DE2932923C2 - Cosmetic preparation for topical use to protect the skin against sunburn and to accelerate tanning - Google Patents

Cosmetic preparation for topical use to protect the skin against sunburn and to accelerate tanning

Info

Publication number
DE2932923C2
DE2932923C2 DE19792932923 DE2932923A DE2932923C2 DE 2932923 C2 DE2932923 C2 DE 2932923C2 DE 19792932923 DE19792932923 DE 19792932923 DE 2932923 A DE2932923 A DE 2932923A DE 2932923 C2 DE2932923 C2 DE 2932923C2
Authority
DE
Germany
Prior art keywords
phase
urocanate
arglnln
protect
topical use
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.)
Expired
Application number
DE19792932923
Other languages
German (de)
Other versions
DE2932923A1 (en
Inventor
Jack J. East Hills N.Y. Mausner
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.)
Parbel of Florida Inc
Original Assignee
Parbel of Florida Inc
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 Parbel of Florida Inc filed Critical Parbel of Florida Inc
Priority to DE19792932923 priority Critical patent/DE2932923C2/en
Publication of DE2932923A1 publication Critical patent/DE2932923A1/en
Application granted granted Critical
Publication of DE2932923C2 publication Critical patent/DE2932923C2/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/04Preparations for care of the skin for chemically tanning the skin
    • 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
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier 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
    • A61Q17/04Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations

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)
  • Dermatology (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Description

65 Gluttuhion
Glycin
65 Gluttuhion
Glycine

0,021 bis 0,033%
Rest
0.021 to 0.033%
rest

100%100%

Beide Komponenten ergeben zusammen 100,0%.Both components add up to 100.0%.

Ein besonders bevorzugtes Mittel der Erfindung, das Jn den folgenden Beispielen für kosmetische Produkte verwendet wird, hat folgende Zusammensetzung:A particularly preferred agent of the invention, which is shown in the following examples of cosmetic products is used, has the following composition:

Tyrosin-Arglnln-Urocanat und Hlstldln-Arglnln-Urocanat zusammen 13,6% mit einer Analyse der vorstehenden Verbindungen:Tyrosine Arglnln Urocanate and Hlstldln Arglnln Urocanate together 13.6% with an analysis of the above compounds:

2020th

Der wichtigste Selbstschutzmechanismus der Haut gegen Sonnenlicht ist die Melanogenesis, d. h. die Bildung des Lichtschutzpigments Melanin In den MeIanocyten (spezifische Zellen) aus farblosen Vorläuferverblndungen, den Prämelamlnen. Bei Sonnenlichteinstrahlung findet eine unmittelbare Pigmentierung oder ein direkter Bräunungseffekt durch Oxidation der In der Epidermis vorhandenen Prämelamlne statt. Diese leichte und begrenzte Farbgebung wird »Bräunung« genannt; sie verschwindet schnell, und es folgt eine verzögerte oder indirekte Pigmentierung oder Melanogenesis, welche durch Oxidation weiterer Prämelamine ■verursacht wird, die nach der Sonneneinstrahlung gebildet werden. Diese Pigmentierung beginnt 24 bis 72 'Stunden nach der Bestrahlung. Leider 1st die In normaler Haut vorhandene Prämelaminmenge sehr begrenzt, und nach längerer Sonneneinwirkung kann ein Verbrennen und/oder eine andere Hautschädigung auftreten, bevor die Haut weiteres Prämelamln bilden kann, Insbesondere bei älterer Haut, die viel weniger Prämelamln als jüngere Haut enthält.The main self-protection mechanism of the skin against sunlight is melanogenesis, i. H. the Formation of the light protection pigment melanin in the melanocytes (specific cells) from colorless precursors, the premelamins. When exposed to sunlight finds an immediate pigmentation or a direct tanning effect through oxidation of the in the Epidermis existing premelamlne instead. This light and limited color scheme is called "tanning" called; it disappears quickly, followed by delayed or indirect pigmentation or melanogenesis, which is caused by the oxidation of other premelamines ■ formed after exposure to the sun will. This pigmentation begins 24 to 72 hours after exposure. Unfortunately the In is normal The amount of premelamine present in the skin is very limited, and after prolonged exposure to the sun it may burn and / or other skin damage occurs before the skin can form further premelamins, in particular with older skin, the much less premelamlin than younger skin contains.

