JP5411146B2 - 皮膚に触れた時に毒性がないピペリジン官能基含有ポリオルガノシロキサン、及び化粧品組成物中におけるそれらの使用 - Google Patents
皮膚に触れた時に毒性がないピペリジン官能基含有ポリオルガノシロキサン、及び化粧品組成物中におけるそれらの使用 Download PDFInfo
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- JP5411146B2 JP5411146B2 JP2010528367A JP2010528367A JP5411146B2 JP 5411146 B2 JP5411146 B2 JP 5411146B2 JP 2010528367 A JP2010528367 A JP 2010528367A JP 2010528367 A JP2010528367 A JP 2010528367A JP 5411146 B2 JP5411146 B2 JP 5411146B2
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- 239000004664 distearyldimethylammonium chloride (DHTDMAC) Substances 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 125000005022 dithioester group Chemical group 0.000 description 1
- WSDISUOETYTPRL-UHFFFAOYSA-N dmdm hydantoin Chemical compound CC1(C)N(CO)C(=O)N(CO)C1=O WSDISUOETYTPRL-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 1
- HUVYTMDMDZRHBN-UHFFFAOYSA-N drometrizole trisiloxane Chemical compound C[Si](C)(C)O[Si](C)(O[Si](C)(C)C)CC(C)CC1=CC(C)=CC(N2N=C3C=CC=CC3=N2)=C1O HUVYTMDMDZRHBN-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 231100000321 erythema Toxicity 0.000 description 1
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 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
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 235000021021 grapes Nutrition 0.000 description 1
- 230000037308 hair color Effects 0.000 description 1
- 239000013529 heat transfer fluid Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 1
- 229960003258 hexylresorcinol Drugs 0.000 description 1
- 229960004881 homosalate Drugs 0.000 description 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000006459 hydrosilylation reaction Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 206010021198 ichthyosis Diseases 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229940117955 isoamyl acetate Drugs 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229940094506 lauryl betaine Drugs 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- 210000000088 lip Anatomy 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- SOXAGEOHPCXXIO-UHFFFAOYSA-N meradimate Chemical compound CC(C)C1CCC(C)CC1OC(=O)C1=CC=CC=C1N SOXAGEOHPCXXIO-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 229940049292 n-(3-(dimethylamino)propyl)octadecanamide Drugs 0.000 description 1
- WWVIUVHFPSALDO-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCCN(C)C WWVIUVHFPSALDO-UHFFFAOYSA-N 0.000 description 1
