DD283930A5 - Verfahren zur herstellung topischer kosmetischer und pharmazeutischer zubereitung mit einem gehalt an fettstoffen und freien tocopherolen - Google Patents

Verfahren zur herstellung topischer kosmetischer und pharmazeutischer zubereitung mit einem gehalt an fettstoffen und freien tocopherolen Download PDF

Info

Publication number: DD283930A5
Authority: DD; German Democratic Republic
Prior art keywords: acid; tocopherol; acid esters; tocopherols; weight
Prior art date: 1988-06-18

Application number

DD89329699A

Other languages

German (de)

English (en)

Inventor

Siegfried Wallat

Hermann Hensen

Hans Pfeiffer

Achim Ansmann

Hinrich Moeller

Original Assignee

Henkel Kommanditgesellschaft Auf Aktien,De

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.)

1988-06-18

Filing date

1989-06-16

Publication date

1990-10-31

1989-06-16 Application filed by Henkel Kommanditgesellschaft Auf Aktien,De filed Critical Henkel Kommanditgesellschaft Auf Aktien,De

1990-10-31 Publication of DD283930A5 publication Critical patent/DD283930A5/de

Links

239000011732 tocopherol Substances 0.000 title claims abstract description 30
229930003799 tocopherol Natural products 0.000 title claims abstract description 30
235000019149 tocopherols Nutrition 0.000 title claims abstract description 22
230000000699 topical effect Effects 0.000 title claims abstract description 16
239000002537 cosmetic Substances 0.000 title claims abstract description 13
239000000825 pharmaceutical preparation Substances 0.000 title claims abstract description 13
QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 title description 17
238000004519 manufacturing process Methods 0.000 title description 2
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical class OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims abstract description 30
GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 claims abstract description 26
GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims abstract description 20
235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 14
239000000194 fatty acid Substances 0.000 claims abstract description 14
229930195729 fatty acid Natural products 0.000 claims abstract description 14
150000004665 fatty acids Chemical class 0.000 claims abstract description 14
238000002360 preparation method Methods 0.000 claims abstract description 12
230000006641 stabilisation Effects 0.000 claims abstract description 11
238000011105 stabilization Methods 0.000 claims abstract description 11
239000000126 substance Substances 0.000 claims abstract description 10
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 8
235000010384 tocopherol Nutrition 0.000 claims abstract description 8
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238000000034 method Methods 0.000 claims abstract description 5
125000005456 glyceride group Chemical group 0.000 claims abstract description 4
125000002640 tocopherol group Chemical class 0.000 claims abstract 5
239000003925 fat Substances 0.000 claims description 12
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230000005855 radiation Effects 0.000 claims description 6
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 abstract description 6
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ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical class NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 4
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239000004480 active ingredient Substances 0.000 description 4
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WSSJONWNBBTCMG-UHFFFAOYSA-N 2-hydroxybenzoic acid (3,3,5-trimethylcyclohexyl) ester Chemical compound C1C(C)(C)CC(C)CC1OC(=O)C1=CC=CC=C1O WSSJONWNBBTCMG-UHFFFAOYSA-N 0.000 description 2
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241001465754 Metazoa Species 0.000 description 2
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235000021355 Stearic acid Nutrition 0.000 description 2
DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 2
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XNEFYCZVKIDDMS-UHFFFAOYSA-N avobenzone Chemical compound C1=CC(OC)=CC=C1C(=O)CC(=O)C1=CC=C(C(C)(C)C)C=C1 XNEFYCZVKIDDMS-UHFFFAOYSA-N 0.000 description 2
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UHUSDOQQWJGJQS-UHFFFAOYSA-N glycerol 1,2-dioctadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCCCCCCCCCCC UHUSDOQQWJGJQS-UHFFFAOYSA-N 0.000 description 2
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
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YAQXGBBDJYBXKL-UHFFFAOYSA-N iron(2+);1,10-phenanthroline;dicyanide Chemical compound [Fe+2].N#[C-].N#[C-].C1=CN=C2C3=NC=CC=C3C=CC2=C1.C1=CN=C2C3=NC=CC=C3C=CC2=C1 YAQXGBBDJYBXKL-UHFFFAOYSA-N 0.000 description 2
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150000001893 coumarin derivatives Chemical class 0.000 description 1
239000006071 cream Substances 0.000 description 1
ZAKOWWREFLAJOT-UHFFFAOYSA-N d-alpha-Tocopheryl acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-UHFFFAOYSA-N 0.000 description 1
