JP2002121121A - Hair-treating method, after-treatment agent and after- care hair-treating agent - Google Patents
Hair-treating method, after-treatment agent and after- care hair-treating agentInfo
- Publication number
- JP2002121121A JP2002121121A JP2000315276A JP2000315276A JP2002121121A JP 2002121121 A JP2002121121 A JP 2002121121A JP 2000315276 A JP2000315276 A JP 2000315276A JP 2000315276 A JP2000315276 A JP 2000315276A JP 2002121121 A JP2002121121 A JP 2002121121A
- Authority
- JP
- Japan
- Prior art keywords
- hair
- agent
- treatment
- acid
- treatment agent
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims description 16
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 68
- 239000003513 alkali Substances 0.000 claims abstract description 31
- 239000000118 hair dye Substances 0.000 claims abstract description 20
- 239000007864 aqueous solution Substances 0.000 claims abstract description 15
- 238000004043 dyeing Methods 0.000 claims description 16
- 238000005406 washing Methods 0.000 claims description 4
- 238000002845 discoloration Methods 0.000 abstract description 25
- 230000006378 damage Effects 0.000 abstract description 16
- 230000001590 oxidative effect Effects 0.000 abstract description 4
- 239000000243 solution Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 16
- 230000000052 comparative effect Effects 0.000 description 7
- 238000005562 fading Methods 0.000 description 7
- 150000007524 organic acids Chemical class 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 6
- 150000007522 mineralic acids Chemical class 0.000 description 6
- 235000018102 proteins Nutrition 0.000 description 6
- 102000004169 proteins and genes Human genes 0.000 description 6
- 108090000623 proteins and genes Proteins 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 238000010306 acid treatment Methods 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- JOOXCMJARBKPKM-UHFFFAOYSA-N 4-oxopentanoic acid Chemical compound CC(=O)CCC(O)=O JOOXCMJARBKPKM-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 238000009825 accumulation Methods 0.000 description 4
- 229940024606 amino acid Drugs 0.000 description 4
- 235000001014 amino acid Nutrition 0.000 description 4
- 150000001413 amino acids Chemical class 0.000 description 4
- 239000002537 cosmetic Substances 0.000 description 4
- 230000002401 inhibitory effect Effects 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- 239000002453 shampoo Substances 0.000 description 4
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- ODKSFYDXXFIFQN-BYPYZUCNSA-N L-arginine Chemical compound OC(=O)[C@@H](N)CCCN=C(N)N ODKSFYDXXFIFQN-BYPYZUCNSA-N 0.000 description 3
- 229930064664 L-arginine Natural products 0.000 description 3
- 235000014852 L-arginine Nutrition 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 3
- 230000003750 conditioning effect Effects 0.000 description 3
- 239000003205 fragrance Substances 0.000 description 3
- 230000037308 hair color Effects 0.000 description 3
- 239000004310 lactic acid Substances 0.000 description 3
- 235000014655 lactic acid Nutrition 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000011975 tartaric acid Substances 0.000 description 3
- 235000002906 tartaric acid Nutrition 0.000 description 3
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 2
- ODHCTXKNWHHXJC-VKHMYHEASA-N 5-oxo-L-proline Chemical compound OC(=O)[C@@H]1CCC(=O)N1 ODHCTXKNWHHXJC-VKHMYHEASA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 2
- 229940043276 diisopropanolamine Drugs 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 229960004275 glycolic acid Drugs 0.000 description 2
- 230000003700 hair damage Effects 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- 229940102253 isopropanolamine Drugs 0.000 description 2
- 229940040102 levulinic acid Drugs 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 239000001024 permanent hair color Substances 0.000 description 2
- CPJSUEIXXCENMM-UHFFFAOYSA-N phenacetin Chemical compound CCOC1=CC=C(NC(C)=O)C=C1 CPJSUEIXXCENMM-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000008213 purified water Substances 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- 229940079889 pyrrolidonecarboxylic acid Drugs 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- PTBJVWZIAZEHRK-UHFFFAOYSA-N 1-amino-2-methylpropane-1,3-diol Chemical compound OCC(C)C(N)O PTBJVWZIAZEHRK-UHFFFAOYSA-N 0.000 description 1
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 description 1
- NFCPRRWCTNLGSN-UHFFFAOYSA-N 2-n-phenylbenzene-1,2-diamine Chemical class NC1=CC=CC=C1NC1=CC=CC=C1 NFCPRRWCTNLGSN-UHFFFAOYSA-N 0.000 description 1
- BLCZXLGRKKRKJJ-UHFFFAOYSA-N 3-amino-2-nitrophenol Chemical class NC1=CC=CC(O)=C1[N+]([O-])=O BLCZXLGRKKRKJJ-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- CKLJMWTZIZZHCS-UHFFFAOYSA-N D-OH-Asp Natural products OC(=O)C(N)CC(O)=O CKLJMWTZIZZHCS-UHFFFAOYSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 206010019030 Hair colour changes Diseases 0.000 description 1
- 102000011782 Keratins Human genes 0.000 description 1
- 108010076876 Keratins Proteins 0.000 description 1
- CKLJMWTZIZZHCS-UWTATZPHSA-N L-Aspartic acid Natural products OC(=O)[C@H](N)CC(O)=O CKLJMWTZIZZHCS-UWTATZPHSA-N 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
- 239000004472 Lysine Substances 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229960005261 aspartic acid Drugs 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- STIAPHVBRDNOAJ-UHFFFAOYSA-N carbamimidoylazanium;carbonate Chemical compound NC(N)=N.NC(N)=N.OC(O)=O STIAPHVBRDNOAJ-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229940043237 diethanolamine Drugs 0.000 description 1
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229960002989 glutamic acid Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229960000448 lactic acid Drugs 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 229940099690 malic acid Drugs 0.000 description 1
- 229940113083 morpholine Drugs 0.000 description 1
- AXKVOSSFZLZIDC-UHFFFAOYSA-N n,n-diaminoaniline Chemical class NN(N)C1=CC=CC=C1 AXKVOSSFZLZIDC-UHFFFAOYSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229960003893 phenacetin Drugs 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- ZZYXNRREDYWPLN-UHFFFAOYSA-N pyridine-2,3-diamine Chemical class NC1=CC=CN=C1N ZZYXNRREDYWPLN-UHFFFAOYSA-N 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000001026 semi permanent hair color Substances 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229960001367 tartaric acid Drugs 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
Landscapes
- Cosmetics (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、酸化型の染毛剤で
染毛した後の毛髪処理方法及びこれに用いるアフタート
リートメント剤、アフターケア毛髪処理剤に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for treating hair after it has been dyed with an oxidative hair dye, an after treatment agent and an after care hair treatment agent.