- DVEKCXOJTLDBFE-UHFFFAOYSA-N n-dodecyl-n,n-dimethylglycinate Chemical compound CCCCCCCCCCCC[N+](C)(C)CC([O-])=O DVEKCXOJTLDBFE-UHFFFAOYSA-N 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- VVGIYYKRAMHVLU-UHFFFAOYSA-N newbouldiamide Natural products CCCCCCCCCCCCCCCCCCCC(O)C(O)C(O)C(CO)NC(=O)CCCCCCCCCCCCCCCCC VVGIYYKRAMHVLU-UHFFFAOYSA-N 0.000 description 1
- 239000001005 nitro dye Substances 0.000 description 1
- 239000000346 nonvolatile oil Substances 0.000 description 1
- 239000001702 nutmeg Substances 0.000 description 1
- JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 description 1
- 229960001679 octinoxate Drugs 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000005375 organosiloxane group Chemical group 0.000 description 1
- 239000008385 outer phase Substances 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 229940055726 pantothenic acid Drugs 0.000 description 1
- 235000019161 pantothenic acid Nutrition 0.000 description 1
- 239000011713 pantothenic acid Substances 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 238000003921 particle size analysis Methods 0.000 description 1
- 229940083254 peripheral vasodilators imidazoline derivative Drugs 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- 230000002688 persistence Effects 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
- 229960003742 phenol Drugs 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 235000021018 plums Nutrition 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920002553 poly(2-methacrylolyloxyethyltrimethylammonium chloride) polymer Polymers 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 150000003139 primary aliphatic amines Chemical class 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 235000021013 raspberries Nutrition 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- ZZPKZRHERLGEKA-UHFFFAOYSA-N resorcinol monoacetate Chemical compound CC(=O)OC1=CC=CC(O)=C1 ZZPKZRHERLGEKA-UHFFFAOYSA-N 0.000 description 1
- 229960002477 riboflavin Drugs 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 150000003902 salicylic acid esters Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 208000008742 seborrheic dermatitis Diseases 0.000 description 1
- 150000005619 secondary aliphatic amines Chemical class 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 230000037307 sensitive skin Effects 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 231100000430 skin reaction Toxicity 0.000 description 1
