EP0808152A1 - Kosmetische reinigungszusammensetzung, die alkylglykosidester enthalten - Google Patents

Kosmetische reinigungszusammensetzung, die alkylglykosidester enthalten

Info

Publication number
EP0808152A1
EP0808152A1 EP96904035A EP96904035A EP0808152A1 EP 0808152 A1 EP0808152 A1 EP 0808152A1 EP 96904035 A EP96904035 A EP 96904035A EP 96904035 A EP96904035 A EP 96904035A EP 0808152 A1 EP0808152 A1 EP 0808152A1
Authority
EP
European Patent Office
Prior art keywords
cosmetic cleansing
cleansing composition
weight
composition according
fatty acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
EP96904035A
Other languages
English (en)
French (fr)
Inventor
Jacob Oosterman
Heleen Peters De Boer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Uniqema BV
Original Assignee
Uniqema BV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Uniqema BV filed Critical Uniqema BV
Priority to EP96904035A priority Critical patent/EP0808152A1/de
Publication of EP0808152A1 publication Critical patent/EP0808152A1/de
Ceased legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/60Sugars; Derivatives thereof
    • A61K8/604Alkylpolyglycosides; Derivatives thereof, e.g. esters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/11Encapsulated compositions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/361Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/42Amides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/463Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4993Derivatives containing from 2 to 10 oxyalkylene groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/22Gas releasing
    • A61K2800/222Effervescent
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/596Mixtures of surface active compounds

