EP1865916A2 - Composition cosmetique comprenant te l'acide hyaluronique et de saponines pour la traitement de la vieillissement de la peau - Google Patents

Composition cosmetique comprenant te l'acide hyaluronique et de saponines pour la traitement de la vieillissement de la peau

Info

Publication number
EP1865916A2
EP1865916A2 EP05801470A EP05801470A EP1865916A2 EP 1865916 A2 EP1865916 A2 EP 1865916A2 EP 05801470 A EP05801470 A EP 05801470A EP 05801470 A EP05801470 A EP 05801470A EP 1865916 A2 EP1865916 A2 EP 1865916A2
Authority
EP
European Patent Office
Prior art keywords
saponins
preparation
weight
cosmetic
hyaluronic 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.)
Withdrawn
Application number
EP05801470A
Other languages
German (de)
English (en)
Inventor
Anette Bürger
Stefan Gallinat
Sabine FÄNGER
Alexander Filbry
Christopher Mummert
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.)
Beiersdorf AG
Original Assignee
Beiersdorf AG
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 Beiersdorf AG filed Critical Beiersdorf AG
Priority to EP08103572.7A priority Critical patent/EP1952799B1/fr
Publication of EP1865916A2 publication Critical patent/EP1865916A2/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73—Polysaccharides
    • A61K8/735—Mucopolysaccharides, e.g. hyaluronic acid; Derivatives thereof
    • 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
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • A61Q19/08—Anti-ageing preparations