- 231100000051 skin sensitiser Toxicity 0.000 description 1
- 238000009751 slip forming Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 210000000434 stratum corneum Anatomy 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- CXVGEDCSTKKODG-UHFFFAOYSA-N sulisobenzone Chemical compound C1=C(S(O)(=O)=O)C(OC)=CC(O)=C1C(=O)C1=CC=CC=C1 CXVGEDCSTKKODG-UHFFFAOYSA-N 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000000213 tara gum Substances 0.000 description 1
- 235000010491 tara gum Nutrition 0.000 description 1
- 208000009056 telangiectasis Diseases 0.000 description 1
- 150000003503 terephthalic acid derivatives Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 125000005207 tetraalkylammonium group Chemical group 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- 239000001585 thymus vulgaris Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 235000019164 vitamin B2 Nutrition 0.000 description 1
- 239000011716 vitamin B2 Substances 0.000 description 1
- 150000003700 vitamin C derivatives Chemical class 0.000 description 1
- 235000019166 vitamin D Nutrition 0.000 description 1
- 239000011710 vitamin D Substances 0.000 description 1
- 150000003710 vitamin D derivatives Chemical class 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
- 229940045997 vitamin a Drugs 0.000 description 1
- 229940046008 vitamin d Drugs 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000012991 xanthate Substances 0.000 description 1
- 229940043810 zinc pyrithione Drugs 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical class [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
-
- 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
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/896—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
- A61K8/898—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing nitrogen, e.g. amodimethicone, trimethyl silyl amodimethicone or dimethicone propyl PG-betaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/32—Post-polymerisation treatment
- C08G77/34—Purification
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
- C08G77/388—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing nitrogen
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Dermatology (AREA)
- General Chemical & Material Sciences (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Silicon Polymers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
