CA1293930C - Cosmetic sunscreen product for the face and body - Google Patents
Cosmetic sunscreen product for the face and bodyInfo
- Publication number
- CA1293930C CA1293930C CA000550573A CA550573A CA1293930C CA 1293930 C CA1293930 C CA 1293930C CA 000550573 A CA000550573 A CA 000550573A CA 550573 A CA550573 A CA 550573A CA 1293930 C CA1293930 C CA 1293930C
- Authority
- CA
- Canada
- Prior art keywords
- weight
- face
- tanning product
- adenosine
- cosmetic tanning
- 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 - Lifetime
Links
- 239000002537 cosmetic Substances 0.000 title claims abstract description 36
- 230000000475 sunscreen effect Effects 0.000 title abstract description 11
- 239000000516 sunscreening agent Substances 0.000 title abstract description 11
- -1 alkaline earth metal salts Chemical class 0.000 claims abstract description 31
- 239000000203 mixture Substances 0.000 claims abstract description 26
- 239000012190 activator Substances 0.000 claims abstract description 21
- 239000004904 UV filter Substances 0.000 claims abstract description 12
- 239000000126 substance Substances 0.000 claims abstract description 12
- 239000002304 perfume Substances 0.000 claims abstract description 8
- 239000003513 alkali Substances 0.000 claims abstract description 5
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 4
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 4
- 239000003531 protein hydrolysate Substances 0.000 claims abstract description 4
- 239000004094 surface-active agent Substances 0.000 claims abstract description 3
- 230000008961 swelling Effects 0.000 claims abstract description 3
- 239000002562 thickening agent Substances 0.000 claims abstract description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract 8
- 150000001340 alkali metals Chemical class 0.000 claims abstract 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract 4
- 150000003667 tyrosine derivatives Chemical class 0.000 claims description 15
- ZKHQWZAMYRWXGA-UHFFFAOYSA-N Adenosine triphosphate Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)C(O)C1O ZKHQWZAMYRWXGA-UHFFFAOYSA-N 0.000 claims description 14
- ZKHQWZAMYRWXGA-KQYNXXCUSA-N Adenosine triphosphate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O ZKHQWZAMYRWXGA-KQYNXXCUSA-N 0.000 claims description 11
- XTWYTFMLZFPYCI-KQYNXXCUSA-N 5'-adenylphosphoric acid Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O XTWYTFMLZFPYCI-KQYNXXCUSA-N 0.000 claims description 9
- SKAWDTAMLOJQNK-UHFFFAOYSA-N 2-acetamido-3-(4-hydroxyphenyl)propanoic acid ethyl ester Chemical compound CCOC(=O)C(NC(C)=O)CC1=CC=C(O)C=C1 SKAWDTAMLOJQNK-UHFFFAOYSA-N 0.000 claims description 8
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 claims description 8
- 229910000397 disodium phosphate Inorganic materials 0.000 claims description 8
- 235000019800 disodium phosphate Nutrition 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
- 229960001682 n-acetyltyrosine Drugs 0.000 claims description 7
- 239000011734 sodium Substances 0.000 claims description 7
- CAHKINHBCWCHCF-JTQLQIEISA-N N-acetyl-L-tyrosine Chemical group CC(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 CAHKINHBCWCHCF-JTQLQIEISA-N 0.000 claims description 6
- IPAZGTSTZYXZAT-UHFFFAOYSA-N N-arachidonoyl-L-tyrosine Natural products CCCCCCCCCCCCCCCC(=O)NC(C(O)=O)CC1=CC=C(O)C=C1 IPAZGTSTZYXZAT-UHFFFAOYSA-N 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 5
- UDMBCSSLTHHNCD-UHFFFAOYSA-N Coenzym Q(11) Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(O)=O)C(O)C1O UDMBCSSLTHHNCD-UHFFFAOYSA-N 0.000 claims description 4
