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WO1996018376A1 - Colorant capillaire naturel a deux composants - Google Patents

Colorant capillaire naturel a deux composants Download PDF

Info

Publication number
WO1996018376A1
WO1996018376A1 PCT/EP1995/004766 EP9504766W WO9618376A1 WO 1996018376 A1 WO1996018376 A1 WO 1996018376A1 EP 9504766 W EP9504766 W EP 9504766W WO 9618376 A1 WO9618376 A1 WO 9618376A1
Authority
WO
WIPO (PCT)
Prior art keywords
component
hair
water
dye
thickener
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
PCT/EP1995/004766
Other languages
German (de)
English (en)
Inventor
Klaus Kirchmayr
Horst Höffkes
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.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
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 Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of WO1996018376A1 publication Critical patent/WO1996018376A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • 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
    • A61Q5/10—Preparations for permanently dyeing the hair
    • 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
    • A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9783—Angiosperms [Magnoliophyta]
    • A61K8/9789—Magnoliopsida [dicotyledons]
    • 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
    • A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/88—Two- or multipart kits

Definitions

  • the invention relates to a new process for coloring hair using natural hair colorants, preferably coloring plant parts, and a hair colorant suitable for this process, consisting of a sales unit consisting of two separately packaged components, one of which coloring plant parts and the other a thickener includes.
  • Herbal hair dyes have long been known for temporary hair coloring. Powdered parts of plants from strongly coloring plants such as e.g. Henna or indigo leaves are used, which are mixed with water and, if appropriate, fillers and thickeners to give coloring pastes which are applied to the hair.
  • This well-known cataplasma process has the disadvantage that the dye powders have to be ground very finely in order to produce a uniform color on the hair. In addition, water-insoluble constituents remain on the hair which are difficult to wash out completely. Fine grinding of the dyes also has the disadvantage that undesirable dust development occurs during manufacture and processing. Attempts have also already been made to extract natural dyes from the plant parts and to incorporate the extracts into coloring preparations. Such dyes isolated from the plant are very unstable with respect to the effects of oxygen and light and are therefore not suitable for the production of storable preparations.
  • a hair dyeing process was therefore sought which avoids the disadvantages of the known natural hair dyeing processes.
  • the invention relates to a two-component natural hair dye consisting of a sales unit with two separately packaged components (A) and (B), the component
  • (B) comprises at least one separately packaged aqueous media thickener.
  • the process according to the invention for coloring the hair using the abovementioned two-component hair colorants is distinguished by the fact that parts of the plant which give off dyes which are soluble in an aqueous medium are in a water-insoluble packaging, the walls of which are at least partially made of porous dyes for water and dissolved dyes permeable material consists (component A) in a predetermined amount of an aqueous medium and, if necessary with agitation, remains in it until the desired amount of dye is dissolved, then the aqueous dye solution contains a water-soluble thickener (component B) in an amount zu ⁇ sets, which gives this a suitable for application to the hair viscosity, and finally applies the thickened dye solution to the hair and rinses the colored hair with water after an exposure time.
  • This process according to the invention ensures that no insoluble parts of the plant get onto the hair and that the dyeing is carried out using a freshly prepared dye extract which has not yet suffered from oxidative degradation and has not undergone photochemical decomposition
  • all strongly coloring plants or parts of plants are suitable for producing component (A) of the two-component natural hair dye.
  • Examples of such plants or parts of plants are:
  • Henna (Lawsonia iner is or Lawsonia alba leaves)
  • Rhubarb root root.
  • dye carriers for the preparation of the hair colorants according to the invention.
  • shredded parts of plants can also contain other dye carriers, for example cochineal, peat or other coloring natural substances.
  • the plant parts of component (A) are preferably in the form of dried powders of henna, indigo, cassia, black tea, chamomile flowers, beetroot, elderberries, rot tree bark, blue wood, redwood, curcuma, sage or rhubarb root.
  • the plants or parts of plants to be used only need to be roughly crushed, but finely ground powders are also suitable. Dusting cannot occur during use because the plant parts remain in the packaging. Plant parts which have a particle size of 1 ⁇ m to 1 mm are preferred. Due to the large surface area, finer powders are less stable in storage, coarser parts of plants take a longer time to remove the dye.
  • any water-resistant packaging material is suitable as water-insoluble packaging, irrespective of whether it is rigid or flexible, whether made of water-resistant paper, plastic or textile. However, it is important that the wall consists at least partially of porous material.
  • the packaging of component (A) is preferably a flexible bag made of a waterproof but fine-pored paper (e.g. hot filter paper), nonwoven fabric or textile fabric. Suitable paper bags are e.g. known for the preparation of tea (so-called tea bags).