・ラウリルエーテルサルフェート等のアニオン性界面活性剤 3.75〜15重量%、
・アルキルアミドベタイン等の両性界面活性剤 1〜4.20重量%、
・ポリオキシエチレン化ソルビタン等のノニオン性界面活性剤 0.7〜3重量%、及び
・脂肪酸、アルキルイセチオネート、アルキルタウリド及びアルキルサルコシドから選択される「石鹸」 0.1〜4重量%
を含む。
・洗剤用界面活性剤 5〜50重量%、
・ふけ防止剤 0.1〜4重量%、
・脂肪酸エステル 0.1〜50重量%、
・ポリオキシエチレン化ソルビタン、及び
・水 少なくとも20重量%
を含む。
・ノニオン性界面活性剤、両性界面活性剤及びアニオン性界面活性剤を含む界面活性剤混合物 5〜20重量%、並びに
・特にカチオン性ポリオール等の保湿剤 0.01〜3重量%
を含む。
(a)式(I)の基:
●基R5は同一であっても異なっていてもよく、1〜3個の炭素原子を有する直鎖状又は分枝鎖状アルキル基及びフェニル基から選択され;基R6は水素基、基R5又はO*原子を表わし;
●R4は以下のもの:
・2〜18個の炭素原子を有する直鎖状又は分枝鎖状アルキレン基;
・アルキレン部分が直鎖状又は分岐鎖状であって2〜20個の炭素原子を有するアルキレン−カルボニル基;
・アルキレン部分が直鎖状又は分岐鎖状であって2〜12個の炭素原子を有し且つシクロヘキシレン部分がOH基及び随意としての1〜4個の炭素原子を有する1又は2個のアルキル基を有するアルキレン−シクロヘキシレン基;
・式R7−O−R7の基(ここで、基R7は同一であっても異なっていてもよく、1〜12個の炭素原子を有するアルキレン基を表わす);
・式R7−O−R7の基(ここで、基R7は上記の意味を持ち、但し、それらの一方又は両方が1又は2個の−OH基で置換されているものとする);
・式R7−COO−R7の基(ここで、基R7は上記の意味を持つ);及び
・式R8−O−R9−O−CO−R8の基(ここで、基R8及びR9は同一であっても異なっていてもよく、2〜12個の炭素原子を有するアルキレン基を表わし、基R9は随意にヒドロキシル基で置換されていてもよい):
より成る群から選択される二価炭化水素基であり;そして
●Uは−O−又は−N(R10)−を表わし、ここで、R10は水素原子、1〜6個の炭素原子を有する直鎖状又は分枝鎖状アルキル基及び次式(II)の二価基:
R11は1〜12個の炭素原子を有する直鎖状又は分枝鎖状二価アルキレン基を表わし、
該二価基(II)の原子価結合の内の一方(R11についてのもの)は−NR10−の原子に結合し、もう一方(R12についてのもの)はケイ素原子に結合し;
基R13は同一であっても異なっていてもよく、1〜3個の炭素原子を有する直鎖状又は分枝鎖状アルキル基及びフェニル基から選択され;そして
基R14は水素基、基R13又はO*原子を表わす}
より成る群から選択される基である];
(b)式(III)の基:
●R'4は
・次式(IV)の三価基:
・式(VI)の三価基:
より成る群から選択され;
●U'は−O−又は−N(R12)−を表わし、ここで、R12は水素原子及び1〜6個の炭素原子を有する直鎖状又は分岐鎖状アルキル基より成る群から選択される基であり;そして
●R5及びR6は式(I)の場合に与えたものと同じ意味を持つ]
より成る群から選択され、そして、
該ポリオルガノシロキサンAは、調製後に、分子量Mが1000ダルトン未満であるモノマー、オリゴマー及びポリマーの選択的分離を可能にする技術によって、分子量Mが1000ダルトン未満であるモノマー、オリゴマー及びポリマーの割合が全分子分布に対して1%未満の値まで減らされたことを特徴とする。
1.ポリジメチルシロキサン、好ましくは環状ポリジメチルシロキサン、ヘキサメチルジシロキサン、及びケイ素原子に結合した官能基Vを含む環状ポリメチルシロキサンを接触させる;
2.加熱し、塩基性触媒(例えば強塩基)を導入し、そして反応させる;そして
3.(例えば弱酸を用いて)中和し、次いで標準的な脱蔵を行い、冷却し、取り出すことによって、官能基Vを含むポリオルガノシロキサンを単離する。
(1)記号Zは同一であっても異なっていてもよく、R15又は官能基Vを表わし;
(2)記号R15、R16及びR17は同一であっても異なっていてもよく、それぞれ、随意に置換された直鎖状又は分岐鎖状C1〜C12アルキル基、随意に置換されたC5〜C10シクロアルキル基、随意に置換されたC6〜C18アリール基、随意に置換されたアラルキル基又は基−OR18(ここで、R18は水素、1〜15個の炭素原子を有する直鎖状、分岐鎖状若しくは環状アルキル基又はエポキシド及び/若しくはポリエーテル官能基を含む炭化水素基を表わす)を表わし;
(3)官能基Vは上記のものと同じ定義(=1個以上の立体障害ピペリジニル官能基を有する基)を有し;そして
(4)官能基Vを持たないシロキシル単位の数は1〜800の範囲であり、官能基Vを持つシロキシル単位の数は1〜50の範囲であり、そしてwは0<w<50、yは8<y<798である。}
・各種単位は鎖中でランダムに分布され;
・pは0以上、好ましくは1〜2000の範囲の数を表わし;
・rは0以上、好ましくは1〜2000の範囲の数を表わし;
・qは1以上、好ましくは1〜50の範囲の数を表わし;
・R10は1〜18個の炭素原子を有する直鎖状又は分枝鎖状アルキル基を表わし;
・基Uは上記のU'と同じ意味を持ち、R11は上記のR'4と同じ意味を持ち、そしてR12は上記のR6と同じ意味を持つ。)
・アルキルエステルスルホネート、例えば式R−CH(SO3M)−CH2COOR'のもの、又はアルキルエステルサルフェート、例えば式R−CH(OSO3M)−CH2COOR'のもの
