WO2000078857A1 - Solid aqueous gel comprising a hydrophilic gelling agent and starch, composition comprising same and uses - Google Patents
Solid aqueous gel comprising a hydrophilic gelling agent and starch, composition comprising same and uses Download PDFInfo
- Publication number
- WO2000078857A1 WO2000078857A1 PCT/FR2000/001632 FR0001632W WO0078857A1 WO 2000078857 A1 WO2000078857 A1 WO 2000078857A1 FR 0001632 W FR0001632 W FR 0001632W WO 0078857 A1 WO0078857 A1 WO 0078857A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- gel
- gel according
- starches
- chosen
- weight
- Prior art date
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- 229920002472 Starch Polymers 0.000 title claims abstract description 44
- 235000019698 starch Nutrition 0.000 title claims abstract description 41
- 239000000203 mixture Substances 0.000 title claims abstract description 38
- 239000003349 gelling agent Substances 0.000 title claims abstract description 20
- 239000008107 starch Substances 0.000 title claims abstract description 15
- 239000007787 solid Substances 0.000 title claims abstract description 10
- 239000002537 cosmetic Substances 0.000 claims abstract description 12
- 239000008247 solid mixture Substances 0.000 claims abstract description 6
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- 150000001875 compounds Chemical class 0.000 claims description 16
- 239000000843 powder Substances 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 229910052791 calcium Inorganic materials 0.000 claims description 11
- 150000003839 salts Chemical class 0.000 claims description 11
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 10
- 239000000945 filler Substances 0.000 claims description 10
- 239000011575 calcium Substances 0.000 claims description 9
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- 108010076876 Keratins Proteins 0.000 claims description 8
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- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 7
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- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- PRBXPAHXMGDVNQ-UHFFFAOYSA-N 2-[2-(2-hydroxyethoxy)ethoxy]acetic acid Chemical compound OCCOCCOCC(O)=O PRBXPAHXMGDVNQ-UHFFFAOYSA-N 0.000 description 1
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
- KZMRYBLIGYQPPP-UHFFFAOYSA-N 3-[[[4-[(2-chlorophenyl)-[4-[ethyl-[(3-sulfonatophenyl)methyl]azaniumylidene]cyclohexa-2,5-dien-1-ylidene]methyl]phenyl]-ethylazaniumyl]methyl]benzenesulfonate Chemical compound C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C(=CC=CC=2)Cl)C=CC=1[NH+](CC)CC1=CC=CC(S([O-])(=O)=O)=C1 KZMRYBLIGYQPPP-UHFFFAOYSA-N 0.000 description 1
- AXDJCCTWPBKUKL-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydron;chloride Chemical compound Cl.C1=CC(=N)C(C)=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 AXDJCCTWPBKUKL-UHFFFAOYSA-N 0.000 description 1
- 241001133760 Acoelorraphe Species 0.000 description 1
- 240000001592 Amaranthus caudatus Species 0.000 description 1
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 1
- 244000144725 Amygdalus communis Species 0.000 description 1
- 235000011437 Amygdalus communis Nutrition 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 241001474374 Blennius Species 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- 241001246270 Calophyllum Species 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000180278 Copernicia prunifera Species 0.000 description 1
- 235000010919 Copernicia prunifera Nutrition 0.000 description 1
- 229920001634 Copolyester Polymers 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- 108010007979 Glycocholic Acid Proteins 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 241000208467 Macadamia Species 0.000 description 1
- 229910021380 Manganese Chloride Inorganic materials 0.000 description 1
- GLFNIEUTAYBVOC-UHFFFAOYSA-L Manganese chloride Chemical compound Cl[Mn]Cl GLFNIEUTAYBVOC-UHFFFAOYSA-L 0.000 description 1
- 240000007817 Olea europaea Species 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 244000025272 Persea americana Species 0.000 description 1
- 235000008673 Persea americana Nutrition 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
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- 235000003434 Sesamum indicum Nutrition 0.000 description 1
- 244000040738 Sesamum orientale Species 0.000 description 1
- 244000044822 Simmondsia californica Species 0.000 description 1
- 235000004433 Simmondsia californica Nutrition 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 240000003829 Sorghum propinquum Species 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 240000000851 Vaccinium corymbosum Species 0.000 description 1
- 235000003095 Vaccinium corymbosum Nutrition 0.000 description 1
- 235000017537 Vaccinium myrtillus Nutrition 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229940061720 alpha hydroxy acid Drugs 0.000 description 1
- 239000004178 amaranth Substances 0.000 description 1
