JP2003520063A - Article for applying topical composition and method for producing the same - Google Patents
Article for applying topical composition and method for producing the sameInfo
- Publication number
- JP2003520063A JP2003520063A JP2001508838A JP2001508838A JP2003520063A JP 2003520063 A JP2003520063 A JP 2003520063A JP 2001508838 A JP2001508838 A JP 2001508838A JP 2001508838 A JP2001508838 A JP 2001508838A JP 2003520063 A JP2003520063 A JP 2003520063A
- Authority
- JP
- Japan
- Prior art keywords
- article according
- topical composition
- layer
- article
- composition
- 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.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 69
- 230000000699 topical effect Effects 0.000 title claims abstract description 48
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 7
- 239000002775 capsule Substances 0.000 claims abstract description 34
- 238000003466 welding Methods 0.000 claims abstract description 11
- 239000002537 cosmetic Substances 0.000 claims description 18
- 239000002657 fibrous material Substances 0.000 claims description 18
- -1 polyethylene Polymers 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 7
- 108010010803 Gelatin Proteins 0.000 claims description 6
- 239000004698 Polyethylene Substances 0.000 claims description 6
- 239000008273 gelatin Substances 0.000 claims description 6
- 229920000159 gelatin Polymers 0.000 claims description 6
- 235000019322 gelatine Nutrition 0.000 claims description 6
- 235000011852 gelatine desserts Nutrition 0.000 claims description 6
- 229920000573 polyethylene Polymers 0.000 claims description 6
- 229920002678 cellulose Polymers 0.000 claims description 5
- 239000001913 cellulose Substances 0.000 claims description 5
- 239000008194 pharmaceutical composition Substances 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- 239000000499 gel Substances 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 238000004026 adhesive bonding Methods 0.000 claims description 2
- 239000000084 colloidal system Substances 0.000 claims description 2
- 230000006835 compression Effects 0.000 claims description 2
- 238000007906 compression Methods 0.000 claims description 2
- 238000000151 deposition Methods 0.000 claims description 2
- 238000000527 sonication Methods 0.000 claims description 2
- 239000000835 fiber Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 229920000297 Rayon Polymers 0.000 description 7
- 229920000728 polyester Polymers 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 239000006260 foam Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 235000010980 cellulose Nutrition 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000012429 reaction media Substances 0.000 description 4
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- YBGZDTIWKVFICR-JLHYYAGUSA-N Octyl 4-methoxycinnamic acid Chemical compound CCCCC(CC)COC(=O)\C=C\C1=CC=C(OC)C=C1 YBGZDTIWKVFICR-JLHYYAGUSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000005538 encapsulation Methods 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 3
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- 101100160821 Bacillus subtilis (strain 168) yxdJ gene Proteins 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 238000005354 coacervation Methods 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- XIRNKXNNONJFQO-UHFFFAOYSA-N ethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC XIRNKXNNONJFQO-UHFFFAOYSA-N 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- 229940057995 liquid paraffin Drugs 0.000 description 2
- 210000004400 mucous membrane Anatomy 0.000 description 2
- 239000007764 o/w emulsion Substances 0.000 description 2
- 229960001679 octinoxate Drugs 0.000 description 2
- 229960005323 phenoxyethanol Drugs 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 230000035807 sensation Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 2
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 description 2
- 239000007762 w/o emulsion Substances 0.000 description 2
- HDDAFVDVXFWWIC-UHFFFAOYSA-N 18-oxooctadecyl octanoate Chemical compound CCCCCCCC(=O)OCCCCCCCCCCCCCCCCCC=O HDDAFVDVXFWWIC-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- OXSYGCRLQCGSAQ-UHFFFAOYSA-N CC1CCC2N(C1)CC3C4(O)CC5C(CCC6C(O)C(O)CCC56C)C4(O)CC(O)C3(O)C2(C)O Chemical compound CC1CCC2N(C1)CC3C4(O)CC5C(CCC6C(O)C(O)CCC56C)C4(O)CC(O)C3(O)C2(C)O OXSYGCRLQCGSAQ-UHFFFAOYSA-N 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- 229920000742 Cotton Polymers 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