(ここで、RはC8〜C20アルキル基、好ましくはC10〜C16アルキル基を表わし、
R'はC1〜C6アルキル基、好ましくはC1〜C3アルキル基を表わし、
Mはアルカリ若しくはアルカリ土類カチオン、例えばナトリウム、又はアンモニウムカチオンを表わす)
(全く特定的には、基RがC14〜C16であるメチルエステルスルホネートを挙げることができる);
・アルキルベンゼンスルホネート(より特定的にはC9〜C20のもの)、第1又は第2アルキルスルホネート(特にC8〜C22のもの)、アルキルグリセロールスルホネート;
・アルキルサルフェート、例えば式ROSO3Mのもの
(ここで、RはC10〜C24、好ましくはC12〜C20のアルキル又はヒドロキシアルキル基を表わし;
Mは上記と同じ定義のカチオンを表わす);
・アルキルエーテルサルフェート、例えば式RO(OA)nSO3Mのもの
(ここで、RはC10〜C24、好ましくはC12〜C20アルキル又はヒドロキシアルキル基を表わし;
OAはエトキシ化及び/又はプロポキシ化基を表わし;
Mは上記と同じ定義のカチオンを表わし;
nは一般的に1〜4の範囲で変化する)
(例えばn=2のラウリルエーテルサルフェート);
・アルキルアミドサルフェート、例えば式RCONHR'OSO3Mのもの
(ここで、RはC2〜C22、好ましくはC6〜C20アルキル基を表わし、
R'はC2〜C3アルキル基を表わし、
Mは上記と同じ定義のカチオンを表わす)
並びにそれらのポリアルコキシル化(エトキシ化及び/又はプロポキシ化)誘導体(アルキルアミドエーテルサルフェート);
・飽和又は不飽和脂肪酸の塩、例えばC8〜C24、好ましくはC14〜C20のものとアルカリ土類カチオンとの塩、N−アシル−N−アルキルタウレート、アルキルイセチオネート、アルキルスクシナメート及びアルキルスルホスクシネート、スルホスクシネートのモノエステル又はジエステル、N−アシルサルコシネート、及びポリエトキシカルボキシレート;
・ホスフェートモノエステル及びジエステル、例えば式(RO)x−P(=O)(OM)xのもの
{ここで、Rはアルキル、アルカリール、アラルキル又はアリール基(これらの基は随意にポリアルコキシル化されていてよい)を表わし、
x及びx'は1又は2であり、但し、xとx'との合計は3であり、そして
Mはアルカリ土類カチオンを表わす}。
・アルコキシル化脂肪族アルコール
・アルコキシル化トリグリセリド
・アルコキシル化脂肪酸
・アルコキシル化ソルビタンエステル
・アルコキシル化脂肪族アミン
・アルコキシル化ジ−(1−フェニルエチル)フェノール
・アルコキシル化トリ−(1−フェニルエチル)フェノール
・アルコキシル化アルキルフェノール
・エチレンオキシドと、プロピレンオキシドとプロピレングリコールとの縮合から得られる疎水性化合物との縮合から得られる生成物、例えばBASF社より販売されているPluronic類;
・エチレンオキシドの縮合から得られる生成物、プロピレンオキシドとエチレンジアミンとの縮合から得られる化合物、例えばBASF社より販売されているTetronic類;
・アルキルポリグリコシド、例えば米国特許第4565647号明細書に記載されたもの;
・(例えばC8〜C20の)脂肪酸のアミド。
・一般的にベタイン類、特に例えばラウリルベタイン(Rhodia社からのMirataine BB)又はオクチルベタインのカルボキシベタイン類;アミドアルキルベタイン類、例えばコカミドプロピルベタイン(CAPB)(Rhodia Chimie社からのMirataine BDJ);
・スルホベタイン類又はサルタイン類、例えばコカミドプロピルヒドロキシサルタイン(Rhodia社からのMirataine CBS);
・アルキルアンフォアセテート及びアルキルアンフォジアセテート、例えばココ又はラウリル鎖を含むもの(特にRhodia社からのMiranol C2M、C32、L32);
・アルキルアンフォプロピオネート又はアルキルアンフォジプロピオネート(Miranol C2M SF);
・アルキルアンフォヒドロキシプロピルサルタイン(Miranol CS)。
・架橋ポリアクリレート、例えばBF Goodrich社若しくはNoveon社から販売されているCARBOPOL若しくはCARBOMERタイプ、RITA社より販売されているACRITAMERタイプ又はGoldschmidt社より販売されているTEGO CARBOMERタイプのポリマー。これらの化合物は組成物に対して典型的には0.1〜3重量%、好ましくは0.3〜2重量%の量で存在させることができる。
・アクリレート/アミノアクリレート/イタコネートのコポリマー、National Starch社よりSTRUCTURE PLUSの商品名で販売されているC10〜C30アルキルPEG 20。これらの化合物は、組成物に対して典型的には0.1〜3重量%、好ましくは0.3〜2重量%の量で存在させることができる。
・組成物中で網状構造を形成する不溶性固体。これらはエチレングリコールの脂肪酸モノ−及び/又はジエステルであることができ、この脂肪酸はC16〜C18のものであるのが好ましい。これは特にエチレングリコールジステアレート(EGDS)、例えばRhodia社よりMIRASHEENの商品名で他の成分を含む濃厚物として販売されているものであることができる。この化合物は、組成物に対して典型的には3〜10重量%、好ましくは5〜8重量%の量で存在させることができる。
・多糖類から誘導されたカチオン性ポリマー、例えばセルロースのカチオン性誘導体、澱粉のカチオン性誘導体、グアールのカチオン性誘導体、カロブのカチオン性誘導体、