  • the pore size it should be noted that undissolved plant material cannot pass through the pores, so the pore size should in any case be smaller than the particle size of the fine fraction of the plant parts used.
  • the packaging material should be slightly permeable to the dissolved dyes be so that the process of removing the dyes can proceed as quickly as possible.
  • the water-insoluble packaging of component (A) may also contain other water-soluble auxiliaries which relate to the process of leaching out the dyes, the formation of brilliant dyeings, the dyeing onto the keratin fiber or the stability of the dyeing solution and improve the dye on the hair.
  • Such aids can e.g. pH adjusting agents or buffer substances which give the dye solution the pH at which the dye is most intensive.
  • Suitable products are primarily e.g. Fruit acids, e.g. Citric acid or tartaric acid and its salts.
  • auxiliaries that can be packed with the plant parts of component (A) are e.g. water soluble antioxidants, e.g. Ascorbic acid, water-soluble hydrotropes or salts such as e.g. Urea, protein hydrolyzates, ammonium sulfate or ammonium lactate and surfactants, e.g. powdery wetting agents such as Saponins or synthetic surfactants.
  • the second, separately packaged component (B) contains at least one water-soluble thickener. Both a solid and a liquid thickener can be used. No particular requirements are to be placed on the packaging of component (B) except that it should sufficiently include the respective thickener. If as a thickener e.g. If an aqueous or other liquid preparation is selected, the packaging must be watertight and, if necessary, stable against the solvents it contains.
  • any thickener can be used.
  • aqueous media suitable and physiologically compatible thickeners be used.
  • Both water-insoluble swelling agents such as layered silicates or colloidal thickening silicas are suitable, as are water-soluble organic hydrocolloids, for example natural rubber and biopolymers, and synthetic water-soluble polymers.
  • emulsifiable fat components or emulsion concentrates which are converted into a viscous emulsion by stirring into the aqueous dye solution.
  • Preferred suitable thickeners for carrying out the present invention are, however, the organic natural products from the group of guar flour, locust bean gum, gum arabic, alginates, water-soluble starch, pectin, gelatin or biopolymers such as e.g. Xanthan gum.
  • Suitable natural product derivatives are e.g. the water-soluble cellulose, starch or guar derivatives, e.g. Methyl cellulose, hydroxyethyl cellulose, carboxymethyl cellulose, carboxyethyl starch, hydroxypropyl guar and others.
  • components (A) and (B) are preferably combined in one sales unit.
  • the amounts of components (A) and (B) are matched to one another in such a way that, with a given amount of water, both the desired dye concentration for hair coloring and the suitable viscosity of the coloring solution for application to the hair, e.g. is achieved with a coloring brush.
  • the concentration of the dye in the coloring solution and thus the intensity of the hair coloring can also be controlled by the user by limiting the amount of dissolved dye by a shorter dissolving time.
  • Te The amount of thickener in the separately packaged Komponen ⁇ (B) should be such that the ge according to instructions ready Haarfärbezurung produced a viscosity in the range of 5 to 50 Pa »s (20 ° C) (measured at a shear stress ( D) of 3 see " 1 , for example in the Haake rotation viscometer type RV12 / MV1).
  • Preferred furthermore are those thickeners which, in addition to the viscosity mentioned, produce a certain thixotropy which promotes adhesion of the dye preparation applied to the hair and the running down of the Colorant and an undesirable skin staining prevented.
  • auxiliaries of component B can also be added, e.g. facilitate the dissolvability of the thickener or favorably influence the theological properties of the ready-to-use hair dye preparation.
  • fragrances, deodorants, hair cosmetic agents and preservatives can also be added.
  • the packaging with the plant parts (component A) is preferably poured with boiling hot water so that the dyes are dissolved as quickly and completely as possible. Then either the solution or the dye container is moved so that the dissolving process is further promoted. If you want to achieve the deepest possible color, leave the dye container in the solution until it cools to room temperature (20 ° C). However, by prematurely removing the dye container, the extraction process of the dyes can be limited and a weaker coloring can be achieved in this way.
  • the thickening agent is preferably added only after the dyeing solution has cooled, since gel clumps which are difficult to dissolve easily form in the hot solution.
  • the coloring preparation After the thickener has been added, the coloring preparation must be homogenized by stirring until the thickener has been completely distributed or dissolved and the desired final viscosity has been reached.
  • the ready-to-use preparation is applied to the hair by the method customary for hair coloring, preferably using a brush.
  • the applied preparation is then left to act until the dye is applied to the hair. Since the dyeing preparation contains no incompatible components, e.g. no longer contains insoluble residues, you can extend the exposure time as long as you like and e.g. let the preparation take effect overnight.
  • an exposure time of 10 to 60 minutes should be sufficient to achieve a good color.
  • the following dye powders or powder mixtures were produced and filled into conventional tea bags in amounts of 5 g each.
  • the coloring gels were applied to light blonde hair with the help of a coloring brush. After an exposure time of 45 minutes at 20 ° C., the colored hair tresses were rinsed off with water and dried.

