claim 1 , wherein the compound has the formula

9. The antimicrobial composition of claim 8 , wherein in the compound having the formula (I-3), at least one of R 1 and R 2 , and at least one of R 3 and R 4 , and at least one of R 5 and R 6 are methyl.

10. The antimicrobial composition of claim 8 , wherein in the compound having the formula (I-3), m and n are 12, one of R 3 and R 4 is selected from a group consisting of ethyl, propyl and allyl, and the other groups among R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 are methyl.

11. The antimicrobial composition of claim 1 , wherein the compound has the formula

12. The antimicrobial composition of claim 11 , wherein in the compound having the formula (II-2) or (II-3), at least one of R 1 and R 2 , and at least one of R 3 and R 4 , at least one of R 5 and R 6 , and at least one of R 10 and R 11 are methyl.

13. The antimicrobial composition of claim 11 , wherein in the compound having the formula (II-2), m and n are 12, one of R 3 and R 4 is selected from a group consisting of ethyl, propyl and allyl, and the other groups among R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 10 , and R 11 are methyl.

14. A method of making the antimicrobial composition of claim 1 comprising mixing an effective amount of a compound having the formula (I) or (II) and a carrier.

15. A method of killing or inhibiting microbial growth, comprising applying the antimicrobial composition of claim 1 comprising a compound having the formula (I) or (II).

16. The method of claim 15 , wherein the antimicrobial composition is used to kill or inhibit growth of at least one group of microorganisms selected from the group consisting of bacteria, viruses, yeast, fungi, and protozoa, or to inhibit formation of a biofilm or eradicate a pre-established biofilm.

17. A film or coating comprising a compound

grafted onto a solid surface

wherein:

R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 10 , or R 11 is H or a C 1-12 alkyl unsubstituted or optionally substituted with a functional group selected from the group consisting of —NH 2 , —NHR′, —NR′ 2 , —N—C(O)R′, —N—C(O)CR′═CR′, —SH, —SR′, —O—C(O)R′, —C(O)R′, —CF 3 , —OCF 3 , halogen, benzyl, o-vinylbenzyl, m-vinylbenzyl, p-vinylbenzyl, phenyl, allyl, and substituted allyl;

R 7 , R 8 or R 9 is a C 3-12 alkyl unsubstituted or optionally substituted with a functional group selected from the group consisting of —NH 2 , —NHR′, —NR′ 2 , —SH, —SR′, —O—C(O)R′, —C(O)R′, —CF 3 , and —OCF 3 ;

R′ is H or a C 1-4 alkyl;

X or Y is a halogen; and

m and n are integers in the range of from 5 to 25.

18. The film or coating of claim 17 , wherein the compound grafted on a solid surface has a structure:

wherein L is a linker comprising a functional group.

19. The film or coating of claim 18 , wherein R 4 is a methylene group optionally substituted with a functional group selected from the group consisting of —OH, —OR′, —NH 2 , —NHR′, —NR′ 2 , —SH, —SR′, —O—C(O)R′, —C(O)R′, —CF 3 , and —OCF 3 .

20. The film or coating of claim 17 , wherein

R 7 , R 8 or R 9 is a C 3-5 alkyl unsubstituted or optionally substituted.

21. The film or coating of claim 17 , wherein

R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 10 , or R 11 is H or a C 1-4 alkyl.

22. The film or coating of claim 17 , wherein

at least one of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 10 , or R 11 is a C 1-12 alkyl substituted with a functional group selected from the group consisting of —SH, allyl, and substituted allyl.

23. The film or coating of claim 17 , wherein

X or Y is chlorine or bromine.

24. The film or coating of claim 17 , wherein

m and n are integers in the range from 10 to 16.

25. The film or coating of claim 17 , wherein

at least one of m and n is 12.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 11, 2017
From: MINBIOLE, KEVIN PATRICK
To: VILLANOVA UNIVERSITY
Reel/Frame 043544/0693 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 11, 2017
From: WUEST, WILLIAM
To: TEMPLE UNIVERSITY OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
Reel/Frame 043811/0866 →
Continuity (4)
Provisional Application 61900037 · Nov 5, 2013
Provisional Application 62039265 · Aug 19, 2014
Provisional Application 62059216 · Oct 3, 2014
Related Publication 20160262384A1 · Sep 15, 2016
Cited By (6)
US 12,226,430 US 12,318,445 US 12,448,619 US 12,502,401 US 12,514,867 US 12,514,869