TW200536890A - Ues of acrylates copolymer as waterproofing agent in personal care applications - Google Patents
Ues of acrylates copolymer as waterproofing agent in personal care applications Download PDFInfo
- Publication number
- TW200536890A TW200536890A TW093136392A TW93136392A TW200536890A TW 200536890 A TW200536890 A TW 200536890A TW 093136392 A TW093136392 A TW 093136392A TW 93136392 A TW93136392 A TW 93136392A TW 200536890 A TW200536890 A TW 200536890A
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- TW
- Taiwan
- Prior art keywords
- acrylate
- copolymer
- phase
- meth
- water
- Prior art date
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- 229920001577 copolymer Polymers 0.000 title claims abstract description 42
- 238000004078 waterproofing Methods 0.000 title description 4
- 239000000203 mixture Substances 0.000 claims description 55
- 230000000475 sunscreen effect Effects 0.000 claims description 16
- 239000000516 sunscreening agent Substances 0.000 claims description 16
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 10
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 8
- -1 (fluorenyl) methyl Chemical group 0.000 claims description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 6
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 4
- 239000000178 monomer Substances 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- CFGGNXFNDNQZKD-UHFFFAOYSA-N 2-(9H-fluoren-1-yl)prop-2-enoic acid Chemical compound C1C2=CC=CC=C2C2=C1C(C(=C)C(=O)O)=CC=C2 CFGGNXFNDNQZKD-UHFFFAOYSA-N 0.000 claims description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N acrylic acid methyl ester Natural products COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 210000004709 eyebrow Anatomy 0.000 claims description 2
- 210000000720 eyelash Anatomy 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims 1
- 150000001409 amidines Chemical class 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 230000002209 hydrophobic effect Effects 0.000 claims 1
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- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims 1
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- JKXYOQDLERSFPT-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-octadecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO JKXYOQDLERSFPT-UHFFFAOYSA-N 0.000 description 3