- UDMBCSSLTHHNCD-KQYNXXCUSA-N adenosine 5'-monophosphate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O UDMBCSSLTHHNCD-KQYNXXCUSA-N 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- IPAZGTSTZYXZAT-QHCPKHFHSA-N N-Palmitoyl tyrosine Chemical compound CCCCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 IPAZGTSTZYXZAT-QHCPKHFHSA-N 0.000 claims description 3
- 239000007789 gas Substances 0.000 claims description 3
- 150000002334 glycols Chemical class 0.000 claims description 3
- JWVQCQGVVNUXFW-NRFANRHFSA-N (2s)-3-(4-hydroxyphenyl)-2-(tetradecanoylamino)propanoic acid Chemical compound CCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 JWVQCQGVVNUXFW-NRFANRHFSA-N 0.000 claims description 2
- YKWCFTGLODSOSB-VWLOTQADSA-N N-Stearoyl tyrosine Chemical compound CCCCCCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 YKWCFTGLODSOSB-VWLOTQADSA-N 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 claims description 2
- 239000000443 aerosol Substances 0.000 claims description 2
- 239000010775 animal oil Substances 0.000 claims description 2
- 239000000839 emulsion Substances 0.000 claims description 2
- 239000006260 foam Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 239000002480 mineral oil Substances 0.000 claims description 2
- 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 claims description 2
- 239000010695 polyglycol Substances 0.000 claims description 2
- 229920000151 polyglycol Polymers 0.000 claims description 2
- 239000003380 propellant Substances 0.000 claims description 2
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 claims description 2
- 159000000000 sodium salts Chemical class 0.000 claims description 2
- 125000004079 stearyl 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])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 2
- 239000008158 vegetable oil Substances 0.000 claims description 2
- 239000001993 wax Substances 0.000 claims description 2
- 229910004814 HzPO4 Inorganic materials 0.000 claims 3
- 101100283604 Caenorhabditis elegans pigk-1 gene Proteins 0.000 claims 2
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 claims 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 2
- TTWYZDPBDWHJOR-IDIVVRGQSA-L adenosine triphosphate disodium Chemical compound [Na+].[Na+].C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP([O-])([O-])=O)[C@@H](O)[C@H]1O TTWYZDPBDWHJOR-IDIVVRGQSA-L 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 claims 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- 125000001419 myristoyl group Chemical group O=C([*])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 claims 1
- 125000001421 myristyl 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])[H] 0.000 claims 1
- 125000001312 palmitoyl group Chemical group O=C([*])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 claims 1
- 125000003696 stearoyl group Chemical group O=C([*])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])C([H])([H])C([H])([H])[H] 0.000 claims 1
- WLMATIVZKLHYJX-DHUJRADRSA-N tetradecyl (2s)-3-(4-hydroxyphenyl)-2-(tetradecanoylamino)propanoate Chemical compound CCCCCCCCCCCCCCOC(=O)[C@@H](NC(=O)CCCCCCCCCCCCC)CC1=CC=C(O)C=C1 WLMATIVZKLHYJX-DHUJRADRSA-N 0.000 claims 1
- 239000013543 active substance Substances 0.000 abstract description 3
- 239000000654 additive Substances 0.000 abstract description 3
- 150000001875 compounds Chemical class 0.000 abstract description 2
- 238000002360 preparation method Methods 0.000 abstract description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 abstract 2