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Botany (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Abstract

L'invention concerne un procédé de coloration capillaire faisant appel à l'utilisation d'un colorant capillaire à deux composants, à savoir le composant (A) et le composant (B) qui sont conditionnés séparément mais combinés en une unité de vente. Le composant (A) comprend des matières végétales présentant une certaine teneur en matières colorantes sobubles, et il est contenu dans un emballage non soluble dans l'eau mais au moins partiellement perméable à l'eau. Le composant (B) comprend au moins un épaississant pour substances aqueuses. Le composant (A), qui se trouve dans un emballage perméable à l'eau, est introduit dans une quantité prédéterminée de substance aqueuse jusqu'à ce que la matière colorante soit dissoute, puis l'épaississant (B) est ajouté à la solution de substance colorante. La préparation de colorant prête à l'emploi ainsi obtenue est appliquée directement sur les cheveux et rincée après un temps de fixation.
PCT/EP1995/004766 1994-12-13 1995-12-04 Colorant capillaire naturel a deux composants Ceased WO1996018376A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB9425118.8 1994-12-13
GBGB9425118.8A GB9425118D0 (en) 1994-12-13 1994-12-13 Two component natural hair colorant

Publications (1)

Publication Number Publication Date
WO1996018376A1 true WO1996018376A1 (fr) 1996-06-20

Family

ID=10765860

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP1995/004766 Ceased WO1996018376A1 (fr) 1994-12-13 1995-12-04 Colorant capillaire naturel a deux composants

Country Status (2)

Country Link
GB (1) GB9425118D0 (fr)
WO (1) WO1996018376A1 (fr)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999011222A1 (fr) * 1997-08-28 1999-03-11 Wella Aktiengesellschaft Produit de soins cosmetiques a deux composantes
EP0761200A3 (fr) * 1995-08-23 1999-03-31 Goldwell Aktiengesellschaft Composition pour colorer ou teindre les cheveux humains
WO1999011223A3 (fr) * 1997-08-29 1999-05-06 Unilever Plc Compositions de traitement capillaire
DE19713696C5 (de) * 1997-04-03 2004-01-15 Kpss-Kao Professional Salon Services Gmbh Verfahren zum gleichzeitigen Tönen und Waschen von menschlichen Haaren
CN1326516C (zh) * 2005-04-14 2007-07-18 冯宝富 一种中药染发水
FR2951374A1 (fr) * 2009-10-16 2011-04-22 Oreal Composition comprenant au moins un derive d'anthrones, procede de coloration des fibres keratiniques a partir de la composition
WO2011157666A1 (fr) * 2010-06-16 2011-12-22 L'oreal Utilisation cosmétique d'un extrait naturel dérivé des épluchures de betterave pour colorer les cheveux, composition comprenant l'extrait, un agent oxydant, un agent basifiant et un dérivé métallique facultatif
CN103222940A (zh) * 2013-05-14 2013-07-31 马志刚 纯天然护发剂
US8529969B2 (en) * 1997-06-12 2013-09-10 Meyhall Ag Method for manufacturing pure guar meal
EP2258847B1 (fr) 2002-08-05 2017-03-15 Silence Therapeutics GmbH Autres nouvelles formes de molécules d'ARN interférant
WO2020128809A1 (fr) * 2018-12-19 2020-06-25 Bhatt Sanjeev Colorant capillaire à base d'herbes et procédé de fabrication associé