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- QAQJMLQRFWZOBN-LAUBAEHRSA-N L-ascorbyl-6-palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](O)[C@H]1OC(=O)C(O)=C1O QAQJMLQRFWZOBN-LAUBAEHRSA-N 0.000 description 1
- 239000011786 L-ascorbyl-6-palmitate Substances 0.000 description 1
- 241001477893 Mimosa strigillosa Species 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- 229920001800 Shellac Polymers 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 241000282898 Sus scrofa Species 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 102100031083 Uteroglobin Human genes 0.000 description 1
- 108090000203 Uteroglobin Proteins 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000003732 agents acting on the eye Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 235000010385 ascorbyl palmitate Nutrition 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- OGQYPPBGSLZBEG-UHFFFAOYSA-N dimethyl(dioctadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC OGQYPPBGSLZBEG-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 229940067592 ethyl palmitate Drugs 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910001412 inorganic anion Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- 229940023490 ophthalmic product Drugs 0.000 description 1
- 150000002891 organic anions Chemical class 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 229940031709 peg-30-dipolyhydroxystearate Drugs 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 235000015277 pork Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A45—HAND OR TRAVELLING ARTICLES
- A45D—HAIRDRESSING OR SHAVING EQUIPMENT; EQUIPMENT FOR COSMETICS OR COSMETIC TREATMENTS, e.g. FOR MANICURING OR PEDICURING
- A45D34/00—Containers or accessories specially adapted for handling liquid toiletry or cosmetic substances, e.g. perfumes
- A45D34/04—Appliances specially adapted for applying liquid, e.g. using roller or ball
-
- A—HUMAN NECESSITIES
- A45—HAND OR TRAVELLING ARTICLES
- A45D—HAIRDRESSING OR SHAVING EQUIPMENT; EQUIPMENT FOR COSMETICS OR COSMETIC TREATMENTS, e.g. FOR MANICURING OR PEDICURING
- A45D37/00—Sachet pads specially adapted for liquid toiletry or cosmetic substances
Landscapes
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
- Containers And Packaging Bodies Having A Special Means To Remove Contents (AREA)
Abstract
(57)【要約】 本発明は、局所組成物透過性の上層(6)、局所組成物不透過性の下層(2)及び少なくとも1つの局所組成物含有カプセル(5)を含み、前記した2つの層は全面的に重なり合っており且つその周囲での溶着により一体に維持されている局所組成物の適用用物品に関する。本発明は前記物品の製造方法にも関する。 SUMMARY OF THE INVENTION The present invention comprises a topical composition permeable upper layer (6), a topical composition impervious lower layer (2) and at least one topical composition containing capsule (5). The two layers relate to an article for the application of the topical composition which is entirely overlapping and is held together by welding around it. The invention also relates to a method for producing said article.
Description
【0001】
本発明は、局所組成物、特に化粧品または医薬品組成物を適用するための物品
並びに前記物品の製造方法に関する。The present invention relates to an article for applying a topical composition, in particular a cosmetic or pharmaceutical composition, as well as a method for producing said article.
【0002】
局所適用用化粧品または医薬品組成物、すなわち皮膚及び粘膜に適用するため
の組成物は通常チューブまたはジャーの形態のパッケージで市販されている。使
用者は組成物を少量取りだした後、その組成物を皮膚または粘膜の所望ゾーンに
指を用いて適用しなければならない。しかしながら、こうすると、局所組成物に
触れたときに使用者の手が汚れ、場合によりいやな手触りが残ることもある。こ
うした不都合を避けるために、皮膚に直接適用するように局所組成物を含浸させ
た繊維媒体が提案された。しかしながら、前記繊維媒体では局所組成物と使用者
の手の接触を部分的にしか解消しない。Cosmetic or pharmaceutical compositions for topical application, ie compositions for application to the skin and mucous membranes, are usually marketed in packages in the form of tubes or jars. The user must withdraw a small amount of the composition and then apply it with the finger to the desired zone of the skin or mucous membranes. However, this may leave the user's hands dirty when touching the topical composition and, in some cases, may leave an unpleasant feel. To avoid these disadvantages, fibrous media impregnated with the topical composition for direct application to the skin have been proposed. However, the fibrous media only partially eliminates contact between the topical composition and the user's hand.
