JP7402603B2 - Pretreatment agent and oxidative hair dyeing or bleaching method - Google Patents
Pretreatment agent and oxidative hair dyeing or bleaching method Download PDFInfo
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- JP7402603B2 JP7402603B2 JP2018132884A JP2018132884A JP7402603B2 JP 7402603 B2 JP7402603 B2 JP 7402603B2 JP 2018132884 A JP2018132884 A JP 2018132884A JP 2018132884 A JP2018132884 A JP 2018132884A JP 7402603 B2 JP7402603 B2 JP 7402603B2
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- 210000004209 hair Anatomy 0.000 title claims description 56
- 230000001590 oxidative effect Effects 0.000 title claims description 38
- 238000000034 method Methods 0.000 title claims description 20
- 238000004061 bleaching Methods 0.000 title claims description 17
- 238000004043 dyeing Methods 0.000 title claims description 17
- 239000003795 chemical substances by application Substances 0.000 claims description 76
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 51
- JOOXCMJARBKPKM-UHFFFAOYSA-N 4-oxopentanoic acid Chemical compound CC(=O)CCC(O)=O JOOXCMJARBKPKM-UHFFFAOYSA-N 0.000 claims description 38
- 239000000118 hair dye Substances 0.000 claims description 21
- 229940040102 levulinic acid Drugs 0.000 claims description 19
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 17
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 17
- 239000011976 maleic acid Substances 0.000 claims description 17
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 17
- 230000002378 acidificating effect Effects 0.000 claims description 8
- 239000003051 hair bleaching agent Substances 0.000 claims description 8
- 239000004475 Arginine Substances 0.000 claims description 5
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims description 5
- 230000008569 process Effects 0.000 claims description 5
- 239000003814 drug Substances 0.000 claims description 2
- 229940079593 drug Drugs 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims description 2
- 238000011282 treatment Methods 0.000 description 23
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 230000003700 hair damage Effects 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000007844 bleaching agent Substances 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 11
- 238000002156 mixing Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 7
- 239000007800 oxidant agent Substances 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 239000000975 dye Substances 0.000 description 6
- 239000002453 shampoo Substances 0.000 description 5
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 4
- 241000124033 Salix Species 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 231100000640 hair analysis Toxicity 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 238000002203 pretreatment Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 2
- AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 2
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- LEVWYRKDKASIDU-IMJSIDKUSA-N L-cystine Chemical compound [O-]C(=O)[C@@H]([NH3+])CSSC[C@H]([NH3+])C([O-])=O LEVWYRKDKASIDU-IMJSIDKUSA-N 0.000 description 2
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 239000001099 ammonium carbonate Substances 0.000 description 2
- 235000012501 ammonium carbonate Nutrition 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 2
- 235000011130 ammonium sulphate Nutrition 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 229960003067 cystine Drugs 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000003695 hair diameter Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 230000007794 irritation Effects 0.000 description 2
- 229940102253 isopropanolamine Drugs 0.000 description 2
- 239000001630 malic acid Substances 0.000 description 2
- 235000011090 malic acid Nutrition 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910000000 metal hydroxide Inorganic materials 0.000 description 2
- 150000004692 metal hydroxides Chemical class 0.000 description 2
- 229910001463 metal phosphate Inorganic materials 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 2
- 150000004986 phenylenediamines Chemical class 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 210000004761 scalp Anatomy 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- 229910000162 sodium phosphate Inorganic materials 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- 229940113490 2,4-diaminophenoxyethanol hydrochloride Drugs 0.000 description 1
- KZTWOUOZKZQDMN-UHFFFAOYSA-N 2,5-diaminotoluene sulfate Chemical compound OS(O)(=O)=O.CC1=CC(N)=CC=C1N KZTWOUOZKZQDMN-UHFFFAOYSA-N 0.000 description 1
- PBVFDMZFBPZIMC-UHFFFAOYSA-N 2-(2,4-diaminophenoxy)ethanol;hydrochloride Chemical compound Cl.NC1=CC=C(OCCO)C(N)=C1 PBVFDMZFBPZIMC-UHFFFAOYSA-N 0.000 description 1
- FECNOIODIVNEKI-UHFFFAOYSA-N 2-[(2-aminobenzoyl)amino]benzoic acid Chemical class NC1=CC=CC=C1C(=O)NC1=CC=CC=C1C(O)=O FECNOIODIVNEKI-UHFFFAOYSA-N 0.000 description 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 1
- DBFYESDCPWWCHN-UHFFFAOYSA-N 5-amino-2-methylphenol Chemical compound CC1=CC=C(N)C=C1O DBFYESDCPWWCHN-UHFFFAOYSA-N 0.000 description 1
- 201000004384 Alopecia Diseases 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
- 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 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 229940081733 cetearyl alcohol Drugs 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 230000003676 hair loss Effects 0.000 description 1
- 208000024963 hair loss Diseases 0.000 description 1
- 230000003699 hair surface Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- PETZRPLPRZXTAD-UHFFFAOYSA-N n-(4-aminophenyl)nitramide;hydrochloride Chemical compound Cl.NC1=CC=C(N[N+]([O-])=O)C=C1 PETZRPLPRZXTAD-UHFFFAOYSA-N 0.000 description 1
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
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Description
本発明は、酸化染毛剤又は脱色剤を塗布する前の毛髪に塗布して使用される前処理剤、及び当該前処理剤を使用する工程を有する酸化染毛方法又は脱色方法に関するものである。 The present invention relates to a pretreatment agent that is used by applying an oxidative hair dye or bleaching agent to the hair, and an oxidative hair dyeing or bleaching method that includes a step of using the pretreatment agent. .