【0002】[0002]
【従来の技術】染毛剤には、永久染毛剤、半永久染毛剤
などがあり、いずれも美容的な目的のために広く一般に
使用されている。永久染毛剤においては、酸化染料及び
アルカリ剤を含む第1剤と、過酸化水素を含む第2剤と
からなる酸化型の染毛剤が染毛力、褪色性能等から広く
使用されている。2. Description of the Related Art Hair dyes include permanent hair dyes and semi-permanent hair dyes, all of which are widely and generally used for cosmetic purposes. Among permanent hair dyes, oxidized hair dyes comprising a first agent containing an oxidation dye and an alkali agent and a second agent containing hydrogen peroxide are widely used due to their hair dyeing power, fading performance and the like. .
【0003】このような酸化型の染毛剤に関しては、一
般的に均一な浸透を助けるためにアルカリ剤を含有して
いるため、pHが高く、そのため毛髪がダメージを受け
やすく、特に連用においては過度のアルカリ剤との接触
や残留するアルカリ剤の影響等によりさらにダメージが
進み、手触りが悪くなったり、色持ちが悪くなったりす
るという欠点がある。そのダメージを軽減するために種
々の毛髪処理剤がヘアカラー毛用として一般的に使用さ
れている。[0003] Such an oxidative hair dye generally contains an alkaline agent to help uniform penetration, so that the pH is high, so that the hair is liable to be damaged. There is a drawback that damage is further promoted due to contact with an excessive amount of an alkaline agent, influence of a residual alkaline agent, and the like, resulting in poor touch and poor color durability. Various hair treatment agents are generally used for hair coloring hair to reduce the damage.
【0004】例えば、特開平2−212410号公報に
は、毛髪がアルカリ処理された後にその毛髪を等電点
(pH6)に戻し、毛髪損傷の修復や毛髪劣化損傷を抑
制するアルカリ処理毛髪のコンディショニング組成剤が
開示されている。このコンディショニング組成剤は、p
H緩衝剤、蛋白質加水分解物、アミノ変性シリコンを含
むものであり、この組成剤で処理した毛髪がpH4〜7
のpH値に戻るように配合されている。For example, Japanese Patent Application Laid-Open No. 2-212410 discloses conditioning of alkali-treated hair after the hair is alkali-treated and returned to an isoelectric point (pH 6) to repair hair damage and suppress hair deterioration damage. A composition is disclosed. This conditioning composition comprises p
H-buffer, protein hydrolyzate, and amino-modified silicone, and the hair treated with this composition has pH 4-7.
It is blended so as to return to the pH value.
【0005】[0005]
【発明が解決しようとする課題】しかしながら、上記コ
ンディショニング組成剤は、毛髪内pHをアルカリ側か
ら急激に毛髪の等電点付近まで下げるため、毛髪の変色
や過収れんを引き起こすおそれがあった。つまり、染毛
後において、毛髪内に残るアルカリ成分は毛髪にダメー
ジを与える大きな要因であるため、この残留アルカリの
除去を図る必要がある一方で、このような残留アルカリ
の除去を目的としてアルカリ性に傾いた毛髪のpH値を
急激に戻すと今度は毛髪の変色や過収れんを引き起こす
という問題があった。However, the above-mentioned conditioning composition sharply lowers the pH in the hair from the alkaline side to near the isoelectric point of the hair, and may cause discoloration and excessive convergence of the hair. In other words, after the hair is dyed, the alkaline component remaining in the hair is a major factor that damages the hair, so it is necessary to remove the residual alkali. If the pH value of the slanted hair is rapidly returned, there is a problem that the discoloration and excessive convergence of the hair are caused.
【0006】本発明は上記問題点を解決することを課題
とするものであり、毛髪の変色や過収れんを防ぎつつ残
留アルカリを除去して毛髪のダメージを抑える毛髪処理
方法を提供することを目的とする。また、この毛髪処理
方法に適するアフタートリートメント剤及びアフターケ
ア毛髪処理剤を提供することをも目的とする。SUMMARY OF THE INVENTION An object of the present invention is to solve the above-mentioned problems, and it is an object of the present invention to provide a hair treatment method for suppressing hair damage by removing residual alkali while preventing discoloration and excessive convergence of hair. And Another object of the present invention is to provide an after treatment agent and an after care hair treatment agent suitable for this hair treatment method.
【0007】[0007]
【課題を解決するための手段、発明の実施の形態及び発
明の効果】本発明者らは、上記課題を解決するために鋭
意研究を重ねた結果、アルカリ剤を含有する酸化型の染
毛剤で染毛することにより毛髪内pHが8〜10になっ
た毛髪に対して、この染毛剤を洗い流し、続いて10重
量%水溶液のpHが3〜5.5のアフタートリートメン
ト剤を毛髪に塗布し、放置したあと洗い流すことにより
毛髪内pHを7.5〜9に調整するという本発明の毛髪
処理方法を見い出した。この毛髪処理方法によれば、毛
髪の変色や過収れんを防ぎつつ残留アルカリを除去して
毛髪のダメージを抑えることができる。Means for Solving the Problems, Embodiments of the Invention, and Effects of the Invention The present inventors have conducted intensive studies in order to solve the above problems, and as a result, have found that an oxidized hair dye containing an alkali agent is obtained. This hair dye is washed away from the hair whose pH in the hair becomes 8 to 10 by the hair dyeing, and then an after treatment agent having a pH of 3 to 5.5 of a 10% by weight aqueous solution is applied to the hair. Then, a hair treatment method of the present invention was found in which the pH in the hair was adjusted to 7.5 to 9 by washing away after standing. According to this hair treatment method, it is possible to remove residual alkali while preventing discoloration and excessive convergence of the hair, thereby suppressing damage to the hair.