- MWEQTWJABOLLOS-UHFFFAOYSA-L disodium;[[[5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-oxidophosphoryl] hydrogen phosphate;trihydrate Chemical class O.O.O.[Na+].[Na+].C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(=O)OP([O-])(=O)OP(O)([O-])=O)C(O)C1O MWEQTWJABOLLOS-UHFFFAOYSA-L 0.000 abstract 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
- 239000000047 product Substances 0.000 abstract 2
- 108010009736 Protein Hydrolysates Proteins 0.000 abstract 1
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 6
- 238000007792 addition Methods 0.000 description 6
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 6
- 150000003838 adenosines Chemical class 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- CMDKPGRTAQVGFQ-RMKNXTFCSA-N cinoxate Chemical compound CCOCCOC(=O)\C=C\C1=CC=C(OC)C=C1 CMDKPGRTAQVGFQ-RMKNXTFCSA-N 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 102000003425 Tyrosinase Human genes 0.000 description 3
- 108060008724 Tyrosinase Proteins 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000005923 long-lasting effect Effects 0.000 description 3
- 230000004224 protection Effects 0.000 description 3
- 229940048102 triphosphoric acid Drugs 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 239000004166 Lanolin Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 235000019388 lanolin Nutrition 0.000 description 2
- 229940039717 lanolin Drugs 0.000 description 2
- 229940057995 liquid paraffin Drugs 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 230000002085 persistent effect Effects 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 2
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 2
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- HEOCBCNFKCOKBX-RELGSGGGSA-N (1s,2e,4r)-4,7,7-trimethyl-2-[(4-methylphenyl)methylidene]bicyclo[2.2.1]heptan-3-one Chemical compound C1=CC(C)=CC=C1\C=C/1C(=O)[C@]2(C)CC[C@H]\1C2(C)C HEOCBCNFKCOKBX-RELGSGGGSA-N 0.000 description 1
- ICFOEHKKFUEQQS-IDTAVKCVSA-N (2R,3R,4S,5R)-2-(6-aminopurin-9-yl)-2-butyl-5-(hydroxymethyl)oxolane-3,4-diol Chemical compound C1=NC2=C(N)N=CN=C2N1[C@]1(CCCC)O[C@H](CO)[C@@H](O)[C@H]1O ICFOEHKKFUEQQS-IDTAVKCVSA-N 0.000 description 1
- YYGNTYWPHWGJRM-UHFFFAOYSA-N (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC=C(C)C YYGNTYWPHWGJRM-UHFFFAOYSA-N 0.000 description 1
- OIRDTQYFTABQOQ-KQYNXXCUSA-N Adenosine Natural products C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 description 1
- 239000002126 C01EB10 - Adenosine Substances 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 240000007817 Olea europaea Species 0.000 description 1
- 208000012641 Pigmentation disease Diseases 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 244000000231 Sesamum indicum Species 0.000 description 1
- 235000003434 Sesamum indicum Nutrition 0.000 description 1
- 206010042496 Sunburn Diseases 0.000 description 1
- BHEOSNUKNHRBNM-UHFFFAOYSA-N Tetramethylsqualene Natural products CC(=C)C(C)CCC(=C)C(C)CCC(C)=CCCC=C(C)CCC(C)C(=C)CCC(C)C(C)=C BHEOSNUKNHRBNM-UHFFFAOYSA-N 0.000 description 1
- 229960005305 adenosine Drugs 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 230000031018 biological processes and functions Effects 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- XONPDZSGENTBNJ-UHFFFAOYSA-N molecular hydrogen;sodium Chemical compound [Na].[H][H] XONPDZSGENTBNJ-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- SKYULNJQRSUAFL-QLKFWGTOSA-N octadecyl (2s)-3-(4-hydroxyphenyl)-2-(octadecanoylamino)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)[C@@H](NC(=O)CCCCCCCCCCCCCCCCC)CC1=CC=C(O)C=C1 SKYULNJQRSUAFL-QLKFWGTOSA-N 0.000 description 1