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- FMJSMJQBSVNSBF-UHFFFAOYSA-N octocrylene Chemical group C=1C=CC=CC=1C(=C(C#N)C(=O)OCC(CC)CCCC)C1=CC=CC=C1 FMJSMJQBSVNSBF-UHFFFAOYSA-N 0.000 description 1
- 229960000601 octocrylene Drugs 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
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- 239000010452 phosphate Substances 0.000 description 1
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- 239000006254 rheological additive Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N sec-butylidene Natural products CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 210000003491 skin Anatomy 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229950004959 sorbitan oleate Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 230000036561 sun exposure Effects 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 230000009182 swimming Effects 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical class [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/046—Aerosols; Foams
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/10—Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
200536890 九、發明說明: 【發明所屬之技術領域】 本發明關於丙烯酸酯共聚物作為個人護理產品之防水 【先前技術】 許多個人護理產品依靠防水劑提供其總體功能。舉例 來說,當哭泣時不掉色之染睫毛膏以及於游泳期間不脫離 之遮光化妝水,有消費者需求。雖然存在有許多宣稱耐水 性或防水性的個人護理產品,但對於具有改 耐水性仍有需求。許多宣㈣水性之現存產品是具有 1 質、油腻或沈重感的,使其對消費者而言是不合意的。再 者,目前用於個人護理產品賦予耐水性之許多藥劑是不易 控制或合併於組成物中的。 刖;奸夕個人遵理調配物中賦予防水性之聚乙稀 吼魏酮(‘讀,)/二十碳烯絲物是油紐的,並且生成具 =合意的油腻、蠓質或沈重感。再者,將其合併於產品中 :不’:為其無法恰當地於處理期間之任-時刻混 i古二二十碳烯共聚物亦可能引人注目地 1費者不ί =1造成調配具所欲性f之產品的困難度。 Β ^ φ 而要其個人護理產品之改良的耐水性,並 配:而盤正、:質且不具沈重及油膩感之平順的乳脂調 其於要轉时性可容㈣合併於產品中(尤 供更7大的讎轉、巾和或其他特殊處理,因而提 200536890 令人驚费地,此刻頃發現丙稀酸g旨共聚物之使用提供 個人護理組成物極佳的耐水性,而沒有不合意的蠛質、油 腻或沈重感。再者,此等丙烯酸酯共聚物容易使製造商使 用,因為其可不需特殊處理而容易地合併於水相中。 【發明内容】 本發明關於丙烯酸酯共聚物之用途,其係提供個人護 理產品極佳的耐水性,而没有不合意的蠟質、油腻或沈重 感。再者,此等丙烯酸酯共聚物容易使製造商使用,因為 其可不需特殊處理而容易地合併於水相中。 此中所用之丙烯酸酯共聚物意欲代表由至少二種將生 成水可分散的共聚物之丙烯酸酯單體所組成之聚合物。 本發明關於丙烯酸醋共聚物之用途,其係提供個人護 理產品極佳的耐水性’並且容易使製造商使用,因為其可 不需特殊處理而容易地合併於水相中。再者,此等丙稀酸 醋共聚物不產生不合意的油腻、蠛質或沈重皮膚感。 丙烯酸醋共聚物係為形成自至少二種選自丙烯酸及甲 烯:丙烯酸上甲基丙烯酸的酯類及/或醯胺類之 之α 並且心欲包含尤其(甲基)丙烯酸甲酯、(甲 ^丙婦酸乙醋、(甲基)丙歸駿丙 酸 "。特別適合的單想為;:==:= 及甲基丙烯酸。此等丙㈣ 0 (f基)丙席酸曱自曰 不包含具有超過微量疏水性疋水可分散的’並且 於C6,更特別為C8)。更特χ,丨、(具垸基基團大於或等 特別適合的⑽_聚合物係為 200536890 於pH超過約4時具有淨陰離子電荷者,雖然熟習本技藝 之人士將瞭解此淨陰離子電荷將隨著pH提高而增加。 於特別適合的具體例中,丙烯酸酯共聚物含有以重量 計為約1至85%之丙烯酸丁酯、約1至87%之(甲基)丙烯 酸曱酯以及約1至25%之曱基丙烯酸。於更特別適合的具 體例中,丙烯酸酯共聚物含有以重量計為約38至48%之丙 烯酸丁醋、約39至49%之(曱基)丙烯酸曱酯以及約8至180/〇 之甲基丙烯酸。 丙烯酸酯共聚物通常係以乳液形式提供,其為薄的非 黏性液體(就45%聚合物於水中之乳液而言)。