・合成カチオン性ポリマー、
・これらの物質の混合物又は組合せ物。
・グアールヒドロキシプロピルトリモニウムクロリド(RHODIA社より販売されているJaguar C13S、Jaguar C14S、Jaguar C17、Jaguar Excel、Jaguar C 2000)、
・ヒドロキシプロピルグアールヒドロキシプロピルトリモニウムクロリド(RHODIA社より販売されているJaguar C162)、
・セルロースポリ(オキシ−1,2−エタンジイル)−2−ヒドロキシ−3−トリメチルアンモニウム−プロピルエーテルクロリド又はポリクオタニウム−10。
・化粧品許容媒体中若しくは化粧品許容媒体を含む混合物中の本発明に従うポリオルガノシロキサンAの溶液;
・化粧品許容媒体中の本発明に従うポリオルガノシロキサンAを含む液滴の安定エマルション;又は
・化粧品許容媒体を含む少なくとも1つの層と本発明に従うポリオルガノシロキサンAを含む層とに分かれた相の組合せであって、ユーザーが撹拌した後に化粧品許容媒体中の本発明に従うポリオルガノシロキサンAを含む液滴の分散体を形成することができるもの。
・非イオン性界面活性剤、
・非イオン性両親媒性ポリマー(随意に1種以上のアニオン性界面活性剤と組み合わされたもの)及び/若しくはアニオン性両親媒性ポリマー、
・特殊界面活性剤(随意に共界面活性剤と組み合わされたもの)、又は
・保護コロイド。
・アルコキシル化脂肪族アルコール
・アルコキシル化トリグリセリド
・アルコキシル化脂肪酸
・アルコキシル化ソルビタンエステル
・アルコキシル化脂肪族アミン
・アルコキシル化ジ−(1−フェニルエチル)フェノール
・アルコキシル化トリ−(1−フェニルエチル)フェノール、及び
・アルコキシル化アルキルフェノール
ここで、アルコキシ(より特定的にはオキシエチレン及び/又はオキシプロピレン)単位の数は、HLB値が10以上になるような数とする。
・少なくとも1種のアニオン性及び/又は両性界面活性剤(単独で又は混合物として)、
・随意としての少なくとも1種の安定剤及び/若しくはコンディショニング剤及び/若しくはコンディショニング助剤、又はそれらの混合物、
・随意としての別のポリオルガノシロキサン、
・これらの成分の混合物。
かかる成分は、上に記載したものである。
・組成物を適用する前又は間に行われる着色(カラリング)の定着、
・髪、特に傷んだ髪及び/又は末端のコンディショニング、
・皮膚のコンディショニング、
・髪及び/又は皮膚のコンディショニングの調整(穏やかなコンディショニング又は重大なコンディショニング)、
・ポリオルガノシロキサン中に存在する窒素の割合に関連する髪及び/又は皮膚のコンディショニングの調整、
・柔らかさ、しなやかさ、髪梳かし(もつれほぐし)、光沢、乾いた髪又は濡れた髪の整髪しやすさのような頭髪化粧効果、
・黄ばみがないこと、
・太陽光線関連の傷み、太陽光線やその他の外的条件によって引き起こされる変色、又は摩耗からの回復、
・組成物中に含まれる化合物の保護及び/又は非分解性、
・皮膚及び/又は髪に適用される活性物質の耐久性。
・時間が経つにつれて色が薄くなる(退色)のを防止し、
・経時着色永続性を促進し、
・色の抽出を減少させ、且つ/又は
・酸化に関して髪を回復する
ことができる。
・オイル2:α,ω−ビス(トリメチルシリル)−ポリ[ジメチル,メチル[3−(2,2,6,6−テトラメチルピペリジン−4−イルオキシ)プロピル]シロキサン(Bluestar Silicones France社より提供されるRhodorsil(登録商標)21650オイル)−粘度:90000mPa・s。
Claims (13)
- 化粧品用途上許容できる媒体中に少なくとも1種のポリオルガノシロキサンAを含み、皮膚に触れた時に毒性がない化粧品/皮膚科用組成物であって、
前記ポリオルガノシロキサンAが、立体障害ピペリジニル官能基を少なくとも1個含む官能基V少なくとも1個で置換されたシロキシル単位を1分子当たりに少なくとも1個含有し、且つ、該ポリオルガノシロキサンAが、その調製後に、分子量Mが1000ダルトン未満であるモノマー、オリゴマー及びポリマーの選択的分離を可能にする技術によって、分子量Mが1000ダルトン未満であるモノマー、オリゴマー及びポリマーの割合を全分子分布に対して1%未満の値に減少させたものであることを特徴とする、前記の皮膚に触れた時に毒性がない化粧品/皮膚科用組成物。 - 分子量Mが1000ダルトン未満であるモノマー、オリゴマー及びポリマーの割合の減少を、分子量Mが1000ダルトン未満であるものの割合が全分子分布の1%未満となるまでの3〜20ミリバールの範囲の減圧下で100〜210℃の範囲の温度における強脱蔵によって実施したことを特徴とする、請求項1に記載の皮膚に触れた時に毒性がない化粧品/皮膚科用組成物。
- 分子量Mが1000ダルトン未満であるモノマー、オリゴマー及びポリマーの割合の減少を、バッチ式反応器、流下薄膜式蒸発器、スクレープ薄膜式蒸発器、遠心分離蒸発器又は連続フラッシュ蒸発器によって実施したことを特徴とする、請求項1又は2に記載の皮膚に触れた時に毒性がない化粧品/皮膚科用組成物。
- 化粧品用途上許容できる媒体中に少なくとも1種のポリオルガノシロキサンAを含み、皮膚に触れた時に毒性がない化粧品/皮膚科用組成物であって、
前記ポリオルガノシロキサンAが、ケイ素原子に直接結合した官能基V少なくとも1個で置換されたシロキシル単位を1分子当たりに少なくとも1個含有し、
前記官能基Vが、立体障害ピペリジニル官能基を1個以上有する基であり、次の(a)及び(b):