Der Erfindung Hegt die Aufgabe zugrunde, ein Mittel bereitzustellen, das beim Auftragen auf die Haut als Prämelamln wirkt und die Haut zu einer schnelleren und stärkeren Melamlnbildung anregt.The invention is based on the object of a means provide that when applied to the skin as Prämelamln works and stimulates the skin to a faster and stronger melamine formation.

Die Erfindung schlägt hierzu das in Anspruch 1 •bezeichnete kosmetische Mittel zum Beschleunigen des Bräunens und zur Erhöhung des Schutzes der Haut vor, das einen Prämelaminkomplex aus Tyrosln-ArgininiUrocanat, Hlstidln-Arglnln-Urocanat und GlyclnjGlutathlon enthält.For this purpose, the invention proposes the cosmetic means for accelerating the Tanning and to increase the protection of the skin, which contains a premelamine complex of tyrosine arginine urocanate, Hlstidln-Arglnln-Urocanat and GlyclnjGlutathlon contains.

Eine bevorzugte Zusammensetzung dieses Mittels enthält Tyrosin-Arglnin-Urocanat und Hlstidln-Arglnln-Urocanat In einer Menge von zusammen 10 bis 17% und 90 bis 83% Glycin-Glutathlon.A preferred composition of this agent contains tyrosine arglnin urocanate and halide arglnin urocanate In a total amount of 10 to 17% and 90 to 83% glycine glutathlon.

Die Analyse der vorstehenden Verbindungen zeigtAnalysis of the above compounds shows

TyrosinTyrosine 29,4%29.4% ArgininArginine 33,2%33.2% HistidinHistidine 0,7%0.7% UrocansäureUrocanic acid 36,7%36.7%

100,0%100.0%

und Glycin-Glutathlon 86,4% mit einer Analyse der ,vorstehenden Verbindung;and Glycine Glutathlon 86.4% with an analysis of the above compound;

Glutathlon
Glycin
Glutathlon
Glycine

0,027%
Rest
0.027%
rest

100,0%100.0%

Beide Komponenten ergeben zusammen 100,0%.Both components add up to 100.0%.

Es wird angenommen, daß das Mittel der Erfindung nach den beiden folgenden Mechanismen wirkt:It is believed that the agent of the invention acts by the following two mechanisms:

1. Es verstärkt die Konzentration von Prämelanogerien in der Epidermis vor der ersten Bestrahlung.1. It increases the concentration of premelanogeries in the epidermis before the first irradiation.

2. Es fördert den Durchgang von UV-A (315 bis 390 nm), welches ein Bräunen Induziert, während das melanolytische UV-B (280 bis 315 nm) abgeschirmt wird. Das Urocanat von Arginin und Tyrosin wirkt als Filter, welches ermöglicht, daß UV-A mit 315 bis 390 nm wie auch sichtbares Licht durchgehen. Dieses jiiatürilche Filter stoppt außerdem UV-B mit 280 bis 315 nm, dessen plgmentolytlscher Effekt von unmittelbarer Bräunung nachgewiesen worden 1st, und schränkt außerdem den erythematogenen Effekt von UV-B ein.2. It promotes the passage of UV-A (315 to 390 nm) which induces tanning while the melanolytic UV-B (280 to 315 nm) is shielded. The urocanate of arginine and tyrosine acts as a Filter that allows UV-A at 315 to 390 nm to pass through as well as visible light. This jiiaturilche filter also stops UV-B with 280 bis 315 nm, the plaginalolytic effect of which has been demonstrated by immediate tanning, and limits also the erythematogenic effect of UV-B.