- 235000012735 amaranth Nutrition 0.000 description 1
- 239000010477 apricot oil Substances 0.000 description 1
- 229940009098 aspartate Drugs 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 235000021014 blueberries Nutrition 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 229940110456 cocoa butter Drugs 0.000 description 1
- 235000019868 cocoa butter Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 125000005534 decanoate group Chemical class 0.000 description 1
- RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical group 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 150000002315 glycerophosphates Chemical class 0.000 description 1
- RFDAIACWWDREDC-FRVQLJSFSA-N glycocholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 RFDAIACWWDREDC-FRVQLJSFSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229940087559 grape seed Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 150000003893 lactate salts Chemical class 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- TWNIBLMWSKIRAT-VFUOTHLCSA-N levoglucosan Chemical group O[C@@H]1[C@@H](O)[C@H](O)[C@H]2CO[C@@H]1O2 TWNIBLMWSKIRAT-VFUOTHLCSA-N 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- HGPXWXLYXNVULB-UHFFFAOYSA-M lithium stearate Chemical compound [Li+].CCCCCCCCCCCCCCCCCC([O-])=O HGPXWXLYXNVULB-UHFFFAOYSA-M 0.000 description 1
- 229960005375 lutein Drugs 0.000 description 1
- KBPHJBAIARWVSC-RGZFRNHPSA-N lutein Chemical compound C([C@H](O)CC=1C)C(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\[C@H]1C(C)=C[C@H](O)CC1(C)C KBPHJBAIARWVSC-RGZFRNHPSA-N 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 235000001055 magnesium Nutrition 0.000 description 1
- YIXJRHPUWRPCBB-UHFFFAOYSA-N magnesium nitrate Inorganic materials [Mg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O YIXJRHPUWRPCBB-UHFFFAOYSA-N 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 150000004701 malic acid derivatives Chemical class 0.000 description 1
- 239000011565 manganese chloride Substances 0.000 description 1
- 235000002867 manganese chloride Nutrition 0.000 description 1
- 229940099607 manganese chloride Drugs 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 210000004379 membrane Anatomy 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
- 210000000282 nail Anatomy 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 description 1
- 125000005474 octanoate group Chemical class 0.000 description 1
- 239000011146 organic particle Substances 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical class [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 description 1
- 229940056211 paraffin Drugs 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 230000010363 phase shift Effects 0.000 description 1
- 238000004987 plasma desorption mass spectroscopy Methods 0.000 description 1
- 229920001921 poly-methyl-phenyl-siloxane Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 239000004172 quinoline yellow Substances 0.000 description 1
- 235000012752 quinoline yellow Nutrition 0.000 description 1
- 229940051201 quinoline yellow Drugs 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 150000003892 tartrate salts Chemical class 0.000 description 1
- 239000004149 tartrazine Substances 0.000 description 1
- UJMBCXLDXJUMFB-GLCFPVLVSA-K tartrazine Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-GLCFPVLVSA-K 0.000 description 1
- 235000012756 tartrazine Nutrition 0.000 description 1
- 229960000943 tartrazine Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- KBPHJBAIARWVSC-XQIHNALSSA-N trans-lutein Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C=CC2C(=CC(O)CC2(C)C)C KBPHJBAIARWVSC-XQIHNALSSA-N 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000010497 wheat germ oil Substances 0.000 description 1
- FJHBOVDFOQMZRV-XQIHNALSSA-N xanthophyll Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C=CC2C=C(C)C(O)CC2(C)C FJHBOVDFOQMZRV-XQIHNALSSA-N 0.000 description 1
- 235000008210 xanthophylls Nutrition 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/042—Gels
-
- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
-
- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/732—Starch; Amylose; Amylopectin; Derivatives thereof
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L3/00—Compositions of starch, amylose or amylopectin or of their derivatives or degradation products
- C08L3/02—Starch; Degradation products thereof, e.g. dextrin
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L3/00—Compositions of starch, amylose or amylopectin or of their derivatives or degradation products
- C08L3/04—Starch derivatives, e.g. crosslinked derivatives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L5/00—Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/594—Mixtures of polymers
Definitions
- the present invention relates to a solid aqueous gel, a solid composition with an aqueous continuous phase comprising such a gel and their use in the cosmetic field, in particular for making up the skin and / or mucous membranes and / or keratin fibers.