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0072298A1 (fr) * 1981-08-03 1983-02-16 Pierre Fabre S.A. Préparation cosmétique extemporanée à pouvoir colorant, en particulier à usage capillaire
GB2281730A (en) * 1993-09-09 1995-03-15 Jean Reidy Herbal sachets

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0072298A1 (fr) * 1981-08-03 1983-02-16 Pierre Fabre S.A. Préparation cosmétique extemporanée à pouvoir colorant, en particulier à usage capillaire
GB2281730A (en) * 1993-09-09 1995-03-15 Jean Reidy Herbal sachets

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0761200A3 (fr) * 1995-08-23 1999-03-31 Goldwell Aktiengesellschaft Composition pour colorer ou teindre les cheveux humains
DE19713696C5 (de) * 1997-04-03 2004-01-15 Kpss-Kao Professional Salon Services Gmbh Verfahren zum gleichzeitigen Tönen und Waschen von menschlichen Haaren
US8529969B2 (en) * 1997-06-12 2013-09-10 Meyhall Ag Method for manufacturing pure guar meal
US8993015B2 (en) 1997-06-12 2015-03-31 Meyhall Ag Method for manufacturing pure guar flour
WO1999011222A1 (fr) * 1997-08-28 1999-03-11 Wella Aktiengesellschaft Produit de soins cosmetiques a deux composantes
WO1999011223A3 (fr) * 1997-08-29 1999-05-06 Unilever Plc Compositions de traitement capillaire
US10266829B2 (en) 2002-08-05 2019-04-23 Silence Therapeutics Gmbh Interfering RNA molecules
US10323246B2 (en) 2002-08-05 2019-06-18 Silence Therapeutics Gmbh Interfering RNA molecules
US11578328B2 (en) 2002-08-05 2023-02-14 Silence Therapeutics Gmbh Interfering RNA molecules
US10774332B2 (en) 2002-08-05 2020-09-15 Silence Therapeutics Gmbh Interfering RNA molecules
US10329568B2 (en) 2002-08-05 2019-06-25 Silence Therapeutics Gmbh Interfering RNA molecules
US9790505B2 (en) 2002-08-05 2017-10-17 Silence Therapeutics Gmbh Interfering RNA molecules
EP2258847B1 (fr) 2002-08-05 2017-03-15 Silence Therapeutics GmbH Autres nouvelles formes de molécules d'ARN interférant
US9695423B2 (en) 2002-08-05 2017-07-04 Silence Therapeutics Gmbh Interfering RNA molecules
US9758784B1 (en) 2002-08-05 2017-09-12 Silence Therapeutics Gmbh Interfering RNA molecules
US9783802B2 (en) 2002-08-05 2017-10-10 Silence Therapeutics Gmbh Interfering RNA molecules
US9790501B2 (en) 2002-08-05 2017-10-17 Silence Therapeutics Gmbh Interfering RNA molecules
CN1326516C (zh) * 2005-04-14 2007-07-18 冯宝富 一种中药染发水
FR2951374A1 (fr) * 2009-10-16 2011-04-22 Oreal Composition comprenant au moins un derive d'anthrones, procede de coloration des fibres keratiniques a partir de la composition
FR2961398A1 (fr) * 2010-06-16 2011-12-23 Oreal Utilisation en cosmetique d'un extrait naturel issu de pelure de betterave rouge, composition comprenant l'extrait et un derive metallique, un agent oxydant et un agent alcalinisant
WO2011157666A1 (fr) * 2010-06-16 2011-12-22 L'oreal Utilisation cosmétique d'un extrait naturel dérivé des épluchures de betterave pour colorer les cheveux, composition comprenant l'extrait, un agent oxydant, un agent basifiant et un dérivé métallique facultatif
CN103222940B (zh) * 2013-05-14 2015-02-11 马志刚 纯天然护发剂
CN103222940A (zh) * 2013-05-14 2013-07-31 马志刚 纯天然护发剂
WO2020128809A1 (fr) * 2018-12-19 2020-06-25 Bhatt Sanjeev Colorant capillaire à base d'herbes et procédé de fabrication associé

Also Published As

Publication number Publication date
GB9425118D0 (en) 1995-02-08

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