US20020031537A1 - Use of nitrogen-containing complexing agents for deodorization and antimicrobial treatment of the skin and textile fibre materials - Google Patents
Use of nitrogen-containing complexing agents for deodorization and antimicrobial treatment of the skin and textile fibre materials Download PDFInfo
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- US20020031537A1 US20020031537A1 US09/180,992 US18099298A US2002031537A1 US 20020031537 A1 US20020031537 A1 US 20020031537A1 US 18099298 A US18099298 A US 18099298A US 2002031537 A1 US2002031537 A1 US 2002031537A1
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- complexing agents
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- ZUHZZVMEUAUWHY-UHFFFAOYSA-N CCCN(C)C Chemical compound CCCN(C)C ZUHZZVMEUAUWHY-UHFFFAOYSA-N 0.000 description 3
- KHRIPQMMFOGLOF-UHFFFAOYSA-N C.CN(C)C Chemical compound C.CN(C)C KHRIPQMMFOGLOF-UHFFFAOYSA-N 0.000 description 2
- AACDSIAWVCYZOH-UHFFFAOYSA-N O=C(O)C(NCCNC(COO)COO)C(=O)O Chemical compound O=C(O)C(NCCNC(COO)COO)C(=O)O AACDSIAWVCYZOH-UHFFFAOYSA-N 0.000 description 2
- ZABVIADJWZDOBO-KGFZYKRKSA-N C=N[C@](CC(O)=O)(C(O)=O)NCCN[C@@H](CC(O)=O)C(O)=O Chemical compound C=N[C@](CC(O)=O)(C(O)=O)NCCN[C@@H](CC(O)=O)C(O)=O ZABVIADJWZDOBO-KGFZYKRKSA-N 0.000 description 1
- VUYLFLAJYCUUEM-UHFFFAOYSA-N CCCN(CCOO)CCOO Chemical compound CCCN(CCOO)CCOO VUYLFLAJYCUUEM-UHFFFAOYSA-N 0.000 description 1
- IDVWPTOMPXLJMB-UHFFFAOYSA-N CCN(CC(=O)O)C(C)COO Chemical compound CCN(CC(=O)O)C(C)COO IDVWPTOMPXLJMB-UHFFFAOYSA-N 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N CN(C)C Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- UGFSMVYIJBCLOD-UHFFFAOYSA-N CN(CC(O)=O)C(CC(O)=O)C(O)=O Chemical compound CN(CC(O)=O)C(CC(O)=O)C(O)=O UGFSMVYIJBCLOD-UHFFFAOYSA-N 0.000 description 1
- XKPVCICRQHPZQR-UHFFFAOYSA-N CN(COOP=O)CP(=O)(O)O Chemical compound CN(COOP=O)CP(=O)(O)O XKPVCICRQHPZQR-UHFFFAOYSA-N 0.000 description 1
- CZURTTXRPCKSCT-UHFFFAOYSA-N O=C(O)CC(COO)N(CCOO)CC(=O)O Chemical compound O=C(O)CC(COO)N(CCOO)CC(=O)O CZURTTXRPCKSCT-UHFFFAOYSA-N 0.000 description 1
- NKVRXBBUYXJMPE-UHFFFAOYSA-N O=C(O)CCN(CCOO)CCOO Chemical compound O=C(O)CCN(CCOO)CCOO NKVRXBBUYXJMPE-UHFFFAOYSA-N 0.000 description 1
- DVXPOBBWIYFGNT-UHFFFAOYSA-N [H]C(C)(CCOO)NC Chemical compound [H]C(C)(CCOO)NC DVXPOBBWIYFGNT-UHFFFAOYSA-N 0.000 description 1
- ZVGYMCGETRUXSS-UHFFFAOYSA-N [H]C(CC)(C(=O)O)N(CCOO)CCOO Chemical compound [H]C(CC)(C(=O)O)N(CCOO)CCOO ZVGYMCGETRUXSS-UHFFFAOYSA-N 0.000 description 1
- HETHGHFSYWRISL-UHFFFAOYSA-N [H]C(CCOO)(NC)C(=O)O Chemical compound [H]C(CCOO)(NC)C(=O)O HETHGHFSYWRISL-UHFFFAOYSA-N 0.000 description 1
- ULLSOJVOFIGQNE-YUMQZZPRSA-N [H][C@@](CC(=O)O)(NCCN[C@@]([H])(CC(=O)O)C(=O)O)C(C)=O Chemical compound [H][C@@](CC(=O)O)(NCCN[C@@]([H])(CC(=O)O)C(=O)O)C(C)=O ULLSOJVOFIGQNE-YUMQZZPRSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/005—Antimicrobial preparations
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
- C11D9/22—Organic compounds, e.g. vitamins
- C11D9/30—Organic compounds, e.g. vitamins containing nitrogen
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/005—Compositions containing perfumes; Compositions containing deodorants
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/325—Amines
- D06M13/342—Amino-carboxylic acids; Betaines; Aminosulfonic acids; Sulfo-betaines
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/51—Chelating agents
Definitions
- the present invention relates to the use of nitrogen-containing complexing agents for deodorization and antimicrobial treatment of the skin and of textile fibre materials.
