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 tanningInfo
- 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
Links
Classifications
-
- 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
- A61Q19/04—Preparations for care of the skin for chemically tanning the skin
-
- 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
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
-
- 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
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%
Rest0.021 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
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
GlycinGlutathlon
Glycine
0,027%
Rest0.027%
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
LanolinPhase A hydrocarbon wax
Carnauba wax
cholesterol
Beeswax
lanolin
Isopropylfettsäureester
Perhydrosqualen
Sorbitanfettsäureester
MineralölIsopropyl fatty acid ester
Perhydrosqualene
Sorbitan fatty acid ester
mineral oil
. Phase B Methyiparaben. Phase B methyl paraben
hydrolysiertes Tierprotein
Prämelanin
entionisiertes Wasserhydrolyzed 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
Lanolinalkohole60 Phase A carnauba wax
Candelilla wax
Vegetable fat
Lanolin alcohols
65 KohJenwasserstoffwachs 65 hydrocarbon wax
Fettalkohol
LanolinölFatty alcohol
Lanolin oil
Gew.-%Wt%
100,00100.00
Gew,"%Weight "%
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
Mineralöllanolin
mineral oil
Konservierungsmittel PrämelaninPreservative premelanin
Phase B Tongel
Phase C Pigmente Phase D ParfümPhase 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)
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 |
Family
ID=6078450
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19792932923 Expired DE2932923C2 (en) | 1979-08-10 | 1979-08-10 | Cosmetic preparation for topical use to protect the skin against sunburn and to accelerate tanning |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE2932923C2 (en) |
Families Citing this family (12)
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 |
-
1979
- 1979-08-10 DE DE19792932923 patent/DE2932923C2/en not_active Expired
Non-Patent Citations (1)
Title |
---|
NICHTS-ERMITTELT |
Also Published As
Publication number | Publication date |
---|---|
DE2932923A1 (en) | 1981-02-19 |
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