【0003】
更に、使用者は、実施するのが容易で、用時使用可能で且つ便利な一回の使用
のための製品を、特にスキンケアの分野でますます求めている。Furthermore, users are increasingly demanding single-use products that are easy to implement, ready to use and convenient, especially in the field of skin care.
【0004】
欧州特許第0,764,409号明細書では、粉末、固体ゲルまたは棒状化粧
品を少なくとも1つのフォームブロックを含み、溶着接合部を有するフォーム状
パウダーパフ中に挿入することが既に提案されている。前記化粧品は、フォーム
ブロックに溶液またはエマルションを含浸させることにより活性化した後皮膚に
適用している。In EP 0,764,409 it has already been proposed to insert a powder, a solid gel or a bar cosmetic into a foam powder puff containing at least one foam block and having a welded joint. ing. The cosmetic is applied to the skin after activation by impregnating a foam block with a solution or emulsion.
【0005】
しかしながら、この種のパッケージは固体形態で提供され得る製品に対しての
み適している。特に、化粧品を活性化するためにフォームに予め液体を含浸させ
る必要があるので、実際のところ用時に簡単に使用できる製品ではない。加えて
、一旦活性化された化粧品はフォームのすべての孔から流出するようになってい
る。このために、使用者の手が活性化された化粧品と接触するのは避けられない
。However, packages of this kind are only suitable for products which can be provided in solid form. In particular, it is not a product that is actually easy to use at the point of use, since the foam must be pre-impregnated with liquid in order to activate the cosmetic product. In addition, once activated, the cosmetic product is intended to flow out of all the pores of the foam. Because of this, it is inevitable that the user's hand will come into contact with the activated cosmetic product.
【0006】
よって、本出願人は、上記した欠点を解消すると共に、一回の使用だけのため
に使用が簡単で、実施が容易であり、使用者の指と組成物の接触を避けることが
できる化粧または医薬用局所組成物を包装及び適用するための物品を開発するこ
とを求めた。Therefore, the applicant has solved the above-mentioned drawbacks, is easy to use because it is only used once, is easy to carry out, and avoids contact between the user's finger and the composition. It sought to develop an article for packaging and applying possible cosmetic or pharmaceutical topical compositions.
【0007】
従って、本発明は化粧品または医薬品局所組成物を適用するための物品を提供
し、その物品は前記局所組成物透過性の上層及び前記局所組成物不透過性の繊維
材料からなる下層を含み、前記した2つの層は全面的に重なり合っており且つ前
記局所組成物を含有しているカプセルが少なくとも1つ配置されるスペースを規
定するようにその周囲を溶着することにより互いに維持されていることを特徴と
する。Accordingly, the present invention provides an article for applying a cosmetic or pharmaceutical topical composition, which article comprises a top layer permeable to said topical composition and a bottom layer comprising a fibrous material impermeable to said topical composition. Including the two layers described above being entirely overlapped and maintained together by welding around their perimeters to define a space in which at least one capsule containing the topical composition is placed. It is characterized by
【0008】
上記した作用効果に加えて、本発明の物品によると特定量の局所組成物がデリ
バリーされ得、空気から隔離されるように維持され、よって前記組成物に対して
安定性が与えられる。In addition to the effects described above, the articles of the present invention can deliver a certain amount of topical composition and maintain it isolated from the air, thus providing stability to the composition. .
【0009】 本発明の他の作用効果は以下の詳細説明及び図面にてらして明らかであろう。[0009] Other effects of the present invention will be apparent from the following detailed description and drawings.