丙烯酸酯共 聚物亦可呈乾燥形式提供。 、 可依足以獲致個人護理產品所需功能及性質之任一用 量使用丙職s旨共聚物…般而言,以個人護理產品之重 量計’其係以含量、約0.2至10% ’特別地以含量約〇 5至 4% ’更特別地以約1至2%存在。 於個Γϊ製程中之任—可行的時刻將丙稀_共聚物添加 化期門組成物巾。於乳液配方巾,可於乳化之前、乳 卻=:r後,㈣ 财。再者,不需中和、聚合 二:處理’以於水中或其他水性媒介物恤充足 200536890 聚合物中和點,故造成聚合物溶解作用。然而,應瞭解本 發明涵蓋其中丙烯酸酯共聚物經中和(甚至經100%中和)之 具體例。 個人護理組成物或產物可為任一種消費者欲用於皮 膚、睫毛或眉毛者,係包含(但不限於)化妝組成物,例如 染睫毛膏、臉部粉底霜、眼線筆、口紅及彩色產品;皮膚 護理組成物,例如保濕化妝水及乳霜、皮膚處理產品、皮 膚防護產品(呈乳液、液體、條狀或凝膠形式);防曬組成 物,例如遮光劑、遮光乳液、化妝水、乳霜、遮光乳液噴 霧劑、液體/酒精遮光喷霧劑、遮光水性凝膠、具Uva及 UVB活性劑之廣泛範圍遮光劑、具有機及無機活性劑之遮 光劑、具有機及無機活性劑的組合之遮光劑、助曬產品、 自曬產πα及日曬後產品等等。特別適合的組成物為個人護 理乳液,更特別適合者為防曬組成物,例如遮光乳液及遮 光乳液喷霧劑。個人護理組成物可呈任一種形式,係包含 (但不限於)喷霧劑、乳液、化妝水、凝膠、液體、條狀: 蠟、糊漿、粉末及乳霜。 個人護理組成物可含有其他工業中常用的成分。此等 將大大地取決於組成物的類型以及所需的功能及性質而 定。不以此為限,此等成分包含增稠劑、懸浮劑、乳化劑、 UV濾材、遮光活性劑、潤濕劑、保濕劑、潤膚劑、油脂、 躐、溶劑、螯合劑、維生素、抗氧化劑、植物萃取物、石夕 酮、中和劑、防腐劑、芳香劑、染料、顏料、調節劑、聚 合物、止汗劑活性成分、抗痤瘡劑、抗頭皮屑活性劑、表 面活性劑、抗剝落劑、薄膜形成劑、推進劑、助曬促進劑、 200536890 固髮劑及色料。本發明之丙烯酸酯共聚物可與大部分習知 個人護理組成物中常用的其他成分相容。舉例來說,遮光 組成物可含有至少一種選自由有機UV濾材、無機UV活 性劑、UVA及/或UVB遮光活性劑、歐克汀諾沙特 (octinoxate)、歐克沙雷特(octisalate)、氧基苯唑 (oxybenzone)、胡莫柳酯、氰雙苯丙烯酸辛酯(octocryiene)、 阿沃苯(avobenzene)、二氧化鈦、澱粉、調節劑、乳化劑、 流變改質劑及增稠劑、中和劑、潤膚劑、溶劑、薄膜形成 劑、保濕劑、抗氧化劑、維生素、螯合劑、防腐劑、芳香 劑及氧化鋅所組成之群之成分。皮膚護理及化妝組成物可 含有至少一種選自由維生素、抗老化劑、保濕劑、潤膚劑、 乳化劑、表面活性劑、防腐劑、顏料、染料、色料及驅蟲 劑所組成之成分。 所生成的個人護理組成物是耐水性的。當使用於以下 實施例一節中所述之試驗時,本發明之丙烯酸酯共聚物耐 水至少40分鐘’更佳為至少6〇分鐘,最佳為至少8〇分鐘。 於浸潰於水巾80分鐘後’由遮光射之聚合物所提供之 SPF保留率超過60%,較佳為超過8〇%,更佳為超過9〇%。 相較於不具聚合物之相同遮光劑,尤其於浸潰於水中之 後’具聚合物之遮光劑已顯示出較高的spF數值。 所生成的個人護理纪成物對於皮膚有極佳 現出無明顯的蠛質、油腻或沈重感。再者,組成物且有極 佳的耐磨除性、賴形輸質及保 錢/、有極 【實施方式】 200536890 實施例 以下所示之實施例係用以進一步說明及解釋本發明, 並且不應認為本發明受此為限。所有使用的百分率係以重 量基準計。 以下成分係用於實施例中:
Dermacryl® AQF聚合物、丙烯酸酯共聚物、45%活性 聚合物於水中之乳液(市售自National Starch and Chemical
Company,Bridgewater,NJ,USA) 〇 實施例1-耐水性遮光乳霜 %w/w 成分 INCI名稱 空白樣品 配方1 相A D.I.水 水 48.90 44.50 Pricerine 9088 甘油99.5% 5.00 5.00 Carbopol 940 (2%) 卡波姆(Carbomer) 10.00 10.00 Pemulen TR-2 丙烯酸酯/C10-30丙烯酸烷酯交聯 0.20 0.20 聚合物 Phenonip 笨氧基乙醇及對羥基苯甲酸甲酯及 1.00 1.00 對羥基笨甲酸丁酯及對羥基苯甲酸 乙酯及對羥基苯甲酸丙酯 TEA 99% 三乙醇胺 0.40 0.40 Dermacryl AQF (45%丙烯酸醋共聚物 0.00 4.40 活性)聚合物 200536890
相B
Neo Heliopan AV 甲氧基肉桂酸乙基己酯 7.50 7.50 Neo Heliopan BB 二苯甲酮-3 6.00 6.00 Neo Heliopan OS 水楊酸乙基己醋 4.00 4.00 Uvinul M-539T 氰雙苯丙稀酸辛醋(Octocrylene) 9.00 9.00 Protachem GMS-450 硬脂酸甘油酯 2.50 2.50 Pristerin 4911 硬脂酸 2.50 2.50 Prisorine 3515 異十八醇 L00 1.00 Amphisol DEA-磷酸十六烷酯 2.00 2.00 合計 100.00 100.00 黏度\叩3) 76,000 84,0〇〇 *黏度係使用BrookfieldDV_I,#6心轴,於23°c下,以l〇rPm 測量。 混合程序:於室溫下,伴隨著螺旋槳混合,合併水與 甘油。將Carbopol 94〇與Pemulen TR-2分散於水/甘油混合 馨 物中’並且混合,直到均勻為止。