- EDTA ethylene-diaminetetraacetic acid
- NTA nitrilotriacetic acid
- EDETA ⁇ -alaninediacetic acid
- EDDS ethylenediaminedisuccinic acid
- the present invention therefore relates to the use of nitrogen-containing complexing agents for antimicrobial treatment of the skin and of textile fibre materials.
- Q 1 is Carb 1 ; Carb 2, ; or a radical of the formula —(CH 2 ) m 1 —OH
- Q 2 is hydrogen or Carb 2 ;
- Q 3 is Carb 3 ; an amino acid radical; or a radical of the formula (1a)
- Carb 1 , Carb 2 and Carb 3 independently of one another are the radical of a C 1 -C 8 -mono- or dicarboxylic acid;
- m 1 is 1 to 5.
- Q 1 is a monocarboxylic acid; or a radical of the formula —(CH 2 ) m 1 —OH;
- Q 2 is hydrogen or a monocarboxylic acid
- Q 3 is formula (1b); or a monocarboxylic acid.
- n 1 is 0 to 5.
- NTA Nitrilotriacetic acid
- AMP aminotrimethylenephosphoric acid
- SDA serinediacetic acid
- MGDA methylglycinediacetic acid
- the nitrogen-containing complexing agents employed according to the invention can be employed not only as the acid but also in the form of the water-soluble salts, preferably as lithium, sodium, potassium, ammonium and ethanolammonium salts.
- Ethylenediaminedisuccinic acid (EDDS) of the formula (2) has two asymmetric carbon atoms. Various stereoisomeric forms of this compound are therefore possible.
- the (S,S) configuration of EDDS has the formula
- Racemic EDDS can be prepared in accordance with U.S. Pat. No. 3,158,635.
- the complexing agents according to the invention show a pronounced bacteriostatic action, in particular against Gram-positive bacteria of the skin flora, for example Corynebacterium xerosis (bacteria which causes body odour). They are therefore particularly suitable as the antimicrobial active substance in body care compositions, for example soaps, shampoos, foot care products and, in particular, deodorants, as well as an additive in detergents.
- body care compositions for example soaps, shampoos, foot care products and, in particular, deodorants, as well as an additive in detergents.
- the invention therefore also relates to a body care composition
- a body care composition comprising at least one nitrogen-containing complexing agent and carriers or auxiliaries which are tolerated in comsetics.
- the body care composition according to the invention comprises 0.01 to 15, preferably 0.5 to 10, % by weight, based on the total weight of the composition, of a nitrogen-containing complexing agent and auxiliaries which are tolerated in cosmetics.
- the body care composition also comprises, in addition to the complexing agent, other constituents, for example sequestering agents, dyes, perfume oils, thickeners or consolidating agents (consistency regulators), emmollients, UV absorbers, skin protection agents, antioxidants, additives which improve the mechanical properties, such as dicarboxylic acids and/or Al, Zn, Ca, or Mg salts of C 14 -C 22 fatty acids, and, if appropriate, preservatives.
- other constituents for example sequestering agents, dyes, perfume oils, thickeners or consolidating agents (consistency regulators), emmollients, UV absorbers, skin protection agents, antioxidants, additives which improve the mechanical properties, such as dicarboxylic acids and/or Al, Zn, Ca, or Mg salts of C 14 -C 22 fatty acids, and, if appropriate, preservatives.
