DE1492322A1 - Use of UV-absorbing substances as additives for cosmetics - Google Patents

Use of UV-absorbing substances as additives for cosmetics

Info

Publication number
DE1492322A1
DE1492322A1 DE19641492322 DE1492322A DE1492322A1 DE 1492322 A1 DE1492322 A1 DE 1492322A1 DE 19641492322 DE19641492322 DE 19641492322 DE 1492322 A DE1492322 A DE 1492322A DE 1492322 A1 DE1492322 A1 DE 1492322A1
Authority
DE
Germany
Prior art keywords
cosmetics
substances
additives
skin
absorbing substances
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.)
Pending
Application number
DE19641492322
Other languages
German (de)
Inventor
Auf Nichtnennung Antrag
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.)
DOMEKOS DR H DOERING GmbH
Original Assignee
DOMEKOS DR H DOERING GmbH
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 DOMEKOS DR H DOERING GmbH filed Critical DOMEKOS DR H DOERING GmbH
Publication of DE1492322A1 publication Critical patent/DE1492322A1/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • 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
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • A61K8/445Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof aromatic, i.e. the carboxylic acid directly linked to the aromatic ring
    • 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
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4973Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
    • A61K8/498Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom having 6-membered rings or their condensed derivatives, e.g. coumarin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/42Colour properties
    • A61K2800/43Pigments; Dyes
    • A61K2800/434Luminescent, Fluorescent; Optical brighteners; Photosensitizers

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)
  • Cosmetics (AREA)

Description

Der überwiegende Teil der unerwünschten Hautrealctionen auf Kosmetika und ähnliche Präparate beruht auf einer individuellen (Jberempfindlichkeit (Allergie). Daneben sind jedoch auch Hautreaktionen bekannt, die dann auftreten können, wenn in den Präparaten Substanzen mit Lichtabsorptionsrr.axima oberhalb 300 nm enthalten sind und das Präparat in aufgetragenem Zustand auf der Haut der Einwirkung von Sonnenstrahlen oder ähnlichen Lichtquellen ausgesetzt ist. Unter diesen Voraussetzungen kann es auf dem V/ege einer Photosensibillsierung (photodynamische Reaktion) zu Ilautreaktionen kommen, die sich als akute Entzündung und/oder Überpigrnentie- rung zu erkennen geben. Derartige Hautreaktionen sind bei- The predominant part of the undesirable skin reactions to cosmetics and similar preparations is based on an individual (hypersensitivity (allergy). In addition, however, skin reactions are known which can occur if the preparations contain substances with light absorption maxima above 300 nm and the preparation is exposed to in-applied state on the skin exposure to sun rays or similar light sources. Under these conditions it may be on the V / ege a Photosensibillsierung (photodynamic reaction) occur Ilautreaktionen which tion as an acute inflammation and / or Überpigrnentie- make known Such skin reactions are both

909883/1571909883/1571

Neue Unterlagen (Art7{1Ab&2Nr.lSatz3desAnderun(mM.v.4.9.19iNew documents (Art7 {1Ab & 2Nr.lSatz3desAnderun (mM.v.4.9.19i

■ KfeiOMN . PMMmUmI* Mta*Mtm74■ KfeiOMN. PMMmUmI * Mta * Mtm74

cpielsv/eise unter der Bezeichnung M3erloque-Derrr.atitio" bekannt, können aber auch eine fleckige Verfärbung des Gesichtes (Chloasma) zur Folge haben.cpielsv / eise known as M 3erloque-Derrr.atitio ", but can also result in blotchy discoloration of the face (chloasma).

Obwohl diese Hautreaktionen relativ selten sind, lassen sie sich doch, cofern sie einmal aufgetreten sind, nur sehr schwierig wieder beseitigen, so daß nach Höflichkeiten gesucht v/erden muß, derartige Hautreaktionen ::u vermeiden.Although these skin reactions are relatively rare, once they have occurred they can be very difficult difficult to get rid of, so looked for courtesies must avoid such skin reactions.

