NO329434B1 - Anvendelse av 6-(4-hydroksybenzylamino)purin til kosmetiske formal - Google Patents
Anvendelse av 6-(4-hydroksybenzylamino)purin til kosmetiske formal Download PDFInfo
- Publication number
- NO329434B1 NO329434B1 NO20040469A NO20040469A NO329434B1 NO 329434 B1 NO329434 B1 NO 329434B1 NO 20040469 A NO20040469 A NO 20040469A NO 20040469 A NO20040469 A NO 20040469A NO 329434 B1 NO329434 B1 NO 329434B1
- Authority
- NO
- Norway
- Prior art keywords
- acid
- oil
- purine
- cells
- hydroxybenzylamino
- Prior art date
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- FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
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- 235000005822 corn Nutrition 0.000 description 1
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- 210000004748 cultured cell Anatomy 0.000 description 1
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- UMNKXPULIDJLSU-UHFFFAOYSA-N dichlorofluoromethane Chemical compound FC(Cl)Cl UMNKXPULIDJLSU-UHFFFAOYSA-N 0.000 description 1
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- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
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- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
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- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 210000005260 human cell Anatomy 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 239000010512 hydrogenated peanut oil Substances 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 230000001506 immunosuppresive effect Effects 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 229960002900 methylcellulose Drugs 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000009456 molecular mechanism Effects 0.000 description 1
- FXGQGYBMZKLBKX-UHFFFAOYSA-N n-[(3-chlorophenyl)methyl]-7h-purin-6-amine Chemical compound ClC1=CC=CC(CNC=2C=3NC=NC=3N=CN=2)=C1 FXGQGYBMZKLBKX-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 239000000276 potassium ferrocyanide Substances 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 229940116317 potato starch Drugs 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000001944 prunus armeniaca kernel oil Substances 0.000 description 1
- 150000003212 purines Chemical class 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229940100486 rice starch Drugs 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 230000009758 senescence Effects 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 229940080236 sodium cetyl sulfate Drugs 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- GGHPAKFFUZUEKL-UHFFFAOYSA-M sodium;hexadecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCCCOS([O-])(=O)=O GGHPAKFFUZUEKL-UHFFFAOYSA-M 0.000 description 1
- NWZBFJYXRGSRGD-UHFFFAOYSA-M sodium;octadecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCCCCCOS([O-])(=O)=O NWZBFJYXRGSRGD-UHFFFAOYSA-M 0.000 description 1
- 229940057429 sorbitan isostearate Drugs 0.000 description 1
- 229950004959 sorbitan oleate Drugs 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- XOGGUFAVLNCTRS-UHFFFAOYSA-N tetrapotassium;iron(2+);hexacyanide Chemical compound [K+].[K+].[K+].[K+].[Fe+2].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] XOGGUFAVLNCTRS-UHFFFAOYSA-N 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229940100445 wheat starch Drugs 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
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- 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
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4953—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom containing pyrimidine ring derivatives, e.g. minoxidil
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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Landscapes
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- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
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- Animal Behavior & Ethology (AREA)
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- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Dermatology (AREA)
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- Agronomy & Crop Science (AREA)
- Physical Education & Sports Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Cardiology (AREA)
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Description
Teknisk område
Oppfinnelsen angår anvendelse av 6-(4-hydroksybenzylamino)purin til kosmetiske formål, og spesielt til inhibering av aldring og aldringstegn i epidermalceller hos pattedyr så som keratinocytter eller fibroblaster. Oppfinnelsen angår også et kosmetikum omfattende 6-(4-hydroksybenzylamino)purin eller farmasøytiske akseptable salter derav med en farmasøytisk bærer.
Bakqrunnsteknikk
Siden alle levende organismer på jorden har utviklet seg sammen over mange mil-lioner år, kan tilstedeværelsen av regulatoriske interaksjoner av planteforbindelser slik som cytokininer, bli antatt i dyr og mennesker. Cytokininavledede forbindelser påvirker sannsynligvis mange forskjellige molekylære mekanismer i animalske og humane celler. Søker har nylig oppdaget at nye generasjoner av antiinflammatoris-ke, antikreft, immunosuppressive, antivirale og andre medikamenter kan være basert på N<6->substituerte puriner og deres derivater.
Målet for foreliggende oppfinnelse er å fremskaffe antisenescente forbindelser som har forbedret selektivitets- og effektivitetsindeks, det vil si som er mindre toksiske og likevel mer effektive enn tidligere kjente analoger.
