JP7338949B2 - 縮毛緩和された毛髪を処理するための方法 - Google Patents
縮毛緩和された毛髪を処理するための方法 Download PDFInfo
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- JP7338949B2 JP7338949B2 JP2017555304A JP2017555304A JP7338949B2 JP 7338949 B2 JP7338949 B2 JP 7338949B2 JP 2017555304 A JP2017555304 A JP 2017555304A JP 2017555304 A JP2017555304 A JP 2017555304A JP 7338949 B2 JP7338949 B2 JP 7338949B2
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| US201562152220P | 2015-04-24 | 2015-04-24 | |
| US62/152,220 | 2015-04-24 | ||
| PCT/US2016/029215 WO2016172708A1 (en) | 2015-04-24 | 2016-04-25 | Methods for treating relaxed hair |
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| JP2018513181A JP2018513181A (ja) | 2018-05-24 |
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| US9095518B2 (en) | 2013-08-01 | 2015-08-04 | Liqwd, Inc. | Methods for fixing hair and skin |
| US12233289B2 (en) | 2013-08-01 | 2025-02-25 | Olaplex, Inc. | Methods for fixing hair and skin |
| US20230201632A1 (en) * | 2013-08-01 | 2023-06-29 | Olaplex, Inc. | Methods for fixing hair and skin |
| US20150037270A1 (en) * | 2013-08-01 | 2015-02-05 | Liqwd, Inc. | Compositions and Kits for Hair and Skin |
| PT3142637T (pt) | 2014-05-16 | 2020-10-15 | Olaplex Inc | Formulações e métodos de tratamento de queratina |
| KR102661331B1 (ko) | 2015-04-24 | 2024-04-30 | 올라플렉스, 인코포레이티드 | 릴렉싱된 헤어의 처리 방법 |
| EP3288520A4 (en) | 2015-05-01 | 2018-12-12 | L'oreal | Use of active agents during chemical treatments |
| JP6873994B2 (ja) | 2015-11-24 | 2021-05-19 | ロレアル | 毛髪を処置するための組成物 |
| WO2017091797A1 (en) | 2015-11-24 | 2017-06-01 | L'oreal | Compositions for treating the hair |
| CN108495613B (zh) | 2015-11-24 | 2021-12-10 | 欧莱雅 | 用于处理头发的组合物 |
| US9713583B1 (en) * | 2016-07-12 | 2017-07-25 | Liqwd, Inc. | Methods and formulations for curling hair |
| US9872821B1 (en) * | 2016-07-12 | 2018-01-23 | Liqwd, Inc. | Methods and formulations for curling hair |
| WO2018085478A1 (en) | 2016-11-02 | 2018-05-11 | L'oreal | Hair lightening compositions and methods of use |
| US11135150B2 (en) | 2016-11-21 | 2021-10-05 | L'oreal | Compositions and methods for improving the quality of chemically treated hair |
| US10555891B2 (en) | 2017-05-24 | 2020-02-11 | L'oreal | Methods for treating chemically treated hair |
| US10561599B2 (en) | 2017-05-24 | 2020-02-18 | L'oreal | Methods and kits for treating chemically relaxed hair |
| US9974725B1 (en) | 2017-05-24 | 2018-05-22 | L'oreal | Methods for treating chemically relaxed hair |
| US10576307B2 (en) | 2017-05-24 | 2020-03-03 | L'oreal | Hair-treatment compositions, methods, and kits for treating hair |
| SE1751041A1 (en) | 2017-08-30 | 2019-03-01 | Jaywant Phopase | Functionalized polypeptide for hair treatment |
| WO2019133785A1 (en) | 2017-12-29 | 2019-07-04 | L'oreal | Compositions for altering the color of hair |
| IT201800003037A1 (it) * | 2018-02-26 | 2019-08-26 | Jean Paul Myne Srl | Trattamento cosmetico per il miglioramento dell’aspetto estetico e delle caratteristiche fisico-meccaniche delle cheratine tramite l’uso di “pinze molecolari” amminiche. |
| IT201800003035A1 (it) * | 2018-02-26 | 2019-08-26 | Jean Paul Myne Srl | Trattamento cosmetico per il miglioramento dell’aspetto estetico e delle caratteristiche fisico-meccaniche delle cheratine tramite l’uso di “pinze molecolari” sulfo-carbossilate. |
| US11090249B2 (en) | 2018-10-31 | 2021-08-17 | 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 |
