IP Library Granted Patent US 12,377,062
Granted Patent B2
US 12,377,062 · App. 17/619,373 · Granted Aug 5, 2025

Antimicrobial solutions

Inventors: Ranjani V. Parthasarathy (Woodbury, MN); Joshua E. Schumaker (Minneapolis, MN)
Assignee: Solventum Intellectual Properties Company
A61K31/155A61K9/0014A61K9/08A61K47/10A61P31/02
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,377,062
App. No.
17/619,373
Granted
Aug 5, 2025
Kind
B2
Abstract

An antimicrobial composition includes an aqueous carrier and a surfactant system. The surfactant system includes a first surfactant including a first polyethylene glycol (PEG) compound with an HLB value of greater than about 10 and less than about 14, and a second surfactant different from the first surfactant, wherein the second surfactant has an HLB value less than about 10.

Claims (29)

1. An antimicrobial composition, comprising:

an aqueous carrier present in an amount of about 5 wt % to about 95 wt % based on the total weight of the composition;

a cationic antiseptic present in an amount of about 1 wt % to about 10 wt % based on the total weight of the composition, the cationic antiseptic selected from octenidine, chlorhexidine, polyhexamethylene biguanide, benzalkonium chloride, alexidine dihydrochloride, cetyl pyridinium chloride, salts thereof, and a combination thereof; and

a surfactant system comprising:

a first surfactant present in an amount of about 1 wt % to about 10 wt % based on the total weight of the composition,

the first surfactant selected from PEG alkyl esters, PEG alkyl ethers, PEG alkyl amides, and a combination thereof, wherein each alkyl group has 8 to 22 carbon atoms,

the first surfactant characterized by an HLB value of greater than about 10 and less than about 14, and

a second surfactant present in an amount of about 1 wt % to about 10 wt % based on the total weight of the composition,

the second surfactant comprising a 1,2-dihydroxy group and selected from an alkyl ester, an alkyl ether an alkyl amide, and a combination thereof, wherein each alkyl group has 8 to 22 carbon atoms

the second surfactant characterized by an HLB value less than about 10, wherein the first surfactant and the second surfactant are different.

2. The antimicrobial composition of claim 1 , further comprising a third surfactant characterized by HLB value of greater than about 14 and less than about 18.

3. The antimicrobial composition of claim 2 , wherein the third surfactant is a PEG compound chosen from PEG alkyl esters, PEG alkyl ethers, PEG alkyl amides, and mixtures and combinations thereof, the PEG compounds having an alkyl group independently selected to have 8 to 22 carbon atoms.

4. The antimicrobial composition of claim 1 , wherein the first surfactant comprises 6 to 60 ethylene oxide units.

5. The antimicrobial composition of claim 1 , wherein the first surfactant is selected from PEG 12 glyceryl laurate, PEG 20 glyceryl laurate, PEG 30 glyceryl laurate, PEG 20 glyceryl stearate, PEG 7 cocoate, PEG glyceryl caprate, polyglycerol oleate and a combination thereof.

6. The antimicrobial composition of claim 1 , wherein the composition further comprises an alcohol chosen from benzyl alcohol, phenoxy ethanol, isopropyl alcohol, ethanol, and mixtures and combinations thereof.

7. The antimicrobial composition of claim 6 , wherein the alcohol is present in the composition at about 1 wt % to about 10 wt %, based on the total weight of the composition.

8. The antimicrobial composition of claim 1 , wherein the aqueous carrier comprises at least about 80 wt % water, based on the total weight of the aqueous carrier.

9. The antimicrobial composition of claim 1 , wherein the aqueous carrier comprises glycerol, propylene glycol, polyethylene glycol, pentylene glycol, and mixtures and combinations thereof.

10. The antimicrobial composition of claim 1 , wherein the second surfactant is a monoglyceride, derived from a fatty acid chosen from oleic, linoleic, linolenic, caproic, caprylic, capric, lauric, and mixtures and combinations thereof.

11. The antimicrobial composition of claim 1 , wherein the cationic antiseptic is chosen from octenidine hydrochloride, polyhexamethylene biguanide, chlorhexidine gluconate, and a combination thereof.

12. The antimicrobial composition of claim 1 , wherein the cationic antiseptic is chlorhexidine gluconate.

13. A method of disinfecting a treatment site chosen from skin, hair, mucosae, wounds, and body cavities, the method comprising

applying to the treatment site an antimicrobial composition of claim 1 .

14. The method of claim 13 , wherein the composition reduces microorganisms at the treatment site by at least 2 log orders after 10 seconds.

15. The method of claim 13 , wherein the composition reduces microorganisms at the treatment site by at least 5 log orders after 10 seconds.

16. The method of claim 13 , wherein the composition prevents regrowth of microorganisms at the treatment site for 24 hours.

17. A kit, comprising:

an antimicrobial composition of claim 1 ; and

an applicator for applying the antimicrobial composition to the skin of a patient.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2024
From: 3M INNOVATIVE PROPERTIES COMPANY
To: SOLVENTUM INTELLECTUAL PROPERTIES COMPANY
Reel/Frame 066430/0149 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 15, 2021
From: PARTHASARATHY, RANJANI V.; SHUMAKER, JOSHUA E.
To: 3M INNOVATIVE PROPERTIES COMPANY
Reel/Frame 058396/0732 →
Continuity (2)
Provisional Application 62864187 · Jun 20, 2019
Related Publication 20220347128A1 · Nov 3, 2022
References Cited (11)
US 6211139B1 · Keys · 2001 [cited by applicant]
US 20090186943A1 · Ikeda · 2009 [cited by applicant]
US 20160074517A1 · Nguyen-Kim · 2016 [cited by applicant]
DE 10016875 · 2001 [cited by applicant]
EP 1955691 · 2008 [cited by applicant]
WO WO2001014313 · 2001 [cited by applicant]
WO WO2011023887 · 2011 [cited by applicant]
WO WO2016019174A1 · 2016 [cited by applicant]
Griffin, “Calculation of HLB Values of Non-Ionic Surfactants”, Journal of the Society of Cosmetic Chemists, Dec. 1954, vol. 5 No. 4, pp. 249-256. [cited by applicant]
Wenninger, “International Cosmetics Ingredient Dictionary and Handbook,” 7th Edition, Published by The Cosmetic, Toiletry, and Fragrance Association, 1997, vol. 2, 4 pages. [cited by applicant]
International Search Report for PCT Application No. PCT/IB2020/055738, mailed on Nov. 23, 2020, 8 pages. [cited by applicant]