Beskrivelse av oppfinnelsen
Mål for foreliggende oppfinnelse er anvendelsen av 6-(4-hydroksybenzyl-amino)purin til kosmetiske formål samt kosmetika omfattende denne forbindelsen sammen med en farmasøytisk bærer.
De kosmetiske sammensetninger ifølge foreliggende oppfinnelse, fremstilles på en i og for seg kjent måte, for eksempel ved hjelp av konvensjonell blanding, granule-ring, belegging, oppløsning eller frysetørkingsprosesser.
Foretrukket blir oppløsninger av den aktive bestanddel, og i tillegg også suspensjoner eller dispersjoner, spesielt isotone, vandige oppløsninger, dispersjoner eller suspensjoner brukt, idet det er mulig for disse å bli fremstilt for bruk, for eksempel i tilfelle med frysetørkede sammensetninger som omfatter den aktive substans i seg selv eller sammen med et bæremateriale, for eksempel mannitol. De kosmetiske sammensetninger kan bli sterilisert og/eller omfatte eksipienter, for eksempel preservativer, stabilisatorer, fuktemidler og/eller emulgatorer, stabiliseringsmidler, og de fremstilles på i og for seg kjent måte, for eksempel ved hjelp av konvensjonell oppløsning eller frysetørkingsprosesser. Oppløsningene eller suspensjonene som er nevnt kan omfatte viskositetsøkende substanser, så som natrium, karboksymetyl-cellulose, dekstran, polyvinylpyrrolidon eller gelatin.
Suspensjoner i olje omfatter som oljekomponenten, vegetabilske, syntetiske eller semi-syntetiske oljer. Oljer som kan bli nevnt er spesielt flytende fettsyreestere som inneholder som syrekomponent, en langkjedet fettsyre som har 8-22, spesielt 12-22 karbonatomer, for eksempel laurinsyre, tridecylsyre, myristinsyre, pentade-cylinsyre, palmitinsyre, margarinsyre, stearinsyre, syre, arakidonsyre, beheninsyre eller tilsvarende umettede syrer, foreksempel oleinsyre, elaidinsyre, eurinsyre, brasidinsyre eller linoleinsyre, om passende med tilsetningen av antioksidanter, for eksempel vitamin E, p-karoten eller 3,5-di-tert-butyl-4-hydroksytoluen. Alkohol-komponenten av disse fettsyreestere har ikke mer enn 6 karbonatomer og er mono- eller polyhydrisk, for eksempel mono-, di- eller trihydrisk alkohol, for eksempel metanol, etanol, propanol, butanol eller pentanol, eller isomerer derav, men spesielt blykol og glycerol. Fettsyreestere er følgelig, for eksempel etyloleat, isopropylmyristat, isopropylpalmitat, "Labrafil M 2375" (polyoksyetylenglykol triol-etat fra Gattefoseé, Paris), "Labrafil M 1944 CS" (umettede polyglykolerte glycerider fremstilt ved en alkoholyse av aprikoskjerneolje og bestående av glycerider og polyetylenglykolestere fra Gattefoseé, Paris), "Labrasol" (mettede polyglykolerte glycerider fremstilt ved en alkoholyse av TCM og dannet av glycerider og polyetylenglykolestere, fra Gattefoseé, Paris) og/eller "Miglyol 812" (triglycerid av mettede fettsyrer av kjedelengde C8 til C12 fra Huls AG, Tyskland) og særskilt vegetabilske oljer, så som bomullsfrøolje, mandelolje, olivenolje, lakserolje, sesamolje, soya-bønneolje og spesielt jordnøttolje.
Passende bærematerialer er spesielt fyllmaterialer, så som sukkere, for eksempel laktose, sukrose, mannitol eller sorbitol, cellulosepreparater og/eller kalsiumfosfa-ter, for eksempel trikalsiumdifosfat, eller kalsium hyd rogenfosfat og ytterligere bin-demidler, så som stivelser, for eksempel mais, hvete, ris eller potetstivelse, metyl-cellulose, hydroksypropylmetylcellulose, natrium ka rboksymetylcel lu lose og/eller polyvinylpyrrolidon og/eller, om ønsket, desintegratorer, så som de ovennevnte stivelser og videre, karboksymetylstivelse, fornettet polyvinylpyrrolidon, algininsyre eller et salt derav, så som natriumalginat. Ytterligere eksipienter er spesielt strøm-ningsregulatorer og smøremidler, for eksempel salisylsyre, stivelse, stearinsyre eller salter derav, så som magnesiumstearat eller kalsiumstearat, og/eller polyetylenglykol eller derivater derav.