接著依序添加剩餘的相 A成分,同時攪拌。伴隨著螺旋槳混合,分開地將相A及 B加熱至70_75t。當相A與相B二者達到溫度時,伴隨 著激烈攪拌,將B加於A中。將溫度保持於751達另外 15分鐘,接著散熱,並且伴隨著適度混合而開始冷卻,直 到達到環境温度為止。 實旌例2-耐皮桃摭光喷霧化妝7lc 11 200536890 成分 INCI名稱 %w/w 相A 配方2 Neo Heliopan OS 水楊酸乙基己酯 5.00 Escalol 567 二苯甲酮-3 3.00 Homosalate 胡莫柳酯 7.00 Neo Heliopan AV 甲氧基肉桂酸乙基己酯 7.50 Finsolv TN 苯甲酸C12-C15烷酯 5.00 Stearyl Alcohol 十八醇 1.50 相B D.I·水 水 62.00 Versene NA EDTA二鈉鹽 0.10 Arlatone V-100 Steareth-100(及)Steareth-2(及)硬脂酸甘油 L50 Pricerine 9088 酯檸檬酸酯(及)蔗糖(及)甘露聚糖(及)黃 原膠 甘油99.5% 2.00
Dermacryl AQF (45%丙稀酸醋共聚物 4·40 活性)聚合物
相C
Phenonip 苯氧基乙醇(及)對羥基苯甲酸甲酯(及)對 1.00 羥基苯甲酸丁酯(及)對羥基苯甲酸乙酯 (及)對羥基苯甲酸丙酯 混合程序:將Arlatone V-100分散於冷水中,直到均 200536890 勻為止。接著依序添加剩餘的相B成分,並且加熱至75-80 °C。將相A緩慢地添加於相B中,同時於高速攪拌,且接 著攪拌10分鐘。使混合物均質2分鐘。添加且混合相C, 直到均勻為止。 實施例3-耐水性遮光乳液喷液 %w/w 成分 配方3 配方4 配方5 配方6 相A D.I.水 74.11 78.51 74.26 76.51 EDTA二鈉鹽 0.04 0.04 0.04 0.04 Pemulen TR-1 0.20 0-20 0.20 0.20 甘油99.5% 3.00 3.00 3.00 3.00 Phenonip 1.00 1.00 1.00 1.00 Dermacryl AQF (45% 活 4.40 0.00 0.00 0.00 性)聚合物 相B 甲氧基肉桂酸乙基己酯 7.50 7.50 7.50 7.50 水楊酸乙基己酯 5.00 5.00 5.00 5-00 二苯甲酮-3 4.00 4.00 4.00 4.00 十六醇 0.30 0.30 0.30 0.30 油酸山梨聚糖 0.45 0.45 0.45 0.45 PVP/二十碳烯共聚物 0.00 0.00 0.00 2.00
13 200536890 相c 丙稀酸酯/C12-22 甲基丙 0·00 0.00 4.25 0.00 烯酸烷酯共聚物 相D 三乙醇胺 合計 適量至pH適量至pH適量至pH適量至pH 6,5 6.5 6.5 6.5 100.00 100.00 100.00 100.00 混合程序:分開地合併相A及B,並且伴隨攪拌加熱 至75°C。伴隨著激烈攪拌,將相B加於A中,並且於75 °C混合15分鐘。接著開始冷卻,並且持續,直到溫度降至 低於40°C為止。添加相C(僅配方5),並且徹底地混合。添 加相D,以調整終點之pH。 黏度一(Brookfield DV-1,#6 心軸,於 23°C 下,以 10 n)m 測量)一 配方 3 (Dermacryl AQF 聚合物): 4200 cps 配方4 (空白樣品): 5800 cps 配方5 (丙稀酸酯/C12-22甲基丙烯酸烷酯共聚物): 9100 cps 配方6 (PVP/二十碳烯共聚物)·· 12100 cps 200536890 藉添加Dermacryl AQF聚合物,所生成的遮光喷霧乳 液不具明顯的黏度增加,並且配方具有極佳的噴霧圖案。 具Dermacryl AQF聚合物之配方之黏度類似於不具聚合物 之基劑的黏度,並且比具有丙烯酸酯/C12-22甲基丙烯酸烷 酯共聚物或PVP/二十碳烯共聚物之類似配方更不黏。具 Dermacryl AQF聚合物之配方具有極佳的喷霧美觀及較少 的顆粒偏移,故造成更均勻的覆蓋範圍。 實施例4-廣泛蔽圍耐水性遮光化妝水 · 成分 INCI名稱 %w/w 相A 配方7 去離子水 47.70 EDTA二鈉鹽 0.10 Carbopol 940 (2% 溶卡波姆(Carbomer) 15,00 液) 丙二醇 2.00 Dermacryl AQF (45% 4.40 活性)聚合物 萘二甲酸二乙基己酯 5.00 阿沃苯嗅(Avobenzone) 3.00 二苯甲酮_3 4.00 水揚酸辛酯 5.00 相B Corapan TQ Parsol 1789 Neo Heliopan BB Neo Heliopan OS Neo Heliopan HMS 胡莫柳醋 5.00 15 200536890
FinsolvTN 笨甲酸 C12-C15 烷酯 Brij 721 Steareth-21 Brij 72 Steareth-2 ProtachemGMS-450硬脂酸甘油酯 相C 三乙醇胺 相D Phenonip 5.00 1.00 0.80 1.00 適量至PH 6.5 1·00 混合程序:於室溫下,伴隨著適度螺旋槳、尾人 相Α成分。接著將相Α加熱至75ΐ。伴隨著螺旋口 ϋ 合併相Β成分且加熱至75GC。當相Α與Β二 匕&
時,伴隨著激烈螺旋攪拌,將Β加於Α中。伴产,到溫^ 旋槳混合,接著將混合物冷卻至低於4〇〇Γ 思著適度J u L,以 TEA 姻 j pH,並且添加及混合Phenonip,直到均句為止 网?