- Products in solid form are known in the cosmetic industry. As products of this type, mention may be made, for example, in the field of make-up, of sticks or “sticks” of lipstick, foundation or eye shadow; in the field of skin or lip care, lip repair pencils, depigmenting, make-up removing or moisturizing sticks or "sticks”; in the field of hygiene, deodorant sticks, sticks or foam bars for shaving or for washing the skin.
- makeup products are generally formulated on the one hand on the basis of an oily phase for reasons of comfort and softness and on the other hand on a pulverulent phase which provides the desired color.
- This pulverulent phase can comprise pigments and / or fillers and / or nacres.
- the fatty phase generally comprises waxes and / or oils and / or pasty compounds.
- the sticks formulated based on waxes have certain disadvantages: they have a fatty character which is not appreciated by the users and they lack freshness on application. In addition, it is difficult to introduce hydrophilic active agents into it.
- a makeup product in particular, that the removal of the product be carried out in an ideal manner, that is to say, allows, in a simple manner, using the finger or a sponge. or even directly on the skin of the body for example, to take not only the quantity of adequate product (not too much not to lose product unnecessarily but enough to ensure a makeup effect) but also to preserve the integrity of the product at the time of its removal: the product must not be broken by a shearing phenomenon, but the entire product must be removed with the pigments and / or pearlescent agents, and / or possibly the fillers, which ensure the function of the makeup. It is only under this condition that the application of the product can be done in a homogeneous manner and that the makeup obtained will be uniform.
- aqueous gels comprising pigments: but we often then observe a phenomenon of sedimentation during manufacture, in particular during the cooling phase.
- the Applicant has unexpectedly discovered that by combining with a hydrophilic gelling agent a compound of a particular nature, namely a starch or its derivatives, it was possible to produce solid aqueous gels optionally comprising pigments and / or nacres, these gels can be easily disintegrated with a finger or a sponge or directly on the skin of the face or body and having remarkable cosmetic qualities.
- the present invention therefore relates to a solid aqueous gel comprising i) at least one hydrophilic gelling agent and ii °) at least one starch or its derivatives.
- the gels according to the invention do not exude, even at low levels of gelling agent, and they do not necessarily require the intervention of a particular preparation technique. They give the application a feeling of great freshness while retaining good cosmetic properties, in particular of softness.
- the gels of the invention have excellent application and disintegration qualities.
- a level of disintegration higher than that of known sticks is obtained, at equivalent hardness.
- Taking the product is easy, it can be done directly on the body or with the finger or even with a sponge, taking a sufficient amount of product, easy to apply then on the skin evenly, without the need for wetting prior.
- the gel spreads easily on the skin.
- the makeup obtained is uniform and homogeneous.
- the present invention also relates to a solid composition with an aqueous continuous phase comprising a gel as defined above.
- the present invention also relates to a product for making up the skin or keratin fibers comprising a gel and / or a composition as defined above.
- the present invention also relates to a process for making up the skin and / or mucous membranes and / or keratin fibers, consisting in applying to the latter, an aqueous gel and / or a solid composition and / or a make-up product such as defined above.
- the term “gel or solid composition” means a gel or composition having a hardness defined by a maximum force before rupture ranging from 5 to 50 grams, at room temperature (20-25 ° C.), after penetration by a 2 mm diameter stainless steel mobile in the gel matrix or composition at a thickness of 1 mm at a speed of 1 mm / s and removal of said mobile from the gel matrix or composition at a speed of 2 mm / s; the maximum force before rupture being measured with a texture analyzer of the "TAXT2" type sold by the company RHEO.
- the maximum force before rupture ranges from 7 to 40 g.
- the gel according to the invention comprises a hydrophilic gelling agent.
- gelling agent is meant a compound which, in the presence of a solvent, creates more or less strong intermacromolecular bonds thus inducing a three-dimensional network which freezes said solvent.
- This hydrophilic gelling agent can be chosen from polysaccharides, protein derivatives, synthetic or semi-synthetic gels of polyester type, polyacrylates or polymethacrylates and their derivatives.
