EP0845975A1 - Haarbehandlungsmittels - Google Patents

Haarbehandlungsmittels

Info

Publication number
EP0845975A1
EP0845975A1 EP96940622A EP96940622A EP0845975A1 EP 0845975 A1 EP0845975 A1 EP 0845975A1 EP 96940622 A EP96940622 A EP 96940622A EP 96940622 A EP96940622 A EP 96940622A EP 0845975 A1 EP0845975 A1 EP 0845975A1
Authority
EP
European Patent Office
Prior art keywords
hair
hair treatment
silicone
treatment composition
trimethyl ammonium
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.)
Withdrawn
Application number
EP96940622A
Other languages
English (en)
French (fr)
Other versions
EP0845975A4 (de
Inventor
Kiichiro Nakamura
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.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
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 Procter and Gamble Co filed Critical Procter and Gamble Co
Publication of EP0845975A1 publication Critical patent/EP0845975A1/de
Publication of EP0845975A4 publication Critical patent/EP0845975A4/de
Withdrawn legal-status Critical Current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
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41Amines
    • A61K8/416Quaternary ammonium compounds
    • 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
    • A61K8/34Alcohols
    • A61K8/342Alcohols having more than seven atoms in an unbroken chain
    • 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners

Definitions

  • the present invention relates to a hair treatment composition, and in particular to rinse off hair products having improved performance in wet detangling and dry combing of conditioned hair.
  • compositions such as hair rinse agents and conditioning compositions have been used to provide gloss and condition to hair.
  • Such compositions may be used either in conjunction with or following shampooing of the hair.
  • Shampooing the hair cleans the hair by removing excess soil that has built up on the hair due to contact with the surrounding atmosphere. Sebum, which is secreted by the head, is also removed by shampooing.
  • the shampooing process generally leaves the hair in a wet, tangled and generally unmanageable state.
  • hair conditioning compositions have a thick creamy rheology making them suitable and desirable for use.
  • Such products are generally based upon surfactants, including a combination of fatty alcohols and quaternary ammonium salts. Both the fatty alcohols and quaternary ammonium salts provide hair conditioning benefits to the hair.
  • surfactants including a combination of fatty alcohols and quaternary ammonium salts. Both the fatty alcohols and quaternary ammonium salts provide hair conditioning benefits to the hair.
  • fatty alcohols and quaternary ammonium salts provide hair conditioning benefits to the hair.
  • such materials have not fully met consumer's needs, especially for dry combing performance.
  • Silicones have also been inco ⁇ orated into hair treatment compositions such as shampoos and conditioning shampoos in order to deliver a desired level of smoothness to the hair.
  • hair treatment compositions such as shampoos and conditioning shampoos in order to deliver a desired level of smoothness to the hair.
  • a number of prior publications such as US Pat. No. 2,826,551, US Pat. No. 3,964,500, US Pat. No. 4,364,837 and US Pat. No. 4,4788,006 disclose the use of silicones in shampoo compositions.
  • a hair treating composition including a dimethyl silicone rubber and a quaternary ammonium salt is disclosed in US Patent 4,950,468.
  • the quaternary ammonium salt consists of a combination of stearyl- and behenyl trimethyl ammonium chloride.
  • the composition in this disclosure is said to have excellent resistance to washing. The effect of washing however will often leave wet hair tangled and unmanageable despite the application of such hair treatment compositions.
  • a hair rinse conditioner including a dodecyl triethyl quaternary ammonium compound, fatty alcohol and a cyclic or linear silicone is disclosed in USP 4,818,523.
  • the composition in this disclosure is said to provide conditioning styling ease and manageability of hair, but it does not disclose the performance in wet detangling and dry combing of hair.
  • the silicone conditioning agent is a polydimethyl siloxane gum having a mass molecular weight of from 200,000 to one million; the fatty alcohol is stearyl alcohol or cetyl alcohol or a mixture thereof; and the monoalkyl trimethyl ammonium salt is behenyl trimethyl ammonium chloride.
  • the composition provides excellent wet detangling and dry hair combing capabilities following application to the hair.
  • DETAILED DESCRIPTION OF THE INVENTION Silicone conditioning agents are known for providing hair conditioning when applied in treatment compositions. Such materials tend not to leave the hair looking "dirty" as typical hair conditioners may.
  • the present invention includes from about 0.01 to 15% of a silicone conditioning agent, preferably from 0.1% to 10%, most preferably from 0.5% to 5%.