毛髪に対して、アンモニアなどのアルカリ剤及び過硫酸塩、過酸化水素などの酸化剤が配合されている酸化染毛剤を使用する酸化染毛方法や、脱色方法においては、アルカリ剤が毛髪表面のキューティクルを開き、酸化染毛剤や脱色剤を毛髪内部に浸透し易くする。この浸透し易くする状態は、毛髪内部のタンパク質が流出し易い状態であるともいえ、タンパク質の流出は、毛髪の損傷に直結する。このような損傷は、通常、毛先に近づくほど蓄積している。 In oxidative hair dyeing methods that use oxidizing hair dyes that contain alkaline agents such as ammonia and oxidizing agents such as persulfates and hydrogen peroxide, and bleaching methods, alkaline agents are applied to the hair surface. Opens the hair cuticle, making it easier for oxidative hair dyes and bleaching agents to penetrate into the hair. This state of easy penetration can be said to be a state in which the proteins inside the hair tend to leak out, and protein leakage is directly linked to hair damage. Such damage usually accumulates closer to the ends of the hair.
損傷の蓄積の程度にかかわらず、毛髪損傷の抑制は望まれる。これに応えるべく、酸化染毛剤又は脱色剤を毛髪に塗布する前に、前処理剤を塗布することが知られている。例えば特許文献1には、第1剤及び第2剤からなる毛髪処理剤組成物を前処理剤とし、第1剤が0.5~4質量%のシスチン、アルカリ剤を含有し、pH8.5~11であり、第2剤が有機酸を含有し、pH3~5であると開示されている(特許文献1の請求項1、請求項2、請求項4参照)。 Regardless of the extent of damage accumulation, inhibition of hair damage is desirable. In response to this, it is known to apply a pretreatment agent before applying an oxidative hair dye or bleaching agent to the hair. For example, in Patent Document 1, a hair treatment composition consisting of a first part and a second part is used as a pretreatment agent, the first part contains 0.5 to 4% by mass of cystine and an alkaline agent, and has a pH of 8.5. -11, and the second agent contains an organic acid and has a pH of 3 to 5 (see claims 1, 2, and 4 of Patent Document 1).
しかしながら、特許文献1に開示されている2剤式の前処理剤は、1剤式の前処理剤に比べて、製造する際、使用する際共に煩雑である。望ましくは、1剤式で、2剤式と同等以上の毛髪損傷の抑制が可能な前処理剤である。 However, the two-part pretreatment agent disclosed in Patent Document 1 is more complicated to manufacture and use than the one-part pretreatment agent. Desirably, the pretreatment agent is a one-part pretreatment agent that can suppress hair damage to the same degree or more as a two-part method.
本発明は、上記事情に鑑み、1剤式で毛髪損傷の抑制に優れる前処理剤、並びにこの前処理剤を使用する酸化染毛方法及び脱色方法の提供を目的とする。 In view of the above circumstances, the present invention aims to provide a one-component pretreatment agent that is excellent in suppressing hair damage, as well as an oxidative hair dyeing method and a bleaching method using this pretreatment agent.
本発明者等が鋭意検討を行った結果、特定の有機酸を配合した酸性の1剤式前処理剤を使用すれば、毛髪損傷の指標となる初期弾性率低下の抑制に優れることを見出し、本発明を完成するに至った。 As a result of extensive research, the present inventors have discovered that the use of an acidic one-part pretreatment agent containing a specific organic acid is effective in suppressing the decrease in initial elastic modulus, which is an indicator of hair damage. The present invention has now been completed.
すなわち、本発明に係る前処理剤は、酸化染毛剤又は脱色剤を塗布する前の毛髪に塗布するものであって、クエン酸、レブリン酸及びマレイン酸から選ばれた一種又は二種以上が配合され、酸性、且つ、1剤式であることを特徴とする。 That is, the pretreatment agent according to the present invention is applied to hair before applying an oxidative hair dye or bleaching agent, and contains one or more selected from citric acid, levulinic acid, and maleic acid. It is characterized by being formulated, acidic, and a one-drug formula.