| US11826451B2 (en) | 2019-12-31 | 2023-11-28 | L'oreal | Compositions for treating hair |
| US12036299B2 (en) | 2021-06-30 | 2024-07-16 | L'oreal | Compositions containing direct dyes for imparting color and tone to the hair |
| US12109289B2 (en) | 2021-06-30 | 2024-10-08 | L'oreal | Compositions for imparting color and tone to the hair |
| US12144879B2 (en) | 2022-07-31 | 2024-11-19 | L'oreal | Compositions and methods for altering the color of hair |
| US12409123B2 (en) | 2022-07-31 | 2025-09-09 | L'oreal | Compositions and methods for altering the color of hair |
| US12109287B2 (en) | 2022-07-31 | 2024-10-08 | L'oreal | Compositions and methods for altering the color of hair |
| WO2024194599A1 (en) | 2023-03-17 | 2024-09-26 | The University Of Warwick | Ionic liquids |
Family Cites Families (175)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB713675A (en) | 1951-11-09 | 1954-08-18 | Mozes Juda Lewenstein | Improvements in the preparation of compounds having a narcotic effect and the products obtained thereby |
| GB741307A (en) | 1952-01-03 | 1955-11-30 | Monsavon L Orfal | Hair-treating compositions |
| GB773559A (en) | 1954-01-29 | 1957-04-24 | Gillette Co | Improvements in or relating to meth ods and compositions for permanent waving of hair |
| US2850351A (en) | 1955-08-19 | 1958-09-02 | Joseph E Moore | Process of reacting reduced keratin with cross-linking polyimides or polyamides and chemically modified keratin containing the aforesaid crosslinkages |
| US3142623A (en) | 1961-11-15 | 1964-07-28 | Oreal | Permanent waving of hair and analogous processes |
| FR1356139A (fr) | 1963-05-06 | 1964-03-20 | Holder G M B H Grunbach | Tracteur agricole |
| FR1356138A (fr) | 1963-05-06 | 1964-03-20 | Kienzle Uhrenfabriken Ag | Couplage à organe de coincement |
| DE1220969B (de) | 1964-11-25 | 1966-07-14 | Ernst Kruegermeyer & Co Seruba | Verfahren zur Verbesserung strukturgeschaedigter Haare |
| GB1125794A (en) * | 1965-01-27 | 1968-08-28 | Iichiro Takeda | Improvements in the straightening of hair |
| US3472243A (en) | 1965-09-27 | 1969-10-14 | Clairol Inc | Treating damaged living human hair with water soluble polymerizable vinyl monomers |
| LU49584A1 (enExample) | 1965-10-05 | 1967-04-05 | ||
| US3538009A (en) | 1967-02-01 | 1970-11-03 | Cincinnati Milling Machine Co | Method for reducing skin irritation in detergent compositions |
| US3568685A (en) | 1968-04-15 | 1971-03-09 | Howard L Scott | Treating human, animal and synthetic hair with a water-proofing composition |
| US3655869A (en) | 1969-01-02 | 1972-04-11 | Monsanto Co | Treatment of diarrhea employing certain basic polyelectrolyte polymers |
| US4007143A (en) | 1972-03-07 | 1977-02-08 | John Lyndon Garnett | Method of grafting monomers to wool with nitric acid |
| DE2549294A1 (de) | 1975-11-04 | 1977-05-12 | Henkel & Cie Gmbh | Mittel zur verminderung der schaedigung von haaren beim bleichen und faerben |
| GB1584364A (en) | 1976-06-21 | 1981-02-11 | Unilever Ltd | Shampoo |
| LU76955A1 (enExample) | 1977-03-15 | 1978-10-18 | ||
| FR2421607A1 (fr) | 1978-04-06 | 1979-11-02 | Oreal | Procede de teinture des fibres keratiniques en deux temps par variation de ph |
| DE2929865A1 (de) | 1979-07-24 | 1981-02-19 | Wella Ag | Verfahren zur dauerhaften haarverformung |
| KR830002888A (ko) | 1980-04-10 | 1983-05-31 | 니시무라 쯔비사부로오 | 소결광(燒結鑛)의 현열(顯熱) 회수방법 |
| EP0083095A3 (en) | 1981-12-24 | 1984-04-04 | Helene Curtis Industries, Inc. | Method of reductively waving or straightening hair |