【0010】
図1は、医薬品または化粧品局所組成物を含有するカプセルを数個含む本発明
の物品の部分切取り斜視図である。FIG. 1 is a partial cutaway perspective view of an article of the present invention containing several capsules containing a pharmaceutical or cosmetic topical composition.
【0011】 本発明の物品では、典型的には上層も繊維材料からなる。[0011] In the articles of the present invention, the upper layer typically also comprises a fibrous material.
【0012】
上層または下層のために等しく使用され得る繊維材料は通常、皮膚と接触した
ときに使用者に対して柔らかくて心地よい感覚を与える材料から選択される。勿
論、非研磨材料が好ましい。繊維材料は織布または不織布のいずれでもよいが、
後者が好ましい。Fibrous materials that can equally be used for the upper or lower layer are usually selected from materials that give the user a soft and comfortable sensation when in contact with the skin. Of course, non-abrasive materials are preferred. The fiber material may be woven or non-woven,
The latter is preferred.
【0013】
繊維材料は、必要な柔らかくて心地よい感覚を与えることができる繊維を適当
な媒体に沈着させてなるものでもよい。The fibrous material may be formed by depositing fibers in a suitable medium that can provide the required soft and pleasant sensation.
【0014】
織または不織繊維材料の例としては、絹または天然セルロース(例えば、綿ま
たは木材パルプ)のような天然製品;再生セルロース(例えば、ビスコースまた
は高強力ビスコース)を含めた人工製品;ポリオレフィン(例えば、ポリエチレ
ン、ポリプロピレンまたはエチレン/プロピレンコポリマー)、ポリエステル(
例えば、ポリ酢酸ビニルのような酢酸から誘導されるコポリマー)、ポリアミド
(例えば、ナイロン)またはポリウレタンを含めた合成製品;上記した製品の2
つ以上の混合物、特にビスコース繊維とポリエステル繊維を主成分とする混合物
が挙げられる。Examples of woven or non-woven fibrous materials are natural products such as silk or natural cellulose (eg cotton or wood pulp); artificial products including regenerated cellulose (eg viscose or high tenacity viscose). ; Polyolefins (eg polyethylene, polypropylene or ethylene / propylene copolymers), polyesters (
Synthetic products including, for example, acetic acid-derived copolymers such as polyvinyl acetate), polyamides (eg nylon) or polyurethanes; 2 of the products mentioned above
There may be mentioned one or more mixtures, in particular mixtures based on viscose fibers and polyester fibers.
【0015】
前記織または不織繊維材料からなる繊維または各繊維は充実、中空、多孔性ま
たはマルチラメラ状であり得、またはポリエステル/ビスコースまたはポリエス
テル/ポリアミド繊維のような二成分繊維として形成され得る。The fibers or individual fibers of the woven or non-woven fibrous material may be solid, hollow, porous or multilamellar or formed as bicomponent fibers such as polyester / viscose or polyester / polyamide fibers. obtain.
【0016】
下層及び上層の繊維材料が熱溶融性または熱可塑性であることが有利であり得
る。上記した材料の幾つかは上記した品質を有し、特にポリエチレンのようなポ
リオレフィンである。更に、前記材料により、2層間の溶着を下記する方法に従
って簡単に、特に工業的規模で実施することができる。It may be advantageous for the fibrous material of the lower and upper layers to be heat fusible or thermoplastic. Some of the materials listed above have the above qualities and are especially polyolefins such as polyethylene. Furthermore, with the said materials, the welding between the two layers can be carried out easily, especially on an industrial scale, according to the method described below.
【0017】
下層及び上層は全体的に上記したような少なくとも1つの繊維材料から構成さ
れ得る。The bottom layer and the top layer may be composed entirely of at least one fibrous material as described above.
【0018】
上層及び下層の少なくとも1つは、少なくとも2つのサブ層を含む多層構造か
ら構成され得る。前記多層構造により幾つかの利点が得られ得る。At least one of the upper and lower layers may be composed of a multi-layer structure including at least two sublayers. Several advantages may be obtained with the multilayer structure.