實施例5-具ZnO之耐水性戒先劍 成分 INCI名稱 %w/w 相A 配方8 Arlacel 165 硬脂酸甘油酯(及)PEG-100硬脂酸酯 3.50 Montanov S 可可葡糖苷(及)椰子醇 1.30 新戊酸異癸酯 8.00 Neo Heliopan OS 水揚酸乙基己酯 5.00 16 200536890
Escalol 567 二苯甲酮-3 3.00 Neo Heliopan AV 甲氧基肉桂酸乙基己酯 7.50 中性氧化鋅 氧化鋅 7.00 Dow 345 壤曱石夕脂(Cyclomethicone) 5.00 相B Keltrol CGT 黃原膠 0·25 Veegum Ultra 矽酸鋁鎂 1·50 D.I.水 水 52.35 EDTA四納鹽 秦—甲酸二乙基己酉旨 0·20 Dermacryl AQF (45% 4.40 活性)聚合物 相c Phenonip L00 混合程序: 除氧化鋅及Dow 345外 ,合併相A中之所 有成分,並且加熱至75_80乞。將氧化鋅分散於以上相A 之部分中。合併相B,並且將所有固形物完全地分散於水 中。將相B加熱至75t:。當相A與B二者達到溫度時, 將A加於B中,並且均質5分鐘。伴隨著連續攪拌而開始 冷卻。於65 C下添加Dow 345,並且均質另外5分鐘。伴 隨著適度攪拌,使混合物冷卻,並且當溫度降至低於4〇它 時添加相C。 200536890 實施例6-具Ti09之财水性遮光劑 成分 INCI名稱 %w/w 相A 配方9 D.I,水 水 50.40 EDTA二鈉鹽 0.10 Phenonip 1.00 1,2丙烷二醇 丙二醇 3.00 Keltrol CG-RD 黃原膠 0.35 CMC 7LF 纖維素膠 0.05 Dermacryl AQF (45% 4.40 活性)聚合物 相B Neo Heliopan AV 甲氧基肉桂酸乙基己酯 7.50 Neo Heliopan BB 二苯甲酮-3 2.00 MT-500-MS5 Ti02 + 甲石夕脂(methicone) 11.00 Myritol 318 辛酸/癸酸三甘油酯 9.00 DC 345 環甲石夕脂(Cyclomethicone) 3.50 Finsolv TN 苯甲酸C12-C15烷酯 1.50 維生素E醋酸酯 生育醇醋酸酯 0.20 Amphisol DEA_磷酸十六烷酯 2.50 Brij 721 Steareth-21 1.85 Brij 72 Steareth-2 0.65 Protachem GMS-450 硬脂酸甘油酯 L00 200536890 相序:於室溫下’伴隨著適度螺旋槳混合,合併 。於確定膠已充分分散後’開始加熱至70-饥。 分,並且激烈地混合20分鐘,俾提供極佳的 2刀散作用。伴隨著螺旋授拌,將相B加熱至75_8(rc。 相A與B —者達到溫度時,伴隨著激烈螺旋槳混合將b 加於A中。將溫度保持於75¾下另外15-20分鐘,同時徹 底地混合。接著添加相c,混合且將其冷卻至環境溫度。 复―施例7-於活體内之耐太性遮光試驗結果 針對極佳耐水性遮光劑’依照專題論文(“Sunscreen Drug
Products for Over-The-Counter Human Drugs”,Rule,21 CFR Part 352, Subpart D (Federal Register/第 64 冊,第 98 號/1999 年5月21日,提議修正案;Docket編號78N-0038/CP 12, 1999年6月21日))。含有DERMACRYL AQF薄膜形成聚 合物之配方類似不含聚合物(空白樣品)之基礎配方。於浸 潰於水中80分鐘後,評估配方。結果揭示如下(表1)。 表1 :於活體内之試驗結果 成分 空白樣品 配方1 無聚合物 DERMACRYL AQF 靜止 32 32 後浸潰 <21 31 標準差 0 1.15 200536890
使用活體外遮光防水/耐水性試驗方法· N-19(得自IMS Inc.)作為供本試驗用之基材。使用 Labsphere UV 1000S紫外透射分析儀測量SPF數值。於用 於水合至如,以於23。(:下透過水/甘油溶液調節16小時之 濕度來水合Vitro_skin。接著將遮光劑施於經水合的 vitro-Skin(每片為6·2公分x9 〇公分)上,具產物劑量為2微 升/平方公分。接著測量初SPF數值,接著將樣品浸潰於水 浴中,並且設定攪拌馬達至3〇〇 rpm。就防水或極耐水試驗 φ 而言,將樣品浸潰於水中80分鐘。於已自樣品去除過量水 且於在室中平衡樣品2小時之後,接著測量水浸潰作用後 之SPF。母一樣品係進行三重複,並且當測量spF時掃描 每一 vitro-skin 10 次。 調配物 SPF(於水中80分 於浸潰後之 優於空白樣品之SPF增加 鐘之後) %SPF保留率* —率**(芒^ 80分鐘之後) 配方2 30·2 (0·9)… 100% 25.6 配方3 33.5(1.1) 100% 15.6 配方7 37.3 (2.2) 86% 32.5 配方8 51.9 (0.8) 100% 41.6 +於浸潰後之%SPF保留率 = SPF(於水中80分鐘之後)/SPF(最初,於水中8〇分鐘之前) "優於空白樣品之SPF增加率
=SPF(具 Dermacryl AQF 聚合物之配方)-SPF(無 Dermacryl AQF聚合物之相同配方) 20 200536890 w標準差 實施例9_含Dermacryl AOF之遮光水性凝勝-凌 成分 INCI名稱 相A 配方