Definitions

  • soya extracts contain as natural products a variety of compounds, whose main representatives are the fats, carbohydrates, proteins, isoflavones, lecithins and saponins. Depending on the extraction method, the extracts may contain different ingredients. There are soybean oils or soy extracts containing at least 90% isoflavonoids. Advantageous in accordance with the invention are those soya extracts which have a high content of saponins. These should represent an accumulation of saponin compared to the content in the soybean. The soybean contains about 6.5 mg / g saponins.
  • the preparation according to the invention is in the form of an emulsion and is particularly preferred according to the invention if the preparation according to the invention is in the form of an O / W emulsion. It is advantageous for the purposes of the present invention if the preparation contains one or more of the following emulsifiers or emulsifier combinations: polyglyceryl-2-dipolyhydroxystearate, PEG-30 dipolyhydroxystearate, cetyldimethicone copolyol, glycol distearate, glycol dilaurate, diethylene glycol dilaurate, sorbitan trioleate, glycol oleate, glycidyl ceryldilaurat, sorbitan tristearate, propylene glycol stearate koldistearat, propylene glycol glycol, propylene, PEG-3 castor OiI, Pentaerythritylmonostearat, Pentaerythri- tylses
  • Silicone oils such as dimethylpolysiloxanes, diethylpolysiloxanes, diphenylpolysiloxanes and mixed forms thereof.
  • cyclomethicone octamethylcyclotetrasiloxane
  • silicone oils are also advantageous for the purposes of the present invention, for example hexamethylcyclotrisiloxane, polydimethylsiloxane, poly (methylphenylsiloxane).
  • the cosmetic preparations according to the invention may contain cosmetic adjuvants such as are conventionally used in such preparations, e.g. Preservatives, bactericides, perfumes, foaming inhibitors, colorants, pigments having a coloring effect, thickeners, surface-active substances, emulsifiers, softening, moisturizing and / or moisturizing substances, fats, oils, waxes or other conventional ingredients of a cosmetic or dermatological formulation such as complexing agents, alcohols, polyols, polymers, foam stabilizers, electrolytes, organic solvents or silicone derivatives, convinced ⁇ extracts, vitamins, perfumes.
  • cosmetic adjuvants such as are conventionally used in such preparations, e.g. Preservatives, bactericides, perfumes, foaming inhibitors, colorants, pigments having a coloring effect, thickeners, surface-active substances, emulsifiers, softening, moisturizing and / or moisturizing substances, fats, oils, waxes or other conventional ingredients of
  • preparations according to the invention may also contain substances which absorb UV radiation in the UVB range, the total amount of filter substances being e.g. 0.1 wt .-% to 30 wt .-%, preferably 0.5 to 10 wt .-%, in particular 1, 0 to 6.0 wt .-%, based on the total weight of the preparations, to cosmetic Zu ⁇ preparations that protect the hair or the skin from the entire range of ultraviolet radiation. They can also serve as sunscreen for hair.
  • the total amount of filter substances being e.g. 0.1 wt .-% to 30 wt .-%, preferably 0.5 to 10 wt .-%, in particular 1, 0 to 6.0 wt .-%, based on the total weight of the preparations, to cosmetic Zu ⁇ preparations that protect the hair or the skin from the entire range of ultraviolet radiation. They can also serve as sunscreen for hair.
  • 4-aminobenzoic acid derivatives preferably (2-ethylhexyl) 4- (dimethylamino) benzoate, 4- (dimethylamino) benzoic acid amyl ester;
  • Esters of cinnamic acid preferably 4-methoxycinnamic acid (2-ethylhexyl) ester, 4-methoxycinnamic acid isopentyl ester;
  • Esters of salicylic acid preferably 2-ethylhexyl salicylate, 4-isopropylbenzyl salicylate, homomenthyl salicylate,
  • Esters of benzalmalonic acid preferably di (2-ethylhexyl) 4-methoxybenzalmalonate,
  • Salts of 2-phenylbenzimidazole-5-sulfonic acid such as its sodium, potassium or triethanolammonium salt, and the sulfonic acid itself;
  • Sulfonic acid derivatives of benzophenones preferably 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid and its salts;
  • Sulfonic acid derivatives of the 3-benzylidene camphor e.g. 4- (2-oxo-3-bomylidenemethyl) benzenesulfonic acid, 2-methyl-5- (2-oxo-3-bomylidenemethyl) sulfonic acid and its salts, and 1,4-di (2-oxo-10-sulfonic acid) 3-bomylidenemethyl) benzene and its salts (the debasing 10-sulfato compounds, for example the corresponding sodium, potassium or triethanolammonium salt), also as benzene-1, 4-di (2-oxo-3-yl) bomylidenemethyl-10-sulfonic acid
  • UVB filters which can be used in combination with the active substance combinations according to the invention should of course not be limiting.
  • UVA filters that are commonly included in cosmetic preparations. These substances are preferably derivatives of dibenzoylmethane, in particular 1- (4'-tert-butylphenyl) -3- (4- l- methoxyphenyl) propane-1,3-dione and 1-phenyl-3 - (4'-isopropylphenyl) propane-1,3-dione.
  • UVA filters originate from the group of triazines, for example 2,4-bis ⁇ [4- (2-ethyl-hexyloxy) -2-hydroxy] -phenyl ⁇ -6- (4-methoxyphenyl) -1, 3,5-triazine (commercial Tinosorb® S) and the group of triazoles, such as the 2,2'-methylene-bis [6- 2H-benzotriazol-2yl] -4- (1,1,3,3-tetramethylbutyl) phenol) (Trade -name Tinosorb® M).
  • An advantageous water-soluble UVA filter is the 2 "bis (1,4-phenylene) -1 H-benzimidazole-4,6-disulfonic acid sodium salt (trade name Neo Heliopan AP®).
  • the amounts used for the UVB combination can be used.
  • the pigments can also be used advantageously in the form of commercially available oily or aqueous predispersions. Dispersants and / or solubilizers may advantageously be added to these pre-dispersions.
  • the pigments may advantageously be surface-treated ("coated"), wherein, for example, a hydrophilic, amphiphilic or hydrophobic character is to be formed or retained.
  • This surface treatment may consist in using a thin film according to methods known per se hydrophilic and / or hydrophobic inorganic and / or organic layer
  • the various surface coatings may also contain water in the sense of the present invention.
  • Inorganic surface coatings for the purposes of the present invention may be composed of aluminum oxide (Al 2 O 3 ), aluminum hydroxide Al (OH) 3 or aluminum oxide hydrate (also: alumina, CAS No .: 1333-84-2), sodium hexametaphosphate (NaPO 3 J 6 , sodium meta-phosphate (NaPO 3 J n , silicon dioxide (SiO 2 ) (also: silica, CAS No .: 7631-86-9), or iron oxide (Fe 2 O 3 )
  • Al 2 O 3 aluminum oxide
  • Al aluminum hydroxide Al
  • Al oxide hydrate also: alumina, CAS No .: 1333-84-2
  • sodium hexametaphosphate NaPO 3 J 6
  • sodium meta-phosphate NaPO 3 J n
  • silicon dioxide SiO 2
  • SiO 2 also: silica, CAS No .: 7631-86-9
  • iron oxide Fe 2 O 3
  • Organic surface coatings in the sense of the present invention can consist of vegetable or animal aluminum stearate, vegetable or animal stearin. acid, lauric acid, dimethylpolysiloxane (also: dimethicone), methyl polysiloxane (methicone), simethicone (a mixture of dimethylpolysiloxane with an average chain length of 200 to 350 dimethylsiloxane units and silica gel) or alginic acid.
  • dimethylpolysiloxane also: dimethicone
  • methicone methyl polysiloxane
  • simethicone a mixture of dimethylpolysiloxane with an average chain length of 200 to 350 dimethylsiloxane units and silica gel
  • alginic acid can occur alone, in combination and / or in combination with inorganic coating materials.
  • the process for the preparation of the cosmetic preparation according to the invention is characterized in that the saponins or the saponins containing soy extract first in at least four times the amount of a glycol with a log P value between -3.6 and 1 or in the Water phase of the preparation containing this amount of the glycol is dissolved and then combined with a fatty phase containing the emulsifiers.