【0008】本発明において、酸化型の染毛剤として
は、例えば、酸化染料とアルカリ剤とを含む第1剤と、
酸化剤を含む第2剤とを含んでなるものが挙げられる。
ここで、第1剤につき、酸化染料としては、特に限定さ
れるものではないが、例えばパラフェニレンジアミン
類、パラトルイレンジアミン類、アミノフェノール類、
アミノニトロフェノール類、ジフェニルアミン類、ジア
ミノフェニルアミン類、N−フェニルフェニレンジアミ
ン類、ジアミノピリジン類等及びそれらの塩類が挙げら
れる。その配合量は、例えば第1剤の全重量に対して
0.01〜10重量%である。また、アルカリ剤として
は、特に限定されるものではないが、例えばアンモニ
ア、トリエタノールアミン、ジエタノールアミン、モノ
エタノールアミン、イソプロパノールアミン、ジイソプ
ロパノールアミン、2−アミノ−2−メチル−1−プロ
パノール、2−アミノ−2−メチル−1,3−プロパン
ジオール等が挙げられ、これらの中から選ばれる1種ま
たは2種以上が用いられる。これにより第1剤のpHは
8〜11に調整される。更に、カップラーとして、ピロ
ガロール、カテコール、メタフェニレンジアミン等を配
合してもよいし、「医薬部外品原料規格」(薬事日報
社、1991年6月発行)に収載されたものや、酸性染
料や、カルボキシメチルセルロース、キサンタンガム、
ポリアクリル酸及びその塩等の増粘剤などのほか、シリ
コンや香料などを配合してもよい。一方、第2剤につ
き、酸化剤としては、特に限定されるものではないが、
例えば過酸化水素や過酸化尿素等が挙げられる。また、
フェナセチン及びEDTA等の安定剤、非イオン性界面
活性剤、アニオン性界面活性剤、カチオン性界面活性
剤、両性界面活性剤、カチオン化ポリマー、高級アルコ
ール、炭化水素、脂肪酸、ロウ類、油脂類、溶剤、酸、
pH調整剤及び香料などを必要に応じて適宜配合しても
よい。第2剤は酸によりpH2〜5に調整される。In the present invention, the oxidation type hair dye includes, for example, a first agent containing an oxidation dye and an alkali agent;
And a second agent containing an oxidizing agent.
Here, regarding the first agent, the oxidation dye is not particularly limited, but for example, paraphenylenediamines, paratoluylenediamines, aminophenols,
Examples include aminonitrophenols, diphenylamines, diaminophenylamines, N-phenylphenylenediamines, diaminopyridines and the like, and salts thereof. The compounding amount is, for example, 0.01 to 10% by weight based on the total weight of the first agent. Examples of the alkali agent include, but are not particularly limited to, for example, ammonia, triethanolamine, diethanolamine, monoethanolamine, isopropanolamine, diisopropanolamine, 2-amino-2-methyl-1-propanol, Examples thereof include amino-2-methyl-1,3-propanediol, and one or more selected from these are used. Thereby, the pH of the first agent is adjusted to 8 to 11. Further, as the coupler, pyrogallol, catechol, metaphenylenediamine, or the like may be blended, or those described in “Quasi-drug Raw Material Standards” (Yakuji Nippo, issued in June 1991), acid dyes, , Carboxymethylcellulose, xanthan gum,
In addition to thickeners such as polyacrylic acid and salts thereof, silicone and fragrance may be blended. On the other hand, regarding the second agent, the oxidizing agent is not particularly limited,
Examples include hydrogen peroxide and urea peroxide. Also,
Stabilizers such as phenacetin and EDTA, nonionic surfactants, anionic surfactants, cationic surfactants, amphoteric surfactants, cationized polymers, higher alcohols, hydrocarbons, fatty acids, waxes, fats and oils, Solvents, acids,
A pH adjuster, a fragrance, and the like may be appropriately added as necessary. The pH of the second agent is adjusted to 2 to 5 with an acid.
【0009】この染毛剤を使用する場合は、染毛処理の
直前に第1剤と第2剤を3:1〜1:3の割合で混合し
て毛髪に塗布する。使用時のpHは8〜10である。本
発明において、染毛剤を洗い流す場合には、例えば温水
で洗い流すだけでもよいが、シャンプーを用いて洗い流
したり、プレーンリンスにより乳化させたあと洗い流し
たりしてもよく、プレーンリンスを用いた場合にはその
後シャンプーで洗い流すようにしてもよい。When this hair dye is used, the first agent and the second agent are mixed at a ratio of 3: 1 to 1: 3 and applied to the hair immediately before the hair dyeing treatment. The pH at the time of use is 8-10. In the present invention, when washing away the hair dye, for example, it may be simply washed off with warm water, but may be washed off with a shampoo, or may be washed off after emulsification with plain rinse, and when plain rinse is used. May then be washed off with shampoo.
【0010】本発明において、アフタートリートメント
剤としては、10重量%水溶液のpHが3〜5.5のも
のを用いる。このpHが3よりも低いと、毛髪内の残留
アルカリを取り除く効果は高いが、染料の分解が始まっ
てしまい、色調への影響が大きくなるため、好ましくな
い。また、pHが5.5よりも高いと、残留アルカリの
除去効果が十分得られないため、好ましくない。In the present invention, a 10% by weight aqueous solution having a pH of 3 to 5.5 is used as an after treatment agent. If the pH is lower than 3, the effect of removing the residual alkali in the hair is high, but the decomposition of the dye is started and the effect on the color tone is undesirably increased. On the other hand, if the pH is higher than 5.5, the effect of removing residual alkali cannot be sufficiently obtained, which is not preferable.
【0011】このアフタートリートメント剤は、有機酸
若しくはその塩又は無機酸若しくはその塩を含んでいる
ものが好ましい。有機酸、無機酸としては、通常化粧品
で使用されるものであれば特に限定されるものではない
が、有機酸としては、例えばクエン酸、酢酸、グリコー
ル酸、ギ酸、レブリン酸、シュウ酸、乳酸、酒石酸、乳
酸、コハク酸、リンゴ酸、L−グルタミン酸、L−アス
パラギン酸、ピロリドンカルボン酸等が挙げられ、無機
酸としては、例えば塩酸、リン酸等が挙げられる。これ
らの中で、有機酸、とりわけ酒石酸、乳酸、クエン酸、
レブリン酸、グリコール酸、ピロリドンカルボン酸が好
ましく、その中でも特に酒石酸が好ましい。酸の配合量
は、特に限定されるものではないが、0.5〜5重量%
が好ましい。The after-treatment agent preferably contains an organic acid or a salt thereof or an inorganic acid or a salt thereof. The organic acid and the inorganic acid are not particularly limited as long as they are usually used in cosmetics. Examples of the organic acid include citric acid, acetic acid, glycolic acid, formic acid, levulinic acid, oxalic acid, and lactic acid. , Tartaric acid, lactic acid, succinic acid, malic acid, L-glutamic acid, L-aspartic acid, pyrrolidone carboxylic acid, and the like. Examples of the inorganic acids include hydrochloric acid, phosphoric acid, and the like. Among these, organic acids, especially tartaric acid, lactic acid, citric acid,
Preference is given to levulinic acid, glycolic acid and pyrrolidonecarboxylic acid, of which tartaric acid is particularly preferred. The compounding amount of the acid is not particularly limited, but is 0.5 to 5% by weight.