- - seaweed extracts such as agar-agar, carrageenans (iota, kappa, lambda), alginates, in particular Na or Ca;
- - gelling agents of animal origin such as protein derivatives, in particular gelatin, beef or fish, caseinates;
- the hydrophilic gelling agent is chosen from polysaccharides, and more preferably, the hydrophilic gelling agent is gellan.
- gellan gum sold under the trade name “Kelcogel F” by the company NUTRASWEET-KELCO or else iota carraghenane sold under the trade names “Seaspen PF 357” or “Viscarin SD 389 "by FMC.
- the hydrophilic gelling agent is preferably present in the gel according to the invention at a concentration of up to 20% by weight, and more preferably from 0.2 to 10%, by weight, relative to the total weight of the gel.
- the gel according to the invention also comprises a starch or one of its derivatives.
- the starches and its derivatives which can be used in the present invention are more particularly macromolecules in the form of polymers consisting of elementary units which are anhydroglucose units.
- the number of these units and their assembly make it possible to distinguish amylose (linear polymer) and amylopectin (branched polymer).
- amylose and amylopectin as well as their degree of polymerization, vary according to the botanical origin of the starches.
- the starches used in the present invention can have, as botanical origin, cereals or tubers.
- the starches are for example chosen from starches of corn, rice, cassava, potato, wheat, sorghum, peas, native (that is to say unmodified) or modified.
- modified starches mention may be made of precooked starches, hydrolyzed starches, crosslinked starches, for example with a methylol urea derivative or with octenyl succinic anhydride or also with epichlorohydrin, esterified starches, etherified starches, oxidized starches, refined starches, starches roasted in the presence of acid, or even starches grafted, for example with sodium polyacrylates, starches coated, for example with amino acids, and / or mixtures thereof.
- Starches are generally in the form of a white powder, insoluble in cold water, the size of the elementary particles of which ranges from 3 to 100 microns. This powder forms a gel when heated.
- starches and derivatives which are particularly suitable for the invention, mention may be made of:
- the starch is chosen from rice starch crosslinked with epichlorohydrin and / or corn starch.
- the starch is preferably present in the gel according to the invention at a content ranging from 0.3 to 20%, preferably from 1 to 10%, by weight, relative to the total weight of the gel.
- the gel can also comprise a pulverulent phase which can comprise fillers, mineral or synthetic, lamellar or non-lamellar, as well as pigments and / or nacres.
- a pulverulent phase which can comprise fillers, mineral or synthetic, lamellar or non-lamellar, as well as pigments and / or nacres.
- fillers it is necessary to understand colorless or white particles, mineral or synthetic, spherical or non-spherical, intended to give body or rigidity to the composition, and / or softness, mattness and uniformity makeup.
- talc As filler, mention may be made of talc, mica, silica, kaolin, powders of nylon, poly- ⁇ -alanine, polyethylene, Teflon, lauroyl-lysine, boron nitride, oxychloride of bismuth, tetrafluoroethylene polymer powders, polymethyl methacrylate powders, polyurethane powders, polystyrene powders, polyester powders, synthetic hollow microspheres, non-deformable silicone resin microbeads, zinc and titanium oxides , zirconium or cerium oxides, calcium carbonate precipitate, magnesium carbonate and hydrocarbonate, hydroxyapatite, hollow silica microspheres, glass or ceramic microcapsules, metal soaps derived from organic carboxylic acids having from 8 to 22 carbon atoms, preferably of 12 to 18 carbon atoms, such as zinc, magnesium or lithium stearate, zinc laurate, magnesium myristate, Si0 2 / TiO 2
- the fillers may be present in the composition in an amount of 0.1-60% by weight, relative to the total weight of the gel, preferably in an amount of 0.1 to 40%, more preferably 1-20%,
- pigments should be understood to mean white or colored, mineral or organic particles, insoluble in the medium, that is to say in the gel, intended to color and / or opacify the composition.
- the pigments can be present in an amount of 0-40% by weight, relative to the total weight of the gel, preferably in an amount of 0.1 to 30% and more preferably in an amount of 1-20%. They can be white or colored, mineral and / or organic, of usual size or nanometric. By nanometric size is meant pigments with an average particle size of 5 to 100 nm.