  • the silicone conditioning agent in the present invention has a molecular weight of from 200,000 to 1 ,000,000.
  • the silicone conditioning agent useful in the invention most preferably includes a non-volatile silicone however a volatile silicone may also be inco ⁇ orated as part of the silicone mixture.
  • volatile refers to a silicone conditioning agent that has a measurable vapour pressure.
  • the non-volatile silicone may be either a polyalkyl siloxane, a polyaryl siloxane, a polyalkylaryl siloxane, an amino siloxane or a polyether siloxane copolymer. Mixtures of these silicones may also be used.
  • the dispersed silicone is preferably insoluble in the hair treatment matrix.
  • materials such as polyalkyl or polyaryl siloxanes may have the following structure:
  • R is alkyl or aryl
  • X is an integer from about 7 to about 8,000.
  • A represents groups which block the end of the silicone chains.
  • the alkyl or aryl groups substituted on the siloxane chain (R) or the ends of the siloxane chain (A) may have any structure, but preferably result in silicones which remain fluid at room temperature, are hydrophobic, are neither irritating, toxic or otherwise harmful when applied to the hair, are compatible with the other components of the composition, are chemically and storage stable, and are capable of being deposited on, and condition the hair.
  • Suitable A groups include methyl, methoxy, ethoxy, propoxy, and aryloxy.
  • the two R groups on the silicone atom may represent the same or different groups. Preferably R represents the same group. Suitable groups include methyl, ethyl, propyl, phenyl, methylphenyl and phenylmethyl.
  • Preferred polyalkyl siloxanes are polydimethyl siloxane and polydiethyl siloxane. Most preferred are polydimethyl siloxanes with viscosities ranging from about 5 to 600,000 centistokes at 25 C. These siloxanes are available, for example, from the General Electric Company as the "Viscasil” series and from Dow Corning as the "Dow Corning 200" series. The viscosity can be measured by means of a glass capillary viscometer as set forth in Dow Corning Corporate Test Method CTM0004. Preferably, the viscosity ranges from about 350 centistokes to about 100,000 centistokes.
  • the preferred polyalkylaryl siloxanes that may be used include for example poiymethylphenylsiloxanes having viscosities of about 15 to 65 centistokes at 25_C. These siloxanes are available from the General Electric Company as SF 1075 methyl phenyl fluid or from Dow Corning as 556 Cosmetic Grade Fluid. Additionally poly(dimethyl siloxane) (diphenyl siloxane) copolymers having a viscosity in the range of from about 10 to about 100,000 centistokes at 25 C are useful.
  • the preferred polyether siloxane copolymer that may be used includes a polypropylene oxide modified dimethylpolysiloxane (eg Dow Corning DC 1748), although ethylene oxide or mixtures of ethylene oxide and propylene oxide may also be used.
  • a polypropylene oxide modified dimethylpolysiloxane eg Dow Corning DC 1748
  • ethylene oxide or mixtures of ethylene oxide and propylene oxide may also be used.
  • silicone gum A silicone conditioning agent found especially useful in the present composition to provide good dry combing is silicone gum.
  • "Silicone gum” materials denote high molecular weight polydiorganosiloxanes generally having a mass molecular weight of from about 200,000 to about 1 ,000,000. Suitable silicone gums are described in "Silicon Compounds" by Petrarch (referred to above) and others including US Pat. No. 4,152,416 and Noll, Walter, "Chemistry and Technology of Silicones", New York, Academic Press 1968. Also describing silicone gums are General Electric Silicone Rubber Products Data Sheets SE30, SE33, SE54 and SE76. All of these described references are incorporated herein by reference.
  • polydimethylsiloxane examples include polydimethylsiloxane, (polydimethylsiloxane)(methylvinylsiloxane) copolymer, poly(dimethylsiloxane) (diphenyl siloxane) (methylvinylsiloxane) copolymer and mixtures thereof.
  • the gums may contain some minor (eg 6% to 14% of total gum weight) of a cyclic or linear volatile silicone.
  • the volatile silicone may be incorporated to act a solvent for the silicone gum.
  • volatile silicone hair conditioning material that may be inco ⁇ orated have a boiling point in the range of about 99_C to about 260_C and have a solubility in water of less than 0.1%.
  • Preferred volatile silicones may be either a cyclic or a linear polydimethylsiloxane.
  • the number of silicone atoms in the cyclic silicones is preferably from about 3 to about 7, more preferably 4 or 5.
  • the general formula of such silicones is
  • n 3 to 7.
  • the linear polydimethyl siloxanes have from about 3 to 9 silicone atoms and have the general formula:
  • Silicones of the above type are available from Dow Corning Co ⁇ oration, Dow Corning 344, 345 and 200 fluids, Union Carbide, Silicone 7202 and Silicone 7158, and Stauffer Chemical SWS 03314.
