IP Library Granted Patent US 12,521,481
Granted Patent B2
US 12,521,481 · App. 18/536,739 · Granted Jan 13, 2026

System and methods for the treatment of wounds with negative pressure and instillation of peroxide pyruvic acid

Inventors: Shannon C. Ingram (San Antonio, TX); Christopher Allen Carroll (San Antonio, TX)
Assignee: Solventum Intellectual Properties Company
A61M1/85A61F13/00063A61F13/01017A61F13/05A61K31/327A61M1/92A61M1/96A61M2205/18A61M2205/3344A61M2205/50A61M2205/502A61M2205/52
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Quick Facts
Patent No.
US 12,521,481
App. No.
18/536,739
Granted
Jan 13, 2026
Kind
B2
Abstract

A system and method for treating a tissue site is described having a dressing adapted to contact the tissue site and provide a fluid seal, and a solution source fluidly coupled to the dressing and adapted to deliver an antimicrobial solution comprising a peroxy α-keto carboxylic acid, such as peroxy pyruvic acid, to the dressing. The system may include a negative-pressure source fluidly coupled to the dressing and adapted to provide negative pressure to the dressing after delivery of the antimicrobial fluid to the dressing.

Claims (28)

1 . A method for treating a tissue site, comprising:

positioning a tissue interface to contact the tissue site;

covering the tissue interface and the tissue site with a drape to provide a fluid seal between a therapeutic environment including the tissue interface on one side of the drape and a local external environment the other side of the drape;

delivering an antimicrobial solution comprising a peroxy α-keto carboxylic acid to the therapeutic environment from a solution source fluidly coupled to the tissue interface; and

providing negative pressure to the therapeutic environment after delivery of the antimicrobial solution to the therapeutic environment from a negative-pressure source fluidly coupled to the tissue interface.

2 . The method to claim 1 , further providing negative pressure to the therapeutic environment before, during or after delivering the antimicrobial solution from the negative-pressure source to the therapeutic environment.

3 . The method according to claim 1 , further providing a target pressure from the negative-pressure source to the therapeutic environment in a pressure control mode.

4 . The method according to claim 1 , further providing a variable target pressure from the negative-pressure source to the therapeutic environment in a dynamic pressure mode.

5 . The method according to claim 1 , further providing the antimicrobial solution to the therapeutic environment in a predetermined dosage.

6 . The method according to claim 1 , further providing the antimicrobial solution to the therapeutic environment for a predetermined time.

7 . The method according to claim 1 , further providing the antimicrobial solution to the therapeutic environment at a predetermined rate over time.

8 . The method according to claim 1 , wherein the delivering of the antimicrobial solution comprises an intermittent flow of fluid soaking the tissue interface, preferably for from about one second to about thirty minutes.

9 . The method according to claim 1 , further providing the negative pressure to the therapeutic environment prior to providing the antimicrobial solution to the therapeutic environment.

10 . The method according to claim 1 , wherein the providing the negative pressure and the providing the antimicrobial solution are sequentially repeated two or more times.

11 . The method according to claim 1 , further providing the negative pressure to the therapeutic environment while providing the antimicrobial solution to the therapeutic environment.

12 . The method according to claim 1 , wherein the tissue interface is a manifold.

13 . The method according to claim 12 , wherein the manifold is a porous foam material having interconnected pores for distributing the antimicrobial fluid to the therapeutic environment.

14 . The method according to claim 13 , wherein the pores have a size in the range of 400-600 microns.

15 . The method according to claim 1 , wherein the antimicrobial solution comprises the peroxy α-keto carboxylic acid at a concentration of from about 2% to about 0.005%, preferably from about 1% to about 0.01%, more preferably from about 0.5% to about 0.25%.

16 . The method according to claim 1 , wherein the peroxy α-keto carboxylic acid is peroxy pyruvic acid.

17 . A dressing for treating a tissue site, comprising:

a tissue interface including a porous foam material having interconnected pores forming passageways for distributing negative pressure to the tissue site and adapted to contact the tissue site;

a cover adapted to provide a fluid seal between a therapeutic environment including

the tissue interface proximate one side of the cover and a local external environment on the other side of the cover; and

an antimicrobial solution comprising a peroxy α-keto carboxylic acid permeating at least a portion of the porous foam material.

18 . The dressing according to claim 17 , wherein the porous foam material has a pore size operable to deliver both negative pressure and the antimicrobial fluid to the therapeutic environment.

19 . The dressing according to claim 17 , wherein the porous foam material has a pore size in the range of 400-600 microns.

20 . The dressing according to claim 17 , wherein the peroxy α-keto carboxylic acid is peroxy pyruvic acid.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2024
From: 3M INNOVATIVE PROPERTIES COMPANY
To: SOLVENTUM INTELLECTUAL PROPERTIES COMPANY
Reel/Frame 066436/0225 →