Is preferred.
【0012】また、このアフタートリートメント剤は、
アルカリ剤を含んでいるものが好ましい。アルカリ剤と
しては、通常化粧品に用いられる無機アルカリ、有機ア
ルカリであれば特に限定されるものではないが、無機ア
ルカリとしては、例えば水酸化ナトリウム、水酸化カリ
ウムなどのアルカリ金属の水酸化物及び炭酸塩、強アン
モニア水が挙げられ、有機アルカリとしては、例えばモ
ルフォリン等の揮発性アルカリ剤、トリエタノールアミ
ン、ジエタノールアミン、イソプロパノールアミン、ジ
イソプロパノールアミン、モノエタノールアミン、2−
アミノ−2−メチル−1−プロパノール、2−アミノ−
2−メチル−1,3−プロパンジオールなどのアルカノ
ールアミン類、L−アルギニン、リジンなどのアミノ酸
類、および炭酸グアニジンが挙げられる。これらの中
で、水酸化ナトリウム、Lーアルギニン、アンモニア、
アミノメチルプロパノールが好ましく、その中でも特に
Lーアルギニンが好ましい。Further, the after-treatment agent comprises:
Those containing an alkaline agent are preferred. The alkali agent is not particularly limited as long as it is an inorganic alkali or an organic alkali usually used in cosmetics. Examples of the inorganic alkali include hydroxides and carbonates of alkali metals such as sodium hydroxide and potassium hydroxide. Examples of the organic alkali include volatile alkaline agents such as morpholine, triethanolamine, diethanolamine, isopropanolamine, diisopropanolamine, monoethanolamine, 2-ethanolamine, and the like.
Amino-2-methyl-1-propanol, 2-amino-
Alkanolamines such as 2-methyl-1,3-propanediol; amino acids such as L-arginine and lysine; and guanidine carbonate. Among these, sodium hydroxide, L-arginine, ammonia,
Aminomethylpropanol is preferred, and L-arginine is particularly preferred.
【0013】なお、このアフタートリートメント剤に
は、補修的効果や色素定着性の向上を目的として蛋白質
誘導体やアミノ酸を配合してもよい。このような蛋白質
誘導体として、例えば、ケラチン、小麦、コラーゲン、
大豆等の蛋白質から誘導された加水分解蛋白質誘導体を
用いることが好ましく、アミノ酸としては、例えば毛髪
を構成するアミノ酸を用いることが好ましい。また、本
発明の効果を妨げない範囲で、安定剤、非イオン性界面
活性剤、アニオン性界面活性剤、カチオン性界面活性
剤、両性界面活性剤、油剤、増粘剤、カチオン化ポリマ
ー、シリコン誘導体、有機溶剤、紫外線防止剤、香料、
キレート剤、抗菌剤、植物抽出液などを必要に応じて適
宜配合してもよい。更に、剤型は、特に限定されるもの
ではなく、液状、ローション状、泡状、エアゾール状、
クリーム状、固形等、化粧品に使用される形態であれば
どのような形態でも構わない。In addition, a protein derivative or an amino acid may be added to the after-treatment agent for the purpose of improving the repairing effect and the dye fixability. As such protein derivatives, for example, keratin, wheat, collagen,
It is preferable to use a hydrolyzed protein derivative derived from a protein such as soybean, and as the amino acid, it is preferable to use, for example, an amino acid constituting hair. Further, within the range not hindering the effects of the present invention, a stabilizer, a nonionic surfactant, an anionic surfactant, a cationic surfactant, an amphoteric surfactant, an oil agent, a thickener, a cationized polymer, silicon Derivatives, organic solvents, UV inhibitors, fragrances,
A chelating agent, an antibacterial agent, a plant extract, and the like may be appropriately added as necessary. Further, the dosage form is not particularly limited, liquid, lotion, foam, aerosol,
Any form used for cosmetics, such as cream or solid, may be used.
【0014】本発明において、アフタートリートメント
剤を毛髪に塗布したあと放置するが、このときの放置時
間は、例えば1〜20分であることが好ましい。1分を
下回ると残留アルカリが十分除去されないおそれがある
ので好ましくなく、20分を越えて放置しても効果上差
がないため好ましくない。また、放置する際には室温で
もよいし、場合によっては40〜50℃程度に加温して
もよい。但し、加温する手間を考慮すれば、室温で放置
するのが好ましい。そして、このように放置した後、ア
フタートリートメント剤を洗い流すことにより、毛髪内
pHを7.5〜9、特に7.5〜8.5に調整する。つ
まり、酸化型の染毛剤で染毛することによりpHが8〜
10になった毛髪内pHを1〜2だけ下げ、酸処理を適
度に抑え、毛髪の変色や過収れんを引き起こさない理想
的なポイント(毛髪内pH8近辺)にコントロールする
ことにより、染毛直後の毛髪の色とコンディションを理
想的に保つ。これに対して、毛髪内pHが下限値を下回
ると、毛髪の変色や過収れんが起きるおそれがあるため
好ましくなく、毛髪pHが上限値を上回ると、残留アル
カリによるダメージが蓄積するため好ましくない。In the present invention, the after-treatment agent is applied to the hair and allowed to stand, and the leaving time at this time is preferably, for example, 1 to 20 minutes. If it is less than 1 minute, the residual alkali may not be sufficiently removed, so that it is not preferable. In addition, at the time of standing, it may be at room temperature, or may be heated to about 40 to 50 ° C in some cases. However, in consideration of the trouble of heating, it is preferable to leave at room temperature. Then, after being left in this manner, the pH in the hair is adjusted to 7.5 to 9, particularly 7.5 to 8.5 by washing away the after-treatment agent. In other words, by dyeing the hair with an oxidative hair dye, the pH becomes 8 to
Immediately after hair dyeing by lowering the pH in the hair which became 10 by 1 to 2 and moderately controlling the acid treatment, and controlling to an ideal point (around pH 8 in the hair) which does not cause discoloration or excessive convergence of the hair. Ideally maintain hair color and condition. On the other hand, if the pH in the hair is lower than the lower limit, discoloration or excessive convergence of the hair may occur, which is not preferable. If the pH is higher than the upper limit, damage due to residual alkali accumulates.