本発明に係る前処理剤は、pHが5.0以下であると良い。このpH範囲であると、初期弾性率低下の抑制により優れる。 The pretreatment agent according to the present invention preferably has a pH of 5.0 or less. Within this pH range, the reduction in initial elastic modulus is better suppressed.
本発明に係る前処理剤は、クエン酸、レブリン酸及びマレイン酸の総配合量が1質量%以上であると良い。この総配合量であると、初期弾性率低下の抑制により優れる。 In the pretreatment agent according to the present invention, the total amount of citric acid, levulinic acid, and maleic acid is preferably 1% by mass or more. This total amount is more effective in suppressing a decrease in initial elastic modulus.
本発明に係る酸化染毛方法又は脱色方法は、クエン酸、レブリン酸及びマレイン酸から選ばれた一種又は二種以上が配合され、酸性、且つ、1剤式である前処理剤を毛髪に塗布する前処理工程と、酸化染毛剤又は脱色剤を重ねて塗布する酸化染毛処理工程又は脱色処理工程とを備えることを特徴とする。 The oxidative hair dyeing method or bleaching method according to the present invention includes applying to hair an acidic, one-part pretreatment agent containing one or more selected from citric acid, levulinic acid, and maleic acid. The method is characterized by comprising a pretreatment step of applying the oxidative hair dye or bleaching agent, and an oxidizing hair dyeing treatment step or a decoloring treatment step of applying the oxidative hair dye or bleaching agent in layers.
本発明に係る1剤式の前処理剤によれば、クエン酸、レブリン酸及びマレイン酸から選ばれた一種又は二種以上が配合された酸性のものであるから、酸化染毛処理又は脱色処理に伴う毛髪損傷の抑制に優れる。 According to the one-component pretreatment agent according to the present invention, since it is an acidic one containing one or more selected from citric acid, levulinic acid, and maleic acid, it can be used for oxidative hair dyeing or bleaching treatment. Excellent in suppressing hair damage caused by hair loss.
また、本発明に係る酸化染毛方法又は脱色方法によれば、クエン酸、レブリン酸及びマレイン酸から選ばれた一種又は二種以上が配合され、酸性、且つ、1剤式である前処理剤を毛髪に塗布する前処理工程を備えるから、酸化染毛処理又は脱色処理に伴う毛髪損傷の抑制に優れる。 Further, according to the oxidative hair dyeing method or bleaching method according to the present invention, the pretreatment agent is acidic and is a one-component type, which contains one or more selected from citric acid, levulinic acid, and maleic acid. Since it includes a pretreatment step of applying the hair to the hair, it is excellent in suppressing hair damage caused by oxidative hair dyeing or bleaching.
本発明の実施形態に基づき、本発明を以下に説明する。
本実施形態に係る前処理剤は、クエン酸、レブリン酸及びマレイン酸から選ばれた一種又は二種以上と、水とが配合されたものである(水の配合量は、例えば80質量%以上)。また、公知の前処理剤に使用されている原料を、更に任意原料として配合しても良い。
The invention will be described below based on embodiments of the invention.
The pretreatment agent according to the present embodiment is a mixture of one or more selected from citric acid, levulinic acid, and maleic acid and water (the amount of water blended is, for example, 80% by mass or more). ). In addition, raw materials used in known pretreatment agents may be further blended as optional raw materials.
上記の通り本実施形態の前処理剤には、クエン酸、レブリン酸及びマレイン酸から選ばれた一種又は二種以上が配合され、クエン酸の配合が好適である。このときのクエン酸、レブリン酸及びマレイン酸の総配合量は、毛髪の損傷を抑制する観点から、1質量%以上が良く、3質量%以上が好ましく、5質量%以上がより好ましい。前記の総配合量の上限は、例えば10質量%である。クエン酸を配合する場合、クエン酸の配合量は、毛髪の損傷を抑制する観点から、1質量%以上が良く、3質量%以上が好ましく、5質量%以上がより好ましい。レブリン酸を配合する場合、レブリン酸の配合量は、毛髪の損傷を抑制する観点から、1質量%以上が良く、3質量%以上が好ましく、5質量%以上がより好ましい。また、マレイン酸を配合する場合、マレイン酸の配合量は、毛髪の損傷を抑制する観点から、1質量%以上が良く、3質量%以上が好ましく、5質量%以上がより好ましい。 As described above, the pretreatment agent of this embodiment contains one or more selected from citric acid, levulinic acid, and maleic acid, and citric acid is preferably blended. The total blending amount of citric acid, levulinic acid, and maleic acid at this time is preferably 1% by mass or more, preferably 3% by mass or more, and more preferably 5% by mass or more from the viewpoint of suppressing hair damage. The upper limit of the total blending amount is, for example, 10% by mass. When blending citric acid, the blending amount of citric acid is preferably 1% by mass or more, preferably 3% by mass or more, and more preferably 5% by mass or more, from the viewpoint of suppressing hair damage. When blending levulinic acid, the blending amount of levulinic acid is preferably 1% by mass or more, preferably 3% by mass or more, and more preferably 5% by mass or more, from the viewpoint of suppressing hair damage. Further, when blending maleic acid, the blending amount of maleic acid is preferably 1% by mass or more, preferably 3% by mass or more, and more preferably 5% by mass or more from the viewpoint of suppressing hair damage.