- the inorganic pigments and nanopigments there may be mentioned titanium, zirconium or cerium dioxides, as well as oxides of zinc, iron or chromium, nanotitanes, ferric blue.
- the organic pigments there may be mentioned carbon black, and the lacquers commonly used to give the lips and the skin a makeup effect, which are calcium, barium, aluminum or zirconium salts, dyes acids such as halo-acid, azo or anthraquinone dyes.
- the pigments can in particular be coated with silicone compounds such as PDMS and / or with polymers, in particular polyethylenes or also with fluorinated compounds. We can thus cite SA pigments from Maprecos or PI pigments from Myoshi.
- the nacres can be present in the gel at a rate of 0-40% by weight, preferably at a rate of 0.1 to 30% and more preferably at a rate of 1-20% by weight, relative to the total weight of the gel .
- the gels of the invention also contain a cosmetically or physiologically acceptable medium, that is to say a medium compatible with all keratin materials such as the skin, the nails, the hair, the eyelashes and eyebrows, the mucous membranes and the semi-mucous membranes, and any other skin area of the body and face.
- a cosmetically or physiologically acceptable medium that is to say a medium compatible with all keratin materials such as the skin, the nails, the hair, the eyelashes and eyebrows, the mucous membranes and the semi-mucous membranes, and any other skin area of the body and face.
- the gels according to the invention can also comprise a floral water such as blueberry water and / or a mineral water such as VITTEL water, LUCAS water or LA ROCHE POSAY water and / or a thermal water.
- a floral water such as blueberry water and / or a mineral water such as VITTEL water, LUCAS water or LA ROCHE POSAY water and / or a thermal water.
- the gels according to the invention may also comprise water-soluble dyes chosen from the usual dyes of the field under consideration such as the disodium salt of culvert, the disodium salt of alizarin green, quinoline yellow, the trisodium salt of amaranth, disodium salt of tartrazine, monosodium salt of rhodamine, disodium salt of fuchsin, xanthophyll.
- the gels according to the invention comprise up to 99.8% by weight, preferably from 20 to 99% by weight, relative to the total weight of the gel, of water.
- the gels according to the invention can also comprise solvents other than water, for example primary alcohols such as ethanol and isopropanol, glycols such as propylene glycol, butylene glycol, dipropylene glycol, diethylene glycol, glycol ethers such as alkyl (C- ⁇ -C4) mono, di- or tripropylene glycol, mono, di- or triethylene glycol ether, and mixtures thereof.
- solvents other than water for example primary alcohols such as ethanol and isopropanol, glycols such as propylene glycol, butylene glycol, dipropylene glycol, diethylene glycol, glycol ethers such as alkyl (C- ⁇ -C4) mono, di- or tripropylene glycol, mono, di- or triethylene glycol ether, and mixtures thereof.
- salts which will increase this rigidity.
- These salts can be chosen from the mono-, di- or trivalent metal salts, and more particularly the alkali and alkaline-earth metal salts and in particular the sodium, calcium or magnesium salts.
- the ions constituting these salts can be chosen, for example, from carbonates, bicarbonates, sulfates, glycerophosphates, borates, chlorides, nitrates, acetates, hydroxides, persulfates as well as the ⁇ -hydroxy acid salts ( citrates, tartrates, lactates, malates) or fruit acids, or the amino acid salts (aspartate, arginate, glycocholate, fumarate).
- the amount of salt can range from 0.01 to 2% and preferably from 0.1 to 1% of the total weight of the gel.
- the salt is chosen from calcium, magnesium or strontium nitrate, calcium or magnesium borate, calcium, sodium, magnesium, strontium, neodymium or manganese chloride, sodium sulfate. magnesium or calcium, calcium or magnesium acetate, and mixtures thereof. More preferably, the salt is chosen from magnesium chloride and sodium chloride.
- the gels of the invention can be incorporated into cosmetic compositions and constitute the continuous phase thereof.
- Such compositions can thus comprise a fatty phase which can for example comprise an oil.