Verwendungsbeispiele:Usage examples:

Der Prämelaminkomplex kann in zahlreichen Hautbehandlungsprodukten und kosmetischen Mitteln verwendet werden, wie z. B. In Gesichts- und Körperlotionen, emulsionen und -cromes, Grundpflegemitteln und Schminken vom Flüsslgkelts-, Emulsions- und Cremetyp sowie auch vom Geltyp, zahlreichen Augenschmlnk- und Geslchtsschmlnkträgerstoffen, wie z.B. cremeartigen und flüssigen Augenschatten und Augen-Itlften, flüssigen und cremeartigen Wimpern- bzw. Brauentuschen, »Eyeliners«, Augencremes, Lippenstiften und Lippenpomaden, flüssigen und cremeartigen Bein- und Körperschminken, wie z. B. Beingrundpflegemitteln, Haarprodukten, wie z. B. Shampoos, Haartonika und -konditloniermltteln.The premelamine complex can be found in numerous skin treatment products and cosmetic agents can be used, such as. B. In face and body lotions, emulsions and creams, basic care products and make-up from liquid, emulsion and Cream type as well as gel type, numerous eye and face care substances, such as e.g. creamy and liquid shadows under the eyes and eyes, liquid and creamy eyelash and brow inks, "eyeliners", eye creams, lipsticks and lip balm, liquid and creamy leg and body make-up, such as. B. Basic leg care products, Hair products such as B. Shampoos, hair tonics and conditioning agents.

Das einzige Grunderfordernis ist, daß der Prämelanlnkomplex einer herkömmlichen kosmetischen Creme, Lotion oder Emulsion, einem Stift, Pulver (lose oder verpreßt) oder einem anderen herkömmlichen Trägerstoff in Konzentrationen zwischen 1 und 10% (vorzugsweise 3 bis 5%) zugesetzt wird, wobei keineThe only basic requirement is that the premelan complex of a conventional cosmetic Cream, lotion or emulsion, stick, powder (loose or compressed) or any other conventional one Carrier in concentrations between 1 and 10% (preferably 3 to 5%) is added, with none

besonderen Vorsichtsmaßnahmen erforderlich sind.special precautionary measures are required.

Spezielle Beispiele für kosmetische Produkte der Erfindung werden unten angegeben. In jedem Fall kann das Produkt gewünschtenfalls außerdem 0 bis 10% von herkömmlichen UV-Licht abschirmenden Mittein enthalten, wie z. B. Derivate von p-Aminobenzoesäure (z. B. 2-ÄthyIhexyl-p-«2imethyIamlnobenzoat), Zimtsaure (z. B. 2-Äthoxyäthyl-p-methoxyclnnamat), Salicylsäure (z. B. Homomenthylsallcylat oder 2-ÄtbylhexyIsalicylat) oder Benzophenon (z. B. 2,4-Dlhydroxybenzophenon, 2-Hydroxy-4-methoxybenzophenon oder 2,2'-Dlhydroxy-4,4'-dImethoxybenzophenon). Be; jedem der nachfolgenden Mittel kann die Menge des Prämelamins gewünschtenfalls Innerhalb des Bereichs von 1 bis 5% variiert werden, wobei die zugegebene Menge an entlonlslertem Wasser entsprechend eingestellt wird.Specific examples of cosmetic products of the invention are given below. In any event, if desired, the product may also contain 0 to 10% of conventional UV light shielding agents, such as e.g. B. Derivatives of p-aminobenzoic acid (e.g. 2-EthyIhexyl-p- «2-methylamylnobenzoate), cinnamic acid (e.g. 2-Ethoxyethyl-p-methoxylnnamate), salicylic acid (e.g. Homomenthylsallcylate or 2-EthylhexyIsalicylate) or Benzophenone (e.g., 2,4-dihydroxybenzophenone, 2-hydroxy-4-methoxybenzophenone, or 2,2'-dihydroxy-4,4'-dimethoxybenzophenone). Be; For each of the following means, the amount of premelamine can, if desired , be varied within the range from 1 to 5% , the added amount of deionized water being adjusted accordingly.