- the complexing agents according to the invention can be incorporated into the corresponding formulations without problems.
- the body care compositions according to the invention can be formulated as a water-in-oil or oil-in-water emulsion, as alcoholic or alcohol containing formulation, as a vesicular dispersion of an ionic or nonionic amphiphilic lipid, as a gel or solid stick or as an aerosol formulation.
- the auxiliary which is tolerated in cosmetics preferably comprises 5 to 50% of an oily phase, 5 to 20% of an emulsifier and 30 to 90% of water.
- the oily phase can comprise any oil suitable for cosmetic formulations, for example one or more hydrocarbon oils, a wax, a naturally occurring oil, a silicone oil, a fatty acid ester or a fatty alcohol.
- Preferred mono- or polyols are ethanol, isopropanol, propylene glycol, hexylene glycol, glycerol and sorbitol.
- An anitmicrobial soap has, for example, the following composition:
- soap base for example the sodium slats of tallow fatty and coconut fatty acid or glycerols.
- a shampoo has, for example, the following composition:
- a deodorant has, for example, the following composition:
- the complexing agents according to the invention are furthermore suitable for the treatment of textile fibre materials.
- the fibre materials are non-dyed and dyed or printed fibre materials, for example of silk, leather, wool, polyamide or polyurethanes, and in particular all types of cellulosic fibre materials.
- Such fibre materials are, for example, naturally occurring cellulosic fibres, such as cotton, linen, jute and hemp, and cellulose and regenerated cellulose.
- Textile fibre materials which are preferably suitable are those of cotton.
- Test method An agar diffusion test is carried out with the following modifications:
- Test organisms Corynebacterium xerosis ATCC 373
- test results show that both EDETA, EDTA and the EDDS prepared by fermentation and chemically ( ⁇ R,R; S,S; R,S) show a pronounced bacteriostatic action against Corynebacterium xerosis.
- the formulation is prepared as follows:
- the solid components are mixed and homogenized in a mortar and stirred with deionized water until a uniform pourable and pumpable paste (slurry) is obtained, which is finally spray-dried.
- the formulation is prepared as follows:
- EDDS is dissolved in ethanol. Under stirring at room temperature PEG-40, glycerol and perfume are added. Finally, the water is added.
- the formulation is prepared as follows:
- S,S-EDDS is obtained by means of microbiological (WO 96/36725) or chemical synthesis (J. A. Neal et al., Inorg.Chem. 7, 2405 (1968)). Racemic EDDS is prepared from maleic anhydride and ethylenediamine (U.S. Pat. No. 3,158,635).
- a 1% suspension of racemic EDDS or S,S-EDDS is prepared in water/ethanol (about 7:3) with vigorous stirring.
- An aqueous solution of NaOH is metered in with an autoamtic titration device until the pH of 7 remains constant for 30 minutes. Any slight milky clouding which occurs is removed by filtering through paper.
- a clear deodorant formulation which is stable at room temperature, comprises about 1% of active substance (based on the tetra-acid) and has a skin-friendly pH is obtained.
- NaOH is replaced by KOH, ammonia or ethanolamine
- the corresponding potassium, ammonium and ethanolammonium salts are obtained.
- Lithium hydroxide, sodium carbonate, sodium bicarbonate or laurylamine can also be employed as the base.
- the underarms are washed with a non-antimicrobial soap twice for 1 minute each time.
- a total of 6 ml of test product is then applied to the washed, dry skin of the underarm.
- the EDDS on the skin is extracted by means of discs of filter paper (2 cm diameter) moistened in 0.9% NaCl solution (pH: 8.2). For this, the moist filter disc is placed on the treated skin without airbubbles for 4 minutes. The filter discs are subsequently dried at room temperature and then placed on solid agar media with test bacteria.
- the agar media are incubated for 2 days at 37° C. and the inhibition under the filter disc or the inhibitory aureolas of the filter discs is/are then determined.