- oils which can be used mention may be made of oils of animal, vegetable or mineral origin, such as paraffin oil, petroleum jelly, perhydrosqualene, apricot oil, wheat germ oil, sweet almond, calophyllum, sesame, macadamia, grape seed, rapeseed, coconut, peanut, palm, castor, avocado, jojoba, olive or cereal sprouts; esters of fatty acids and of polyol, in particular liquid triglycerides; alcohols; acetylglycerides; octanoates, decanoates or ricinoleates of alcohols or polyalcohols; fatty acid triglycerides; glycerides, fluorinated and perfluorinated oils; synthetic oils such as fatty esters; silicone oils such as volatile silicone oils, polymethylsi
- the fatty phase of the compositions according to the invention can also comprise other fatty substances, which can be chosen by a person skilled in the art on the basis of his general knowledge, so as to confer on the final composition the desired properties, for example in consistency, texture and / or transfer.
- additional fatty substances can be waxes, gums and / or pasty fatty substances of animal, vegetable, mineral or synthetic origin, as well as their mixtures.
- waxes such as microcrystalline waxes, paraffin, petrolatum, petrolatum, Pozokerite, montan wax; beeswax, lanolin and its derivatives; Candellila, Ouricury, Carnauba and Japanese waxes, cocoa butter, cork fiber or sugar cane waxes; hydrogenated oils concrete at 25 ° C, ozokerites, fatty esters and glycerides concrete at 25 ° C; the waxes of polyethylene and the waxes obtained by Fischer-Tropsch synthesis; concrete hydrogenated oils at 25 ° C; lanolines; concrete fatty esters at 25 ° C; silicone waxes; fluorinated waxes; their mixtures.
- microcrystalline waxes paraffin, petrolatum, petrolatum, Pozokerite, montan wax
- beeswax lanolin and its derivatives
- Candellila Ouricury, Carnauba and Japanese waxes, cocoa butter, cork fiber or sugar cane waxes
- the fatty phase can be present in proportions ranging, for example, up to 30%, preferably from 0.1 to 20% and better still from 0.5 to 10% of the total weight of the composition, these proportions varying according to selected application.
- Oils or waxes can be introduced into the aqueous phase in the presence of one or more surfactants to ensure better dispersion.
- compositions according to the invention can therefore also contain one or more O / W surfactants or ionic or nonionic cosurfactants, of HLB (hydrophilic-lipophilic balance) greater than or equal to 8, usually used in the cosmetic field.
- HLB hydrophilic-lipophilic balance
- the amount of surfactant or cosurfactant preferably ranges from 0.05 to 8% of the total weight of the composition.
- composition can also comprise any additional compound usually used in the cosmetic field.
- complementary compounds can be chosen from antioxidants, essential oils, preservatives, cosmetic or pharmaceutical active ingredients that are lipophilic or hydrophilic, moisturizers, vitamins, essential fatty acids, sphingolipids, self-tanning compounds such as DHA, sun filters, perfumes, and mixtures thereof.
- the gels and the compositions with an aqueous continuous phase according to the invention can be prepared according to the conventional methods for preparing the sticks, these methods being well known to those skilled in the art.
- the gels and compositions according to the invention may constitute make-up or care products for the skin, in particular the body, the face and / or the scalp, or keratin fibers, in particular the hair, nails, eyelashes and / or eyebrows, or also mucous membranes, in particular the lips. They can thus constitute body makeup products, foundations, eyeshadows, blushes, concealers, lipsticks, lip contour pencils, mascaras, contour pencils eyes, sticks for dyeing or making up locks of hair.
- the amounts are given as a percentage by weight relative to the total weight of the composition.
- a gellan gel is formed in water while heating at 80 ° for 15 min. Then incorporate the starch at 70 ° C for 20 min, then the salt. We wait 10 min then add the pigments. After 10 min, the triethanolamine is incorporated. After 5 min, it is poured hot.
- the hardness of this gel is 30 ⁇ 1.5 g.
- This gel was prepared according to the same method of preparation as in Example 1.
- the hardness of this gel is 17.4 ⁇ 2 g.