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)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Botany (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Gerontology & Geriatric Medicine (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

La présente invention concerne des préparations cosmétiques contenant une combinaison de principes actifs constituée d'acide hyaluronique et de saponines.
EP05801470A 2005-03-16 2005-11-01 Composition cosmetique comprenant te l'acide hyaluronique et de saponines pour la traitement de la vieillissement de la peau Withdrawn EP1865916A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP08103572.7A EP1952799B1 (fr) 2005-03-16 2005-11-01 Preparation cosmetique comprenant l'acide hyaluonique pour traiter les signes de vieillissement

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102005012554A DE102005012554A1 (de) 2005-03-16 2005-03-16 Kosmetische Zubereitung mit Hyaluronsäure
PCT/EP2005/055677 WO2006018454A2 (fr) 2005-03-16 2005-11-01 Preparation cosmetique contenant de l'acide hyaluronique

Related Child Applications (1)

Application Number Title Priority Date Filing Date
EP08103572.7A Division EP1952799B1 (fr) 2005-03-16 2005-11-01 Preparation cosmetique comprenant l'acide hyaluonique pour traiter les signes de vieillissement

Publications (1)

Publication Number Publication Date
EP1865916A2 true EP1865916A2 (fr) 2007-12-19

Family

ID=35539053

Family Applications (2)

Application Number Title Priority Date Filing Date
EP05801470A Withdrawn EP1865916A2 (fr) 2005-03-16 2005-11-01 Composition cosmetique comprenant te l'acide hyaluronique et de saponines pour la traitement de la vieillissement de la peau
EP08103572.7A Expired - Lifetime EP1952799B1 (fr) 2005-03-16 2005-11-01 Preparation cosmetique comprenant l'acide hyaluonique pour traiter les signes de vieillissement

Family Applications After (1)

Application Number Title Priority Date Filing Date
EP08103572.7A Expired - Lifetime EP1952799B1 (fr) 2005-03-16 2005-11-01 Preparation cosmetique comprenant l'acide hyaluonique pour traiter les signes de vieillissement

Country Status (5)