上記任意原料としては、界面活性剤、多価アルコール、高分子化合物、防腐剤、pH調整剤、香料などである。 Examples of the above-mentioned optional raw materials include surfactants, polyhydric alcohols, polymer compounds, preservatives, pH adjusters, fragrances, and the like.
本実施形態の前処理剤は、酸性であり、毛髪の損傷を抑制する観点から、当該前処理剤のpHは、5.0以下が良く、4.0以下が好ましい。このpHの下限は、例えば3.0である。pHの調整が必要な場合、アルギニンなどの公知のアルカリなどを使用して調整すると良い。 The pretreatment agent of this embodiment is acidic, and from the viewpoint of suppressing hair damage, the pH of the pretreatment agent is preferably 5.0 or less, preferably 4.0 or less. The lower limit of this pH is, for example, 3.0. If the pH needs to be adjusted, it may be adjusted using a known alkali such as arginine.
本実施形態の前処理剤の剤型は、毛髪への浸透性に優れる液状が良い。このときの前処理剤の粘度は、例えば1000mPa・s以下である。当該粘度は、B型粘度計を使用し、適宜なローターを用いて、25℃でローター回転数12rpmとして計測したときの、計測開始から60秒後の値を意味している。 The pretreatment agent of this embodiment preferably has a liquid form that has excellent permeability into the hair. The viscosity of the pretreatment agent at this time is, for example, 1000 mPa·s or less. The viscosity means the value measured 60 seconds after the start of measurement using a B-type viscometer with an appropriate rotor at 25° C. and a rotor rotation speed of 12 rpm.
本実施形態の前処理剤は、一つの剤で構成される1剤式のものであり、酸化染毛処理又は脱色処理を行う前の毛髪に塗布して使用される。なお、本実施形態の前処理剤を塗布する前の毛髪は、洗浄の必要がある場合には、アニオン界面活性剤などが配合されたシャンプー組成物を使用して洗浄する。 The pretreatment agent of the present embodiment is a one-component type consisting of one agent, and is used by applying it to hair before oxidative hair dyeing or bleaching. In addition, if the hair before applying the pretreatment agent of this embodiment needs to be washed, it is washed using a shampoo composition containing an anionic surfactant or the like.
本実施形態の酸化染毛方法は、本実施形態の前処理剤を毛髪に塗布する前処理工程と、酸化染毛剤を重ねて塗布する酸化染毛処理工程とを備える。前処理工程と酸化染毛処理工程は連続しており、両工程間において、毛髪の水洗、加熱などの他の処理を一切行わない。 The oxidative hair dyeing method of the present embodiment includes a pretreatment step of applying the pretreatment agent of the present embodiment to hair, and an oxidative hair dyeing step of applying the oxidative hair dye in layers. The pretreatment step and the oxidative hair dyeing treatment step are continuous, and no other treatments such as washing or heating the hair are performed between the two steps.
酸化染毛処理工程では、公知の酸化染毛処理と同様、酸化染毛剤を使用して染毛する。ここで使用する酸化染毛剤は、公知の酸化染毛剤であると良い。 In the oxidative hair dyeing process, hair is dyed using an oxidative hair dye, similar to known oxidative hair dyeing processes. The oxidative hair dye used here is preferably a known oxidative hair dye.
上記酸化染毛剤は、例えば、酸化染料、アルカリ剤及び酸化剤が配合されたアルカリ性のものが挙げられる。なお、酸化染毛剤の剤型は、毛髪への塗布、垂れ落ち等のハンドリング性を考慮すれは、クリーム状が良い。 Examples of the above-mentioned oxidative hair dyes include alkaline ones containing an oxidizing dye, an alkaline agent, and an oxidizing agent. Note that the formulation of the oxidative hair dye is preferably cream-like in consideration of handling properties such as application to hair and dripping.
