Electroporation of tissue products
US-2015343101-A1 · Dec 3, 2015 · US
US9763442B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9763442-B2 |
| Application number | US-201414497427-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 26, 2014 |
| Priority date | Dec 29, 2010 |
| Publication date | Sep 19, 2017 |
| Grant date | Sep 19, 2017 |
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The present disclosure is related to percarboxylic acid compositions formed in situ in non-equilibrium reactions. The peroxycarboxylic acid compositions are formed using ester based starting materials. Methods for using the percarboxylic acid compositions are also disclosed.
Opening claim text (preview).
What is claimed is: 1. A peroxycarboxylic acid forming composition comprising: an ester of a polyhydric alcohol and a C5 to C18 carboxylic acid, wherein said ester has an HLB value of 3 or greater; an oxidizing agent comprising a hydrogen peroxide donor; and a source of alkalinity; wherein said composition is not at equilibrium, forms a peroxycarboxylic acid in situ, and has a pH greater than 12; and wherein the composition is free of surfactant. 2. The composition of claim 1 , wherein the polyhydric alcohol is selected from the group consisting of a sugar, a sugar alcohol, and mixtures and derivatives thereof. 3. The composition of claim 2 , further comprising an organic solvent to solubilize the ester; wherein the solvent is an ether, or a ketone, or a water soluble alcohol selected from the group consisting of methanol, ethanol, propanol, isopropanol, butanol and mixtures thereof. 4. The composition of claim 1 , wherein the ester is selected from the group consisting of glycerol monooctanoate, glycerol dioctanoate, glycerol trioctanoate, sorbitan monooctanoate, sorbitan dioctanoate, sorbitan trioctanoate, laurate sucroside and mixtures and derivatives thereof. 5. The composition of claim 1 , wherein the oxidizing agent comprises hydrogen peroxide or a source of hydrogen peroxide selected from the group consisting of a percarbonate, a perborate, urea hydrogen peroxide, PVP-peroxides and mixtures thereof. 6. The composition of claim 1 , wherein the source of alkalinity is selected from the group consisting of an alkaline metal hydroxide, an alkaline earth metal hydroxide, an alkali metal silicate, an alkali metal carbonate, borates and mixtures thereof. 7. The composition of claim 1 , further comprising an ester of a polyhydric alcohol and a C1 to C4 carboxylic acid. 8. The composition of claim 1 , wherein the concentration of the at least one ester of a polyhydric alcohol and a C5 to C18 carboxylic acid is between about 0.01 wt-% to about 95 wt-% of the composition. 9. A peroxycarboxylic acid forming composition comprising: about 0.01 wt-% to about 95 wt-% of an ester of a polyhydric alcohol and a C5 to C18 carboxylic acid, wherein said ester has an HLB value of 3 or greater; an oxidizing agent comprising a hydrogen peroxide donor; and about 0.001 wt-% to about 25 wt-% of a source of alkalinity; wherein said composition is not at equilibrium, forms a peroxycarboxylic acid in situ, and has a pH of at least 12.5; and wherein the composition does not contain surfactant. 10. The composition of claim 9 , further comprising an ester of a polyhydric alcohol and a C1 to C4 carboxylic acid; wherein the ester of the polyhydric alcohol and C5 to C18 carboxylic acid is selected from the group consisting of glycerol monooctanoate, glycerol dioctanoate, glycerol trioctanoate, sorbitan monooctanoate, sorbitan dioctanoate, sorbitan trioctanoate, laurate sucroside and mixtures and derivatives thereof. 11. The composition of claim 10 , further comprising a solvent, wherein the solvent is water and/or an organic solvent to solubilize the ester. 12. The composition of claim 9 , wherein the oxidizing agent comprises hydrogen peroxide or a hydrogen peroxide source selected from the group consisting of a percarbonate, a perborate, urea hydrogen peroxide, PVP-peroxides and mixtures thereof. 13. The composition of claim 9 , wherein the source of alkalinity is selected from the group consisting of an alkaline metal hydroxide, an alkaline earth metal hydroxide, an alkali metal silicate, an alkali metal carbonate and mixtures thereof. 14. A method for delivering an antimicrobial composition to a surface comprising contacting the surface with the peroxycarboxylic acid composition of claim 1 . 15. A method for forming an antimicrobial composition, said method comprising: (a) providing the peroxycarboxylic acid composition according to claim 9 ; (b) diluting the peroxycarboxylic acid composition; (c) providing an acidic aqueous solution; and (d) diluting the peroxycarboxylic acid composition of step (b) with the acidic aqueous solution to a pH of about 1.0 to about 8.0 to form the antimicrobial composition. 16. The method of claim 15 , wherein the peroxycarboxylic acid composition is allowed to react for a sufficient amount of time such that a C5 to C18 percarboxylic acid is formed. 17. The method of claim 16 , wherein the step (b) dilution of the peroxycarboxylic acid composition results in an active peroxycarboxylic acid content of about 0.01% to about 0.1%. 18. The method of claim 17 , wherein the antimicrobial composition having a pH of about 1.0 to about 8.0 is further diluted to a use solution having an active peroxycarboxylic acid content of about 1 ppm to about 100 ppm. 19. A method of using a peroxycarboxylic acid composition, said method comprising: (a) providing the peroxycarboxylic acid composition according to claim 9 ; (b) allowing the peroxycarboxylic acid composition to react for a sufficient amount of time such that a C5 to C18 peroxycarboxylic acid is formed; and (c) delivering the peroxycarboxylic acid composition to a surface without an acidification step. 20. The method of claim 19 , wherein the peroxycarboxylic acid composition is further diluted within a use application. 21. The method of claim 19 , wherein the peroxycarboxylic acid composition is substantially free of a stabilizing agent.
Antibacterial agents · CPC title
the —O—O— group being bound between a >C=O group and hydrogen, i.e. peroxy acids · CPC title
containing the group [IMAGE cpc-sch-A01N-0934.gif]; Thio analogues thereof · CPC title
containing the group [IMAGE cpc-sch-A01N-0932.gif], wherein Cn means a carbon skeleton not containing a ring; Thio analogues thereof · CPC title
Acyclic compounds · CPC title
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