| US4812307A (en) | 1983-07-06 | 1989-03-14 | Chesebrough-Pond's Inc. | Crosslinking of hair thiols using glutathione disulfide |
| US4567039A (en) | 1984-10-12 | 1986-01-28 | Revlon, Inc. | Hair conditioning composition and method |
| US4658839A (en) | 1985-10-04 | 1987-04-21 | Zotos International Inc. | Hair conditioning and enhancing applicator wrap, composition and method |
| FR2596985B1 (fr) | 1986-04-10 | 1990-08-24 | Oreal | Compositions cosmetiques pour teindre ou pour decolorer les cheveux |
| DE3627746A1 (de) | 1986-08-16 | 1988-02-18 | Henkel Kgaa | Verfahren zur dauerhaften haarverformung |
| US4795629A (en) | 1987-07-06 | 1989-01-03 | Chesebrough-Pond's Inc. | Crosslinking of hair thiols using cystamine |
| US4793993A (en) | 1987-07-06 | 1988-12-27 | Chesebrough-Pond's Inc. | Crosslinking of hair thiols |
| ZA885143B (en) | 1987-07-16 | 1990-03-28 | Unilever Plc | Hair treatment product |
| EP0299764B1 (en) | 1987-07-16 | 1992-05-27 | Unilever Plc | Hair treatment product |
| DE69005283D1 (de) | 1990-01-09 | 1994-01-27 | Dow Corning | Siloxanzusammensetzung für die Haarpflege. |
| JP2693859B2 (ja) | 1990-09-28 | 1997-12-24 | 高砂香料工業株式会社 | 尋常性▲ざ▼瘡用皮膚外用剤 |
| WO1993000882A1 (en) | 1991-07-08 | 1993-01-21 | R.M. Walker Healthcare Products, Inc. | Neutralizing rinse and improved method for chemically relaxing hair |
| HU215636B (hu) | 1991-10-29 | 1999-01-28 | The Procter & Gamble Co. | Szilikont, kationos polimert és olajos kondícionálószereket tartalmazó samponkészítmények és alkalmazásuk |
| US5221286A (en) | 1992-07-17 | 1993-06-22 | Eastman Kodak Company | Cold mix emulsions used as a developer composition for oxidative hair dyes and for hair bleaches |
| KR960009640B1 (ko) | 1992-10-16 | 1996-07-23 | 주식회사 태평양 | 헤어칼라린스 조성물 |
| DE4300320A1 (de) * | 1993-01-08 | 1994-07-14 | Hartmann Haarkosmetik Gmbh | Mittel und Verfahren zum Zwecke der Herstellung gebrauchsfertiger Dauerwellenpräparate für jede Haarqualität durch mischen von 2 Lösungen, wodurch ein sukzessiver Thio-Gruppen-Verminderungseffekt durch Addition und eine teilweise Neutralisation eintritt |
| ATE173915T1 (de) | 1993-02-01 | 1998-12-15 | Goldwell Gmbh | Blondiermittel für menschliche haare |
| US5350572A (en) | 1993-02-18 | 1994-09-27 | Shiseido Co., Ltd. | Permanent waving composition |
| US5437860A (en) | 1993-06-22 | 1995-08-01 | Aminco, Inc. | Skin and scalp barrier for use with hair treatment products |
| KR100297626B1 (ko) | 1993-06-30 | 2001-10-24 | 데이비드 엠 모이어 | 다가 금속 양이온 함유 컨디셔닝 샴푸 |
| DE69420142T2 (de) | 1993-07-01 | 2000-03-23 | The Procter & Gamble Co., Cincinnati | Thermoplastische Elastomere Copolymere und diese enthaltendes Haar und Hautflegemittel |
| US5565216A (en) | 1993-07-21 | 1996-10-15 | Carson Products Company | Hair relaxer compositions |
| FR2708197B1 (fr) | 1993-07-28 | 1995-09-08 | Oreal | Nouvelles compositions à base d'eau oxygénée et leur utilisation comme fixateurs pour permanentes. |
| ATE185578T1 (de) | 1993-08-23 | 1999-10-15 | Procter & Gamble | Thermoplastische und elastomere silikonpfropfcopolymere und diese enthaltende haar- und hautpflegemittel |
| GB9415911D0 (en) | 1994-08-05 | 1994-09-28 | Unilever Plc | Hair styling composition and method |
| US5490980A (en) | 1994-09-28 | 1996-02-13 | Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. | Covalent bonding of active agents to skin, hair or nails |
| US5651960A (en) | 1995-09-22 | 1997-07-29 | Helene Curtis, Inc. | Method and composition for removing semi-permanent color from human hair |