Salver er olje-i-vann emulsjoner, hvilke omfatter ikke mer enn 70 %, men foretrukket 20-50 % vann eller vandig fase. Fettfasen består spesielt av hydrokarboner, for eksempel vaselin, parafinolje eller harde parafiner, som fortrinnsvis omfatter egnede hydroksyforbindelser, så som fettsyrealkoholer eller estere derav, for eksempel cetylalkohol eller ullvoksolje, så som ullvoks for å forbedre den vann-bindende kapasitet. Emulgatorer er tilsvarende lipofile substanser, så som sorbitan, fettsyreestere (Spans), for eksempel sorbitanoleat og/eller sorbitanisostearat. Additiver til den vandige fase er for eksempel humektanter, så som polyalkoholer, for eksempel glycerol, propylenglykol, sorbitol og/eller polyetylenglykol eller preservativer og luktfremmende substanser.
Fettkremer er vannfrie og omfatter som base spesielt hydrokarboner, for eksempel parafin, vaselin eller parafinolje og videre, naturlig forekommende eller semi-syntetiske fettsorter, for eksempel hydrogenerte kokosnøttfettsyretriglyserider eller foretrukket hydrogenerte oljer, for eksempel hydrogenert jordnøtt- eller lakserolje og videre, partielle fettsyreestere av glycerol, for eksempel glycerol mono- og/eller distearat, for eksempel fettalkoholene. De inneholder også emulgatorer og/eller additiver nevnt i forbindelse med salvene som øker opptak av vann.
Kremer er olje-i-vann emulsjoner som omfatter mer enn 50 % vann. Oljebaser som blir brukt er spesielt fettalkoholer, for eksempel lauryl, cetyl eller stearylalkoholer, fettsyrer, for eksempel palmitin- eller stearinsyre, flytende til faste vokstyper, for eksempel isopropylmyristat, ullvoks eller bivoks, og/eller hydrokarboner, for eksempel vaselin (petrolatum) eller parafinolje. Emulgatorer er overflateaktive substanser med i hovedsak hydrofile egenskap så som tilsvarende ikke-joniske emulgatorer, for eksempel fettsyreestere av polyalkoholer eller etylenoksyaddukter derav, så som polyglyserinsyre fettsyreestere eller polyetylensorbitan fettestere (Tweens) og videre polyoksyetylen fettalkoholetere eller polyoksyetylen fettsyreestere, eller tilsvarende joniske emulgatorer, så som alkalimetallsalter av fettalkoholsulfater, for eksempel natrium laurylsulfat, natrium cetylsulfat eller natrium stearylsulfat, som vanligvis blir brukt i nærvær av fettalkoholer, for eksempel cetylstearylalkohol eller stearylalkohol. Additiver til den vandige fase er bl.a. midler som forhindrer kremene fra å tørke ut, for eksempel polyalkoholer så som glycerol, sorbitol, propylenglykol og/eller polyetylenglykoler og ytterligere preservativer og luktfremmende substanser.
Pastaer er kremer og salver som har sekresjonsabsorberende pulverbestanddeler så som metalloksider, for eksempel titanoksid eller zinkoksyd og videre talkum og/eller aluminiumsilikater, som har oppgaven å binde fuktigheten eller sekresjo-nene som er til stede.
Skum blir administrert fra trykksatte beholdere og der er flytende olje-i-vann emulsjoner som er til stede i aerosolskum. Som drivgasser blir halogenerte hydrokarboner så som polyhalogenerte alkaner, for eksempel diklorfluormetan og diklor-tetrafluoretan, eller fortrinnsvis ikke-halogenerte, gassformige hydrokarboner, luft, N20 eller karbondioksid brukt. Oljefasene som benyttes er bl.a. dem nevnt ovenfor for salver og kremer og additivene som er nevnt der blir likeledes benyttet.
Figurer
I figur 2 er det vist senescente celler i kultur av humane fibroblaster (B) (de andre celler (A)) farget blå grunnet virkningen av p-galaktosidase på substratet X-gal (5-brom-4-klor-3-indolyl-p-D-galaktopyranosid) (1 mg/ml).
De følgende eksempler virker til å illustrere oppfinnelsen uten å begrense omfanget derav.
Eksempler
Referanse Eksempel 1
6-(3-klorbenzylamino)purin
3 mmol av 6-klorpurin ble oppløst i 15 ml butanol. Derpå ble 4 mmol 3-klorbenzyl-amin og 5 mmol trietylamin tilsatt og blandingen ble oppvarmet til 90 °C i 4 timer. Etter avkjøling ble det utfelte produkt filtrert fra, vasket med kaldt vann og n-butanol og krystallisert fra etanol eller dimetylformamid. Smeltepunkt = 252°C, TLC (CHCI3:MeOH: kons. NH4OH (8:2:0.2, v/v/v)): enkel spot; HPLC: renhet> 98 %. Utbytte 95 %.