- BARWIPMJPCRCTP-UHFFFAOYSA-N oleic acid oleyl ester Natural products CCCCCCCCC=CCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC BARWIPMJPCRCTP-UHFFFAOYSA-N 0.000 description 1
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 210000004694 pigment cell Anatomy 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229940031439 squalene Drugs 0.000 description 1
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- 150000003668 tyrosines Chemical class 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives 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)
- Dermatology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH4819/86A CH671514A5 (en, 2012) | 1986-12-03 | 1986-12-03 | |
| CH4819/86-0 | 1986-12-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1293930C true CA1293930C (en) | 1992-01-07 |
Family
ID=4283091
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000550573A Expired - Lifetime CA1293930C (en) | 1986-12-03 | 1987-10-29 | Cosmetic sunscreen product for the face and body |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4844884A (en, 2012) |
| AU (1) | AU600535B2 (en, 2012) |
| CA (1) | CA1293930C (en, 2012) |
| CH (1) | CH671514A5 (en, 2012) |
| DE (1) | DE3732154C2 (en, 2012) |
| ES (1) | ES2008256A6 (en, 2012) |
| FR (1) | FR2607699B1 (en, 2012) |
| GB (1) | GB2198042B (en, 2012) |
| IT (1) | IT1213915B (en, 2012) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH675967A5 (en, 2012) * | 1987-12-09 | 1990-11-30 | Induchem Ag | |
| AU2971689A (en) * | 1988-02-11 | 1989-08-17 | Estee Lauder Inc. | Tanning compositions and their use |
| FR2634374B1 (fr) * | 1988-07-19 | 1993-10-15 | Laboratoires Serobiologiques | Agents photoprotecteurs, cytophotoprotecteurs cutanes ayant une activite photoprotectrice des cellules constitutives, fonctionnelles de la peau, en particulier des cellules de langerhans, a base de composes nucleiques : nucleoprotides, ribonucleotides et desoxyribonucleotides, ribonucleosides et desoxyribonucleosides, compositions cosmetiques ou dermo-pharmaceutiques contenant un tel agent ainsi que des nouveaux composes en soi |
| US4968497A (en) * | 1988-08-26 | 1990-11-06 | Clairol Incorporated | Skin tanning composition and method |
| US5061480A (en) * | 1989-11-03 | 1991-10-29 | Marchese Co., Inc. | Tanning composition |
| FR2702766B1 (fr) * | 1993-03-15 | 1995-04-28 | Sederma Sa | Nouveaux composés synthétiques, procédé de leur obtention et utilisation dans des préparations cosmétiques et dermopharamceutiques pour améliorer le bronzage. |
| JP3485375B2 (ja) | 1995-02-17 | 2004-01-13 | 株式会社資生堂 | 皮膚外用剤 |
| FR2823112B1 (fr) * | 2001-04-09 | 2004-03-05 | Oreal | Produit bronzant et filtrant |
| FR2828099A1 (fr) * | 2001-08-02 | 2003-02-07 | Soc Extraction Principes Actif | Utilisation d'un hydrolysat de proteines riche en tyrosine pour augmenter la synthese de melanine |
| FR2849375B1 (fr) * | 2002-12-30 | 2006-10-20 | Jean Noel Thorel | Compositions cosmetiques, par exemple pour traiter le vieillissement cutane photo-induit |
| EP1581177B1 (fr) * | 2002-12-30 | 2018-04-11 | Thorel, Jean-Noël | Bio-activateur metabolique cutane |
| US20070183995A1 (en) * | 2006-02-09 | 2007-08-09 | Conopco, Inc., D/B/A Unilever | Compounds useful as agonists of A2A adenosine receptors, cosmetic compositions with A2A agonists and a method for using the same |
| US20070255119A1 (en) * | 2006-03-13 | 2007-11-01 | David Mordaunt | Separate computing device for medical device with computing capabilities |