2s wurde nun gefunden, daß durch Verwendung von Substanzen, die kurzwelliges Ultraviolett etwa in dem Bereich zwischen 300 und 450 nr. zu absorbieren vermögen, als Zusätze zu photosensibilisierende Bestandteile enthaltenden Kosmetika in Mengen von weniger als 10 c/?, bezogen auf die Kosmetika, unerwünschte Hautreaktionen vermieden v/erden können.2s it has now been found that by using substances which have short-wave ultraviolet in the range between 300 and 450 nr. able to absorb, as additives to cosmetics containing photosensitizing constituents in amounts of less than 10 c /?, based on the cosmetics, undesired skin reactions can be avoided.

Von photosensibilisierenden Substanzen, die in Kosmetika, wie beispielsweise Parfüms, Kölnisch V/ässer, Toilettewässer, Lippenstiften oder Hautpflegemitteln, enthalten sein können, seien Citrusöle, Azulene, Teere oder Sosine erwähnt.Of photosensitizing substances used in cosmetics, such as perfumes, cologne, toilet waters, Lipsticks or skin care products, citrus oils, azulenes, tars or sosines may be mentioned.

Ss sind bereits Kosmetika bekannt, denen Stoffe beigemischt sind, die das Eindringen bestimmter Lichtbereiche in die Haut einschränken bzw. ganz verhindern (DAS 1 021 541, DDR-Patentschrift 32 279, Karl Rothemann, Das große Rezeptbuch der Haut- und Körperpflegemittel, 1902, 3. 64^ sowie Sagarin, Cosmetics Science and Technology, 1957, S. 205).Ss cosmetics are already known to which substances are mixed that the penetration of certain areas of light into the Restrict skin or prevent it entirely (DAS 1 021 541, GDR patent specification 32 279, Karl Rothemann, Das Großes recipe book der skin and body care products, 1902, 3. 64 ^ as well as Sagarin, Cosmetics Science and Technology, 1957, p. 205).

909883/1571909883/1571

BAD ORIGINALBATH ORIGINAL

Bisher erfolgte der Zusatz üV-absorbierender J ifes tanzen :'.u Kosr.:etika nur deshalb, um entweder den Kosmetika eine gegen Jonr.enbrand schützende V/irkunß zu verleihen oder urr. eire Zersetzung von in ihnen enthaltenen Substanzen zu verhindern, ileiner der angegebenen Literaturstellcn ist der Hinweis darauf zu entnehmen, daß es möglich ist, durch Zvfatz uY-absorbierender Substanzen zu photosensibilisiererxle Bestandteile enthaltenden Kosmetika unerwünschte H onen zu vermeiden.So far, the addition of UV-absorbing J ifes has been added : '. u Kosr.:etika only to either the cosmetics a to give protective measures against fire or urr. prevent the decomposition of substances contained in them, one of the cited references is the Indication to infer that it is possible to photosensitizerxle by adding uY-absorbing substances Cosmetics containing ingredients to avoid undesirable honing.

Als errindungs£eraäß verwendbare Substanzen, die kurzv/ Ultraviolett zu absorbieren vermögen, kommen Verbindungen in Frage, die folgende Voraussetzungen erfüllen:Substances that can be used as rindings, which are briefly Able to absorb ultraviolet, compounds come in Question that meet the following requirements:

1. Sie müssen weitgehend lichtbeständig sein,1. They must be largely lightfast,

2. sie müssen eine gute Hautverträgliehkeit besitzen,2. they must be well tolerated by the skin,

3. sie sollen möglichst wenig in die Kaut eindringen,3. They should penetrate the chew as little as possible,

4. sie sollen zur Vermeidung unerwünschter Umsetzungen mit anderen Bestandteilen der Kosmetika chemisch ir.ö™-lichst indifferent sein, und4. They are intended to avoid undesired conversions chemically ir.ö ™ with other components of cosmetics be indifferent, and

5. sie müssen die Fähigkeit besitzen, Licht zu absorbieren, zu reflektieren oder zu zerstreuen, insbesondere in der. Bereich zwischen 300 und ^50 nm.5. they must have the ability to absorb light, to reflect or disperse, especially in the. Range between 300 and ^ 50 nm.