Definitions

  • the present invention relates to a cosmetic cleansing composition in a water-soluble capsule.
  • the cosmetic cleansing composition should have a relatively high viscosity, so as to enable its encapsulation, whereas upon use the composition after breakage of the capsule should quickly dissolve or disperse in the aqueous environment.
  • a cosmetic cleansing composition in a water- soluble capsule, preferably made of gelatin, which composition comprises an alkali metal salt of an alkyl sulphate, a fatty acid ester of an alkylglycoside having an alkyl group with from 1 to 4 carbon atoms and a sorbitan
  • the viscosity of the product was dependent on the shear exerted upon it. For example 1 it was found that at very low shear (below to 10 sec “1 ) the viscosity of the product was 8,000 mPas; then with increasing shear (to 50 sec “1 ) the viscosity increased to 8,300 mPas and at constant shear of 50 sec "1 the viscosity increased further to 9,100 mPas. If the shear was then decreased, the viscosity further increased to 15,000 mPas. After some time, the viscosity started to decrease again. It may therefore be stated that the product is both shear thickening or dilatant and exhibits rheopexy.
  • This rheological behaviour is of advantage during finishing and in using the product.
  • a relatively high viscosity is required (in the order of 8,000 to 12,000 mPas) . If the product after finishing is left to rest, its viscosity will decrease to its original value at low shear, so that upon use the product will easily dissolve or disperse in water.
  • the present invention relates to a cosmetic cleansing composition in a water-soluble capsule, which composition comprises:
  • the fatty acid ester of the alkylglycoside having an alkyl group with from 1 to 4 carbon atoms preferably is a fatty acid ester of methyl glucoside, methyl fructoside, ethyl glycoside or ethyl fructoside.
  • the fatty acid may be a straight or branched chain, saturated or unsaturated fatty acid having from 10 to 22 carbon atoms.
  • lauric acid, palmitic acid, stearic acid and iso-stearic acid is preferred.
  • fatty acid mixtures may be used, such as coconut fatty acids, palm kernel fatty acids and tallow fatty acids.
  • coconut fatty acids of which the fatty acids up to and including octanoic acid have mainly been removed, is preferred.
  • the fatty acid esters of the alkylglycosides comprise mono-, di-, tri- and higher esters.
  • the use of esters comprising at least 50% by weight, preferably at least 75% by weight, of mono esters is preferred.
  • the esters may comprise up to 15% by weight of free fatty acids, but preferably the free fatty acid content is as low as possible, e.g.below 3% by weight.
  • from 30 to 85% by weight of alkylglycoside ester is used, preferably from 60% to 85% by weight, and most preferably from 70% to 80% by weight.
  • the alkali metal salt of the alkyl sulphate preferably is the sodium salt.
  • the alkyl sulphate contains from 10 to 20 carbon atoms, such as dodecyl, lauryl, hexadecyl, myristyl and octadecyl sulphate. The use of lauryl sulphate is preferred. In general amine salts or alkanolamine salts are not used in view of the possibility of skin irritation. Generally from 10% to 20% by weight of the alkali metal salt of C 10 - C 20 alkyl sulphate is used.
  • the alkoxylated sorbitan fatty acid esters are derived from sorbitan (or anhydrohexitol) .
  • the fatty acids may be straight or branched chain, saturated or unsaturated fatty acids having from 10 to 22 carbon atoms, such as lauric acid, stearic acid, palmitic acid, oleic acid, iso-stearic acid and the like.
  • the sorbitan fatty acid esters have been alkoxylated with C1-C4 alkylene oxides, preferably ethylene oxide, or mixtures of such alkylene oxides. On an average from 10 to 80 moles of alkylene oxide per mole of sorbitan fatty acid ester are reacted.
  • the use of polyoxyethylene (20) orbitan monolaurate is preferred.
  • the alkoxylated sorbitan fatty acid ester is used in an amount of from 1% to 30% by weight, preferably from 5% to 25% by weight of the total composition.
  • the fatty acid dialkylolamide is derived from a straight or branched chain, saturated or unsaturated fatty acid having from 10 to 22 carbon atoms, such as lauric acid or coconut acids of which the fatty acids up to and including octanoic acid have mainly been removed. In the latter case the term "coconut fatty acid dialkylolamide" is used and these dialkylolamides are preferred.
  • the hydroxyalkyl groups of the dialkylolamide have from 2 to 5 carbon atoms and these groups may the same or different and may be mono- or polyhydroxyalkyl.
  • the use of coconut fatty acid diethanolamide is preferred.
  • the fatty acid dialkylolamide is used in an amount of up to 30% by weight of the total composition, preferably from 15% to 25% by weight.
  • the amount of water in the cosmetic cleansing composition is at most 4% by weight and preferably at most 3% by weight.
  • the cosmetic cleansing compositions according to the present invention may also comprise an effective amount (in general up to 10% by weight, but greater amounts may be used) of a functional additive, selected from the group consisting of perfumes, chelating or sequestering agents (like EDTA) , preservatives, bactericides, herbs (or herb extracts) , vitamins, buffering substances, moisturizers, emollients (such as esters of fatty acids and/or fatty alcohols) , viscosity controlling agents (such as monohydric alcohols with 2 to 8 carbon atoms) , anti-oxidants, dyes, lather boosters (such as higher alkyl amine oxides) , and mixtures thereof .
  • a functional additive selected from the group consisting of perfumes, chelating or sequestering agents (like EDTA) , preservatives, bactericides, herbs (or herb extracts) , vitamins, buffering substances, moisturizers, emollients (such as esters of fatty acids
  • the viscosity of the cosmetic cleansing composition as measured with a rotation viscosimeter at 20°C using spindle No SV1 is from 6,500 to 15,000 mPas, preferably from 7,000 to 12,000 mPas.
  • the water-soluble capsule material is preferably gelatin, but other material like polyvinyl alcohol may be used.
  • the release time of the capsule may be controlled by the selection of the wall thickness of the capsule and the type of gelatin (different Bloom strength) .
  • the capsule may have a well thickness of 0.1 mm to 1 mm and a volume of for example 5 ml .
  • a cosmetic cleansing composition was prepared by mixing the following ingredients (in % by weight)
  • Citric acid 60 wt% aqueous solution
  • Citric acid 60 wt% aqueous solution
  • the lauric acid ester of ethyl glucoside contained 65.5% by weight of mono-ester, 14.8% by weight of di-ester, 19.1% by weight of tri-ester and 0.6% by weight of higher ester.
  • Polysorbate-20 (Trade Mark; ex. Atlas Chem.) is poly- oxyethylene (20) sorbitan monolaurate in which on an average 20 moles of ethylene oxide are present, having a HLB value of 16.7 and a viscosity at 25°C of 330 cSt (mm 2 S "1 ) .
  • Sheets of gelatin were made and passed through a capsule making machine in a manner known per se, producing capsules having a wall thickness of 0.2-0.7 mm and a volume of 5 ml, which were filled with the above prepared cosmetic cleansing composition.
  • Example 1 was repeated, now using the following formulations (ingredients in % by weight of the total composition) :
  • Polysorbate-20 (as in Example 1) 20 % 20 % Ethanol (96%) 1 % 4 % Perfume 0.10% 0.10%
  • gelatin capsules filled with the formulations as described in Example 1 upon use yielded a copiously foaming, mild to the skin cosmetic cleansing composition.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)
  • Detergent Compositions (AREA)
EP96904035A 1995-02-07 1996-02-05 Kosmetische reinigungszusammensetzung, die alkylglykosidester enthalten Ceased EP0808152A1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP96904035A EP0808152A1 (de) 1995-02-07 1996-02-05 Kosmetische reinigungszusammensetzung, die alkylglykosidester enthalten