【0019】
すなわち、下層は、心地よい感触の透過性繊維材料からなる外側サブ層及び局
所組成物に対して不透過性の内側サブ層を有し得る。この不透過性の内側サブ層
はポリマー材料製フィルム、例えばポリオレフィン(例えば、ポリエチレン、ポ
リプロピレンまたはエチレン/プロピレンコポリマー)フィルムから構成され得
る。That is, the underlayer may have an outer sublayer of a permeable fibrous material of pleasant feel and an inner sublayer impermeable to the topical composition. The impermeable inner sublayer may be composed of a film of polymeric material, such as a polyolefin (eg, polyethylene, polypropylene or ethylene / propylene copolymer) film.
【0020】
更に、下層及び上層の各層を、下記するような方法に従って溶着し得るように
上記した熱可塑性または熱溶融性材料からなる内側サブ層を対向して配置した多
層構造から構成してもよい。こうすると、使用者が触れる外側サブ層は、感触が
心地よくて柔らかいが、良好な溶着を確保するために適当な品質を必ずしも有し
ていない材料から構成され得る。Further, each of the lower layer and the upper layer may have a multi-layer structure in which the inner sub-layers made of the above-mentioned thermoplastic or heat-fusible material are arranged so as to face each other so that they can be welded by the following method. Good. In this way, the outer sub-layer that the user touches may be composed of a material that is pleasant to the touch and soft, but does not necessarily have the appropriate quality to ensure good welding.
【0021】
前記多層構造は、当業者に公知の方法、例えば対向する辺を接着したりカレン
ダーがけする等により得ることができる。The multi-layer structure can be obtained by a method known to those skilled in the art, for example, by adhering opposite sides or calendering.
【0022】
少なくとも下層が繊維材料から構成されていることが重要である。これは、前
記材料により使用者による本発明の物品の把持が改善され、局所組成物の皮膚へ
の適切な適用が助長されるからである。これは、局所組成物を注意深く且つ正確
に広げなければならない顔、特に顔の皺に適用するときにはより重要である。It is important that at least the lower layer is composed of fibrous material. This is because the material improves the grip of the article of the invention by the user and facilitates the proper application of the topical composition to the skin. This is more important when applied to the face, especially facial wrinkles, where the topical composition must be carefully and accurately spread.
【0023】
更に、心地よい感触を有する繊維材料により、化粧品または医薬品に関して特
に多くを要求している使用者も本発明の物品を許容し得る。[0023] Furthermore, the pleasant-feeling fibrous material may also allow the articles of the invention to be used by users who are particularly demanding in terms of cosmetics or pharmaceuticals.
【0024】
本発明によれば、局所組成物が材料の孔を通過し得るときに材料は局所組成物
に対して透過性である。According to the invention, the material is permeable to the topical composition as it can pass through the pores of the material.
【0025】
考えられる織または不織繊維材料は20〜250g/m2、好ましくは100
〜180g/m2の重量(ISO基準9073−1)を有し得る。Possible woven or non-woven fibrous materials are 20 to 250 g / m 2 , preferably 100.
It may have a weight (ISO standard 9073-1) of ˜180 g / m 2 .
【0026】
本発明の物品が局所組成物含有カプセルを1個しか含んでいなくてもよい。し
かしながら、通常は各々に局所組成物の一部を含有させてなる小さなカプセルを
複数個使用する。前記の小さなカプセルは通常0.5〜5mm、好ましくは1〜
2.5mmの平均直径を有する。前記カプセルの外被は親水性コロイド、例えば
アルブミン、アルギネート、カゼイン、ペクチン、澱粉、ゼラチン、セルロース
誘導体(例えば、エチルセルロース、ニトロセルロース、セルロースアセテート
)、セラック、ポリアクリル酸、ポリメタクリル酸、ポリサッカライド、ポリビ
ニル誘導体、ポリカーボネートまたはポリスチレンから構成され得る。ゼラチン
がカプセル外被の好ましい成分である。The article of the invention may contain only one capsule containing the topical composition. However, usually multiple small capsules are used, each containing a portion of the topical composition. The small capsules are usually 0.5-5 mm, preferably 1-
It has an average diameter of 2.5 mm. The capsule is coated with a hydrophilic colloid such as albumin, alginate, casein, pectin, starch, gelatin, cellulose derivative (eg, ethyl cellulose, nitrocellulose, cellulose acetate), shellac, polyacrylic acid, polymethacrylic acid, polysaccharide, It can be composed of polyvinyl derivatives, polycarbonate or polystyrene. Gelatin is the preferred component of the capsule envelope.