上記の例示した酸化染毛剤における酸化染料は、酸化反応により単独で発色する公知の染料中間体から選択した一種又は二種以上を採用する。染料中間体としては、硫酸トルエン-2,5-ジアミン、塩酸ニトロパラフェニレンジアミン、パラフェニレンジアミン等のフェニレンジアミン誘導体などが挙げられる。また、酸化染料として、染料中間体により酸化されて色調を呈する公知のカップラーから選択された一種または二種以上を採用しても良い。カップラーとしては、塩酸2,4-ジアミノフェノキシエタノール、塩酸メタフェニレンジアミン等のフェニレンジアミン誘導体;5-アミノオルトクレゾール、メタアミノフェノール等のアミノフェノール誘導体;レゾルシン;などが挙げられる。 As the oxidation dye in the above-mentioned oxidation hair dye, one or more selected from known dye intermediates that develop color by themselves through an oxidation reaction are employed. Examples of the dye intermediate include phenylenediamine derivatives such as toluene-2,5-diamine sulfate, nitroparaphenylenediamine hydrochloride, and paraphenylenediamine. Further, as the oxidation dye, one or more kinds selected from known couplers that exhibit a color tone when oxidized by a dye intermediate may be used. Examples of the coupler include phenylenediamine derivatives such as 2,4-diaminophenoxyethanol hydrochloride and metaphenylenediamine hydrochloride; aminophenol derivatives such as 5-aminoorthocresol and meta-aminophenol; and resorcinol.
上記の例示した酸化染毛剤におけるアルカリ剤は、酸化染毛剤に含まれる酸化剤の作用を促進するとともに、毛髪を膨潤させて毛髪への染料の浸透性を向上させることにより、染色性を向上させる。当該アルカリ剤としては、水酸化ナトリウム、水酸化カリウム等の金属水酸化物;炭酸ナトリウム、炭酸カリウム等の金属炭酸塩;リン酸ナトリウム等の金属リン酸塩;アンモニア;炭酸アンモニウム、硫酸アンモニウム等のアンモニウム塩;モノエタノールアミン、トリエタノールアミン、イソプロパノールアミン等のアルカノールアミン;アルギニン等の塩基性アミノ酸;等が挙げられる。 The alkaline agents in the oxidative hair dyes listed above promote the action of the oxidizing agent contained in the oxidative hair dyes, and also improve the dyeability by swelling the hair and improving the permeability of the dye into the hair. Improve. The alkaline agents include metal hydroxides such as sodium hydroxide and potassium hydroxide; metal carbonates such as sodium carbonate and potassium carbonate; metal phosphates such as sodium phosphate; ammonia; ammonium such as ammonium carbonate and ammonium sulfate; Salts; alkanolamines such as monoethanolamine, triethanolamine, and isopropanolamine; basic amino acids such as arginine; and the like.
上記の例示した酸化染毛剤における酸化剤は、例えば、過酸化水素が挙げられる。 Examples of the oxidizing agent in the above-mentioned oxidative hair dye include hydrogen peroxide.
上記の例示した酸化染毛剤は、アルカリ性であるが、当該酸化染毛剤のpHは、良好な染色性と頭皮への刺激を低減するためには9.0以上11.0以下であり、9.5以上10.5以下が良い。 The above-exemplified oxidative hair dye is alkaline, but the pH of the oxidative hair dye is 9.0 or more and 11.0 or less in order to have good dyeability and reduce irritation to the scalp. 9.5 or more and 10.5 or less is good.
本実施形態の脱色方法は、本実施形態の前処理剤を毛髪に塗布する前処理工程と、前処理剤が塗布された状態の毛髪に脱色剤を重ねて塗布する脱色処理工程とを備える。前処理工程と脱色処理工程は連続しており、両工程間において、毛髪の水洗、加熱などの他の処理を一切行わない。 The bleaching method of the present embodiment includes a pretreatment step of applying the pretreatment agent of the present embodiment to hair, and a bleaching treatment step of overlappingly applying the bleaching agent to the hair to which the pretreatment agent has been applied. The pretreatment step and the bleaching treatment step are continuous, and no other treatments such as washing or heating the hair are performed between the two steps.
脱色処理工程では、公知の脱色処理と同様、脱色剤を使用して毛髪のメラニンを酸化脱色させる。ここで使用する脱色剤は、公知の脱色剤であると良い。 In the bleaching treatment step, similar to known bleaching treatments, a bleaching agent is used to oxidize and bleach hair melanin. The decolorizing agent used here is preferably a known decolorizing agent.
上記脱色剤は、例えば、アルカリ剤及び酸化剤が配合されたアルカリ性のものが挙げられる。なお、脱色剤の剤型は、毛髪への塗布、垂れ落ち等のハンドリング性を考慮すれは、クリーム状が良い。 Examples of the above-mentioned decolorizing agent include alkaline agents containing an alkaline agent and an oxidizing agent. Note that the dosage form of the bleaching agent is preferably cream-like in consideration of handling properties such as application to hair and dripping.