Neo Heliopan Hydro苯基苯并咪嗤績酸 5·〇〇 去離子水 1〇·〇
TEA 99% 三乙醇胺 5.5
相B D.I.水 水 適量 EDTA 二鈉鹽 〇·1〇 結構XL 羥丙基澱粉磷酸酯 5·0
Escalol 587 二苯甲 3.0
Dermacryl AQF (45%丙稀酸醋共聚物 4.40 活性)聚合物
相C
Germaben II 1.00 混合程序:預熱Neo Heliopan Hydro及水。添加三乙 醇胺,並且充分混合。接著依序合併及混合相B成分,直 到均勻為止。將相A添加於B中,並且混合,直到均勻為 止。伴隨攪拌,將相C添加於批量中。 21 200536890 實施例ίο-臉部粉底霜 成分 INCI名稱 %w/w 相A 配方11 D.I.水 水 適量 聚二醇E-400 PEG-8 5.0 1,2丙烷二醇 丙二醇 5.0 Dermacryl AQF (45%丙烯酸醋共聚物 4.40 活性)聚合物
相B
Ceraphyl 140 A 油酸癸酯 2.2 Cerasynt Q 單硬脂酸甘油酯SE 0.9 硬脂酸山梨聚糖 硬脂酸山梨聚糖 1.5 Stearyl Alcohol 十八醇 0.5 相C 氧化鐵 2.0 二氧化鈦 6.0 高嶺土 7.0 相D DC 345 環甲石夕脂(Cyclomethicone) 15·0
相E 防腐劑 適量 200536890 混合程序:分開地合併相A與相B,並且加熱至75°C。 伴隨良好的混合,將相B添加於相A中。伴隨著持續攪拌, 將混合物冷卻至60°C,並且添加相C。接著添加相D。混 合混合物,並且將其冷卻至小於40°C。添加相E,並且接 著使混合物均質1-2分鐘。 於此臉部粉底霜或其他彩色化妝產品中,Dermacryl AQF提供延長的耐撕裂、耐皺性以及耐水性。 成分 實施例11-潤膚霜 INCI名稱 %w/w 相A 配方12 Tegin Μ 單硬脂酸甘油酯 0.95 Stearic acid 硬脂酸 1.9 Finsolv TN 苯甲酸C12-C15烷酯 2.5 Miglycol 812 辛酸/癸酸三甘油酯 3.0 Isopropyl Myristate 莖蔻酸異丙酯 2.5 Jojoba oil 荷荷巴油 2.0 相B 去離子水 適量 TEA 99% 三乙醇胺 035 Glycerin 甘油 3.0 Xanthan gum 黃原膠 0.6 23 200536890 相c
Dermacryl AQF (45%丙烯酸S旨共聚物 活性)聚合物
相D 適量 防腐劑
a) 此&程序:口併相A,並且加熱至75〇c。混合相j 及Dennacryi AQF,以確保黃原膠完全分散,接著加熱至 抑。伴隨良好混合’將相A添加於相B中 攪拌,將混合物冷卻至低於4(TC。接著添加相匚 …… b) 除於合併相A與相B之後於75下六 AQF外,重複(a)之混合程序。 乂加Dermacry 於此式中,Dermacryl AQF聚合物係充當 俾除延長產品的耐用性(包含耐水性)外, 、形成劑, 提供水分防護或保濕作用。 ㈢、、、、閉塞性而
24
Claims (1)
- 200536890 十、申請專利範圍: 1·一種個人護理組成物,其包含防水有效量之丙烯酸酯共 聚物。 2·如申請專利範圍第1項之組成物,其中該丙烯酸酯共聚 物為水可分散的及於pH超過4時,並且大體上不含有 具烷基基團大於或等於C8之疏水性單體。 3·如申請專利範圍第1項之組成物,其中該丙烯酸酯共聚 物係形成自至少二種選自由丙烯酸、甲基丙烯酸及/或其 酯類及/或醯胺類及其組合所組成之群之單體。 _ 4·如申請專利範圍第1項之組成物,其中該丙烯酸酯共聚 物係形成自至少二種選自由(甲基)丙烯酸曱酯、(甲基) 丙烯酸乙酯、(甲基)丙烯酸丙酯、(甲基)丙烯酸丁酯、(甲 基)丙烯酸異丁酯、丙烯酸、甲基丙烯酸及其組合所組成 之群之單體。 5·如申請專利範圍第4項之丙烯酸酯共聚物,其中該至少 二種單體係選自由丙烯酸丁酯、(甲基)丙烯酸曱酯、丙 稀酸及其組合所組成之群。 _ 6·如申請專利範圍第1項之組成物,其中該丙烯酸酯共聚 物含有以該共聚物之重量計為1%至85%之丙烯酸丁 酯、以該共聚物之重量計為1%至87%之(甲基)丙烯酸甲 酯以及以該共聚物之重量計為1%至25%之曱基丙烯酸。 7.如申請專利範圍第6項之組成物,其中該丙烯酸酯共聚 物含有以該共聚物之重量計為約38%至約48%之丙烯酸 丁酯、以該共聚物之重量計為約39%至約49%之(曱基) 丙烯酸甲酯以及以該共聚物之重量計為約8%至約18% 25 200536890 之甲基丙烯酸。 8.如申請專利範圍第1項之個人護理組成物,其中該組成 物係為防曬組成物、護膚組成物、睫毛護理組成物或眉 毛護理組成物。26 200536890 七、指定代表圖·· (一) 本案指定代表圖為··第( )圖。無 (二) 本代表圖之元件符號簡單說明: 無八、本案若有化學式時,請揭示最能顯示發明特徵的化學式: 無4
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2621722C3 (de) * | 1976-05-15 | 1983-11-17 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von Copolymerisaten aus (Meth)acrylsäure und (Meth)acrylsäureestern |