  • Fatty alcohol materials are desirably included into hair treatment compositions to provide hair manageability benefits, and ease of styling for the user.
  • Suitable fatty alcohols that are useful as conditioning agents herein are described in "Baileys Industries Oil and Fat Products” (Third Edition D Swen, Ed. 1979), incorporated herein by reference. Further examples of suitable fatty alcohols are disclosed in the following documents, each of which are incorporated herein by reference; US Pat. No. 3,155,591 , US Pat. No. 4,165,369, US Pat. No. 4,269,824 and British Specification 1 ,532,585.
  • the fatty alcohol in the present invention has a melting point higher than 30_C.
  • fatty alcohol materials include stearyl-, cetyl-, myristyl-, behenyl-, lauryl-, and oleyl alcohols and mixtures thereof. Most preferred of the fatty alcohols are cetyl and stearyl alcohol or mixtures thereof.
  • the composition should include from 0.6 to 10% by weight of the total composition of a fatty alcohol, preferably 2 to 9% and most preferably 3% to 8%. In combination with for example a silicone conditioning agent, and a monoalkyl trimethyl ammonium chloride, it has been found that the hair treatment composition that includes a fatty alcohol provides improved wet detangling and dry combing capabilities.
  • Monoalkyl trimethyl ammonium salts which may be useful in the present invention have the formula:
  • Ri may be selected from an aliphatic group of at least 14 carbon atoms
  • X is an anion selected from halogen, acetate, phosphate and alkyl sulfate radicals.
  • the aliphatic groups may contain, in addition to carbon and hydrogen atoms, ether linkages as well as amido groups among other groups.
  • the preferred monoalkyl trimethyl ammonium salt ingredient is behenyl trimethyl ammonium chloride. Preferably, it is present in an amount of from 0.1 to 5% by weight based on the total weight of the composition. The majority of the remainder of the composition is made up of water. It is generally present at a level of from about 20% to 98%, preferably from about 60% to 95%, more preferably from 80% to 90% content ofthe total composition.
  • the hair treatment composition may also include a variety of other components suitable for rendering such compositions acceptable for use.
  • Such components are generally well known to those skilled in the art and may include for examples preservatives such as benzyl alcohol, trimethyl parabin, propyl parabin and imidazolidinyl urea, thickeners and viscosity modifiers such as a hydroxy ethyl cellulose and xantham gum, pH adjusting agents such as citric acid, sodium citrate, succinic acid, phosphoric acid, sodium hydroxide, sodium carbonate etc; perfume, dyes and sequestering agents such as disodium ethylene diamine tetraacetate.
  • Such agents generally are used individually at a level of from about 0.01% to about 10% preferably from about 0.1% to about 5% by weight of the total composition.
  • compositions There are many approaches suitable for making the present compositions. If it is desired to form a rinse off treatment, monoalkyl trimethyl ammonium chloride and fatty alcohol are added to hot (70-80_C) water. Then, the mixture is slowly cooled down to room temperature where silicone and other ingredients are added.
  • the compositions may be processed in such a manner that the volatile agent is dispersed in the aqueous phase in particles of from about 1 to about 10 microns.
  • the hair treatment composition of the invention may be formed into a hair treatment preparation, for example a conditioner or conditioning shampoo, a hair rinse or hair treatment spray and the like, according to conventional preparation techniques.
  • the hair treatment compositions of the present invention are preferably used as a rinse on freshly shampooed hair.
  • the composition is used in an amount of from about 1 g. to about 60 g. preferably from about 2 g. to about 30 g. and is then rinsed from the hair.
  • Prototypes were prepared to compare compositions of the present invention with the prior art technologies via wet detangling and dry combing tests. Unless otherwise indicated, all percentages herein are by weight.
  • 1 MBTMAC is Monobehenyl trimethyl ammonium chloride and is commercially available under the trade name of DC-80 from TOHO Chemical.
  • 2 MLTMAC is Monolauryl trimethyl ammonium chloride and is commercially available under the trade name of LTC-35A from TOHO Chemical.
  • Polydimethylsiloxane is 15%/85% (wt. basis) mixture of D5 cyclomethicone and dimethicone gum (average molecular weight of about 400,000 to about 600,000).
  • Cyclomethicone (D5) is Decamethyl cyclopentasiloxane and is commercially available under the trade name of SF1202 from General Electric.
  • Comparative example 1 caused separation, while example 1 became homogenous product.
  • Example 2 and comparative example 2 were progressed to the wet detangling and dry combing test.
  • Example 2 showed higher performance in wet detangling than Comparative Example 2.
  • Example 2 showed higher performance in dry combing than Comparative Example 2.

