Bacterial ferment of Lactobacillus species

US12076436B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12076436-B2
Application numberUS-202217737206-A
CountryUS
Kind codeB2
Filing dateMay 5, 2022
Priority dateMay 7, 2021
Publication dateSep 3, 2024
Grant dateSep 3, 2024

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  2. Abstract

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Abstract

Official abstract text for this publication.

A bacterial ferment obtained by a method including the following steps: (a) culturing Lactobacillus species in at least one growth medium for at least 24 hours; (b) separating the mixture via centrifugation; (c) adding lactic acid to the supernatant obtained from step b) in an amount sufficient to lower the pH value of the supernatant; (d) stabilizing the resulting mixture with the addition of at least one preservative and/or at least one multifunctional; and optionally (e) filtering the mixture to remove any final precipitation.

First claim

Opening claim text (preview).

What is claimed: 1. A bacterial ferment obtained by a method comprising the following steps: (a) culturing Lactobacillus species in at least one growth medium for at least 24 hours; (b) separating the mixture via centrifugation to obtain a supernatant; (c) adding lactic acid to the supernatant obtained from step b) in an amount sufficient to lower the pH value of the supernatant to obtain a resulting mixture, wherein the amount of lactic acid is from 2 to 10 percent, by weight, of the total amount of the mixture; (d) stabilizing the resulting mixture by adding at least one preservative and/or at least one multifunctional, wherein the at least one preservative comprises benzoic acid, or esters and salts thereof; propionic acid or salts thereof; salicylic acid or salts thereof; 2,4-hexanoic acid (sorbic acid) or salts thereof; formaldehyde, paraformaldehyde; 2-hydroxybiphenyl ether or salts thereof; 2-zincsulphidopyridine N-oxide; inorganic sulphites, inorganic bisulphites; sodium iodate; chlorobutanol; 4-hydroxybenzoic acid or salts or esters thereof; dehydroacetic acid; formic acid; 1,6-bis(4-amidino-2-bromophenoxy)-n-hexane or salts thereof; sodium salt of ethylmercury-(II)-thiosalicylic acid; phenylmercury or salts thereof; 10-undecylenic acid or salts thereof; 5-amino-1,3-bis(2-ethylhexyl)-5-methylhexahydropyrimidine; 5-bromo-5-nitro-1,3-dioxane; 2-bromo-2-nitro-1,3-propanediol; 2,4-dichlorobenzyl alcohol; N-(4-chlorophenyl)-N′-(3,4-dichlorophenyl)urea; 4-chloro-m-cresol; 2,4,4′-trichloro-2′-hydroxy-diphenyl ether; 4-chloro-3,5-dimethylphenol; 1,1′-methylene-bis(3-(1-hydroxymethyl-2,4-dioximidazolidin-5-yl)urea); poly(hexamethylene biguanide) hydrochloride; 2-phenoxyethanol; hexamethylenetetramine; 1-(3-chloroallyl)-3,5,7-triaza-1-azoniaadamantane chloride; 1-(4-chloro-phenoxy)-1(1H-imidazol-1-yl)-3,3-dimethyl-2-butanone; 1,3-bis(hydroxymethyl)-5,5-dimethyl-2,4-imidazolidinedione; benzyl alcohol; piroctone olamine; 1,2-dibromo-2,4-dicyanobutane; 2,2′-methylene-bis(6-bromo-4-chloro-phenol); bromochlorophene; mixture of 5-chloro-2-methyl-3(2H)-isothiazolinone and 2-methyl-3(2H)isothiazolinone with magnesium chloride and/or magnesium nitrate; 2-benzyl-4-chlorophenol; 2-chloroacetamide; chlorhexidine; chlorhexidine acetate; chlorhexidine gluconate; chlorhexidine hydrochloride; 1-phenoxy-propan-2-ol; N-alkyl(C12-C22)trimethylammonium bromide and/or chloride; 4,4-dimethyl-1,3-oxazolidine; N-hydroxymethyl-N-(1,3-di(hydroxymethyl)-2,5-dioxoimidazolidin-4-yl)-N′-hydroxymethylurea; 1,6-bis(4-amidinophenoxy)-n-hexane or salts thereof; glutaraldehyde 5-ethyl-1-aza-3,7-dioxabicyclo(3.3.0)octane; 3-(4-chlorophenoxy)-1,2-propanediol; hyamine; alkyl(C8-C18)dimethylbenzylammonium chloride; alkyl(C8-C18)dimethylbenzylammonium bromide; alkyl(C8-C18)dimethylbenzylammonium saccharinate; benzylhemiformal; 3-iodo-2-propynyl butylcarbamate; or sodium ((hydroxymethyl)amino)acetate; and wherein the at least one multifunctional comprises 1,2-propanediol; 1,3-propanediol; 1,2-butanediol; 1,3-butanediol (butylene glycol); 1,2-pentanediol; 1,2-hexanediol; 1,2-heptanediol; 1,2-octanediol; 1,2-nonanediol; 1,2-decanediol; glycerol; phenoxyethanol; ethylhexylglycerin; glyceryl caprylate; hydroxyacetophenone; methylbenzyl alcohol; o-cymen-5-ol; benzyl alcohol; tropolone; or mixtures of two or more of said multifunctionals; and optionally (e) filtering the mixture to remove any final precipitation. 2. A composition comprising the bacterial ferment according to claim 1 , wherein the composition is a pharmaceutical composition or a cosmetic composition. 3. The composition according to claim 2 , wherein the composition is selected from the group consisting of oil in water emulsion, water in oil emulsion, crème, lotion, and ointment. 4. A product comprising the bacterial ferment according to claim 1 , wherein the product is a pharmaceutical product or a cosmetic product.

Assignees

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Classifications

  • Anti-perspirants or body deodorants (deodorisation of air A61L9/00) · CPC title

  • Preparations containing hair conditioners · CPC title

  • Preparations for cleaning the hair · CPC title

  • Washing or bathing preparations · CPC title

  • Anti-ageing preparations · CPC title

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What does patent US12076436B2 cover?
A bacterial ferment obtained by a method including the following steps: (a) culturing Lactobacillus species in at least one growth medium for at least 24 hours; (b) separating the mixture via centrifugation; (c) adding lactic acid to the supernatant obtained from step b) in an amount sufficient to lower the pH value of the supernatant; (d) stabilizing the resulting mixture with the addition o…
Who is the assignee on this patent?
Symrise Ag
What technology area does this patent fall under?
Primary CPC classification C12N1/20. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 03 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).