【0015】本発明において、上述のようにして毛髪内
pHを7.5〜9に調整した後、10重量%水溶液のp
Hが3.5〜6.5のアフターケア毛髪処理剤で複数回
処理することにより毛髪内pHを毛髪の等電点の近傍
(pH5.5〜6.5)に調整することが好ましい。こ
こで、アフターケア毛髪処理剤としては、例えばシャン
プー、リンス、コンディショナー、トリートメント等が
挙げられる。このアフターケア毛髪処理剤による処理を
複数回、好ましくは3回以上、特に好ましくは5回以上
繰り返して毛髪内pHを毛髪の等電点付近に調整するた
め、毛髪内のアルカリを時間をかけて無理なく除去し、
残留アルカリによるダメージの蓄積を防止すると共に、
染毛を繰り返し行っても髪を元の状態に近づけることが
できる。なお、アフターケア毛髪処理剤による処理は、
1日1回ずつ複数日にわたって行うことが好ましい。In the present invention, after the pH in the hair is adjusted to 7.5 to 9 as described above, the pH of a 10% by weight aqueous solution is adjusted.
It is preferable to adjust the pH in the hair to a value near the isoelectric point of the hair (pH 5.5 to 6.5) by treating the hair several times with an aftercare hair treatment agent having H of 3.5 to 6.5. Here, examples of the aftercare hair treatment agent include shampoo, rinse, conditioner, treatment and the like. In order to adjust the pH in the hair to around the isoelectric point of the hair by repeating the treatment with the aftercare hair treatment agent a plurality of times, preferably at least three times, particularly preferably at least five times, alkalis in the hair are taken over time. Remove without difficulty,
While preventing accumulation of damage due to residual alkali,
Even if the hair is repeatedly dyed, the hair can be brought close to the original condition. In addition, the treatment with the aftercare hair treatment agent,
It is preferable to carry out once a day for a plurality of days.
【0016】このアフターケア毛髪処理剤は、有機酸若
しくはその塩又は無機酸若しくはその塩を含んでいるも
のが好ましい。また、アルカリ剤を含んでいるものが好
ましい。有機酸、無機酸、アルカリ剤としては、アフタ
ートリートメント剤と同様のものを用いればよい。但
し、アフターケア毛髪処理剤は、複数回にわたって施用
して残存アルカリを除去するものであるため、アフター
トリートメント剤に比べて弱いアルカリ除去能を有する
ことが好ましい。したがって、pHはアフタートリート
メント剤ほど酸性でないことが好ましく、例えば、アフ
タートリートメント剤の10重量%水溶液のpHを3〜
4.5とし、アフターケア毛髪処理剤の10重量%水溶
液のpHを4〜6.5とすることが好ましい。また、有
機酸、無機酸の配合量もアフタートリートメント剤に比
べて同等又はそれ未満であることが好ましい。The aftercare hair treatment agent preferably contains an organic acid or a salt thereof, or an inorganic acid or a salt thereof. Further, those containing an alkali agent are preferred. As the organic acid, the inorganic acid, and the alkali agent, the same as those for the after treatment agent may be used. However, since the aftercare hair treatment agent is applied a plurality of times to remove the residual alkali, it preferably has a weaker alkali removal ability than the aftertreatment agent. Therefore, it is preferable that the pH is not so acidic as that of the after-treatment agent.
It is preferred that the pH be 4.5, and the pH of a 10% by weight aqueous solution of the aftercare hair treatment agent be 4 to 6.5. Further, the amount of the organic acid or inorganic acid is preferably equal to or less than that of the after treatment agent.
【0017】ここで、本発明の毛髪処理方法を適用した
場合の毛髪内pHの回復曲線の一例を、従来例と比較し
て図1に示す。図1は毛髪内pHの回復曲線を表すグラ
フである。この図1において、染毛後特別な処理をしな
かった場合には、一点鎖線で示すように、残存アルカリ
により毛髪内pHが高く、毛髪にダメージが蓄積される
ので好ましくない。また、染毛剤施用後に従来の処理方
法を適用した場合には、点線で示すように、残存アルカ
リが除去されるため、ダメージの蓄積は回避されるもの
の、アルカリ性に傾いた毛髪内pHを急激に戻す過度な
酸処理により毛髪の変色や過収れんを引き起こすおそれ
があるので好ましくない。これに対して、本発明の毛髪
処理方法を適用した場合には、実線で示すように、染毛
直後では酸処理を適度に抑え、毛髪の変色や過収れんを
引き起こさない理想的なポイントであるpH8の近傍ま
でのpHコントロールを行い、その後数日にわたって毛
髪内pHを毛髪の等電点近傍までコントロールする。つ
まり、染毛直後から数日にわたって、毛髪内のアルカリ
を少しずつ無理なく除去し、ダメージの蓄積を回避す
る。この結果、染毛を繰り返し行っても、髪を元の状態
に近づけることができ、良好なコンディションを保つこ
とができる。なお、図1において、便宜上、染毛直後に
行う処理を1次ケア、染毛直後から数日にわたって行う
処理を2次ケアと称する(以下同じ)。Here, an example of a recovery curve of the pH in hair when the hair treatment method of the present invention is applied is shown in FIG. 1 in comparison with a conventional example. FIG. 1 is a graph showing a recovery curve of pH in hair. In FIG. 1, when no special treatment is performed after the hair is dyed, the pH in the hair is high due to the remaining alkali, and damage to the hair is undesirably accumulated, as indicated by the dashed line. In addition, when the conventional treatment method is applied after application of the hair dye, the residual alkali is removed, as shown by the dotted line, so that the accumulation of damage is avoided, but the pH in the hair inclined to alkalinity is rapidly increased. It is not preferable because excessive acid treatment to restore the color may cause hair discoloration and excessive convergence. In contrast, when the hair treatment method of the present invention is applied, as shown by the solid line, acid treatment is suppressed moderately immediately after hair dyeing, which is an ideal point that does not cause discoloration or excessive convergence of hair. The pH is controlled to around pH 8, and then the pH in the hair is controlled to around the isoelectric point of the hair for several days. In other words, the alkali in the hair is removed little by little over a few days immediately after the hair dyeing to avoid accumulation of damage. As a result, even if the hair is repeatedly dyed, the hair can be brought close to the original state, and a good condition can be maintained. In FIG. 1, for convenience, processing performed immediately after hair dyeing is referred to as primary care, and processing performed for several days immediately after hair dyeing is referred to as secondary care (the same applies hereinafter).
【0018】[0018]
【実施例】次に実施例を挙げて本発明を更に詳しく説明
するが、本発明はこれらの実施例により何ら限定される
ものではない。また、実施例及び比較例中の[%]は特
に断わらない限り[重量%]を示す。Next, the present invention will be described in more detail with reference to examples, but the present invention is not limited to these examples. [%] In Examples and Comparative Examples indicates [% by weight] unless otherwise specified.