| ES2531520T3 (es) * | 2007-05-04 | 2015-03-16 | Marina Biotech, Inc. | Lipoaminoácidos y usos de los mismos |
| JP5697450B2 (ja) * | 2007-10-02 | 2015-04-08 | マリーナ バイオテック，インコーポレイテッド | 核酸の送達のためのリポペプチド |
| KR101489638B1 (ko) | 2008-04-01 | 2015-02-11 | (주)네오팜 | 인간유래 항균 펩타이드의 분비를 촉진하는 신규화합물, 그제조방법, 및 이를 유효성분으로 함유하는피부외용제조성물 |
| DE102008031556A1 (de) | 2008-07-07 | 2009-04-30 | Henkel Ag & Co. Kgaa | Kosmetische oder dermatologische Zubereitungen zur Hautbräunung |
| DE102008047945A1 (de) | 2008-09-18 | 2009-06-25 | Henkel Ag & Co. Kgaa | Selbstbräunungszusammensetzungen |
| BRPI0920171A2 (pt) * | 2008-10-16 | 2016-07-12 | Marina Biotech Inc | processos e composições para liberação lipossômica e eficiente de terapêuticos de silenciamento de gene. |
| WO2012026639A1 (ko) * | 2010-08-27 | 2012-03-01 | (주)네오팜 | 인간유래 항균 펩타이드의 분비를 촉진하는 신규화합물, 그 제조방법 및 이를 유효성분으로 함유하는 조성물 |
| US20160008245A1 (en) * | 2014-07-11 | 2016-01-14 | Mary Kay Inc. | Sunscreen compositions and methods of their use |
| EP4028502A4 (en) * | 2019-09-13 | 2024-02-28 | Sederma | N-ACYL-TYROSINE DERIVATIVES AND THEIR USE |
| WO2021224133A1 (en) * | 2020-05-07 | 2021-11-11 | Unilever Ip Holdings B.V. | An antiperspirant composition |
| FR3128375B1 (fr) * | 2021-10-26 | 2024-11-29 | Sederma Sa | Traitement cosmétique, dermatologique ou cosméceutique, notamment propigmentant |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE964172C (de) * | 1954-07-22 | 1957-05-16 | Hugo Janistyn | Hautpflegemittel |
| FR1440795A (fr) * | 1965-04-21 | 1966-06-03 | Docteur Jacques Auclair Lab Du | Composition cosmétique |
| FR2077725A1 (en) * | 1970-02-10 | 1971-11-05 | Lapinet Eugene | Adenosine phosphoric acid - to stimulate cellular function of the ski |
| US3937808A (en) * | 1972-02-29 | 1976-02-10 | Gaf Corporation | Sun tanning and hari protecting acid salts of aminomethyl-o-hydroxyphenones compositions |
| US3937804A (en) * | 1972-10-04 | 1976-02-10 | Colgate-Palmolive Company | Toothpaste |
| US3937809A (en) * | 1974-05-01 | 1976-02-10 | Kolmar Laboratories, Inc. | Addition compound of a nucleotide and an amino acid and the use thereof in protection against actinic radiation |
| FR2324293A1 (fr) * | 1975-04-29 | 1977-04-15 | Orlane | Produit cosmetique stimulant le metabolisme de la peau et procede de preparation dudit produit cosmetique |
| US4021538A (en) * | 1975-09-29 | 1977-05-03 | Yu Ruey J | Method for producing pigmentation in hair or skin |
| FR2439013A1 (fr) * | 1978-10-19 | 1980-05-16 | Serobiologiques Lab Sa | Composition, utilisable notamment comme produit cosmetique permettant un bronzage de la peau, comprenant l'emploi d'acides amines |
| CH642537A5 (en) * | 1980-01-25 | 1984-04-30 | Uni Chemie Ag | Cosmetic sunscreen product |
| GB8302683D0 (en) * | 1983-02-01 | 1983-03-02 | Unilever Plc | Skin treatment composition |
| US4515773A (en) * | 1983-07-05 | 1985-05-07 | Repligen Corporation | Skin tanning composition and method |
-
1986
- 1986-12-03 CH CH4819/86A patent/CH671514A5/de not_active IP Right Cessation
-
1987
- 1987-09-24 DE DE3732154A patent/DE3732154C2/de not_active Expired - Lifetime
- 1987-10-07 ES ES8702859A patent/ES2008256A6/es not_active Expired
- 1987-10-16 IT IT8712557A patent/IT1213915B/it active
- 1987-10-23 US US07/113,005 patent/US4844884A/en not_active Expired - Lifetime
- 1987-10-29 CA CA000550573A patent/CA1293930C/en not_active Expired - Lifetime
- 1987-11-23 FR FR878716196A patent/FR2607699B1/fr not_active Expired - Lifetime