Country Link
US (1) US8252348B2 (fr)
EP (2) EP1865916A2 (fr)
DE (1) DE102005012554A1 (fr)
ES (1) ES2622084T3 (fr)
WO (1) WO2006018454A2 (fr)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2022829B1 (fr) * 2006-04-21 2013-06-12 Nippon Sheet Glass Company, Limited Pigment photoluminescent, procédé de production du pigment, et composition de résine aqueuse comprenant le pigment
JP2010509570A (ja) 2006-11-03 2010-03-25 パーデュー・リサーチ・ファウンデーション エクスビボフローサイトメトリーの方法および装置
WO2008130040A1 (fr) * 2007-04-18 2008-10-30 Nippon Sheet Glass Company, Limited Pigment photoluminescent et composition cosmétique utilisant celui-ci
CN101668819B (zh) * 2007-04-27 2012-11-21 日本板硝子株式会社 光亮性颜料、含有其的光亮性涂料组合物及汽车外板涂敷物
US8409708B2 (en) * 2007-10-18 2013-04-02 Nippon Sheet Glass Company, Limited Bright pigment
US8039024B2 (en) * 2008-01-23 2011-10-18 Apr Applied Pharma Research, S.A. Device and composition for the delivery of a preservative-free balsamic cream
FR2945936A1 (fr) * 2009-05-26 2010-12-03 Jean Claude Epiphani Procede de fabrication d'une emulsion aqueuse d'une substance active huileuse pour application cosmetique, alimentaire ou pharmaceutique
FR3012334A1 (fr) * 2013-10-29 2015-05-01 World Cosmetics Composition cosmetique anti age
TR201609395A2 (tr) * 2016-07-01 2018-01-22 Bioarge Bitkisel Kozmetik Arastirma Gelistirme Muehendislik Ltd Sti İyileştirilmiş yağ dispersiyonu ve transdermal dağıtımı.
EP3549575A4 (fr) * 2016-12-01 2020-07-15 Daniel Dal'Asta Coimbra Méthode non thérapeutique, utilisations d'une substance stimulant ou provoquant une augmentation de volume

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FR2680686B1 (fr) * 1991-08-28 1993-11-05 Oreal Lotion tri-phases destinee a un usage corporel, pharmaceutique ou cosmetique.
FR2695561B1 (fr) * 1992-09-17 1994-12-02 Lvmh Rech Gie Composition cosmétique ou dermatologique contenant au moins une saponine de type ginsenoside, et ses applications, notamment pour le soin des cheveux.
DE4410778C2 (de) * 1994-03-28 2002-09-12 Beisel Guenther Mittel zur Herstellung eines medizinisch und/oder kosmetisch und/oder keimabtötend und/oder parasitenabtötend wirkenden wässrigen stabilen Schaums und dessen Verwendung
US6461622B2 (en) * 1994-09-07 2002-10-08 Johnson & Johnson Consumer Companies, Inc. Topical compositions
JPH08217660A (ja) * 1995-02-16 1996-08-27 Shiseido Co Ltd 皮膚外用剤
FR2746316B1 (fr) * 1996-03-19 1998-06-12 Guerlain Nouvelles compositions cosmetologiques ou dermatologiques
IT1288257B1 (it) 1996-11-29 1998-09-11 Paoli Ambrosi Gianfranco De Composizione per uso cosmetico,farmaceutico o dietetico a base di un aminozucchero e/o di un acido poliidrossilico
JPH1135445A (ja) * 1997-07-23 1999-02-09 Osaka Yakuhin Kenkyusho:Kk 化粧料組成物
FR2767057B1 (fr) 1997-08-08 1999-10-29 Lvmh Rech Utilisation du ginsenoside rb1 comme agent destine a stimuler la synthese de l'elastine
FR2767059B1 (fr) * 1997-08-11 2000-03-24 Lvmh Rech Utilisation d'extraits de polygonatum pour stimuler la synthese de l'elastine cutanee
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DE10301632A1 (de) 2003-01-17 2004-07-29 Beiersdorf Ag Kosmetische oder dermatologische Zubereitungen mit einem Gehalt an Kreatin, Kreatinin und/oder seinen Derivaten in Kombination mit Sojabohnenkeimextrakten

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Also Published As

Publication number Publication date
ES2622084T3 (es) 2017-07-05
US8252348B2 (en) 2012-08-28
WO2006018454A2 (fr) 2006-02-23
US20080306021A1 (en) 2008-12-11
DE102005012554A1 (de) 2006-09-28
EP1952799A2 (fr) 2008-08-06
EP1952799B1 (fr) 2017-01-11
WO2006018454A3 (fr) 2006-05-11
EP1952799A3 (fr) 2008-08-20

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