| GB9526633D0 (en) | 1995-12-29 | 1996-02-28 | Procter & Gamble | Hair colouring compositions |
| DE19755491C1 (de) | 1997-12-13 | 1999-05-12 | Henkel Kgaa | Mikrodispersionsverfahren zur Herstellung von Haarfärbepräparaten mit erhöhter Viskosität |
| BR9807422A (pt) | 1997-12-19 | 2000-03-21 | Wella Ag | Processo para dar forma e volume aos cabelos humanos |
| US6010690A (en) * | 1998-03-05 | 2000-01-04 | Bristol-Myers Squibb Company | Alkaline hair conditioning compositions containing cationic guar |
| GB9808310D0 (en) | 1998-04-20 | 1998-06-17 | Unilever Plc | Shampoo compositions |
| EP0978272A1 (en) | 1998-08-07 | 2000-02-09 | Kao Corporation | Medulla care preparation |
| CA2352778A1 (en) | 1998-12-01 | 2000-06-08 | Novozymes A/S | Method for treating hair |
| JP3208381B2 (ja) | 1998-12-28 | 2001-09-10 | 花王株式会社 | 毛髪化粧料 |
| US6299697B1 (en) | 1999-08-25 | 2001-10-09 | Shibaura Mechatronics Corporation | Method and apparatus for processing substrate |
| ECSP993171A (es) | 1999-10-08 | 2000-02-24 | Composiciones para el cuidado del cabello dandole volumen | |
| JP3420143B2 (ja) | 1999-12-02 | 2003-06-23 | 花王株式会社 | 毛髪処理剤 |
| FR2802093B1 (fr) | 1999-12-08 | 2002-01-18 | Oreal | Composition pour la decoloration ou la deformation permanente des fibres keratiniques comprenant un polymere epaississant a squelette aminoplaste-ether |
| DE19962869A1 (de) | 1999-12-24 | 2001-06-28 | Henkel Kgaa | Verringerung der Haarschädigung bei oxidativen Prozessen |
| US20010042276A1 (en) | 2000-03-30 | 2001-11-22 | Shiseido Co., Ltd. | Hair dye fixatives, hair dyes and hair dyeing methods |
| KR100551583B1 (ko) | 2000-05-30 | 2006-02-13 | 제이에프이 스틸 가부시키가이샤 | 유기피복 강판 및 그의 제조방법 |
| TWI278328B (en) | 2000-07-21 | 2007-04-11 | Kao Corp | Hair cosmetic composition |
| FR2813016B1 (fr) | 2000-08-21 | 2002-10-11 | Oreal | Composition de decoloration des fibres keratiniques teintes |
| DE10051773A1 (de) | 2000-10-19 | 2002-04-25 | Henkel Kgaa | Neue Verwendung von kurzkettigen Carbonsäuren |
| DE10051774A1 (de) | 2000-10-19 | 2002-04-25 | Henkel Kgaa | Neue Verwendung von kurzkettigen Carbonsäuren |
| FR2816210B1 (fr) | 2000-11-08 | 2005-02-25 | Oreal | Composition pour la decoloration ou la deformation permanente des fibres keratiniques comprenant un polyurethane associatif cationique |
| FR2818538B1 (fr) | 2000-12-22 | 2003-02-07 | Oreal | Composition pour la teinture d'oxydation des fibres keratiniques comprenant au moins un 4,5 ou 3,4-diamino pyrazole ou un triamino pyrazole et au moins un compose carbonyle selectionne, et procede de teinture |
| US6602493B2 (en) * | 2001-02-15 | 2003-08-05 | Avlon Industries, Inc. | Hair relaxer system and method therefor |
| US7186275B2 (en) | 2001-03-20 | 2007-03-06 | The Procter & Gamble Company | Compositions suitable for the treatment of hair comprising chelants and methods for reducing oxidative hair damage |
| GB2386068A (en) | 2001-03-20 | 2003-09-10 | Procter & Gamble | Oxidative treatment of hair with reduced hair damage |
| US7179302B2 (en) | 2001-03-20 | 2007-02-20 | The Procter & Gamble Company | Oxidative treatment of hair with reduced hair damage |
| US20020197227A1 (en) | 2001-05-23 | 2002-12-26 | Scholz William F. | Anti-frizz hair care compositions |
| JP2002363048A (ja) | 2001-05-31 | 2002-12-18 | Nicca Chemical Co Ltd | ２剤式染毛・脱色剤組成物用第１剤、２剤式染毛・脱色剤組成物キット、及びそれを用いた毛髪処理方法 |
| KR100761217B1 (ko) | 2001-07-04 | 2007-10-04 | 주식회사 엘지생활건강 | 염모제 조성물 |