上記の例示した脱色剤におけるアルカリ剤は、酸化剤の作用を促進するとともに、毛髪を膨潤させて毛髪への脱色剤の浸透性を向上させる。当該アルカリ剤としては、水酸化ナトリウム、水酸化カリウム等の金属水酸化物;炭酸ナトリウム、炭酸カリウム等の金属炭酸塩;リン酸ナトリウム等の金属リン酸塩;アンモニア;炭酸アンモニウム、硫酸アンモニウム等のアンモニウム塩;モノエタノールアミン、トリエタノールアミン、イソプロパノールアミン等のアルカノールアミン;アルギニン等の塩基性アミノ酸;等が挙げられる。 The alkaline agent in the bleaching agent exemplified above not only promotes the action of the oxidizing agent, but also swells the hair and improves the permeability of the bleaching agent into the hair. The alkaline agents include metal hydroxides such as sodium hydroxide and potassium hydroxide; metal carbonates such as sodium carbonate and potassium carbonate; metal phosphates such as sodium phosphate; ammonia; ammonium such as ammonium carbonate and ammonium sulfate; Salts; alkanolamines such as monoethanolamine, triethanolamine, and isopropanolamine; basic amino acids such as arginine; and the like.
上記の例示した脱色剤における酸化剤は、例えば、過硫酸塩、過酸化水素が挙げられる。 Examples of the oxidizing agent in the above-mentioned decolorizing agent include persulfate and hydrogen peroxide.
上記の例示した脱色剤は、アルカリ性であるが、当該脱色剤のpHは、良好な脱色性と頭皮への刺激を低減するためには9.0以上11.0以下であり、9.5以上10.5以下が良い。 The above-mentioned bleaching agent is alkaline, but the pH of the bleaching agent is 9.0 or more and 11.0 or less, and 9.5 or more in order to have good bleaching properties and reduce irritation to the scalp. 10.5 or less is good.
以下、実施例に基づき本発明を詳述するが、この実施例の記載に基づいて本発明が限定的に解釈されるものではない。 The present invention will be described in detail below based on Examples, but the present invention should not be interpreted as being limited based on the description of these Examples.
実施例及び比較例の前処理剤を製造し、これら前処理剤及び脱色剤による処理を行った。詳細は、次の通りである。 Pretreatment agents of Examples and Comparative Examples were manufactured, and treatments were performed with these pretreatment agents and decolorizing agents. Details are as follows.
(実施例1a~1c、比較例1a~1c)
クエン酸、レブリン酸、マレイン酸、グリコール酸又はリンゴ酸と、水とを配合し、アルギニンでpHを3.5に調整することにより、実施例1a~1c及び比較例1a~1bの液状の前処理剤を得た(クエン酸などの配合量は下記表1の通り)。
(Examples 1a to 1c, Comparative Examples 1a to 1c)
By blending citric acid, levulinic acid, maleic acid, glycolic acid, or malic acid with water and adjusting the pH to 3.5 with arginine, the liquid preparations of Examples 1a to 1c and Comparative Examples 1a to 1b were prepared. A processing agent was obtained (the amounts of citric acid and the like are shown in Table 1 below).
日本人女性から採取した長さ18cm程度、0.5gの複数の毛束を作成した。各毛束に実施例1a~1c及び比較例1a~1bのいずれかの前処理剤0.2gを塗布した後、この前処理剤を洗い流すことなく、2.0gの脱色剤(ミルボン社製「パウダーブリーチ」0.5質量部とミルボン社製「オルディーブ アディクシー オキシダン6.0」1.5質量部との混合物)を重ねて塗布し、室温で30分放置した。その後、毛束を水洗し、ミルボン社製シャンプー「ノイドゥーエ・ウィローリュクス・シャンプー」を使用して更に洗浄してから、ミルボン社製洗い流すトリートメント「ノイドゥーエ・ウィローリュクス・トリートメント」を使用して処理した後、温風で乾燥させた。そして、前処理剤の塗布から乾燥までを、合計3回行った。 A plurality of hair bundles approximately 18 cm long and weighing 0.5 g were prepared from Japanese women. After applying 0.2 g of the pre-treatment agent of any of Examples 1a to 1c and Comparative Examples 1a to 1b to each hair bundle, without washing off the pre-treatment agent, apply 2.0 g of a bleaching agent (manufactured by Milbon Co., Ltd.). A mixture of 0.5 parts by mass of "Powder Bleach" and 1.5 parts by mass of "Ordeve Addixie Oxidan 6.0" manufactured by Milbon was applied in layers and left at room temperature for 30 minutes. After that, the hair strands are washed with water, further washed with Milbon's shampoo "Neidoue Willow Luxe Shampoo", and then treated with Milbon's wash-off treatment "Neidoue Willow Luxe Treatment". , and dried with warm air. The process from applying the pretreatment agent to drying was performed a total of three times.