- test results are listed in Table 2: TABLE 2 Substance Inhibitory aureola dia- meter (mm)/inhibition under the filter disc* Coryneb. xerosis ATCC 373 Placebo 0/0 R,S-EDDS (sodium salt) immed- 5/4 iately 2 hours 3/4 after application R,S-EDDS (Amine salt) immed- 2,5/4 iately 2 hours 2/4 after application
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Abstract
The present invention relates to the use of nitrogen-containing complexing agents for deodorization and antimicrobial treatment of the skin and of textile fibre materials.
in which
Q1, is Carb1; Carb2,; or a radical of the formula —(CH2)m 1 —OH
Q2 is hydrogen or Carb2; and
where Carb1, Carb2 and Carb3 independently of one another are the radical of a C1-C8-mono- or -dicarboxylic acid and
m1 is 1 to 5.
The complexing agents according to the invention show a pronounced bacteriostatic action against Corynebacterium xerosis (bacteria which cause body odour) and are therefore suitable as the antimicrobial active substance in body care compositions and antimicrobial fabric finishing of textile materials.
Description
- The present invention relates to the use of nitrogen-containing complexing agents for deodorization and antimicrobial treatment of the skin and of textile fibre materials.
- It is known that various nitrogen-containing complexing agents, for example ethylene-diaminetetraacetic acid (EDTA), nitrilotriacetic acid (NTA), β-alaninediacetic acid (EDETA) or ethylenediaminedisuccinic acid (EDDS) are widely employed in domestic detergents because of their complexing properties.
- Surprisingly, it has been found that certain nitrogen-containing complexing agents also have an antimicrobial action against Gram-positive bacteria and are therefore particularly suitable for deodorization and antimicrobial treatment of the human skin and of textile fibre materials.
- The present invention therefore relates to the use of nitrogen-containing complexing agents for antimicrobial treatment of the skin and of textile fibre materials.
-
- in which
- Q1, is Carb1; Carb2,; or a radical of the formula —(CH2)m
1 —OH - Q2 is hydrogen or Carb2; and
-
- where Carb1, Carb2 and Carb3 independently of one another are the radical of a C1-C8-mono- or dicarboxylic acid; and
- m1 is 1 to 5.
-
- and especially compounds of the formula (1) in which
- Q1 is a monocarboxylic acid; or a radical of the formula —(CH2)m
1 —OH; - Q2 is hydrogen or a monocarboxylic acid; and
- Q3 is formula (1b); or a monocarboxylic acid.
- Complexing agents which are of particular interest are those of the formula (1) in which Carb2 and Carb3, independently of one another are the radical of the formula
- —[(CH2)]n
1 —COOH, (1c) - in which
- n1 is 0 to 5.
-
-
- Nitrilotriacetic acid (NTA) is furthermore suitable as the complexing agent.
-
-
-
-
- The nitrogen-containing complexing agents employed according to the invention can be employed not only as the acid but also in the form of the water-soluble salts, preferably as lithium, sodium, potassium, ammonium and ethanolammonium salts.
-
- An inexpensive chemical synthesis leads to a mixture of the three forms S,S; R,R; and meso-EDDS. However, separation of these stereoisomeric compounds requires a high industrial expenditure. Optically pure (S,S)-EDDS can be prepared with the aid of an Actinomycetes strain (T. Nishikiori et al., Production by Actinomycetes of (S,S)-N,N′-ethylenediaminedisuccinic acid, an inhibitor of phospholipase c; J.Antibiotics 37, 426-427 (1984)).
- The purely chemical preparation of the compound of the formula (9) is carried out in a manner known per se, such as is described, for example, by J. A. Neal, N. Rose in Inorganic Chemistry,7, 2405 (1985).
- Racemic EDDS can be prepared in accordance with U.S. Pat. No. 3,158,635.
- The complexing agents according to the invention show a pronounced bacteriostatic action, in particular against Gram-positive bacteria of the skin flora, for example Corynebacterium xerosis (bacteria which causes body odour). They are therefore particularly suitable as the antimicrobial active substance in body care compositions, for example soaps, shampoos, foot care products and, in particular, deodorants, as well as an additive in detergents.
- The invention therefore also relates to a body care composition comprising at least one nitrogen-containing complexing agent and carriers or auxiliaries which are tolerated in comsetics.