| GB0119011D0 (en) | 2001-08-03 | 2001-09-26 | Univ Aberdeen | Treatment of nail infections |
| US7468180B2 (en) * | 2001-08-20 | 2008-12-23 | L'oreal, S.A. | Compositions comprising at least one hydroxide compound and at least one oxidizing agent, and methods to straighten curly hair |
| FR2829385B1 (fr) * | 2001-09-11 | 2005-08-05 | Oreal | Compositions cosmetiques contenant un copolymere d'acide methacrylique, une huile et leurs utilisations |
| WO2003070206A1 (fr) | 2002-02-21 | 2003-08-28 | Yugen Kaisha Okada Giken | Agent de traitement servant a proteger une fibre animale |
| EP1487904A1 (de) | 2002-03-20 | 2004-12-22 | GE Bayer Silicones GmbH & Co. KG | Verzweigte polyorganosiloxanpolymere |
| US20030223951A1 (en) | 2002-06-04 | 2003-12-04 | The Procter & Gamble Company | Conditioning shampoo compositions containing select cationic conditioning polymers |
| WO2004024176A1 (de) | 2002-08-30 | 2004-03-25 | Henkel Kommanditgesellschaft Auf Aktien | Synergistische kombination von seidenproteinen |
| US7306662B2 (en) | 2006-05-11 | 2007-12-11 | Lam Research Corporation | Plating solution for electroless deposition of copper |
| US7597880B2 (en) | 2003-02-24 | 2009-10-06 | L'oreal | Multimineral no-mix relaxer |
| US20050036970A1 (en) | 2003-03-25 | 2005-02-17 | L'oreal S.A. | Reducing compositions for bleaching or permanently reshaping keratin fibres comprising polycarboxylic acids and salts thereof as complexing agents |
| KR20040098688A (ko) | 2003-05-15 | 2004-11-26 | 삼성전자주식회사 | 광 모듈 |
| US7202270B2 (en) | 2003-06-20 | 2007-04-10 | Sami Labs Limited | Convenient stable non-hygroscopic crystalline solid forms of racemic and chiral LA-plus salts: process for their manufacture and uses |
| US7066968B2 (en) | 2004-03-02 | 2006-06-27 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Efficient two-step method of coloring and lightening hair with less damage |
| JP4878446B2 (ja) | 2004-07-08 | 2012-02-15 | 花王株式会社 | パーマネントウェーブ用又はストレートパーマ用還元性組成物 |
| WO2006011771A1 (en) | 2004-07-30 | 2006-02-02 | Korea Research Institute Of Chemical Technology | Self-molding permanent agent and method for proceeding free-rod and free-band type permanent |
| KR100684984B1 (ko) | 2004-07-30 | 2007-03-02 | 한국화학연구원 | 탈-롯드 및 탈-밴드형 퍼머방법 |
| US7041142B2 (en) | 2004-10-12 | 2006-05-09 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Two step hair coloring compositions delivering deeper, long-lasting color |
| DE102004052480A1 (de) | 2004-10-28 | 2006-05-04 | Henkel Kgaa | Reduktionsmittel-haltiges Mittel zum Färben von keratinhaltigen Fasern |
| WO2006051287A1 (en) | 2004-11-10 | 2006-05-18 | Arrow International Limited | Composition and method for treatment of alopecia areata |
| KR20060059564A (ko) | 2004-11-29 | 2006-06-02 | 건국대학교 산학협력단 | 약산을 포함하는 모발처리제 |
| FR2880888B1 (fr) | 2005-01-20 | 2010-12-24 | Oreal | Utilisation d'aminodithiol en tant qu'agent reducteur pour la deformation permanente des cheveux |
| US7754194B2 (en) * | 2005-04-06 | 2010-07-13 | L'oréal | Hair relaxer compositions utilizing bioactive glass |
| JP2006327994A (ja) | 2005-05-26 | 2006-12-07 | Okada Giken:Kk | 毛髪保護剤 |
| JP2007045802A (ja) | 2005-08-12 | 2007-02-22 | Kao Corp | 縮毛矯正剤組成物 |
| ZA200606791B (en) * | 2005-08-18 | 2008-05-28 | Unilever Plc | Method for relaxing hair |
| US20090126756A1 (en) | 2005-09-12 | 2009-05-21 | Avlon Industries, Inc. | Keratin-protective curl minimizer, compostions, method, and kit therefor |