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- Health & Medical Sciences (AREA)
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- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Polymers & Plastics (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dispersion Chemistry (AREA)
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Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP00951580A EP1112320A1 (en) | 1999-06-18 | 2000-06-13 | Solid aqueous gel comprising a hydrophilic gelling agent and starch, composition comprising same and uses |
KR1020017002061A KR20010072740A (en) | 1999-06-18 | 2000-06-13 | Solid aqueous gel comprising a hydrophilic gelling agent and starch, composition comprising same and uses |
MXPA01001680A MXPA01001680A (en) | 1999-06-18 | 2000-06-13 | Solid aqueous gel comprising a hydrophilic gelling agent and starch, composition comprising same and uses. |
BR0006824-1A BR0006824A (en) | 1999-06-18 | 2000-06-13 | Solid aqueous gel comprising a hydrophilic and starch gelling agent, solid composition of continuous aqueous phase, products for the make-up of the skin or keratin fibers and their make-up process |
JP2001505611A JP2003503316A (en) | 1999-06-18 | 2000-06-13 | Solid aqueous gel containing hydrophilic gelling agent and starch, composition containing the same and use thereof |
AU64475/00A AU6447500A (en) | 1999-06-18 | 2000-06-13 | Solid aqueous gel comprising a hydrophilic gelling agent and starch, compositioncomprising same and uses |
CA002340025A CA2340025A1 (en) | 1999-06-18 | 2000-06-13 | Solid aqueous gel comprising a hydrophilic gelling agent and starch, composition comprising same and uses |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR99/07770 | 1999-06-18 | ||
FR9907770A FR2795081A1 (en) | 1999-06-18 | 1999-06-18 | Solid aqueous gel for use in make-up products for skin, mucous membranes and keratin fibers, comprises hydrophilic gelling agent and at least starch or its derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000078857A1 true WO2000078857A1 (en) | 2000-12-28 |
Family
ID=9546998
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR2000/001632 WO2000078857A1 (en) | 1999-06-18 | 2000-06-13 | Solid aqueous gel comprising a hydrophilic gelling agent and starch, composition comprising same and uses |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP1112320A1 (en) |
JP (1) | JP2003503316A (en) |
KR (1) | KR20010072740A (en) |
AU (1) | AU6447500A (en) |
BR (1) | BR0006824A (en) |
CA (1) | CA2340025A1 (en) |
FR (1) | FR2795081A1 (en) |
MX (1) | MXPA01001680A (en) |
WO (1) | WO2000078857A1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10237459A1 (en) * | 2002-08-16 | 2004-02-26 | Beiersdorf Ag | Cosmetic preparation containing active ingredients |
US8754136B2 (en) | 2005-05-19 | 2014-06-17 | Aqua Bio Technology Asa | Gelatin-containing topical composition |
CN104829874A (en) * | 2015-05-21 | 2015-08-12 | 浙江海洋学院 | Application of gelatin-ZnO nano composite film |
KR101965607B1 (en) | 2018-08-27 | 2019-04-04 | (주)씨앤케이코스메디칼 | External force-disintegrable solid cleanser comprising discontinous phase hydrogel and adhesive starch as binder and method for preparing the same |
US10273424B2 (en) | 2012-03-09 | 2019-04-30 | B.C.B. International Limited | Alcohol-containing compositions useful as solid fuels and processes for their manufacture |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20040004973A (en) * | 2002-07-08 | 2004-01-16 | 용인송담대학 | Hair styling gel and method of manufacturing the same |
WO2006112690A1 (en) * | 2005-04-22 | 2006-10-26 | R & H Minerals B.V. | Mineral salt gel compositions |
FR2932488B1 (en) * | 2008-06-13 | 2012-10-26 | Roquette Freres | CIPO - Patent - 2581626 Canadian Intellectual Property Office Symbol of the Government of Canada CA 2461392 STARCH - BASED THERMOPLASTIC OR ELASTOMERIC COMPOSITIONS AND PROCESS FOR THE PREPARATION OF SUCH COMPOSITIONS. |