NZZIMKJIVMHWJC-UHFFFAOYSA-N dibenzoylmethane Chemical class C=1C=CC=CC=1C(=O)CC(=O)C1=CC=CC=C1 NZZIMKJIVMHWJC-UHFFFAOYSA-N 0.000 description 1
235000019961 diglycerides of fatty acid Nutrition 0.000 description 1
239000008157 edible vegetable oil Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
229960000655 ensulizole Drugs 0.000 description 1
LFMDCCGJAJYZML-UHFFFAOYSA-N ethyl 2-amino-3-(3-hydroxypropyl)benzoate Chemical compound C(C)OC(C1=C(C(=CC=C1)CCCO)N)=O LFMDCCGJAJYZML-UHFFFAOYSA-N 0.000 description 1
125000004494 ethyl ester group Chemical group 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
235000013305 food Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
235000021588 free fatty acids Nutrition 0.000 description 1
LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical class OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
239000000077 insect repellent Substances 0.000 description 1
239000010699 lard oil Substances 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
239000006210 lotion Substances 0.000 description 1
239000000155 melt Substances 0.000 description 1
WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
239000004200 microcrystalline wax Substances 0.000 description 1
239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
229940078812 myristyl myristate Drugs 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
239000002674 ointment Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
AFDXODALSZRGIH-UHFFFAOYSA-N p-coumaric acid methyl ether Natural products COC1=CC=C(C=CC(O)=O)C=C1 AFDXODALSZRGIH-UHFFFAOYSA-N 0.000 description 1
LXTZRIBXKVRLOA-UHFFFAOYSA-N padimate a Chemical compound CCCCCOC(=O)C1=CC=C(N(C)C)C=C1 LXTZRIBXKVRLOA-UHFFFAOYSA-N 0.000 description 1
239000002540 palm oil Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
IWHVCHNCTHGORM-UHDJGPCESA-M potassium;(e)-3-phenylprop-2-enoate Chemical compound [K+].[O-]C(=O)\C=C\C1=CC=CC=C1 IWHVCHNCTHGORM-UHDJGPCESA-M 0.000 description 1
238000004321 preservation Methods 0.000 description 1
230000003244 pro-oxidative effect Effects 0.000 description 1
229940058287 salicylic acid derivative anticestodals Drugs 0.000 description 1
150000003872 salicylic acid derivatives Chemical class 0.000 description 1
150000003902 salicylic acid esters Chemical class 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000002453 shampoo Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
CXVGEDCSTKKODG-UHFFFAOYSA-N sulisobenzone Chemical compound C1=C(S(O)(=O)=O)C(OC)=CC(O)=C1C(=O)C1=CC=CC=C1 CXVGEDCSTKKODG-UHFFFAOYSA-N 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
BORJONZPSTVSFP-UHFFFAOYSA-N tetradecyl 2-hydroxypropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)C(C)O BORJONZPSTVSFP-UHFFFAOYSA-N 0.000 description 1
DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
210000001519 tissue Anatomy 0.000 description 1
229950009883 tocopheryl nicotinate Drugs 0.000 description 1
239000012049 topical pharmaceutical composition Substances 0.000 description 1
LOIYMIARKYCTBW-UHFFFAOYSA-N urocanic acid Chemical compound OC(=O)C=CC1=CNC=N1 LOIYMIARKYCTBW-UHFFFAOYSA-N 0.000 description 1
229940099259 vaseline Drugs 0.000 description 1
239000011718 vitamin C Substances 0.000 description 1
235000019154 vitamin C Nutrition 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
230000003442 weekly effect Effects 0.000 description 1
WGVKWNUPNGFDFJ-DQCZWYHMSA-N β-tocopherol Chemical compound OC1=CC(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C WGVKWNUPNGFDFJ-DQCZWYHMSA-N 0.000 description 1
QUEDXNHFTDJVIY-DQCZWYHMSA-N γ-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-DQCZWYHMSA-N 0.000 description 1
GZIFEOYASATJEH-VHFRWLAGSA-N δ-tocopherol Chemical compound OC1=CC(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1 GZIFEOYASATJEH-VHFRWLAGSA-N 0.000 description 1

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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
- A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
- 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
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/67—Vitamins
- 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
- A61K8/67—Vitamins
- A61K8/676—Ascorbic acid, i.e. vitamin C
- 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
- A61K8/67—Vitamins
- A61K8/678—Tocopherol, i.e. vitamin E
- 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
- 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
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
- 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
- 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
- A61K2800/52—Stabilizers

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Veterinary Medicine (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Birds (AREA)
Epidemiology (AREA)
Dermatology (AREA)
Oil, Petroleum & Natural Gas (AREA)
Chemical & Material Sciences (AREA)
Emergency Medicine (AREA)
Cosmetics (AREA)
Medicinal Preparation (AREA)