| US7736633B2 (en) | 2005-09-28 | 2010-06-15 | E.I. Du Pont De Nemours And Company | Method for enhancing effects of colorants and conditioners |
| FR2892629B1 (fr) | 2005-10-28 | 2012-04-27 | Oreal | Composition cosmetique comprenant au moins un polymere fixant particulier et au moins un tensioactif ionique et/ou non ionique |
| EP1797861A1 (en) | 2005-12-16 | 2007-06-20 | KPSS-Kao Professional Salon Services GmbH | Composition for the permanent shaping of human hair |
| FR2894816B1 (fr) | 2005-12-16 | 2008-02-01 | Oreal | Composition cosmetique ou pharmaceutique comprenant un copolymere comportant au moins un groupe ionisable, et procede de traitement cosmetique |
| WO2007127065A2 (en) | 2006-04-21 | 2007-11-08 | Living Proof, Inc. | In situ polymerization for hair treatment |
| GB0617024D0 (en) | 2006-08-30 | 2006-10-11 | Unilever Plc | Hair treatment compositions incorporating hair substantive polymers |
| RU2009122982A (ru) | 2006-11-17 | 2010-12-27 | Унилевер Н.В. (NL) | Способ дериватизации волос с помощью реакционноспособного полиэтиленгликоля |
| JP2008150308A (ja) | 2006-12-15 | 2008-07-03 | Mitsui Fine Chemicals Inc | 毛髪改質剤、毛髪改質剤成分を含有する毛髪化粧料、及び毛髪の改質方法 |
| JP4709737B2 (ja) | 2006-12-27 | 2011-06-22 | 花王株式会社 | 縮毛矯正組成物 |
| US20080210253A1 (en) | 2007-02-05 | 2008-09-04 | Jose Antonio Carballada | Hair care composition |
| US20080187506A1 (en) | 2007-02-05 | 2008-08-07 | Jose Antonio Carballada | Hair care composition |
| JP2009007283A (ja) | 2007-06-27 | 2009-01-15 | Lion Corp | 毛髪化粧料 |
| US20090087398A1 (en) | 2007-08-20 | 2009-04-02 | Mark Anthony Brown | Method for Treating Damaged Hair |
| WO2009047251A1 (en) | 2007-10-10 | 2009-04-16 | Unilever Plc | Method of treating hair |
| JP2009120563A (ja) | 2007-11-16 | 2009-06-04 | Akihiko Mori | パーマ方法及びパーマ用キット |
| FR2929508B1 (fr) | 2008-04-08 | 2010-06-04 | Oreal | Procede de deformation permanente des fibres keratiniques presentant une etape de pretraitement acide |
| CA2723010C (en) | 2008-04-29 | 2014-09-16 | Hair Systems, Inc. | Composition and method for cream bleach product |
| JP5789901B2 (ja) | 2008-05-29 | 2015-10-07 | セラピューティック・ペプタイズ・インコーポレーテッドＴｈｅｒａｐｅｕｔｉｃ Ｐｅｐｔｉｄｅｓ，Ｉｎｃ． | 皮膚化粧用組成物におけるオリゴマーバイオサーファクタント |
| EP2177203A1 (en) | 2008-10-20 | 2010-04-21 | KPSS-Kao Professional Salon Services GmbH | Colouring and perming compositions for hair |
| FR2937640B1 (fr) | 2008-10-27 | 2011-02-25 | Oreal | Utilisation d'au moins un compose derive de lysine pour le conditionnement des fibres keratiniques, composition cosmetique le contenant et procede de conditionnement des fibres |
| EP2340010B1 (en) * | 2008-10-29 | 2017-08-16 | L'Oréal | Process for relaxing or straightening hair, using weak mono-, di- or tricarboxylic acids with heat |
| EP2191812A1 (en) | 2008-11-27 | 2010-06-02 | KPSS-Kao Professional Salon Services GmbH | Bleaching/Highlighting composition |
| JP5411655B2 (ja) | 2008-12-03 | 2014-02-12 | 株式会社ミルボン | 毛髪処理方法及び毛髪処理剤 |
| BRPI1015471A2 (pt) * | 2009-04-14 | 2016-04-26 | Alberto Culver Co | ativador de gel relaxante |
| EP2295029A1 (en) | 2009-09-14 | 2011-03-16 | The Procter & Gamble Company | Method of chemically modifying the internal region of a hair shaft |
| US20110097293A1 (en) | 2009-10-27 | 2011-04-28 | Gary Grey | Multiple component systems and methods for hair relaxation of variable strength |
| BR112012014912A2 (pt) | 2009-12-18 | 2017-03-21 | Nokia Siemens Networks Oy | partilha de recursos em sistemas de comunicações |
| US20120244082A1 (en) | 2009-12-18 | 2012-09-27 | Kao Germany Gmbh | Hair styling gel foam |