JP2009155332A (en) * | 2009-01-09 | 2009-07-16 | Fancl Corp | Sunscreen cosmetic |
KR101282572B1 (en) * | 2011-01-14 | 2013-07-04 | 한국콜마주식회사 | Cosmetic Composition for eye makeup |
JP5734686B2 (en) * | 2011-02-03 | 2015-06-17 | ロート製薬株式会社 | Skin external composition |
JP6509791B2 (en) * | 2015-09-25 | 2019-05-08 | 積水化成品工業株式会社 | Hydrogel and method for producing the same |
KR101997440B1 (en) * | 2017-10-27 | 2019-07-08 | 코스맥스 주식회사 | Powder cosmetic composition comprising starch |
FR3091172B1 (en) * | 2018-12-31 | 2021-12-10 | Lvmh Rech | Solid cosmetic composition consisting of a solid aqueous continuous phase |
FR3094226B1 (en) | 2019-03-29 | 2021-11-26 | Chanel Parfums Beaute | Long-lasting cosmetic composition |
FR3094222B1 (en) | 2019-03-29 | 2021-09-10 | Chanel Parfums Beaute | Long-lasting cosmetic composition |
WO2021060079A1 (en) | 2019-09-27 | 2021-04-01 | 株式会社 資生堂 | Cosmetic |
KR102334447B1 (en) * | 2019-10-29 | 2021-12-03 | 코스맥스 주식회사 | Non-press type solid cosmetic composition comprising polyethylene terephthalate based pearl powder |
Citations (3)
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EP0291228A1 (en) * | 1987-05-14 | 1988-11-17 | Merck & Co. Inc. | Gellan gum/starch blends |
EP0342738A2 (en) * | 1988-05-16 | 1989-11-23 | Merck & Co. Inc. | Blends of high acyl gellan gum with starch |
JPH1192333A (en) * | 1997-09-17 | 1999-04-06 | Kose Corp | Oil-in-water type solid cosmetic |
-
1999
- 1999-06-18 FR FR9907770A patent/FR2795081A1/en not_active Withdrawn
-
2000
- 2000-06-13 MX MXPA01001680A patent/MXPA01001680A/en unknown
- 2000-06-13 AU AU64475/00A patent/AU6447500A/en not_active Abandoned
- 2000-06-13 BR BR0006824-1A patent/BR0006824A/en not_active IP Right Cessation
- 2000-06-13 JP JP2001505611A patent/JP2003503316A/en active Pending
- 2000-06-13 WO PCT/FR2000/001632 patent/WO2000078857A1/en not_active Application Discontinuation
- 2000-06-13 KR KR1020017002061A patent/KR20010072740A/en not_active Application Discontinuation
- 2000-06-13 CA CA002340025A patent/CA2340025A1/en not_active Abandoned
- 2000-06-13 EP EP00951580A patent/EP1112320A1/en not_active Withdrawn
Patent Citations (3)
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EP0291228A1 (en) * | 1987-05-14 | 1988-11-17 | Merck & Co. Inc. | Gellan gum/starch blends |
EP0342738A2 (en) * | 1988-05-16 | 1989-11-23 | Merck & Co. Inc. | Blends of high acyl gellan gum with starch |
JPH1192333A (en) * | 1997-09-17 | 1999-04-06 | Kose Corp | Oil-in-water type solid cosmetic |
Non-Patent Citations (2)
Title |
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GRAHAM SWORN ET AL.: "Effect of conformation and molecular weight of co-solute on the mechanical properties of gellan gum gels", FOOD HYDROCOLLOIDS, vol. 12, 1998, pages 283 - 290, XP000884240 * |
PATENT ABSTRACTS OF JAPAN vol. 1999, no. 09 30 July 1999 (1999-07-30) * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10237459A1 (en) * | 2002-08-16 | 2004-02-26 | Beiersdorf Ag | Cosmetic preparation containing active ingredients |
US8754136B2 (en) | 2005-05-19 | 2014-06-17 | Aqua Bio Technology Asa | Gelatin-containing topical composition |
US10273424B2 (en) | 2012-03-09 | 2019-04-30 | B.C.B. International Limited | Alcohol-containing compositions useful as solid fuels and processes for their manufacture |
CN104829874A (en) * | 2015-05-21 | 2015-08-12 | 浙江海洋学院 | Application of gelatin-ZnO nano composite film |
KR101965607B1 (en) | 2018-08-27 | 2019-04-04 | (주)씨앤케이코스메디칼 | External force-disintegrable solid cleanser comprising discontinous phase hydrogel and adhesive starch as binder and method for preparing the same |
Also Published As
Publication number | Publication date |
---|---|
MXPA01001680A (en) | 2002-04-08 |
KR20010072740A (en) | 2001-07-31 |
BR0006824A (en) | 2001-06-05 |
CA2340025A1 (en) | 2000-12-28 |
FR2795081A1 (en) | 2000-12-22 |
JP2003503316A (en) | 2003-01-28 |
EP1112320A1 (en) | 2001-07-04 |
AU6447500A (en) | 2001-01-09 |
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