Aufgrund der vorstehend genannten Kriterien kommen Substanzen, die zum Schutz der menschlichen Haut vor Sonnenbrand verwendet werden (Sonnen- oder Lichtschutzmittel) sowie solche Substanzen oder Gemische in Betracht, die aufgrund ihrer BeschaffenheitOn the basis of the criteria mentioned above, substances are which are used to protect human skin from sunburn (sun or light protection agents) as well as substances or mixtures that are due to their nature

909883/1571909883/1571

in der Lage sind, Licht zu absorbieren, zu reflektieren oder zu streuen, beispielsweise Talkum, Dentonit, Zinkoxyd, Stärke, Titandioxyd oder dergleichen. Unter den löslichen, lichtabsorbierenden .Substanzen richtet sich die Auswahl in erster Linie nach den optischen Eigenschaften des photosensicilisierenden Kosmetikumbestandteils, da die beste Wirkung dann erzielt wird, wenn die lichtfilternde Substanz den gleichen oder einen wenig längerwelligen Lichtbereich maximal absorbiert, wie der Photosensibilisator.are able to absorb, reflect or light to sprinkle, for example talc, dentonite, zinc oxide, starch, titanium dioxide or the like. Among the soluble, light-absorbing The selection of substances depends primarily on the optical properties of the photosensicilizing agent Cosmetic ingredient, as the best effect then achieved becomes when the light-filtering substance is the same or one A little longer-wave light range is maximally absorbed, like the photosensitizer.

Beispielsweise wird die Photosensibilisierungsreaktion durch die Purocumarine.der Citrus- oder Angelikaöle (maximale Absorption zwischen 300 und 315 nm) am besten durch Substanzen verhindert, deren Absorptionsmaximum zwischen 3OO und 3^0 nm liegt. Entsprechend zeigen bei Teeren oder Azulenen Substanzen mit Absorptionsmaxima zwischen 350 und 450 nm die günstigste Wirkung.For example, the photosensitization reaction is caused by the purocoumarins of the citrus or angelica oils (maximum absorption between 300 and 315 nm) best by substances prevents their absorption maximum between 3OO and 3 ^ 0 nm lies. Correspondingly, in the case of tars or azulenes, substances with absorption maxima between 350 and 450 nm show the most favorable Effect.

Die folgenden Beispiele erläutern die Erfindung.The following examples illustrate the invention.

Beispiel 1example 1

2 g p-Aminobenzoesäure-monoglycerinester und 0,5 ^ p-Isopropylzimtsäure-isopropylester werden mit 30,0 g $2 g of p-aminobenzoic acid monoglycerol ester and 0.5 ^ p-isopropylcinnamic acid isopropyl ester are with 30.0 g $

CO ·· y.CO ·· y.

o Äthylalkohol gemischt und zu 67,5 G Citrusöl-haltigem o Ethyl alcohol mixed and added to 67.5 g of citrus oil

co Toilettenwasser gegeben.co given toilet water.

w w Beispiel 2Example 2

-» 5,0 ζ P-Methylenaminobenzoesäure-polyglykolester und 5,0 g Trimethoxy-dihydroxybenzophenon werden mit 990,0 g Kölnischwasser vermischt.- "5.0 ζ P Methylenaminobenzoesäure-polyglycol and 5.0 g of trimethoxy-dihydroxybenzophenone are mixed with 990.0 g colognes.

BAD ORDINALBAD ORDINAL Beispiel 3Example 3

Dei dor Herstellung der Kölnischwaooer-otifto werden in die warme Grundmasse 0,5 % Umbelliferonessissäure und 2 £ 3entonit eingearbeitet.During the production of the Kölnischwaooer otifto, 0.5 % umbelliferonessis acid and 2 £ 3entonite are incorporated into the warm base mass.

909883/1571909883/1571

Claims (1)

PatentanspruchClaim r.r:^ von oubatanzen, die kurzwellijec Ultraviolett, insbesondere den Bereich zwischen JOC und Ji5C nni, zu absorbieren vermögen, al3 Zucätze zu p'notoseiiöibilicierendo 3eotandteile enthaltenden Kosmetika in ϊ-'enfjen von v/enijer als 10 /I, bezogen auf die Kosmetika, zur Vermeidung unerwünschter Hautreaktionen.rr: ^ of substances that are able to absorb short-wave ultraviolet, especially the area between JOC and J i5C nni, al3 additives to cosmetics containing p'notoseiiöibilicierendo 3eotandteile in ϊ-'enfjen of v / enijer than 10 / I, based on the Cosmetics to avoid unwanted skin reactions. BAD ORIGINAL 909883/1571BATH ORIGINAL 909883/1571 Neue Unterlagen (Art 7 SI Abs. 2 Nr. 1 Sau 3 de· Xndwung^w. v. 4.9.19New documents (Art 7 SI Paragraph 2 No. 1 Sau 3 de Xndwung ^ w. V. 4.9.19
DE19641492322 1964-06-08 1964-06-08 Use of UV-absorbing substances as additives for cosmetics Pending DE1492322A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DED0044629 1964-06-08