| JP2013528578A (ja) | 2010-04-28 | 2013-07-11 | ユニリーバー・ナームローゼ・ベンノートシヤープ | ヘアケア組成物 |
| BR112012026635B1 (pt) | 2010-04-30 | 2018-05-08 | Oreal | composições e métodos para clarear a cor de cabelo relaxado ou alisado |
| FR2959917B1 (fr) | 2010-05-11 | 2012-07-27 | Oreal | Procede de traitement des cheveux |
| WO2012078658A1 (en) * | 2010-12-06 | 2012-06-14 | International Flora Technologies, Ltd. | Hair relaxing and straightening compositions |
| US8191673B1 (en) | 2010-12-08 | 2012-06-05 | Scott Peaslee | Collapsible megaphone device |
| WO2012080321A2 (en) | 2010-12-17 | 2012-06-21 | L'oreal | Dye composition comprising a heterocyclic oxidation base and a 4-aminoindole coupler |
| DE102010064052A1 (de) | 2010-12-23 | 2012-06-28 | Henkel Ag & Co. Kgaa | Verfahren zur Umformung keratinhaltiger Fasern |
| EP2561855B1 (en) | 2011-01-19 | 2017-10-11 | The Procter and Gamble Company | Method for chemically modifying the internal region of a hair shaft |
| EP2478892A1 (en) | 2011-01-19 | 2012-07-25 | The Procter & Gamble Company | Composition for chemically modifying the internal region of a hair shaft |
| US20120225106A1 (en) | 2011-03-01 | 2012-09-06 | Isp Investments Inc. | Personal care compositions with suspended metal oxides |
| EP3659576A1 (en) | 2011-03-09 | 2020-06-03 | Baum, Marc Michael | Keratin-based hair straightening formulations, methods and systems |
| FR2975901B1 (fr) | 2011-06-01 | 2014-12-05 | Oreal | Procede de traitement des fibres keratiniques defrisees |
| US9180086B2 (en) * | 2011-06-01 | 2015-11-10 | L'oreal | Process for treating straightened keratin fibres |
| FR2975900B1 (fr) | 2011-06-01 | 2015-02-20 | Oreal | Procede de traitement des fibres keratiniques defrisees |
| EP2549412B1 (de) | 2011-07-19 | 2014-03-19 | Deutsche Post AG | Betriebsmodusänderung eines einer Transporteinheit zugeordneten elektronischen Geräts |
| US20130034515A1 (en) | 2011-08-03 | 2013-02-07 | Melaleuca, Inc. | Hair care compositions |
| TWI437027B (zh) | 2011-12-29 | 2014-05-11 | Ind Tech Res Inst | 一種含有軟鏈段之馬來醯亞胺聚合物及其製備方法 |
| US8343238B1 (en) | 2011-12-30 | 2013-01-01 | L'oreal Sa. | Process for altering the appearance of hair using a composition containing dyes and non-hydroxide bases |
| US20130309190A1 (en) | 2012-05-15 | 2013-11-21 | L'oreal S.A. | Hair cosmetic and styling compositions based on maleic acid copolymers and polyamines |
| ITMI20121323A1 (it) | 2012-07-27 | 2014-01-28 | Giuliani Spa | Composizione farmaceutica o cosmeticaper il trattamento dell' alopecia |
| EP2914239B1 (en) | 2012-11-05 | 2020-04-29 | Hercules LLC | Composition comprising conditioning and/or styling polymer |
| FR2997846B1 (fr) | 2012-11-09 | 2023-10-20 | Oreal | Composition comprenant un derive dicarbonyle et un acide, le procede de lissage des fibres keratiniques a partir de cette composition |
| FR3001385B1 (fr) | 2013-01-31 | 2015-10-30 | Oreal | Composition comprenant un diacide carboxylique et une huile et procede de lissage des cheveux |
| ITMI20130218A1 (it) | 2013-02-18 | 2014-08-19 | Giuliani Spa | Composizione per uso cosmetico atta a produrre un effetto di pigmentazione dei capelli |
| ITMI20130555A1 (it) | 2013-04-09 | 2014-10-10 | Giuliani Spa | Composizione farmaceutica o cosmetica per contrastare l¿invecchiamento della pelle attraverso un¿azione antiinfiammatoria |
| WO2014207097A1 (en) | 2013-06-26 | 2014-12-31 | L'oreal | Cosmetic composition for lightening or dyeing the hair, comprising two basic agents, an acid and an oxidizing agent |