(a)式(I)の基:
●基R 5 は同一であっても異なっていてもよく、1〜3個の炭素原子を有する直鎖状又は分枝鎖状アルキル基及びフェニル基から選択され;基R 6 は水素基又は基R 5 を表わし;
●R 4 は以下のもの:
・2〜18個の炭素原子を有する直鎖状又は分枝鎖状アルキレン基;
・アルキレン部分が直鎖状又は分岐鎖状であって2〜20個の炭素原子を有するアルキレン−カルボニル基;
・アルキレン部分が直鎖状又は分岐鎖状であって2〜12個の炭素原子を有し且つシクロヘキシレン部分がOH基及び随意としての1〜4個の炭素原子を有する1又は2個のアルキル基を有するアルキレン−シクロヘキシレン基;
・式R 7 −O−R 7 の基(ここで、基R 7 は同一であっても異なっていてもよく、1〜12個の炭素原子を有するアルキレン基を表わす);
・式R 7 −O−R 7 の基(ここで、基R 7 は上記の意味を持ち、但し、それらの一方又は両方が1又は2個の−OH基で置換されているものとする);
・式R 7 −COO−R 7 の基(ここで、基R 7 は上記の意味を持つ);及び
・式R 8 −O−R 9 −O−CO−R 8 の基(ここで、基R 8 及びR 9 は同一であっても異なっていてもよく、2〜12個の炭素原子を有するアルキレン基を表わし、基R 9 は随意にヒドロキシル基で置換されていてもよい):
より成る群から選択される二価基であり;そして
●Uは−O−又は−N(R 10 )−を表わし、ここで、R 10 は水素原子、1〜6個の炭素原子を有する直鎖状又は分枝鎖状アルキル基及び次式(II)の二価基:
R 11 は1〜12個の炭素原子を有する直鎖状又は分枝鎖状二価アルキレン基を表わし、
該二価基(II)の原子価結合の内の一方(R 11 についてのもの)は−NR 10 −の原子に結合し、もう一方(R 12 についてのもの)はケイ素原子に結合し;
基R 13 は同一であっても異なっていてもよく、1〜3個の炭素原子を有する直鎖状又は分枝鎖状アルキル基及びフェニル基から選択され;そして
基R 14 は水素基又は基R 13 を表わす}
より成る群から選択される基である];
(b)式(III)の基:
●R' 4 は
・次式(IV)の三価基:
・式(VI)の三価基:
より成る群から選択され;
●U'は−O−又は−N(R 12 )−を表わし、ここで、R 12 は水素原子及び1〜6個の炭素原子を有する直鎖状又は分岐鎖状アルキル基より成る群から選択される基であり;そして
●R 5 及びR 6 は式(I)の場合に与えたものと同じ意味を持つ]
より成る群から選択され、そして、
該ポリオルガノシロキサンAが、調製後に、分子量Mが1000ダルトン未満であるモノマー、オリゴマー及びポリマーの選択的分離を可能にする技術によって、分子量Mが1000ダルトン未満であるモノマー、オリゴマー及びポリマーの割合を全分子分布に対して1%未満の値まで減少させたものであることを特徴とする、前記の皮膚に触れた時に毒性がない化粧品/皮膚科用組成物。 - 前記ポリオルガノシロキサンAのケイ素原子の0.8〜4%が前記官能基Vで置換されていることを特徴とする、請求項1〜5のいずれかに記載の皮膚に触れた時に毒性がない化粧品/皮膚科用組成物。
- エマルション、ローション、ジェル、小胞分散体、ペースト若しくは固体スティックの形にあるか、又はエーロゾルとして包装されてムース若しくはスプレーの形で提供されるかのいずれかであることを特徴とする、請求項1〜6のいずれかに記載の皮膚に触れた時に毒性がない化粧品組成物。
- ケラチン物質用のケア及び/又は衛生製品として用いられることを特徴とする、請求項1〜7のいずれかに記載の皮膚に触れた時に毒性がない化粧品組成物。
- 毛髪の洗浄、染色、ケア、コンディショニング、直毛化、ヘアスタイルの維持又は永久若しくは非永久整髪用のリンス・オフ又はリーブ・イン毛髪用製品、アンチサン組成物或はメーキャップ製品から成ることを特徴とする、請求項1〜6のいずれかに記載の皮膚に触れた時に毒性がない化粧品組成物。
- リンス・オフ毛髪用組成物として、又はアフターシャンプーコンディショナーとして用いられることを特徴とする、請求項1〜6のいずれかに記載の皮膚に触れた時に毒性がない化粧品組成物。
- 請求項1〜10のいずれかに記載の組成物をこの組成物を使用するための慣用的な技術に従ってケラチン物質に適用することを特徴とする、ケラチン物質の非治療的コスメチック処置方法。
- 毛髪の洗浄及び/又はケア及び/又はコンディショニング及び/又は整髪のための化粧品における、請求項1〜10のいずれかに記載の組成物の使用。
- 請求項1〜10に記載の有効量の化粧品組成物を毛髪に適用することを含む、コスメチック処理方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0706892A FR2921663A1 (fr) | 2007-10-02 | 2007-10-02 | Polyorganosiloxanes a fonction piperidine depourvus de toxicite par contact cutane et utilisation de ces derniers dans des compositions cosmetiques |
FR0706892 | 2007-10-07 | ||