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP95200301 1995-02-07
EP95200301 1995-02-07
EP96904035A EP0808152A1 (de) 1995-02-07 1996-02-05 Kosmetische reinigungszusammensetzung, die alkylglykosidester enthalten
PCT/EP1996/000541 WO1996024328A1 (en) 1995-02-07 1996-02-05 Cosmetic cleansing compositions comprising esters of alkylglycosides

Publications (1)

Publication Number Publication Date
EP0808152A1 true EP0808152A1 (de) 1997-11-26

Family

ID=8219998

Family Applications (1)

Application Number Title Priority Date Filing Date
EP96904035A Ceased EP0808152A1 (de) 1995-02-07 1996-02-05 Kosmetische reinigungszusammensetzung, die alkylglykosidester enthalten

Country Status (7)

Country Link
EP (1) EP0808152A1 (de)
JP (1) JPH10513189A (de)
KR (1) KR19980701954A (de)
CN (1) CN1173814A (de)
AU (1) AU4789296A (de)
BR (1) BR9607118A (de)
WO (1) WO1996024328A1 (de)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19721708A1 (de) * 1997-05-23 1998-11-26 Henkel Kgaa Verkapseltes Reinigungsmittel
CN1150969C (zh) * 1998-06-23 2004-05-26 联合碳化化学品及塑料技术公司 用于表面活性剂体系的液体增稠剂
AU2001254824A1 (en) * 2000-05-12 2001-11-20 Unilever Plc Unit dose cleaning product
DE10032118B9 (de) * 2000-07-01 2006-12-07 Wella Ag Antithixotropes kosmetisches Mittel
US7125828B2 (en) 2000-11-27 2006-10-24 The Procter & Gamble Company Detergent products, methods and manufacture
US8658585B2 (en) 2000-11-27 2014-02-25 Tanguy Marie Louise Alexandre Catlin Detergent products, methods and manufacture
US8940676B2 (en) 2000-11-27 2015-01-27 The Procter & Gamble Company Detergent products, methods and manufacture
ES2273912T3 (es) 2000-11-27 2007-05-16 THE PROCTER & GAMBLE COMPANY Metodo para lavar vajillas.
EP1660023B1 (de) 2003-08-27 2009-01-07 Beiersdorf AG Kapsel deren kapselhülle bei topischer anwendung nicht mehr gesondert wahrnehmbar ist
US9055745B2 (en) 2011-04-13 2015-06-16 Natureza, Inc. Compositions for internal and external insecticides, ovicides, repellents and wound healing
EP2861204B1 (de) * 2012-06-15 2016-08-31 Lubrizol Advanced Materials, Inc. Alkylglycosidbasierte mizellare verdickungsmittel für tensidsysteme
US11717473B2 (en) 2019-11-25 2023-08-08 Kao Corporation Skin cleansing agent containing a particle comprised of an ester, moisturizing agent, and polymer

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3705102A (en) * 1971-01-18 1972-12-05 Armour Dial Inc Composition and method of defoaming bubble baths
US4597885A (en) * 1985-01-02 1986-07-01 Pharmacaps, Inc. Encapsulated foaming bath composition
GB2192404B (en) * 1986-07-09 1990-08-01 Scherer Ltd R P Encapsulated products
DK76889D0 (da) * 1989-02-17 1989-02-17 Novo Industri As Fremgangsmaade til fremstilling af organiske forbindelser
JP2751503B2 (ja) * 1989-12-25 1998-05-18 ライオン株式会社 シャンプー組成物
JPH04331295A (ja) * 1991-04-30 1992-11-19 Lion Corp 洗浄剤組成物

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9624328A1 *

Also Published As

Publication number Publication date
BR9607118A (pt) 1997-11-04
AU4789296A (en) 1996-08-27
JPH10513189A (ja) 1998-12-15
KR19980701954A (ko) 1998-06-25
CN1173814A (zh) 1998-02-18
WO1996024328A1 (en) 1996-08-15

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