| US9095518B2 (en) | 2013-08-01 | 2015-08-04 | Liqwd, Inc. | Methods for fixing hair and skin |
| US20150034119A1 (en) | 2013-08-01 | 2015-02-05 | Liqwd, Inc. | Hair Color Smoothing Compositions and Methods |
| US20150037270A1 (en) | 2013-08-01 | 2015-02-05 | Liqwd, Inc. | Compositions and Kits for Hair and Skin |
| UA116148C2 (uk) | 2013-08-01 | 2018-02-12 | Ліквд, Інк. | Способи відновлення волосся і шкіри |
| WO2015026994A1 (en) | 2013-08-23 | 2015-02-26 | The Procter & Gamble Company | Hair colouring methods and kits thereof |
| MX2016008163A (es) | 2013-12-19 | 2016-09-16 | Procter & Gamble | Formacion de fibras de queratina mediante el uso de una composicion reductora y una composicion fijadora. |
| JP6314235B2 (ja) * | 2013-12-19 | 2018-04-18 | ザ プロクター アンド ギャンブル カンパニー | オキソエタン酸及び／又はその誘導体を使用したヒトの毛髪をまっすぐにする方法 |
| EP2942049A1 (en) * | 2014-05-09 | 2015-11-11 | The Procter and Gamble Company | Method of forming a polymer inside the hair shaft comprising using a salt of thiosulfonic acid |
| PT3142637T (pt) | 2014-05-16 | 2020-10-15 | Olaplex Inc | Formulações e métodos de tratamento de queratina |
| WO2015175989A2 (en) | 2014-05-16 | 2015-11-19 | Arizona Board Of Regents, A Body Corporate Of The State Of Arizona, Acting For And On Behalf Of Arizona State University | Methods of rapid 3d nano/microfabrication of multifunctional shell-stabilized liquid metal pipe networks and insulating/metal liquids electro-mechanical switch and capacitive strain sensor |
| KR101922543B1 (ko) | 2014-11-28 | 2018-11-28 | (주)아모레퍼시픽 | 말레산을 유효성분으로 포함하는 모발용 화장료 조성물 |
| KR102661331B1 (ko) * | 2015-04-24 | 2024-04-30 | 올라플렉스, 인코포레이티드 | 릴렉싱된 헤어의 처리 방법 |
| EP3313363A1 (en) | 2015-06-26 | 2018-05-02 | H.S.A. Hair Styling Applications S.P.A. | Protective and restructuring hair composition |
| US10632053B2 (en) | 2015-09-08 | 2020-04-28 | Kao Germany Gmbh | Process for bleaching hair |
| US10076475B2 (en) | 2015-10-23 | 2018-09-18 | International Business Machines Corporation | Shell-structured particles for sunscreen applications |
| US9713583B1 (en) | 2016-07-12 | 2017-07-25 | Liqwd, Inc. | Methods and formulations for curling hair |
| US9872821B1 (en) | 2016-07-12 | 2018-01-23 | Liqwd, Inc. | Methods and formulations for curling hair |
| MX2023000870A (es) | 2020-07-21 | 2023-05-19 | Chembeau LLC | Formulaciones cosmeticas de diester y usos de las mismas. |
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2016
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- 2016-04-25 US US15/137,788 patent/US9597273B2/en active Active
- 2016-04-25 EP EP16720308.2A patent/EP3285733B1/en active Active
- 2016-04-25 JP JP2017555304A patent/JP7338949B2/ja active Active
- 2016-04-25 WO PCT/US2016/029215 patent/WO2016172708A1/en not_active Ceased
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| US11191707B2 (en) | 2021-12-07 |
| EP3285733A1 (en) | 2018-02-28 |
| US9597273B2 (en) | 2017-03-21 |
| US20180125768A1 (en) | 2018-05-10 |
| US20160310394A1 (en) | 2016-10-27 |
| KR20180008513A (ko) | 2018-01-24 |
| US9717668B2 (en) | 2017-08-01 |
| US12251456B2 (en) | 2025-03-18 |
| US20200009035A1 (en) | 2020-01-09 |
| WO2016172708A1 (en) | 2016-10-27 |
| US20220323327A1 (en) | 2022-10-13 |
| EP3285733B1 (en) | 2019-10-23 |
| KR102661331B1 (ko) | 2024-04-30 |
| JP2018513181A (ja) | 2018-05-24 |
| US20170071838A1 (en) | 2017-03-16 |
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