PCT/EP2008/063247 WO2009047212A2 (fr) | 2007-10-02 | 2008-10-02 | Polyorganosiloxane a fonction piperidine depourvus de toxicite par contact cutane, et utilisation de ces derniers dans des compositions cosmetiques |
Publications (2)
Publication Number | Publication Date |
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JP2011519378A JP2011519378A (ja) | 2011-07-07 |
JP5411146B2 true JP5411146B2 (ja) | 2014-02-12 |
Family
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Family Applications (1)
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JP2010528367A Expired - Fee Related JP5411146B2 (ja) | 2007-10-02 | 2008-10-02 | 皮膚に触れた時に毒性がないピペリジン官能基含有ポリオルガノシロキサン、及び化粧品組成物中におけるそれらの使用 |
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US (1) | US8481014B2 (ja) |
EP (1) | EP2201062B1 (ja) |
JP (1) | JP5411146B2 (ja) |
KR (1) | KR101310591B1 (ja) |
CN (1) | CN101998972A (ja) |
ES (1) | ES2400024T3 (ja) |
FR (1) | FR2921663A1 (ja) |
WO (1) | WO2009047212A2 (ja) |
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CN102958979B (zh) * | 2011-02-04 | 2015-06-03 | 株式会社艾迪科 | 具有受阻胺骨架的化合物以及树脂组合物 |
KR102209214B1 (ko) * | 2014-02-25 | 2021-02-01 | 주식회사 불스원 | 피막 형성용 코팅제 조성물 |
JP6497340B2 (ja) * | 2016-03-11 | 2019-04-10 | 信越化学工業株式会社 | 防曇剤 |
BR112018068458B1 (pt) * | 2016-05-05 | 2020-10-13 | Avlon Industries, Inc. | composições e métodos de relaxamento do cabelo |
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-
2007
- 2007-10-02 FR FR0706892A patent/FR2921663A1/fr not_active Withdrawn
-
2008
- 2008-10-02 EP EP08805025A patent/EP2201062B1/fr not_active Not-in-force
- 2008-10-02 ES ES08805025T patent/ES2400024T3/es active Active
- 2008-10-02 KR KR1020107010047A patent/KR101310591B1/ko not_active IP Right Cessation
- 2008-10-02 JP JP2010528367A patent/JP5411146B2/ja not_active Expired - Fee Related
- 2008-10-02 WO PCT/EP2008/063247 patent/WO2009047212A2/fr active Application Filing
- 2008-10-02 CN CN2008801145585A patent/CN101998972A/zh active Pending
- 2008-10-02 US US12/681,021 patent/US8481014B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
KR20100082005A (ko) | 2010-07-15 |
FR2921663A1 (fr) | 2009-04-03 |
WO2009047212A3 (fr) | 2009-11-19 |
EP2201062B1 (fr) | 2012-11-21 |
ES2400024T3 (es) | 2013-04-05 |
CN101998972A (zh) | 2011-03-30 |
WO2009047212A2 (fr) | 2009-04-16 |
US20110020249A1 (en) | 2011-01-27 |
KR101310591B1 (ko) | 2013-09-23 |
JP2011519378A (ja) | 2011-07-07 |
EP2201062A2 (fr) | 2010-06-30 |
US8481014B2 (en) | 2013-07-09 |
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