- The body care composition according to the invention comprises 0.01 to 15, preferably 0.5 to 10, % by weight, based on the total weight of the composition, of a nitrogen-containing complexing agent and auxiliaries which are tolerated in cosmetics.
- Depending on the form in which the body care composition is present, it also comprises, in addition to the complexing agent, other constituents, for example sequestering agents, dyes, perfume oils, thickeners or consolidating agents (consistency regulators), emmollients, UV absorbers, skin protection agents, antioxidants, additives which improve the mechanical properties, such as dicarboxylic acids and/or Al, Zn, Ca, or Mg salts of C14-C22 fatty acids, and, if appropriate, preservatives.
- Because of their good water-solubility, the complexing agents according to the invention can be incorporated into the corresponding formulations without problems.
- The body care compositions according to the invention can be formulated as a water-in-oil or oil-in-water emulsion, as alcoholic or alcohol containing formulation, as a vesicular dispersion of an ionic or nonionic amphiphilic lipid, as a gel or solid stick or as an aerosol formulation.
- As a water-in-oil or oil-in-water emulsion, the auxiliary which is tolerated in cosmetics preferably comprises 5 to 50% of an oily phase, 5 to 20% of an emulsifier and 30 to 90% of water. The oily phase can comprise any oil suitable for cosmetic formulations, for example one or more hydrocarbon oils, a wax, a naturally occurring oil, a silicone oil, a fatty acid ester or a fatty alcohol. Preferred mono- or polyols are ethanol, isopropanol, propylene glycol, hexylene glycol, glycerol and sorbitol.
- An anitmicrobial soap has, for example, the following composition:
- 0.01 to 5% by weight of the compound of the formula (2)
- 0.3 to 1% by weight of titanium dioxide
- 1 to 10% by weight of stearic acid
- to 100% of soap base, for example the sodium slats of tallow fatty and coconut fatty acid or glycerols.
- A shampoo has, for example, the following composition:
- 0.01 to 5% by weight of the compound of the formula (2),
- 12.0% by weight of sodium laureth-2-sulfate,
- 4.0% by weight of cocamidopropylbetaine,
- 3.0% by weight of NaCl and
- water to 100%.
- A deodorant has, for example, the following composition:
- 0.01 to 5% by weight of the compound of the formula (2),
- 60% by weight of ethanol,
- 0.3% by weight of perfume oil and
- water to 100%.
- The complexing agents according to the invention are furthermore suitable for the treatment of textile fibre materials. The fibre materials are non-dyed and dyed or printed fibre materials, for example of silk, leather, wool, polyamide or polyurethanes, and in particular all types of cellulosic fibre materials. Such fibre materials are, for example, naturally occurring cellulosic fibres, such as cotton, linen, jute and hemp, and cellulose and regenerated cellulose. Textile fibre materials which are preferably suitable are those of cotton.
- The following examples serve to illustrate the invention.
- Determination of the Antimicrobial Activities of S,S-EDDS, R,R-EDDS, Racemate of EDDS and EDETA, EDTA and NTA
- Test method: An agar diffusion test is carried out with the following modifications:
- Medium: casein-soya flour peptone agar (caso-agar)
- Test organisms: Corynebacterium xerosis ATCC 373
- Corynebacterium xerosis ATCC 7711
- Corynebacterium minutissimum ATCC 23358
- Procedure: 500 ml of caso-agar are innoculated with 3.5 ml of an overnight culture of the bacteria, diluted 1:100, and caso plates (18 ml) are covered with a layer of about 5 ml of the bacteria-containing agar. After the plates have cooled, holes of diameter 1 cm are stamped out with a cork borer. Each stamped-out hole is filled with in each case 100 μl of a test substance dilution and the plates are incubated at 37° C. for 2 days. Double-distilled water is employed as the solvent for all the substances. In the case of EDETA GS, the pH is adjusted to 3.3 by addition of 1 N NaOH. Chemically prepared S,S-EDDS is adjusted to the pH of 5.6 by addition of 1 N NaOH.