- 1987-11-26 AU AU81810/87A patent/AU600535B2/en not_active Expired
- 1987-12-02 GB GB8728139A patent/GB2198042B/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| FR2607699A1 (fr) | 1988-06-10 |
| IT1213915B (it) | 1990-01-05 |
| GB2198042A (en) | 1988-06-08 |
| GB8728139D0 (en) | 1988-01-06 |
| IT8712557A0 (it) | 1987-10-16 |
| DE3732154A1 (de) | 1988-06-30 |
| ES2008256A6 (es) | 1989-07-16 |
| US4844884A (en) | 1989-07-04 |
| AU600535B2 (en) | 1990-08-16 |
| FR2607699B1 (fr) | 1990-06-22 |
| DE3732154C2 (de) | 1994-10-06 |
| GB2198042B (en) | 1990-07-25 |
| CH671514A5 (en, 2012) | 1989-09-15 |
| AU8181087A (en) | 1988-06-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA1293930C (en) | Cosmetic sunscreen product for the face and body | |
| DE69201667T2 (de) | S-Triazinderivate mit Benzalmalonaten als Substituenten, Verfahren zu ihrer Herstellung, diese enthaltende kosmetische Zubereitungen mit filternder Wirkung und ihre Verwendung als Schutzmittel für Haut und Haar. | |
| DE69001458T2 (de) | Mit einer benzotriazolgruppe substituierte diorganopolysiloxane enthaltende kosmetika sowie deren verwendung zum schutz von haut und haaren. | |
| DE2545986C2 (de) | Kosmetika auf der Basis von Enzymen | |
| KR100613825B1 (ko) | 플라보노이드 제제 및 화장품에서의 탁월한 그 용도 | |
| RU2126244C1 (ru) | Косметическая композиция для искусственного загара, способ обработки кожи и агент для стабилизации дигидроксиацетона и/или интенсивности окрашивания кожи | |
| DE69305578T2 (de) | Produkt, bazierend auf gefaerbten mineralteilchen, die ein melanin-pigment enthalten, sein herstellungsverfahren und seine verwendung in der kosmetik | |
| FR2595245A1 (fr) | Compositions tinctoriales pour fibres keratiniques a base de derives d'indole et composes nouveaux | |
| US4145413A (en) | Artificial skin darkening composition and method of using the same | |
| JPH04364197A (ja) | パーソナルケアに有用なアルコキシル化アルキルグルコシドエーテル四級化物 | |
| DE69102707D1 (de) | In einem DNA - Gel stabilisierte Heilwasserliposomen. | |
| US4839160A (en) | Polymers capable of absorbing ultraviolet radiation, their preparation and their use in cosmetic compositions | |
| FR2673532A1 (fr) | Procede de teinture des fibres keratiniques associant l'isatine ou ses derives a une aminopyridine ou aminopyrimidine, et agents de teinture. | |
| US6010707A (en) | Cosmetic and dermatological compositions containing aminoalcohol derivatives containing a urea functional group and uses thereof | |
| US3184388A (en) | Process and product for artificially browning the skin | |
| JPS6422878A (en) | Fluorescein derivative and liposome preparation containing the same | |
| CH667650A5 (de) | Salze von thiazolidin-4-carbonsaeuren und 6-piperidino-2,4-diaminopyrimidin-3-oxid sowie diese salze enthaltende zusammensetzungen. | |
| DE69000884T2 (de) | Kosmetische verwendung von diorganopolysiloxanen mit 2-hydroxybenzophenon-substituenten, kosmetische mittel, die diese verbindungen enthalten zum schutz der haut und der haare. | |
| ES8101884A1 (es) | Procedimiento de obtencion de composiciones cosmeticas | |
| JPH04312519A (ja) | 自然な日焼け色付与組成物 | |
| CH642537A5 (en) | Cosmetic sunscreen product | |
| CA1043495A (fr) | Polymeres anti-solaires et compositions cosmetiques les contenant | |
| JPH0899859A (ja) | 皮膚外用剤 | |
| GB2185396A (en) | Cosmetic compositions designed to protect the skin against the adverse effects of ultraviolet radiation | |
| JPS6413018A (en) | Skin-beautifying cosmetic |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKLA | Lapsed | ||
| MKEC | Expiry (correction) |
Effective date: 20121205 |