【0019】[1]染毛処理 表1に示す酸化型の染毛剤の第1剤と第2剤とを同量混
合し、その混合物を毛束に適量塗布した後、室温(25
℃)にて20分間放置するという染毛処理を行った。な
お、毛束は、日本人女性のバージンヘア(ヘアカラー及
びパーマ経験のない毛髪)で長さ15cmのものを用い
た。[1] Hair dyeing treatment The first and second oxidized hair dyes shown in Table 1 were mixed in the same amount, and the mixture was applied to a hair bundle in an appropriate amount.
C.) for 20 minutes. The hair bundle used was virgin hair of a Japanese woman (hair having no hair color and no perm experience) having a length of 15 cm.
【0020】[0020]
【表1】 [Table 1]
【0021】[2]1次ケアによる効果の調査 上記染毛処理後の毛束をシャンプーして染毛剤を洗い流
し、表2に示す実施例1〜3及び比較例1,2のいずれ
かのアフタートリートメント剤を適量塗布し、3分放置
したあと洗い流した(1次ケア)。その後、毛束を乾燥
させ、その毛髪1gを液体窒素にて1mm以下まで凍結
粉砕し、50℃の蒸留水100mlに10分間浸漬後、
25℃に冷却し、その水溶液のpHを測定し、これを毛
髪内pHとした。その結果を表2に示す。[2] Investigation of the Effect of Primary Care The hair bundle after the above hair dye treatment was shampooed to wash away the hair dye, and any of Examples 1 to 3 and Comparative Examples 1 and 2 shown in Table 2 After treatment agent was applied in an appropriate amount, left for 3 minutes and then washed away (primary care). Thereafter, the hair bundle is dried, and 1 g of the hair is freeze-ground with liquid nitrogen to 1 mm or less, and immersed in 100 ml of 50 ° C. distilled water for 10 minutes.
After cooling to 25 ° C., the pH of the aqueous solution was measured, and this was taken as the pH in the hair. Table 2 shows the results.
【0022】[0022]
【表2】 [Table 2]
【0023】また、1次ケア後の毛束につき、(1)毛
髪の変色度合い、(2)褪色抑制効果、(3)ダメージ
抑制効果を調べた。 (1)毛髪の変色度合い 1次ケア後の毛束を乾燥さ
せ、その毛髪の変色度合いを専門パネラー10名にて視
覚的に判断した。ここでは、アフタートリートメント剤
として精製水を使用した場合の毛髪(未処理の毛髪)と
対比させて変色度合いを判断した。その結果を表2に示
す。なお、表2中、「○」は変色なし、「△」はやや変
色あり、「×」は変色あり、である。The hair bundle after the primary care was examined for (1) the degree of discoloration of the hair, (2) the effect of suppressing fading, and (3) the effect of suppressing damage. (1) Degree of Discoloration of Hair The hair bundle after the primary care was dried, and the degree of discoloration of the hair was visually judged by ten specialized panelists. Here, the degree of discoloration was determined in comparison with the hair (untreated hair) when purified water was used as an after treatment agent. Table 2 shows the results. In Table 2, “○” indicates no discoloration, “△” indicates slight discoloration, and “×” indicates discoloration.
【0024】(2)褪色抑制効果 1次ケア後の毛束を
乾燥させ、50℃でラウリル硫酸ナトリウム1%水溶液
に10分間浸漬したあと乾燥し、専門パネラー10名に
て視覚的に判断をした。ここでも、アフタートリートメ
ント剤として精製水を使用した場合の毛髪(未処理の毛
髪)と対比させて褪色抑制効果を判断した。結果を表2
に示す。なお、表2中、「◎」は未処理に比べて、かな
り色残りがよい、「○」は未処理に比べて色残りがやや
良い、「△」は未処理と変わらない、「×」は未処理よ
り悪い、である。(2) Effect of inhibiting fading The hair bundle after the primary care was dried, immersed in a 1% aqueous solution of sodium lauryl sulfate at 50 ° C. for 10 minutes, dried, and visually judged by ten professional panelists. . Also in this case, the discoloration inhibiting effect was judged by comparing with the hair (untreated hair) using purified water as an after treatment agent. Table 2 shows the results
Shown in In Table 2, “◎” indicates that the color retention is considerably better than that of the untreated color, “「 ”indicates that the color retention is slightly better than that of the untreated color,“ △ ”indicates the same as that of the untreated color, and“ × ” Is worse than untreated.
【0025】(3)ダメージ抑制効果 1次ケア後の毛
束を乾燥させ、専門パネラー10名にてゴワつきやなめ
らかさなどの手触り感を評価した。結果を表2に示す。
なお、表2中、「◎」は未処理と比べてかなり手触りが
よい、「○」は未処理に比べてややよい、「△」は未処
理と比べて変わらない、「×」は未処理よりも悪い、で
ある。(3) Damage Suppressing Effect The hair bundle after the primary care was dried, and ten special panelists evaluated the feeling of touch such as stickiness and smoothness. Table 2 shows the results.
In Table 2, “◎” indicates that the texture is considerably better than untreated, “処理” is slightly better than untreated, “△” is the same as untreated, and “×” is untreated. Worse than.
【0026】上記表2から、1次ケア後の毛髪内pHが
6.5の場合には、過度の酸処理により髪が変色したう
え十分な褪色抑制効果が得られなかった(比較例1)。
また、1次ケア後の毛髪内pHが9.0の場合には、毛
髪の変色はみられなかったが、残存アルカリが除去され
ず、褪色抑制効果も得られなかった(比較例2)。これ
に対して、pHが8.0近傍の場合には、適度な酸処理
のため、毛髪の変色や過収れんが起きることはなく、毛
髪の変色度合い、褪色抑制効果のいずれについても良好
な結果が得られた(実施例1〜3)。特に、蛋白質誘導
体(加水分解小麦タンパク)を併用した場合には褪色抑
制効果が極めて良好になった(実施例3)。From Table 2 above, when the pH in the hair after the primary care was 6.5, the hair was discolored due to excessive acid treatment, and a sufficient fading inhibiting effect was not obtained (Comparative Example 1). .
When the pH in the hair after the primary care was 9.0, no discoloration of the hair was observed, but the residual alkali was not removed, and no fading inhibiting effect was obtained (Comparative Example 2). On the other hand, when the pH is around 8.0, moderate acid treatment does not cause discoloration or excessive convergence of the hair, and shows good results in both the degree of discoloration of the hair and the effect of suppressing fading. Was obtained (Examples 1 to 3). In particular, when a protein derivative (hydrolyzed wheat protein) was used in combination, the effect of suppressing fading was extremely good (Example 3).