- Controls: Double-distilled water
- The test results are listed in Table 1:
TABLE 1 Concen- Inhibitory aureola diameter tration Cory. xerosis Cory. xerosis Substance [ppm] AUG 7711 ATTC 373 EDETA 10000 5/51 1/11 S,S-EDDS 10000 15/151 10/101 (prepared chemically) S,S-EDDS 10000 15/151 10/101 (prepared by fermentation EDTA 10000 2/2 5/5 R,S-EDDS 10000 n.d. 12/13 R,R-EDDS 10000 n.d. 15/15 - The test results show that both EDETA, EDTA and the EDDS prepared by fermentation and chemically (═R,R; S,S; R,S) show a pronounced bacteriostatic action against Corynebacterium xerosis.
- Examples of formulations having a bacteriostatic action
- Preparation of a Washing Powder
Laurylammonium sulfate 8.0% Nonionic surfactants 2.9% Soaps 3.5% Sodium tripolyphosphate 43.8% Sodium silicate 7.5% Magnesium silicate 1.9% Carboxymethylcellulose 1.2% EDTA 0.2% Sodium sulfate 21.2% EDDS 1% Water to 100% - The formulation is prepared as follows:
- The solid components are mixed and homogenized in a mortar and stirred with deionized water until a uniform pourable and pumpable paste (slurry) is obtained, which is finally spray-dried.
- Preparation of a Cleansing Tonic
Ethanol 20% Glycerol 5% PEG-40 hydrogenated castor oil 1% (hydrogenated ethoxylated castor oil) EDDS 0.5% Perfume ad libidum Water to 100% - The formulation is prepared as follows:
- EDDS is dissolved in ethanol. Under stirring at room temperature PEG-40, glycerol and perfume are added. Finally, the water is added.
- Preparation of a Deodorant Stick
Ethanol 20% Glycerol 30% Propylene glycol 20% Ceteareth-25 3% (= ethoxylated cetyl/stearyl alcohol) Sodium stearate 7% EDDS 0,5% Perfume ad libidum Water to 100% - The formulation is prepared as follows:
- Sodium stearate is melted at 60° C. Propylene glycol, Cetearath-25 and glycerol are added to the melting until a homogeneous clear suspension is obtained. Finally, the suspension is stirred with a EDDS-solution in an alcohol/water mixture at 50° C. and cooled slowly.
- Preparation of Soluble EDDS Salts and Deodorant Formulations
- S,S-EDDS is obtained by means of microbiological (WO 96/36725) or chemical synthesis (J. A. Neal et al., Inorg.Chem. 7, 2405 (1968)). Racemic EDDS is prepared from maleic anhydride and ethylenediamine (U.S. Pat. No. 3,158,635).
- A 1% suspension of racemic EDDS or S,S-EDDS is prepared in water/ethanol (about 7:3) with vigorous stirring. An aqueous solution of NaOH is metered in with an autoamtic titration device until the pH of 7 remains constant for 30 minutes. Any slight milky clouding which occurs is removed by filtering through paper.
- By addition of a thickener like hydroxy ethyl cellulose a clear deodorant formulation which is stable at room temperature, comprises about 1% of active substance (based on the tetra-acid) and has a skin-friendly pH is obtained.
- If NaOH is replaced by KOH, ammonia or ethanolamine, the corresponding potassium, ammonium and ethanolammonium salts are obtained. Lithium hydroxide, sodium carbonate, sodium bicarbonate or laurylamine can also be employed as the base.
- Detection of the Substantial Antimicrobial Activity of R,S-EDDS Salts on the Skin
Formulations 1% of R,S-EDDS/sodium salt (Solutions in 30% ethanol): 1% of R,S-EDDS/amine salt (for the preparation, cf. Example 4) Medium: Casein-soya flour peptone agar (caso-agar) Test organism: Corynebacterium xerosis ATCC 373 - Test method:
- Before application of the test solutions, the underarms are washed with a non-antimicrobial soap twice for 1 minute each time. A total of 6 ml of test product is then applied to the washed, dry skin of the underarm. Immediately and 2 hours after application of the test products, the EDDS on the skin is extracted by means of discs of filter paper (2 cm diameter) moistened in 0.9% NaCl solution (pH: 8.2). For this, the moist filter disc is placed on the treated skin without airbubbles for 4 minutes. The filter discs are subsequently dried at room temperature and then placed on solid agar media with test bacteria.