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)
  • Dermatology (AREA)
  • Emergency Medicine (AREA)
  • Cosmetics (AREA)
EP96940622A 1995-08-23 1996-08-22 Haarbehandlungsmittels Withdrawn EP0845975A4 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
AUPN4998A AUPN499895A0 (en) 1995-08-23 1995-08-23 Hair treatment composition
AUPN4998/95 1995-08-23
PCT/US1996/013561 WO1997007774A1 (en) 1995-08-23 1996-08-22 Hair treatment composition

Publications (2)

Publication Number Publication Date
EP0845975A1 true EP0845975A1 (de) 1998-06-10
EP0845975A4 EP0845975A4 (de) 2000-05-10

Family

ID=3789326

Family Applications (1)

Application Number Title Priority Date Filing Date
EP96940622A Withdrawn EP0845975A4 (de) 1995-08-23 1996-08-22 Haarbehandlungsmittels

Country Status (6)

Country Link
EP (1) EP0845975A4 (de)
JP (1) JPH11511460A (de)
CN (1) CN1193903A (de)
AU (1) AUPN499895A0 (de)
BR (1) BR9610382A (de)
WO (1) WO1997007774A1 (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020012646A1 (en) * 1997-05-06 2002-01-31 Royce Douglas Allan Shampoo compositions with cationic polymers
US6322778B1 (en) 1998-02-10 2001-11-27 Johnson & Johnson Consumer Companies, Inc. Hair conditioning compositions comprising a quaternary ammonium compound
GB9902632D0 (en) * 1999-02-05 1999-03-31 Unilever Plc Hair treatment compositions
WO2002022089A1 (en) * 2000-09-13 2002-03-21 The Procter & Gamble Company Concentrated conditioning composition
WO2005079737A1 (en) * 2004-02-13 2005-09-01 The Procter & Gamble Company Hair conditioning composition comprising pre-mixture of three kinds of silicones
DE102007060530A1 (de) * 2007-12-13 2009-09-17 Henkel Ag & Co. Kgaa Haarkonditionierende Mittel mit kationischen Behenylverbindungen und ausgewählten Siliconen und/oder kosmetischen Ölen
EP3162408A1 (de) * 2015-10-28 2017-05-03 The Procter and Gamble Company Haarglanzzusammensetzung und verfahren zur verwendung

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0155806A2 (de) * 1984-03-15 1985-09-25 The Procter & Gamble Company Haarbehandlungsmittel mit konditionierenden Eigenschaften
US5100657A (en) * 1990-05-01 1992-03-31 The Procter & Gamble Company Clean conditioning compositions for hair
EP0538762A1 (de) * 1991-10-22 1993-04-28 Kao Corporation Haarkosmetikum
DE4229922A1 (de) * 1992-09-08 1994-03-10 Kao Corp Gmbh Mittel zur Konditionierung von menschlichen Haaren
DE4425096A1 (de) * 1993-07-19 1995-01-26 Kao Corp Haarbehandlungszusammensetzungen
WO1995024180A1 (en) * 1994-03-09 1995-09-14 Unilever Plc Hair conditioning composition
WO1996031188A1 (en) * 1995-04-06 1996-10-10 Unilever Plc Hair treatment compositions

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63222109A (ja) * 1987-03-11 1988-09-16 Sunstar Inc 毛髪処理剤
US4818523A (en) * 1987-06-17 1989-04-04 Colgate-Palmolive Company Hair rinse conditioner
JP2820329B2 (ja) * 1991-04-01 1998-11-05 株式会社資生堂 毛髪化粧料
US5334376A (en) * 1993-08-13 1994-08-02 Colgate-Palmolive Company Compositions for conditioning hair

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0155806A2 (de) * 1984-03-15 1985-09-25 The Procter & Gamble Company Haarbehandlungsmittel mit konditionierenden Eigenschaften
US5100657A (en) * 1990-05-01 1992-03-31 The Procter & Gamble Company Clean conditioning compositions for hair
EP0538762A1 (de) * 1991-10-22 1993-04-28 Kao Corporation Haarkosmetikum
DE4229922A1 (de) * 1992-09-08 1994-03-10 Kao Corp Gmbh Mittel zur Konditionierung von menschlichen Haaren
DE4425096A1 (de) * 1993-07-19 1995-01-26 Kao Corp Haarbehandlungszusammensetzungen
WO1995024180A1 (en) * 1994-03-09 1995-09-14 Unilever Plc Hair conditioning composition
WO1996031188A1 (en) * 1995-04-06 1996-10-10 Unilever Plc Hair treatment compositions

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Section Ch, Week 199250 Derwent Publications Ltd., London, GB; Class A26, AN 1992-410111 XP002130635 & JP 04 305516 A (SHISEIDO CO LTD), 28 October 1992 (1992-10-28) *
See also references of WO9707774A1 *

Also Published As

Publication number Publication date
BR9610382A (pt) 1999-07-06
MX9801455A (es) 1998-05-31
JPH11511460A (ja) 1999-10-05
AUPN499895A0 (en) 1995-09-14
CN1193903A (zh) 1998-09-23
EP0845975A4 (de) 2000-05-10
WO1997007774A1 (en) 1997-03-06

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