【0027】[3]1次ケア及び2次ケアによる効果の
調査 1次ケア及び2次ケアによる効果を調査した。即ち、上
記染毛処理後の毛束をシャンプーして染毛剤を洗い流
し、実施例3のアフタートリートメント剤を適量塗布
し、3分放置したあと洗い流した(1次ケア)。1次ケ
ア後の毛髪内pHは表2に示した通り7.5であった。
そして、その翌日から、表3に示す実施例4及び比較例
3,4のいずれかのシャンプー、リンス(アフターケア
毛髪処理剤)を用いて毎日1回、5日間にわたって洗浄
した(2次ケア)。その後、毛束を乾燥させ、その毛髪
1gを液体窒素にて1mm以下まで凍結粉砕し、50℃
の蒸留水100mlに10分間浸漬後、25℃に冷却
し、その水溶液のpHを測定し、これを毛髪内pHとし
た。結果を表3に示す。[3] Investigation of the effects of primary care and secondary care The effects of primary care and secondary care were investigated. That is, the hair bundle after the hair dyeing treatment was shampooed to wash away the hair dye, the after-treatment agent of Example 3 was applied in an appropriate amount, left for 3 minutes, and then washed off (primary care). The pH in the hair after the primary care was 7.5 as shown in Table 2.
Then, from the next day, the shampoo and the rinse (aftercare hair treatment agent) of any of Example 4 and Comparative Examples 3 and 4 shown in Table 3 were washed once daily for 5 days (secondary care). . Thereafter, the hair bundle is dried, and 1 g of the hair is freeze-pulverized with liquid nitrogen to 1 mm or less, and 50 ° C.
Immersed in 100 ml of distilled water for 10 minutes, cooled to 25 ° C., the pH of the aqueous solution was measured, and this was taken as the pH in the hair. Table 3 shows the results.
【0028】[0028]
【表3】 [Table 3]
【0029】また、1次ケア及び2次ケアを施した毛束
を用いて、変色度合い及びダメージ抑制効果を調べた。
即ち、2次ケア後の毛束を乾燥させ、染毛直後の色調と
比較しての変色度合いを専門パネラー10名にて視覚的
に判断した。結果を表3に示す。なお、表3中、「○」
は変色なし、「△」はやや変色あり、「×」は変色あ
り、である。The degree of discoloration and the effect of suppressing damage were examined using the hair bundles subjected to primary care and secondary care.
That is, the hair bundle after the secondary care was dried, and the degree of discoloration as compared with the color tone immediately after the hair dyeing was visually judged by ten specialized panelists. Table 3 shows the results. In Table 3, "○"
Indicates no discoloration, “、” indicates a slight discoloration, and “×” indicates a discoloration.
【0030】また、2次ケア後の毛束を乾燥させ、専門
パネラー10名にてゴワつきやなめらかさなどの手触り
感を評価した。結果を表3に示す。なお、表3中、
「◎」は未処理と比べてかなり手触りがよい、「○」は
未処理に比べてややよい、「△」は未処理と比べて変わ
らない、「×」は未処理よりも悪い、である。The hair bundle after the secondary care was dried, and ten special panelists evaluated the feeling of touch such as stiffness and smoothness. Table 3 shows the results. In Table 3,
“◎” is considerably better than untreated, “○” is slightly better than untreated, “△” is not different from untreated, “×” is worse than untreated. .
【0031】上記表3から、2次ケア後の毛髪内pHが
4.5の場合には、染毛直後に比べて変色してしまい
(比較例3)、一方、2次ケア後の毛髪内pHが7.3
の場合には、残存アルカリの除去が不十分なため毛髪に
ダメージが蓄積された(比較例4)。これに対して、2
次ケア後の毛髪内pHが6.0の場合には、染毛直後か
ら数日にわたって、毛髪内のアルカリを少しずつ無理な
く除去したことになり、ダメージの蓄積を回避できるう
え、過度な酸化による変色も見られなかった(実施例
4)。つまり、1次ケアとして実施例3を採用し、2次
ケアとして実施例4を採用すれば、図1の実線に近いp
H回復曲線が得られ、染毛を繰り返し行っても、髪を元
の状態に近づけることができ、良好なコンディションを
保つことができる。From Table 3 above, when the pH in the hair after the secondary care is 4.5, the color is discolored as compared to immediately after the hair dyeing (Comparative Example 3), while the pH in the hair after the secondary care is increased. pH 7.3
In the case of (1), damage was accumulated on the hair due to insufficient removal of the residual alkali (Comparative Example 4). In contrast, 2
If the pH in the hair after the next care is 6.0, it means that the alkali in the hair has been removed little by little over a few days immediately after the hair dyeing, so that accumulation of damage can be avoided and excessive oxidation No discoloration was observed (Example 4). That is, if the third embodiment is adopted as the primary care and the fourth embodiment is adopted as the secondary care, p close to the solid line in FIG.
An H recovery curve is obtained, and the hair can be brought close to the original state even when the hair is repeatedly dyed, and a good condition can be maintained.
【図1】 毛髪内pHの回復曲線を表すグラフである。FIG. 1 is a graph showing a recovery curve of pH in hair.
───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4C083 AB032 AC072 AC122 AC302 AC532 AC582 AC662 AC692 AC712 AC782 AD132 AD152 AD412 BB44 CC33 CC38 CC39 EE12 ──────────────────────────────────────────────────続 き Continued on the front page F term (reference) 4C083 AB032 AC072 AC122 AC302 AC532 AC582 AC662 AC692 AC712 AC782 AD132 AD152 AD412 BB44 CC33 CC38 CC39 EE12
Claims (7)
染毛することにより毛髪内pHが8〜10になった毛髪
に対して、この染毛剤を洗い流し、続いて10重量%水
溶液のpHが3〜5.5のアフタートリートメント剤を
毛髪に塗布し、放置したあと洗い流すことにより毛髪内
pHを7.5〜9に調整することを特徴とする毛髪処理
方法。1. A hair dyeing with an oxidized hair dye containing an alkaline agent, the pH of which has been adjusted to 8 to 10 in hair, the hair dye is washed off, and then a 10% by weight aqueous solution A hair treatment method, wherein an after treatment agent having a pH of 3 to 5.5 is applied to hair, and the pH in the hair is adjusted to 7.5 to 9 by leaving the hair to stand and then washing it away.