Referanse Eksempel 2
Blanding av 10 mmol adenin, 12 mmol 2-metoksybenzaldehyd og 5 ml 98-100 % maursyre ble kokt under tilbakeløp i 3 dager. Etter inndampning av maursyre ble det resulterende materialet avkjølt og deretter vasket med 40 ml dietyleter. Fast residium ble kokt med 60 ml vann, filtrert og grovproduktet krystallisert fra etanol. Utbytte 45 %.
Eksempel 3
Inhibering av senescens med utvalgte forbindelser
I dette eksempel ble humane, diploide fibroblaster (HCA-celler av forskjellige pas-sasjenivåer: passasje 25 - betegnet HCA25; passasje 45 - betegnet HCA45; passasje 80 - betegnet HCA80) farget for p-galaktosidaseaktivitet. Mediet som ble brukt for celledyrking ble fjernet, cellene ble vasket to ganger i PNS og fiksert i 2-3 ml av fikseringsoppløsning bestående av 2 % formaldehyde og 0,2 % glutaraldehyd i PBS. Cellene ble inkubert ved romtemperatur i 5 minutter, derpå vasket to ganger med PBS. Cellene ble derpå inkubert ved 37 °C (uten C02) i 1 til 16 timer i 2-3 ml av en oppløsning omfattende kalium ferricyanid (5 mM), kalium ferrocyanid (5 mM), MgCI2 (2 mM), X-gal (5-brom-4-klor-3-indol-p-D-galaktopyranosid) (1 mg/ml), i sitronsyre/fosfatbuffer, pH 6,0). Etter denne inkuberingsperioden ble cel-leprøvene observert for å påvise tilstedeværelsen av blå celler, noe som indikerer at X-gal hadde blitt spaltet (positivt senescente celler). I dette forsøk ble senescente celler, men ikke andre celler, farget blå grunnet virkningen av p-galaktosidase på substratet.
Som vist i tabell 5 ble, med økende antall passasjer, fargingen mørkere. For de eldste celler var det kun blå celler i området fra klart blått til en nesten gjennomsik-tig farge. N6 -substituerte adeninderivater var meget effektive i å oppnå et meget lavere nivå av senescente celler etter 80 passasjer. I tilfellet med langvarende dyr-king var de dyrkede celler i stand til å leve en 30 % lenger periode enn kontrollcel-lene.
Claims (3)
1. Anvendelse av 6-(4-hydroksybenzylamino)purin til kosmetiske formål.
2. Anvendelse ifølge krav 1, hvor det kosmetiske formål er inhibering av aldring og aldringstegn i epidermalceller hos pattedyr så som keratinocytter eller fibroblaster.
3. Kosmetikum omfattende 6-(4-hydroksybenzylamino)purin eller dets farma-søytisk akseptable salt innbefattende en farmasøytisk bærer.
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JP2636118B2 (ja) * | 1991-09-10 | 1997-07-30 | 三省製薬株式会社 | 育毛剤 |
AU659861B2 (en) * | 1991-09-10 | 1995-06-01 | Sansho Seiyaku Co., Ltd. | Preparation for promoting hair growth |
JPH07233037A (ja) * | 1993-12-29 | 1995-09-05 | Sansho Seiyaku Co Ltd | 皮膚化粧料 |
MX9709867A (es) * | 1995-06-07 | 1998-03-31 | Pfizer | Derivados de pirimidina condensados con un anillo heterociclico, composiciones que contienen los mismos, y uso de los mismos. |
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AU3540101A (en) * | 2000-01-07 | 2001-07-16 | Universitaire Instelling Antwerpen | Purine derivatives, process for their preparation and use thereof |
CZ294535B6 (cs) * | 2001-08-02 | 2005-01-12 | Ústav Experimentální Botaniky Avčr | Heterocyklické sloučeniny na bázi N6-substituovaného adeninu, způsoby jejich přípravy, jejich použití pro přípravu léčiv, kosmetických přípravků a růstových regulátorů, farmaceutické přípravky, kosmetické přípravky a růstové regulátory tyto sloučeniny obsahující |
CA2491094A1 (en) * | 2002-07-01 | 2004-01-08 | Univesity Of Rochester Medical Center | Method for determination of likelihood of occurrence of preterm labor in pregnant females |
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