Die folgenden Mittel werden nach bekanntenThe following remedies are known according to

herkömmlichen Verfahren hergestellt. Die Phasen A und B werden gesondert erwärmt, und die heißen Phasen,,werden vermischt, abgekühlt und mieden rest-conventional process. Phases A and B are heated separately and they are hot Phases ,, are mixed, cooled and avoided

- liehen Phasen versetzt. '- borrowed phases staggered. '

Cremecream

■· Gew.-°/o■ ·% by weight

Fortsetzungcontinuation

Phase A Kohlenwasserstoffwachs
Karnaubawachs
Cholesterin
Bienenwachs
Lanolin
Phase A hydrocarbon wax
Carnauba wax
cholesterol
Beeswax
lanolin

Isopropylfettsäureester
Perhydrosqualen
Sorbitanfettsäureester
Mineralöl
Isopropyl fatty acid ester
Perhydrosqualene
Sorbitan fatty acid ester
mineral oil

. Phase B Methyiparaben. Phase B methyl paraben

hydrolysiertes Tierprotein
Prämelanin
entionisiertes Wasser
hydrolyzed animal protein
Premelanin
deionized water

Phase C ParfümPhase C perfume

Emulsionemulsion

' »Eyeliner«'»Eyeliner«

3,8503,850

2,2912.291

0,4680.468

6,360 12,220 16,0006,360 12,220 16,000

5,0005,000

2,884 10,0242,884 10,024

0,400 • 8,0000.400 • 8.000

3,000 29,3473,000 29,347

0,1560.156

100,000100,000

5050

Gew.-%Wt%

5555

Phase A Siliconöl 2,00Phase A silicone oil 2.00

Fettaikohoi 0,50Fettaikohoi 0.50

Polyoxyäthylenfettsäureester 1,25Polyoxyethylene fatty acid ester 1.25

Sorbitanfettsäurfcester 0,30Sorbitan fatty acid ester 0.30

Isopropylfettsäureester 5,00Isopropyl fatty acid ester 5.00

Mineralöl 3,00Mineral oil 3.00

Siliconwachs 2,00Silicone wax 2.00

höherer Alkylfettsäureester 7,50higher alkyl fatty acid ester 7.50

2-Äthylhexyl-p-dimetbylamino- 0,75 benzoat2-ethylhexyl-p-dimethylamino-0.75 benzoate

Lippenstiftlipstick

60 Phase A Karnaubawachs
Candelillawachs
Pflanzenfett
Lanolinalkohole
60 Phase A carnauba wax
Candelilla wax
Vegetable fat
Lanolin alcohols

65 KohJenwasserstoffwachs 65 hydrocarbon wax

Fettalkohol
Lanolinöl
Fatty alcohol
Lanolin oil

Gew.-%Wt%

Phase BPhase B enttonisiertes Wasserde-toned water 56,0156.01 Propylenglyko!Propylene glycol! 5,005.00 PrärnelaninPrärnelanin 3,003.00 MilchproteinMilk protein 2,002.00 MethylparabenMethyl paraben 0,400.40 AlkanoiaminAlkanoiamine 0,250.25 CellulosederivatCellulose derivative 0,500.50 Phase CPhase C. ParfümPerfume 0,300.30 Phase DPhase D. CarboxyvinylpolymerisatCarboxy vinyl polymer 10,0010.00 Phase EPhase E. Roter FarbstoffRed dye 0,240.24 (0,05 %ige wäßrige Lösung)(0.05% aqueous solution)

100,00100.00

Gew,"%Weight "%

Phase APhase a entionisiertes Wasserdeionized water 60,9560.95 Magnesiumaluminiumsililiaf!Magnesium Aluminum Sililiaf! 0,600.60 MethylparabenMethyl paraben 0,400.40 hydrolisiertes Tierproteinhydrolyzed animal protein 0,100.10 PrämelaninPremelanin 3,003.00 Phase BPhase B Tonvolume 0,700.70 Phase CPhase C. Pigmente '''*''■ Pigments ''' * '' ■ 6,006.00 Phase DPhase D. PropylenglykolPropylene glycol 4,504.50 CellulosederivatCellulose derivative 1,001.00 Phase EPhase E. PigmentePigments 8,008.00 Phase p Phase p AlkanoiaminAlkanoiamine 0,550.55 Phase GPhase G KarnaubawachsCarnauba wax 2,002.00 GlycerylfetisäureesterGlyceryl fatty acid ester 1,501.50 Fettsäurefatty acid 1,801.80 FettalkoholFatty alcohol 0,300.30 IsopropyllanolinfettsäureesterIsopropyl ethanolin fatty acid ester 0,400.40 Mineralölmineral oil 7,107.10 SorbitanfettsäureesterSorbitan fatty acid ester 1,101.10 100,00100.00