Publications (1)

Publication Number Publication Date
DE1492322A1 true DE1492322A1 (en) 1970-01-15

Family

ID=7048445

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
DE (1) DE1492322A1 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4136165A (en) * 1976-04-23 1979-01-23 Henkel Kommanditgesellschaft Auf Aktien Cosmetic preparations with alkoxybenzoic acid esters as inflammation inhibitors and method
FR2409751A1 (en) * 1977-11-29 1979-06-22 Thorel Jean Noel Sun tan compsn. giving rapid bronzing - contg. 5-methoxy psoralen, lanolin, and UV filter cpd.
FR2539625A1 (en) * 1983-01-26 1984-07-27 Oreal ALCOHOLIC OR HYDRO-ALCOHOLIC COMPOSITIONS CONTAINING NATURAL SPECIES AND DERIVATIVES OF BENZYLIDENE CAMPHOR
FR2539623A1 (en) * 1983-01-26 1984-07-27 Oreal COSMETIC COMPOSITIONS CONTAINING NATURAL ESSENCES AND DERIVATIVES OF BENZYLIDENE CAMPHOR
EP0257928A2 (en) * 1986-08-22 1988-03-02 Kays Kaidbey Suntanning composition
EP0376821A1 (en) * 1988-12-30 1990-07-04 L'oreal Compositions for inducing and stimulating hair growth and/or stop their fall based on pyrimidine derivatives and UV filters
WO2001093823A1 (en) * 2000-06-02 2001-12-13 Quest International B.V. Improvements in or relating to perfumes

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4136165A (en) * 1976-04-23 1979-01-23 Henkel Kommanditgesellschaft Auf Aktien Cosmetic preparations with alkoxybenzoic acid esters as inflammation inhibitors and method
FR2409751A1 (en) * 1977-11-29 1979-06-22 Thorel Jean Noel Sun tan compsn. giving rapid bronzing - contg. 5-methoxy psoralen, lanolin, and UV filter cpd.
FR2539625A1 (en) * 1983-01-26 1984-07-27 Oreal ALCOHOLIC OR HYDRO-ALCOHOLIC COMPOSITIONS CONTAINING NATURAL SPECIES AND DERIVATIVES OF BENZYLIDENE CAMPHOR
FR2539623A1 (en) * 1983-01-26 1984-07-27 Oreal COSMETIC COMPOSITIONS CONTAINING NATURAL ESSENCES AND DERIVATIVES OF BENZYLIDENE CAMPHOR
US4731200A (en) * 1983-01-26 1988-03-15 L'oreal Alcoholic or aqueous-alcoholic compositions containing natural essences and benzylidene-camphor derivatives
US4950478A (en) * 1983-01-26 1990-08-21 L'oreal Cosmetic compositions containing natural essences and benzylidenecamphor derivatives
EP0257928A2 (en) * 1986-08-22 1988-03-02 Kays Kaidbey Suntanning composition
EP0257928A3 (en) * 1986-08-22 1988-05-18 Kays Kaidbey Suntanning composition
EP0376821A1 (en) * 1988-12-30 1990-07-04 L'oreal Compositions for inducing and stimulating hair growth and/or stop their fall based on pyrimidine derivatives and UV filters
FR2641184A1 (en) * 1988-12-30 1990-07-06 Oreal COMPOSITION FOR INDUCING AND STIMULATING HAIR GROWTH AND / OR BRAKING THEIR FALL BASED ON PYRIMIDINE DERIVATIVES AND SOLAR FILTERS
WO2001093823A1 (en) * 2000-06-02 2001-12-13 Quest International B.V. Improvements in or relating to perfumes
US7129204B2 (en) 2000-06-02 2006-10-31 Quest International Services B.V. Perfumes

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