- To prepare the solid agar media, 500 ml of liquid agar are innoculated with 3.5 ml of a 12-16-hour culture, diluted 1:100, of the test bacteria at 47° C. and caso plates (18 ml) are covered with a layer of about 5 ml of the bacteria-containing agar.
- After the filter discs have been placed on top, the agar media are incubated for 2 days at 37° C. and the inhibition under the filter disc or the inhibitory aureolas of the filter discs is/are then determined.
- The test results are listed in Table 2:
TABLE 2 Substance Inhibitory aureola dia- meter (mm)/inhibition under the filter disc* Coryneb. xerosis ATCC 373 Placebo 0/0 R,S-EDDS (sodium salt) immed- 5/4 iately 2 hours 3/4 after application R,S-EDDS (Amine salt) immed- 2,5/4 iately 2 hours 2/4 after application - Explanation:
- 0=good growth (no inhibition)
- 2=inhibited but clear growth (weak inhibition)
- 4=no growth (potent inhibition)
- The test results show that a pronounced inhibition of Corynebacterium xerosis is achieved with both test substances.
- The test shows that sufficiently high concentrations of EDDS to achieve inhibition of Corynebacterium xerosis are also still present on the skin 2 hours after the last application.
Claims (15)
1. The use of a nitrogen-containing complexing agent for antimicrobial treatment of the skin and of textile fibre materials.
2. The use according to claim 1 , wherein a compound of the formula
in which
Q1, is Carb1; Carb2,; or a radical of the formula —(CH2)m 1 —OH;
Q2 is hydrogen or Carb2; and
Q3 is Carb3; an amino acid radical; or a radical of the formula (1a)
where Carb1, Carb2 and Carb3 independently of one another are the radical of a C1-C8-mono- or dicarboxylic acid; and
m1 is 1 to 5, is used as the complexing agent.
4. The use according to claim 3 , wherein
Q1 is a monocarboxylic acid; or a radical of the formula —(CH2)m 1 —OH;
Q2 is hydrogen or a monocarboxylic acid; and
Q3 is formula (ib); or a monocarboxylic acid.
5. The use according to claim 1 or 2, wherein Carb2 and Carb3, independently of one another are the radical of the formula
—[(CH2)]n 1 —COOH, (1c)
in which
n1 is 0 to 5.
8. The use according to claim 1 , wherein nitrilotriacetic acid is used as the complexing agent.
9. The use of a complexing agent according to any one of claims 1 to 8 , wherein the complexing agent is also in the form of one of its water-soluble salts.
10. The use according to claim 9 , wherein the complexing agent is present in the form of its lithium, sodium, potassium, ammonium or ethanolammonium salt.
11. The use of a complexing agent according to any one of claims 1 to 10 as an antimicrobial active substance against Gram-positive bacteria.