Gew.-%Wt%

3,60 4,30 8,20 7,00 7,50 6,00 21,003.60 4.30 8.20 7.00 7.50 6.00 21.00

Fortsetzungcontinuation

Lanolin
Mineralöl
lanolin
mineral oil

Konservierungsmittel PrämelaninPreservative premelanin

Phase B Tongel
Phase C Pigmente Phase D Parfüm
Phase B clay gel
Phase C Pigments Phase D Perfume

Gew,-%Weight%

IOIO

1515th

Flüssige SchminkeLiquid make-up

Phase A Bienenwachs '\ '■' RizinusölPhase A beeswax '\' ■ ' castor oil

!Phase B Mineralspiritus Phase C entionisiertes Wasser! Phase B mineral spirit Phase C deionized water

PrämelaninPremelanin

NatriumboratSodium borate

Konservierungsmittel Phase D PigmentePreservative phase D pigments

Phenylquecksilberacetat Phase E entionisiertes WasserPhenyl mercury acetate phase E deionized water

hydrolisiertes Proteinhydrolyzed protein

Gew.-°/o% By weight

2525th

: 'f Phase A *'entionisiertes Wasser 57,365 ^Cellulosederivat 0,100 : 'f Phase A *' deionized water 57.365 ^ cellulose derivative 0.100

Tropylenglykol 3,000Tropylene glycol 3,000

Methylparaben 0,400Methyl paraben 0.400

Alkanolamin 1,000Alkanolamine 1,000

Borax 1,000Borax 1,000

Magnesiumaluminiumsilikat 0,250 30 Magnesium aluminum silicate 0.250 30

Lecithin 0,500Lecithin 0.500

Dioctylnatriumsulfosuccinat 0,050Dioctyl sodium sulfosuccinate 0.050

Pulvergemisch 13,000 Prämelanin 3,000 35Powder mix 13,000 premelanin 3,000 35

Phase B Fettsäure 2,600Phase B fatty acid 2,600

flüssiger Absorptionsgrundstoff 8,000 Glycerylfettsäureester 3,000 ,liquid absorption base 8,000 glyceryl fatty acid ester 3,000,

f 40f 40

Propylparaben 0,050Propyl paraben 0.050

Pflanzenöl 3,250Vegetable oil 3,250

• Mineralöl 3,250• mineral oil 3,250

Phase C Parfümölgrundstoff 0,185 45Phase C perfume oil base 0.185 45

100,000100,000

Wimpern- oder BraueniuschöEyelashes or browbones

Gew.-% 50 Wt% 50

26,84 0,52 52,94526.84 0.52 52.945

6,94 3,00 0,65 0,406.94 3.00 0.65 0.40

7,50 0,0057.50 0.005

1,001.00

0,200.20

100,00100.00

6565

Claims (3)

Patentansprüche:Patent claims: 1. Kosmetisches Mittel zur örtlichen Anwendung zum Schützen der Fjut gegen Sonnenbrand und zum Beschleunigen des Bräunens, dadurch gekennzeichnet, daß es einen Prämelaninkomplex aus Tyrosln-Arglnln-Urocanat, Hlstldln-Arglnln-Urocanat und Glycln-GIutathlon enthält.1. Cosmetic for topical use to protect the fjut against sunburn and to accelerate tanning, characterized in that it is a premelanin complex from tyrosin-arglnln urocanate, hlstldln-arglnln urocanate and Glycln-Glutathlon. 2. Mittel nach Anspruch 1, dadurch gekennzelchnet, daß es zusammen von 10 bis 17% Tyrosln-Arglnln-Urocanat und Histldln-Arglnln-Urocanat und 90 bis 83% Glycln-Glutathion enthält2. Means according to claim 1, characterized in that that there is a total of 10 to 17% tyrosin-arglnln urocanate and histldln-arglnln urocanate and 90 contains up to 83% glycine glutathione 3. Mittel nach Anspruch 2, dadurch gekennzeichnet, daß es Tyrosln-Arglnln-Urocanat/Hlstldln-Arglnln-Urocanat zusammen 13,6% und 86,4% Glycln-Glutathlon enthält.3. Composition according to claim 2, characterized in that it is tyrosin-arglnln urocanate / Hlstldln-arglnln urocanate together contains 13.6% and 86.4% Glycln-Glutathlon. Die Analyse des Glycln-Glutathlons «Igt an:The analysis of the Glycln-Glutathlon «Igt an: TyrosinTyrosine 2424 bis 35%up to 35% ArgininArginine 2727 bis 40%up to 40% HistidinHistidine 0,50.5 bis 0,9%up to 0.9% UrocansäureUrocanic acid 3030th bis 43%up to 43%
100%100% 6060
DE19792932923 1979-08-10 1979-08-10 Cosmetic preparation for topical use to protect the skin against sunburn and to accelerate tanning Expired DE2932923C2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DE19792932923 DE2932923C2 (en) 1979-08-10 1979-08-10 Cosmetic preparation for topical use to protect the skin against sunburn and to accelerate tanning