DD89329699A 1988-06-18 1989-06-16 Verfahren zur herstellung topischer kosmetischer und pharmazeutischer zubereitung mit einem gehalt an fettstoffen und freien tocopherolen DD283930A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE3820693A DE3820693A1 (de)	1988-06-18	1988-06-18	Topische kosmetische und pharmazeutische zubereitungen

Publications (1)

Publication Number	Publication Date
DD283930A5 true DD283930A5 (de)	1990-10-31

Family

ID=6356783

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD89329699A DD283930A5 (de)	1988-06-18	1989-06-16	Verfahren zur herstellung topischer kosmetischer und pharmazeutischer zubereitung mit einem gehalt an fettstoffen und freien tocopherolen

Country Status (8)

Country	Link
EP (2)	EP0347664A1 (fr)
JP (1)	JPH03505089A (fr)
KR (1)	KR900701249A (fr)
AU (1)	AU3760789A (fr)
DD (1)	DD283930A5 (fr)
DE (1)	DE3820693A1 (fr)
DK (1)	DK296690D0 (fr)
WO (1)	WO1989012437A1 (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5102659A (en)	1990-07-12	1992-04-07	Shaklee Corporation	Natural antioxidant compositions
GB9109965D0 (en) *	1991-05-07	1991-07-03	Unilever Plc	Cosmetic composition
DE4128748A1 (de) *	1991-08-29	1993-03-04	Beiersdorf Ag	Kosmetische stifte
NL9201438A (nl) *	1992-08-11	1994-03-01	Prospa Bv	Nieuwe farmaceutische samenstellingen die esters van omega-3 polyonverzadigde zuren omvatten en de toepassing ervan bij de plaatselijke behandeling van ziekelijke aandoeningen.
DE4343264A1 (de) *	1993-12-17	1995-06-22	Henkel Kgaa	Deodorierende Zubereitungen
GB9403855D0 (en) *	1994-03-01	1994-04-20	Scotia Holdings Plc	Fatty acid derivatives
DE19529773A1 (de) *	1995-08-12	1997-02-13	Beiersdorf Ag	Hautpflegemittel und pflegendes Hautreinigungsmittel
JPH11199425A (ja) *	1998-01-05	1999-07-27	Nippon Haipokkusu:Kk	化粧料
DE19802206A1 (de)	1998-01-22	1999-07-29	Beiersdorf Ag	Lipidreduzierte, fließfähige Zubereitungen
DE19802204A1 (de) *	1998-01-22	1999-07-29	Beiersdorf Ag	Kosmetische oder pharmazeutische Zubereitungen mit vermindertem Klebrigkeitsgefühl, enthaltend Glycerinester von -Hydroxycarbonsäuren und gesättigten Fettsäuren
AU746555B2 (en)	1998-10-30	2002-05-02	Kabushiki Kaisha Toshiba	Apparatus for controlling synchronous motor
DE19933670A1 (de) *	1999-07-17	2001-01-18	Beiersdorf Ag	Verwendung von kosmetischen oder dermatologischen Zubereitungen zur Stabilisierung von Ascorbinsäure und/oder Ascorbylverbindungen
DE10031324A1 (de) *	2000-07-03	2002-01-17	Henkel Kgaa	Stabilisiertes kosmetisches Mittel
JP4091746B2 (ja) *	2001-02-06	2008-05-28	日清オイリオグループ株式会社	紫外線吸収物質の安定性向上のための使用、紫外線吸収剤及び化粧料

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DK136039B (da) *	1970-09-08	1977-08-01	Kongo Yakuhin Kabushiki Kaisha	Fremgangsmåde og middel til at forhindre oxydation af lipider og/eller farvestoffer, som indgår eller skal indgå i næringsmidler.
FR2244468A1 (en) *	1973-07-31	1975-04-18	Passwater Richard	Anticarcinogenic food supplements - contg antioxidants and S-contg amino acids
DE3522572C2 (de) *	1984-03-07	1997-07-03	Roshdy Ismail	Verwendung von Vitamin E zum Schutz der Haut
US4711894A (en) *	1986-01-16	1987-12-08	Henkel Corporation	Stabilized tocopherol in dry, particulate, free-flowing form
FR2610626B1 (fr) *	1987-02-09	1989-05-19	Oreal	Nouveau systeme anti-oxydant a base d'un ester d'ascorbyle stabilise, contenant en association au moins un agent complexant et au moins un thiol, et compositions contenant un tel systeme anti-oxydant