また、比較例1cとして、前処理剤の塗布を省略した以外は実施例1aと同様にした処理を行った。 Further, as Comparative Example 1c, the same treatment as in Example 1a was performed except that the application of the pretreatment agent was omitted.
上記3回の処理後の毛束の毛髪について、オリエンテック社製「TENSILON UTM-II-20」を使用し、単位断面積(25℃、50%RHに保った恒温恒湿室内で12時間以上調湿後、毛径測定装置を用いて測定した毛径から算出)当たりの初期弾性率を測定した。測定条件は、測定前に毛髪試料を水に12時間以上浸漬、測定時に毛髪試料を水中浸漬、温度25℃、引張り速度2mm/分、毛髪試料の引張り間隔20mmとした。 The hair bundles after the above three treatments were treated using "TENSILON UTM-II-20" manufactured by Orientech Co., Ltd. for 12 hours or more in a constant temperature and humidity room maintained at a unit cross-sectional area (25°C, 50% RH). After conditioning the humidity, the initial elastic modulus (calculated from the hair diameter measured using a hair diameter measuring device) was measured. The measurement conditions were that the hair sample was immersed in water for 12 hours or more before the measurement, the hair sample was immersed in water during the measurement, the temperature was 25°C, the pulling speed was 2 mm/min, and the hair sample pulling interval was 20 mm.
下表1に、配合した成分、pHと共に、初期弾性率の結果を示す。なお、下記表1における各初期弾性率は、毛髪5本の平均値である。
上記表1において、クエン酸、レブリン酸又はマレイン酸を配合した前処理剤を使用した実施例1a~1cは、前処理剤を使用しなかった比較例1cよりも初期弾性率に優れていたことを確認できる。一方、グリコール酸又はリンゴ酸を配合した前処理剤を使用した比較例1a~1bは、前処理剤を使用しなかった比較例1cと同等以下の初期弾性率であったことを確認できる。 In Table 1 above, Examples 1a to 1c, which used a pretreatment agent containing citric acid, levulinic acid, or maleic acid, had better initial elastic modulus than Comparative Example 1c, which did not use a pretreatment agent. You can check. On the other hand, it can be confirmed that Comparative Examples 1a and 1b, which used a pretreatment agent containing glycolic acid or malic acid, had an initial elastic modulus equal to or lower than Comparative Example 1c, which did not use a pretreatment agent.
(参考例、実施例2、比較例2)
特開2014-80384号公報に記載の2剤式毛髪処理剤組成物(2剤式前処理剤)との比較を行った。その詳細を以下に示す。
(Reference example, Example 2, Comparative example 2)
A comparison was made with a two-part hair treatment composition (two-part pre-treatment agent) described in JP-A-2014-80384. The details are shown below.
特開2014-80384号公報の実施例8に準じる第1剤及び第2剤を、製造した。第1剤については、シスチン、水酸化ナトリウム、塩化ステアリルトリメチルアンモニウム、イソプロパノール、セテアリルアルコール及び水を配合し、レブリン酸でpHを10.5に調整することにより、液状乳化白色のものを製造した(水と配合した成分の配合量は下記表2の通り。)。また、第2剤は、酒石酸、レブリン酸及び水を配合し、水酸化ナトリウムでpHを3.5に調整することにより、液状のものを製造した(水と配合した成分の配合量は下記表2の通り。)。 A first part and a second part were produced according to Example 8 of JP-A-2014-80384. For the first agent, a white liquid emulsion was produced by blending cystine, sodium hydroxide, stearyltrimethylammonium chloride, isopropanol, cetearyl alcohol, and water, and adjusting the pH to 10.5 with levulinic acid. (The amounts of ingredients mixed with water are shown in Table 2 below.) In addition, the second agent was prepared in liquid form by blending tartaric acid, levulinic acid, and water, and adjusting the pH to 3.5 with sodium hydroxide (the amounts of the components blended with water are shown in the table below). As per 2).
参考例を次の通り行った。日本人女性から採取した長さ18cm程度、0.5gの毛束を作成した。この毛束に、上記の第1剤0.1gを塗布してから室温で3分間経過後、第1剤を洗い流すことなく、上記の第2剤0.1gを重ねて塗布し、室温で5分間放置した。そして、第2剤を洗い流すことなく、4gの脱色剤(ミルボン社製「パウダーブリーチ」1質量部とミルボン社製「オルディーブ アディクシー オキシダン6.0」3質量部との混合物)を重ねて塗布し、室温で30分放置した。その後、毛束を水洗し、ミルボン社製シャンプー「ノイドゥーエ・ウィローリュクス・シャンプー」を使用して更に洗浄してから、ミルボン社製洗い流すトリートメント「ノイドゥーエ・ウィローリュクス・トリートメント」を使用して処理した後、温風で乾燥させた。 A reference example was carried out as follows. Hair bundles approximately 18 cm in length and 0.5 g were collected from a Japanese woman. After applying 0.1 g of the above first agent to this hair bundle, after 3 minutes at room temperature, without rinsing off the first agent, apply 0.1 g of the above second agent, and leave it at room temperature for 5 minutes. Leave it for a minute. Then, without washing away the second agent, 4 g of decolorizing agent (a mixture of 1 part by mass of Milbon's "Powder Bleach" and 3 parts by mass of Milbon's "Ordeve Addixie Oxidan 6.0") was applied in layers. , and left at room temperature for 30 minutes. After that, the hair strands are washed with water, further washed with Milbon's shampoo "Neidoue Willow Luxe Shampoo", and then treated with Milbon's wash-off treatment "Neidoue Willow Luxe Treatment". , and dried with warm air.