【0027】 ゼラチンは特に豚、牛、羊及び魚ゼラチンであり得る。[0027] The gelatin may especially be pig, cow, sheep and fish gelatin.
【0028】
カプセル化比、すなわち各カプセルに含有させる局所組成物/カプセルの全重
量の重量比は通常80〜99%である。カプセル中に含有されている組成物の放
出にてらし、カプセルは本発明の物品を単に曲げ、手で押圧するだけで崩壊され
得なければならない。本発明の別の利点によれば、カプセルを層を介して崩壊さ
せるとき使用者は心地よさを感ずる。The encapsulation ratio, ie the weight ratio of the total weight of the topical composition / capsule contained in each capsule, is usually 80-99%. Upon release of the composition contained in the capsule, the capsule must be able to be disintegrated by simply bending and manually pressing the article of the invention. According to another advantage of the invention, the user feels comfortable when the capsule is disintegrated through the layers.
【0029】
本発明の物品中のカプセルの量は、局所組成物の所望用量及びカプセル化比に
応じて選択される。局所組成物の用量それ自体は該組成物の種類及び所期用途に
依存する。The amount of capsules in the article of the invention is selected depending on the desired dose of the topical composition and the encapsulation ratio. The dosage of the topical composition itself depends on the type of composition and its intended use.
【0030】
カプセルの製造は当業者に公知である。これに関して、例えば援用により本明
細書に含まれるとする米国特許第3,691,090号明細書、同第5,051
,304号明細書または同第4,752,496号明細書を参照することができ
る。より具体的には、カプセルはコアセルベート化剤を用いるコアセルベーショ
ンにより製造することができる。コアセルベート化剤の例としては、有機または
無機アニオン(例えば、硫酸、ポリリン酸、酢酸及びギ酸アニオン)のアルカリ
金属塩、アルカリ土類金属塩またはアンモニウム塩のような有機及び/または無
機塩を含む水性電解質溶液が挙げられ得る。ヘキサメタリン酸ナトリウムが最も
適当なコアセルベート化剤である。この方法で得られたカプセルは脆く、該カプ
セルが形成されてなる反応媒体から抽出するときには特にそうであり得る。カプ
セルの脆性を改善し、溶解度を低下させるために、反応媒体に架橋剤(例えば、
グルタルアルデヒドまたはホルムアルデヒド)を添加することが可能である。The manufacture of capsules is known to those skilled in the art. In this regard, for example, US Pat. Nos. 3,691,090 and 5,051 which are hereby incorporated by reference.
, 304 or 4,752,496. More specifically, capsules can be manufactured by coacervation using a coacervating agent. Examples of coacervating agents are aqueous containing organic and / or inorganic salts such as alkali metal salts, alkaline earth metal salts or ammonium salts of organic or inorganic anions (eg sulfuric acid, polyphosphoric acid, acetic acid and formate anions). An electrolyte solution may be mentioned. Sodium hexametaphosphate is the most suitable coacervating agent. The capsules obtained in this way are brittle and may be especially so when extracting from the reaction medium in which they are formed. To improve the brittleness of the capsule and reduce its solubility, the reaction medium may be cross-linked (for example
It is possible to add glutaraldehyde or formaldehyde).