| US4172122A (en) * | 1977-07-29 | 1979-10-23 | Minnesota Mining And Manufacturing Company | Substantive sunscreening compositions |
| JPS54151139A (en) * | 1978-05-16 | 1979-11-28 | Shiseido Co Ltd | Make-up cosmetics |
| US5139877A (en) * | 1984-10-19 | 1992-08-18 | Abco Industries, Ltd. | Chemical composition for improving the wettability of synthetic polymeric materials for use in composite applications, synthetic materials coated therewith and composites produced therefrom |
| LU86429A1 (fr) † | 1986-05-16 | 1987-12-16 | Oreal | Compositions cosmetiques renfermant un polymere cationique et un polymere anionique comme agent epaississant |
| CA1299319C (en) † | 1986-10-23 | 1992-04-21 | Izumi Saitoh | Acrylic copolymer and skin protective |
| JP2740542B2 (ja) † | 1989-04-01 | 1998-04-15 | 塩野義製薬株式会社 | 皮膚の保護剤組成物 |
| JPH04103514A (ja) * | 1990-08-21 | 1992-04-06 | Kao Corp | 水系美爪料 |
| US5288493A (en) * | 1991-05-17 | 1994-02-22 | National Starch And Chemical Investment Holding Corporation | Skin care compositions with improved rub-off resistance |
| US5204090A (en) * | 1991-05-30 | 1993-04-20 | Bristol Myers Squibb | Waterproof high-SPF sunscreen compositions |
| JPH0517320A (ja) | 1991-07-10 | 1993-01-26 | Kao Corp | 化粧料 |
| JP3212637B2 (ja) † | 1991-07-30 | 2001-09-25 | 全薬工業株式会社 | 被膜型皮膚保護剤 |
| FR2740330B1 (fr) * | 1995-10-27 | 1997-12-05 | Oreal | Composition comprenant un systeme polymerique et utilisation dudit systeme |
| FR2741530B1 (fr) * | 1995-11-23 | 1998-01-02 | Oreal | Utilisation pour la coloration temporaire des cheveux ou poils d'animaux d'une composition a base d'une dispersion de polymere filmogene et d'un pigment non-melanique |
| FR2745494B1 (fr) * | 1996-03-04 | 1998-08-07 | Oreal | Composition comprenant une dispersion aqueuse de particules de polymere filmogene,et utilisation d'un systeme polymerique comprenant ladite dispersion notamment en cosmetique |
| US6503495B1 (en) | 1996-10-31 | 2003-01-07 | The Procter & Gamble Company | Cosmetic compositions having improved wear and beauty |
| US5853700A (en) * | 1996-11-06 | 1998-12-29 | National Starch And Chemical Investment Holding Corporation | Hydro-alcoholic aerosol hair cosmetic compositions containing a hydrolytically stable silicone glycol block copolymer dispersion |
| US6015574A (en) * | 1997-06-09 | 2000-01-18 | L'oreal | Lipophilic carrier systems |