12. The use of a complexing agent according to any one of claims 1 to 11 in body care compositions.
13. A body care composition comprising a nitrogen-containing complexing agent according to claim 1 .
14. A body care composition according to claim 13 in the form of a soap, a shampoo or a deodorant.
15. The use of a complexing agent according to any one of claims 1 to 10 in textile fibre materials.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19620644.8 | 1996-05-22 | ||
DE19620644U | 1996-05-22 | ||
DE19620644A DE19620644A1 (en) | 1996-05-22 | 1996-05-22 | Use of nitrogen-containing complexing agents for deodorization and antimicrobial treatment of the skin and textile fiber materials |
PCT/EP1997/002380 WO1997044006A1 (en) | 1996-05-22 | 1997-05-09 | Use of nitrogen-containing complexing agents for deodorization and antimicrobial treatment of the skin and textile fibre materials |
Publications (2)
Publication Number | Publication Date |
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US20020031537A1 true US20020031537A1 (en) | 2002-03-14 |
US6391325B1 US6391325B1 (en) | 2002-05-21 |
Family
ID=7795040
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US09/180,992 Expired - Fee Related US6391325B1 (en) | 1996-05-22 | 1997-05-09 | Use of nitrogen-containing complexing agents for deodorization and antimicrobial treatment of the skin and textile fibre materials |
Country Status (8)
Country | Link |
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US (1) | US6391325B1 (en) |
EP (1) | EP0901367A1 (en) |
JP (1) | JP2000511523A (en) |
CN (1) | CN1219124A (en) |
AU (1) | AU2895197A (en) |
BR (1) | BR9709595A (en) |
DE (1) | DE19620644A1 (en) |
WO (1) | WO1997044006A1 (en) |
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WO2010003819A1 (en) * | 2008-07-10 | 2010-01-14 | Unilever Nv | A personal wash composition |
EP2206506A1 (en) | 2008-12-18 | 2010-07-14 | Bracco Imaging S.p.A | Probiotic formulations |
US20110263472A1 (en) * | 2010-04-23 | 2011-10-27 | Nigel Patrick Somerville Roberts | Particle |
FR3117831A1 (en) * | 2020-12-18 | 2022-06-24 | L'oreal | Cosmetic use of fatty chain derivatives of diglutamide lysine as a deodorant active ingredient |
US20230065230A1 (en) * | 2018-12-21 | 2023-03-02 | L'oreal | Antimicrobial mixture containing 4-(3-ethoxy-4-hydroxyphenyl)butan-2-one and an acid or silver-based compound, and cosmetic composition containing same |
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DE19650102A1 (en) * | 1996-12-03 | 1998-06-04 | Basf Ag | Use of bis (dicarboxylic acid) diaminoalkylene derivatives as biodegradable complexing agents for alkaline earth and heavy metal ions |
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US20150004126A9 (en) * | 2011-01-27 | 2015-01-01 | Givaudan S.A. | Compositions |
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DE1287256B (en) * | 1967-06-23 | 1969-01-16 | Henkel & Cie Gmbh | Antimicrobial agents |
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-
1996
- 1996-05-22 DE DE19620644A patent/DE19620644A1/en not_active Withdrawn
-
1997
- 1997-05-09 AU AU28951/97A patent/AU2895197A/en not_active Abandoned
- 1997-05-09 BR BR9709595-8A patent/BR9709595A/en not_active Application Discontinuation
- 1997-05-09 EP EP97923037A patent/EP0901367A1/en not_active Withdrawn
- 1997-05-09 WO PCT/EP1997/002380 patent/WO1997044006A1/en not_active Application Discontinuation
- 1997-05-09 JP JP09541462A patent/JP2000511523A/en active Pending
- 1997-05-09 CN CN97194728A patent/CN1219124A/en active Pending
- 1997-05-09 US US09/180,992 patent/US6391325B1/en not_active Expired - Fee Related
Cited By (7)
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WO2010003819A1 (en) * | 2008-07-10 | 2010-01-14 | Unilever Nv | A personal wash composition |
EA023242B1 (en) * | 2008-07-10 | 2016-05-31 | Юнилевер Н.В. | Method of cleansing skin |
EP2206506A1 (en) | 2008-12-18 | 2010-07-14 | Bracco Imaging S.p.A | Probiotic formulations |
US20110263472A1 (en) * | 2010-04-23 | 2011-10-27 | Nigel Patrick Somerville Roberts | Particle |
US8455422B2 (en) * | 2010-04-23 | 2013-06-04 | The Procter & Gamble Company | Process for making a methyl glycine diacetic acid particle |
US20230065230A1 (en) * | 2018-12-21 | 2023-03-02 | L'oreal | Antimicrobial mixture containing 4-(3-ethoxy-4-hydroxyphenyl)butan-2-one and an acid or silver-based compound, and cosmetic composition containing same |
FR3117831A1 (en) * | 2020-12-18 | 2022-06-24 | L'oreal | Cosmetic use of fatty chain derivatives of diglutamide lysine as a deodorant active ingredient |
Also Published As
Publication number | Publication date |
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BR9709595A (en) | 2000-04-25 |
AU2895197A (en) | 1997-12-09 |
JP2000511523A (en) | 2000-09-05 |
US6391325B1 (en) | 2002-05-21 |
EP0901367A1 (en) | 1999-03-17 |
WO1997044006A1 (en) | 1997-11-27 |
DE19620644A1 (en) | 1997-11-27 |
CN1219124A (en) | 1999-06-09 |
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