1988
- 1988-06-18 DE DE3820693A patent/DE3820693A1/de not_active Withdrawn
1989
- 1989-06-09 AU AU37607/89A patent/AU3760789A/en not_active Abandoned
- 1989-06-09 EP EP89110452A patent/EP0347664A1/fr not_active Ceased
- 1989-06-09 JP JP1506438A patent/JPH03505089A/ja active Pending
- 1989-06-09 EP EP89906773A patent/EP0444033A1/fr active Pending
- 1989-06-09 WO PCT/EP1989/000648 patent/WO1989012437A1/fr not_active Ceased
- 1989-06-09 KR KR1019900700071A patent/KR900701249A/ko not_active Withdrawn
- 1989-06-16 DD DD89329699A patent/DD283930A5/de not_active IP Right Cessation
1990
- 1990-12-13 DK DK296690A patent/DK296690D0/da not_active Application Discontinuation

Also Published As

Publication number	Publication date
DK296690A (da)	1990-12-13
KR900701249A (ko)	1990-12-01
EP0444033A1 (fr)	1991-09-04
DE3820693A1 (de)	1989-12-21
DK296690D0 (da)	1990-12-13
EP0347664A1 (fr)	1989-12-27
JPH03505089A (ja)	1991-11-07
AU3760789A (en)	1990-01-12
WO1989012437A1 (fr)	1989-12-28

Legal Events

Date	Code	Title	Description
1995-02-02	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
DE69201510T2 (de)	1995-07-13	Verwendung von Lysin und/oder Arginin Pyrrolidone-Carboxylate als Antioxidationsmittel in Kosmetika oder Pharmazeutika.
DE69325896T2 (de)	1999-12-02	Ungesättigte Fettsäure-Triglyceride enthaltende Lipidzusammensetzung für Kosmetik
DE19603018C2 (de)	1998-02-26	Kosmetisches Selbstbräunungsmittel mit Lichtschutzwirkung
EP0343694B1 (fr)	1992-11-25	Agent pour le traitement et la protection de la peau
DE69100848T2 (de)	1994-05-11	Hautpflegezusammensetzungen.
DE69201216T2 (de)	1995-05-18	Öllösliche Antioxydationsmischung.
DE69130020T2 (de)	1999-03-04	Stabilisierte, retinoide enthaltende hautpflegepräparate
DE3102181C2 (de)	1986-05-22	Oxidationsbeständige Lösung mindestens einer essentiellen Fettsäure und eines pflanzlichen Öls sowie sie enthaltende kosmetische Zubereitungen
DD283930A5 (de)	1990-10-31	Verfahren zur herstellung topischer kosmetischer und pharmazeutischer zubereitung mit einem gehalt an fettstoffen und freien tocopherolen
DE69933518T2 (de)	2007-08-23	Stabile flüssige zusammensetzungen von kalzium-ascorbat und verfahren zu ihrer herstellung und verwendung
DE69720737T3 (de)	2007-06-14	Pflanzliche ölzusammensetzungen
DE69800170T2 (de)	2000-09-28	System bestehend aus Phosphonsäurederivate und Metabisulfit zur Stabilisierung von Ascorbinsäure
EP3024433A1 (fr)	2016-06-01	Compositions de protection solaire transparentes et leur utilisation
DE69123363T2 (de)	1997-04-24	Neue zusammensetzungen
DE60003434T2 (de)	2004-05-06	Zerstäuber zur topischen anwendung einer zubereitung, die vitamin e und essentielle fettsäuren enthält
DE2734823C2 (de)	1986-03-13	Sonnenschutzmittel
EP0804150B1 (fr)	2003-04-23	Lotions contenant des derives d'acide gras
EP0911016B1 (fr)	2003-04-09	Utilisation d'esters d'ascorbyl de l'acide phosphorique pour stabiliser le vitamine a et/ou les derivatives de vitamine a dans des compositions cosmetique et pharmaceutique
EP0579079B1 (fr)	1997-01-22	Composition cosmétique pour le traitement du photo-vieillissement de la peau
DE69114796T2 (de)	1996-07-04	Antioxydantsystem auf Basis einer basischen Aminosäure und eines Tocopherols.
EP2082725B1 (fr)	2016-10-12	Ensemble cosmétique de protection solaire et procédé cosmétique destiné au traitement de la peau sensible
DE60106014T2 (de)	2005-10-06	Verwendung von n,n'-dibenzylethylendiamindiessigsäurederivaten zum schutz gegen verschmutzung
DE19645920A1 (de)	1998-05-14	Stabile Formulierung eines Insekt-Repellents
DE10013167A1 (de)	2001-09-20	Verwndung eines Schutzsystems zur Stabilisierung von Ascorbinsäure in kosmetischen und pharmazeutischen Zubereitungen
DE10355711A1 (de)	2005-06-16	Kosmetische und dermatologische Emulsionen, enthaltend Kreatin und/oder Kreatinin und Elektrolytkonzentrationen, einer Ionenstärke von mindestens 50 mmol/l