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19792932923 DE2932923C2 (en) 1979-08-10 1979-08-10 Cosmetic preparation for topical use to protect the skin against sunburn and to accelerate tanning

Publications (2)

Publication Number Publication Date
DE2932923A1 DE2932923A1 (en) 1981-02-19
DE2932923C2 true DE2932923C2 (en) 1984-08-30

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Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4453941A (en) * 1980-12-29 1984-06-12 Board Of Overseers Of Goshen College Composition and process for producing pigmentation in hair or skin
DE3435842A1 (en) * 1984-09-29 1986-04-10 Wella Ag Use of N- alpha -acetyllysinamide in skin treatment compositions for increased bronzing of the skin
FR2579461B1 (en) * 1985-03-28 1988-08-26 Strasbourg Universite L Pasteu AMIDES OF PARA-METHOXYCINNAMIC ACID AND UROCANIC ACID FOR USE AS SOLAR FILTERS; PROCESSES FOR OBTAINING, DERMO-PHARMACEUTICAL AND COSMETIC COMPOSITIONS CONTAINING THEM AND APPLICATIONS
FR2594332B1 (en) * 1986-02-14 1988-12-16 Jung Louis DERIVATIVES OF AMINO-BENZOIC ACIDS, HYDROXY-BENZOIC ACIDS, CINNAMIC ACIDS, UROCANIC ACID AND BENZIMIDAZOLE WITH OR WITHOUT A GROUP OF AMINO ACID ABSORBING UVB AND / OR UVA AND FOR AVOIDING PHOTODERMATOSES, IN MAN, CONSECUTIVE TO THE ADMINISTRATION OF MEDICINES, TO THE USE OF COSMETIC PERFUMES OR PERFUMES
JP2565513B2 (en) * 1987-09-25 1996-12-18 三省製薬株式会社 Topical drug for suppressing melanin production
US5290562A (en) * 1987-11-27 1994-03-01 L V M H Recherche Compositions and methods employing liposomes including tyrosine or a tyrosine derivative
AU2971689A (en) * 1988-02-11 1989-08-17 Estee Lauder Inc. Tanning compositions and their use
JP3091270B2 (en) * 1990-09-28 2000-09-25 協和醗酵工業株式会社 Whitening cosmetics
DE4307983A1 (en) * 1993-03-13 1994-09-15 Beiersdorf Ag Active ingredients and cosmetic and dermatological preparations
DE19713776A1 (en) * 1997-04-03 1998-10-08 Beiersdorf Ag Light protection preparations with a content of basic amino acids and water-soluble UV filter substances
DE19757826A1 (en) * 1997-12-24 1999-07-01 Beiersdorf Ag Use of chaotropic compounds for protection of skin against UV radiation e.g. during exposure to sunlight, phototherapy and photo-chemotherapy
DE19958121A1 (en) * 1999-12-02 2001-06-28 Max Planck Gesellschaft Tyrosine and tryptophan-containing peptides as antioxidants

Non-Patent Citations (1)

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Title
NICHTS-ERMITTELT

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Publication number Publication date
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