また、実施例2として、参考例の処理における第1剤の塗布を省略し、塗布する第2剤の量を0.2gとした以外は、参考例と同様にした処理を行い、比較例2として、実施例2の処理における第2剤の塗布を省略した以外は、実施例2と同様にした処理を行った。 In addition, as Example 2, the same treatment as in the reference example was performed except that the application of the first agent in the treatment of the reference example was omitted and the amount of the second agent to be applied was 0.2 g, and comparative example 2 The same treatment as in Example 2 was performed except that the application of the second agent in the treatment in Example 2 was omitted.
下表2に、水と配合した成分、pHと共に、初期弾性率(測定方法は、実施例1aと同様)の結果を示す。なお、下記表2における各初期弾性率は、毛髪20本の平均値である。 Table 2 below shows the components mixed with water, the pH, and the results of the initial elastic modulus (measurement method is the same as in Example 1a). In addition, each initial elastic modulus in Table 2 below is an average value of 20 hairs.
上記表2において、参考例及び実施例2共に、比較例2よりも初期弾性率に優れていたことを確認できる。そして、第1剤の塗布を省略した実施例2は、その省略のない参考例と同等の初期弾性率であったことを確認できる。 In Table 2 above, it can be confirmed that both Reference Example and Example 2 were superior to Comparative Example 2 in initial elastic modulus. It can be confirmed that Example 2 in which the application of the first agent was omitted had the same initial elastic modulus as the Reference Example without such omission.
Claims (5)
クエン酸、レブリン酸及びマレイン酸から選ばれた一種又は二種以上が配合され、
酸性、且つ、1剤式であり、
前記レブリン酸及び前記マレイン酸から選ばれた一種又は二種が必須成分として配合されていることを特徴とする前処理剤。 A pretreatment agent applied to hair before applying an oxidative hair dye or bleaching agent,
Contains one or more selected from citric acid, levulinic acid and maleic acid,
It is acidic and a one-drug formula,
A pretreatment agent characterized in that one or two selected from the above levulinic acid and the above maleic acid are blended as essential components .
酸化染毛剤又は脱色剤を重ねて塗布する酸化染毛処理工程又は脱色処理工程とを
備え、
前記前処理剤には、前記レブリン酸及び前記マレイン酸から選ばれた一種又は二種が必須成分として配合されていることを特徴とする酸化染毛方法又は脱色方法。 a pretreatment step of applying to the hair an acidic, one-part pretreatment agent containing one or more selected from citric acid, levulinic acid, and maleic acid;
an oxidative hair dyeing process or a bleaching process in which oxidative hair dyes or bleaching agents are applied in layers ;
An oxidative hair dyeing or bleaching method , wherein the pretreatment agent contains one or two selected from the levulinic acid and the maleic acid as essential ingredients .
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Citations (4)
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JP2001342119A (en) | 2000-06-02 | 2001-12-11 | Ceramide Sha:Kk | Treating agent for hair color and method for dyeing hair using the same |
JP2004189745A (en) | 2002-12-12 | 2004-07-08 | Kao Corp | Pretreatment composition applied before coloring hair with acidic direct dyes |
CN107837212A (en) | 2017-11-06 | 2018-03-27 | 广州市花安堂生物科技有限公司 | A kind of scalp release compositions being used for before dyeing and perm |
JP2018048091A (en) | 2016-09-21 | 2018-03-29 | ホーユー株式会社 | Hair cosmetic composition and method for using the same |
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JP2001342119A (en) | 2000-06-02 | 2001-12-11 | Ceramide Sha:Kk | Treating agent for hair color and method for dyeing hair using the same |
JP2004189745A (en) | 2002-12-12 | 2004-07-08 | Kao Corp | Pretreatment composition applied before coloring hair with acidic direct dyes |
JP2018048091A (en) | 2016-09-21 | 2018-03-29 | ホーユー株式会社 | Hair cosmetic composition and method for using the same |
CN107837212A (en) | 2017-11-06 | 2018-03-27 | 广州市花安堂生物科技有限公司 | A kind of scalp release compositions being used for before dyeing and perm |
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