染毛することにより毛髪内pHが8〜10になった毛髪
に対して、この染毛剤を洗い流し、続いて10重量%水
溶液のpHが3〜5.5のアフタートリートメント剤を
毛髪に塗布し、放置したあと洗い流すことにより毛髪内
pHを7.5〜9に調整し、その後、10重量%水溶液
のpHが3.5〜6.5のアフターケア毛髪処理剤で複
数回処理することにより毛髪内pHを5.5〜6.5に
調整することを特徴とする毛髪処理方法。2. A hair dyeing with an oxidized hair dye containing an alkali agent, the pH of the hair having been adjusted to 8 to 10 is washed away from the hair, followed by a 10% by weight aqueous solution. The after-treatment agent having a pH of 3 to 5.5 is applied to the hair, and the pH in the hair is adjusted to 7.5 to 9 by leaving the hair, and then the pH of the 10% by weight aqueous solution is adjusted to 3.5 to 9. A hair treatment method comprising adjusting the pH in the hair to 5.5 to 6.5 by treating it multiple times with the aftercare hair treating agent of 6.5.
処理することにより毛髪内pHを5.5〜6.5に調整
する請求項2記載の毛髪処理方法。3. The hair treatment method according to claim 2, wherein the pH in the hair is adjusted to 5.5 to 6.5 by treating the hair with the aftercare hair treating agent at least three times.
フタートリートメント剤よりも10重量%水溶液のpH
が高いことを特徴とする請求項2又は3記載の毛髪処理
方法。4. The aftercare hair treatment agent has a pH of 10% by weight aqueous solution more than that of the aftertreatment agent.
The hair treatment method according to claim 2, wherein the hair treatment is high.
量%水溶液のpHが4〜6.5であり、前記アフタート
リートメント剤は、10重量%水溶液のpHが3〜4.
5であることを特徴とする請求項4記載の毛髪処理方
法。5. The aftercare hair treatment agent has a 10% by weight aqueous solution having a pH of 4 to 6.5, and the aftertreatment agent has a 10% by weight aqueous solution having a pH of 3 to 4.
The hair treatment method according to claim 4, wherein
理方法に用いられるアフタートリートメント剤。6. An after treatment agent used in the hair treatment method according to claim 1.
理方法に用いられるアフターケア毛髪処理剤。7. An aftercare hair treatment agent used in the hair treatment method according to any one of claims 2 to 5.
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| JP2000315276A JP4417538B2 (en) | 2000-10-16 | 2000-10-16 | Hair treatment method |
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| JP2000315276A JP4417538B2 (en) | 2000-10-16 | 2000-10-16 | Hair treatment method |
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Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010195707A (en) * | 2009-02-24 | 2010-09-09 | Arimino Kagaku Kk | Aftertreatment agent for hair dyeing treatment and method for using the same |
| JP2013129629A (en) * | 2011-12-21 | 2013-07-04 | Nakano Seiyaku Kk | After-treatment agent for hair dyeing and hair treatment method |
| JP2018535268A (en) * | 2015-11-24 | 2018-11-29 | ロレアル | Composition for treating hair |
| US10993896B2 (en) | 2015-05-01 | 2021-05-04 | L'oreal | Compositions for altering the color of hair |
| JP2021109864A (en) * | 2020-01-15 | 2021-08-02 | タカラベルモント株式会社 | Hair treatment agent, hair treatment agent set, and hair treatment method |
| US11083675B2 (en) | 2015-11-24 | 2021-08-10 | L'oreal | Compositions for altering the color of hair |
| US11090249B2 (en) | 2018-10-31 | 2021-08-17 | L'oreal | Hair treatment compositions, methods, and kits for treating hair |
| US11135150B2 (en) | 2016-11-21 | 2021-10-05 | L'oreal | Compositions and methods for improving the quality of chemically treated hair |
| US11419809B2 (en) | 2019-06-27 | 2022-08-23 | L'oreal | Hair treatment compositions and methods for treating hair |
| US11433011B2 (en) | 2017-05-24 | 2022-09-06 | L'oreal | Methods for treating chemically relaxed hair |
| US11596588B2 (en) | 2017-12-29 | 2023-03-07 | L'oreal | Compositions for altering the color of hair |
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| JPS60119279A (en) * | 1983-11-29 | 1985-06-26 | サンスター株式会社 | Keratine fiber dyeing agent and method |
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| JPH02212410A (en) * | 1989-02-14 | 1990-08-23 | Mandamu:Kk | Composition agent for conditioning alkali-treated hair |
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Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010195707A (en) * | 2009-02-24 | 2010-09-09 | Arimino Kagaku Kk | Aftertreatment agent for hair dyeing treatment and method for using the same |
| JP2013129629A (en) * | 2011-12-21 | 2013-07-04 | Nakano Seiyaku Kk | After-treatment agent for hair dyeing and hair treatment method |
| US10993896B2 (en) | 2015-05-01 | 2021-05-04 | L'oreal | Compositions for altering the color of hair |
| JP2018535268A (en) * | 2015-11-24 | 2018-11-29 | ロレアル | Composition for treating hair |
| US12048759B2 (en) | 2015-11-24 | 2024-07-30 | L'oreal | Compositions for treating the hair |
| US11083675B2 (en) | 2015-11-24 | 2021-08-10 | L'oreal | Compositions for altering the color of hair |
| US11191706B2 (en) | 2015-11-24 | 2021-12-07 | L'oreal | Compositions for altering the color of hair |
| US11213470B2 (en) | 2015-11-24 | 2022-01-04 | L'oreal | Compositions for treating the hair |
| US11135150B2 (en) | 2016-11-21 | 2021-10-05 | L'oreal | Compositions and methods for improving the quality of chemically treated hair |
| US11433011B2 (en) | 2017-05-24 | 2022-09-06 | L'oreal | Methods for treating chemically relaxed hair |
| US11596588B2 (en) | 2017-12-29 | 2023-03-07 | L'oreal | Compositions for altering the color of hair |
| US11090249B2 (en) | 2018-10-31 | 2021-08-17 | L'oreal | Hair treatment compositions, methods, and kits for treating hair |
| US11975092B2 (en) | 2018-10-31 | 2024-05-07 | L'oreal | Hair treatment compositions, methods, and kits for treating hair |
| US11419809B2 (en) | 2019-06-27 | 2022-08-23 | L'oreal | Hair treatment compositions and methods for treating hair |
| JP2021109864A (en) * | 2020-01-15 | 2021-08-02 | タカラベルモント株式会社 | Hair treatment agent, hair treatment agent set, and hair treatment method |
| JP7656886B2 (en) | 2020-01-15 | 2025-04-04 | タカラベルモント株式会社 | Hair treatment agent, hair treatment agent set, and hair treatment method |
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