| AU5617700A (en) | 1999-06-18 | 2001-01-09 | Schering-Plough Healthcare Products, Inc. | Anhydrous ultraviolet light screening composition containing octocrylene |
| US6762158B2 (en) | 1999-07-01 | 2004-07-13 | Johnson & Johnson Consumer Companies, Inc. | Personal care compositions comprising liquid ester mixtures |
| JP4461308B2 (ja) * | 1999-11-25 | 2010-05-12 | 麻沼総業株式会社 | 美爪料 |
| US20020076390A1 (en) | 2000-10-25 | 2002-06-20 | 3M Innovative Properties Company | Acrylic-based copolymer compositions for cosmetic and personal care |
| FR2817476B1 (fr) | 2000-12-05 | 2003-01-03 | Oreal | Composition de soin de maquillage contenant des fibres et un copolymere dispersant |
| DE10136883B4 (de) | 2001-07-24 | 2008-08-21 | Coty B.V. | Wasser- und abriebfestes Kosmetikum für Haare und dekorative Kosmetik |
| JP3755753B2 (ja) | 2001-11-30 | 2006-03-15 | 株式会社東海理化電機製作所 | 圧電振動ジャイロ及び圧電振動ジャイロ装置 |
| JP4382398B2 (ja) | 2003-06-11 | 2009-12-09 | アクゾノーベル株式会社 | 化粧料用樹脂 |
-
2003
- 2003-11-26 US US10/723,341 patent/US8545859B2/en active Active
-
2004
- 2004-11-23 AU AU2004231259A patent/AU2004231259B2/en not_active Expired
- 2004-11-23 EP EP04027724.6A patent/EP1535938B2/en not_active Expired - Lifetime
- 2004-11-25 BR BRPI0405213A patent/BRPI0405213B1/pt not_active IP Right Cessation
- 2004-11-25 MX MXPA04011702A patent/MXPA04011702A/es active IP Right Grant
- 2004-11-26 AR ARP040104409A patent/AR046727A1/es not_active Application Discontinuation
- 2004-11-26 CN CNB2004101047919A patent/CN100536821C/zh not_active Expired - Fee Related
- 2004-11-26 TW TW093136392A patent/TW200536890A/zh unknown
- 2004-11-26 JP JP2004341916A patent/JP4664049B2/ja not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US20050112080A1 (en) | 2005-05-26 |
| EP1535938A1 (en) | 2005-06-01 |
| BRPI0405213A (pt) | 2005-07-19 |
| JP2005170940A (ja) | 2005-06-30 |
| BRPI0405213B1 (pt) | 2015-09-15 |
| US8545859B2 (en) | 2013-10-01 |
| CN100536821C (zh) | 2009-09-09 |
| AU2004231259B2 (en) | 2011-04-21 |
| EP1535938B1 (en) | 2013-04-17 |
| MXPA04011702A (es) | 2005-06-08 |
| CN1660030A (zh) | 2005-08-31 |
| EP1535938B2 (en) | 2016-11-02 |
| AU2004231259A1 (en) | 2005-06-09 |
| JP4664049B2 (ja) | 2011-04-06 |
| AR046727A1 (es) | 2005-12-21 |
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