【0031】
局所組成物は通常液体、ペースト、半ペーストまたはゲル形態である。前記局
所組成物は化粧品組成物、特にメークアップ製品、スキンケア製品、または皮膚
衛生またはクレンジング製品であり得る。メークアップ製品は特にメーキャツプ
ファンデーションであり得る。皮膚衛生またはクレンジング製品はメーク落とし
であり得る。局所組成物はまた医薬品組成物、特に皮膚科または眼科医薬品であ
り得る。局所組成物はまた精油、水−アルコール溶液またはエマルションの形態
で香料をも含み得る。局所組成物それ自体は公知であり、活性成分及び/または
慣用の賦形剤を含む。Topical compositions are usually in liquid, paste, semi-paste or gel form. The topical composition may be a cosmetic composition, in particular a make-up product, a skin care product or a skin hygiene or cleansing product. The make-up product may in particular be a make-up foundation. The skin hygiene or cleansing product can be a makeup remover. The topical composition may also be a pharmaceutical composition, especially a dermatological or ophthalmic drug. The topical composition may also include a perfume in the form of an essential oil, water-alcohol solution or emulsion. Topical compositions are known per se and contain the active ingredient and / or customary excipients.
【0032】
本発明の物品は通常5〜20mmの厚さを有する。前記物品は長方形、三角形
、正方形または円形をとり得る。前記物品の直径または長辺は通常1〜10cm
である。上層及び下層の各層の厚さは0.5〜4mm、好ましくは1〜3mmで
あり得る。The articles of the present invention typically have a thickness of 5-20 mm. The article can be rectangular, triangular, square or circular. The diameter or long side of the article is usually 1 to 10 cm
Is. The thickness of each of the upper and lower layers may be 0.5-4 mm, preferably 1-3 mm.
【0033】
図1は本発明の物品1を示し、この物品1は不織天然セルロースからなる外側
サブ層3とポリエチレンフィルムからなる内側サブ層4を含む不透過性下層2、
及びポリエステルからなる内側サブ層7とポリエステル30重量%及びビスコー
ス70重量%の混合物を主成分とするビスコースからなる外側サブ層8を含む透
過性上層6を含み、前記内側サブ層4の上には局所組成物を含有する複数個のカ
プセル5が堆積されている。上層及び下層は全面的に溶着9により結合されてい
る。使用に際し、本発明の物品のカプセルは該物品を指で曲げ、押圧することに
より壊され、こうすると局所組成物が活性化され、その活性化された組成物は透
過性上層を介して移行する。次いで、有利には、局所組成物が使用者の手または
指と接触することなく、該局所組成物は上層を構成する繊維材料により皮膚に適
用され得る。FIG. 1 shows an article 1 of the invention, which is an impermeable underlayer 2, comprising an outer sublayer 3 made of non-woven natural cellulose and an inner sublayer 4 made of polyethylene film,
And a permeable upper layer 6 including an inner sub-layer 7 made of polyester and an outer sub-layer 8 made of viscose having a mixture of 30% by weight of polyester and 70% by weight of viscose as a main component, and above the inner sub-layer 4. A plurality of capsules 5 containing a topical composition have been deposited therein. The upper layer and the lower layer are entirely bonded by welding 9. In use, the capsules of the article of the present invention are broken by bending and pressing the article with a finger, which activates the topical composition, which activated composition migrates through the permeable top layer. . Then, advantageously, the topical composition may be applied to the skin by means of the fibrous material constituting the upper layer, without the topical composition coming into contact with the user's hands or fingers.
【0034】
本発明の別の態様によれば、上記した物品の製造方法が提供される。この方法
では、局所組成物を含有するカプセルを物品を構成する上層または下層のいずれ
かの内側表面上に堆積させる。次いで、堆積カプセルを含む層と他の層とを全面
的に重ね合わせ、2つの層をその周囲で全面的に溶着させる。According to another aspect of the present invention, there is provided a method of manufacturing the article described above. In this method, capsules containing the topical composition are deposited on the inner surface of either the top or bottom layers of the article. The layer containing the deposited capsules and the other layer are then superposed over one another and the two layers are welded over their peripheries.
【0035】
溶着は加熱、超音波、接着、高周波または機械的圧縮により実施され得る。加
熱、超音波または高周波により溶着を実施する場合には、上層及び下層の少なく
とも周囲を熱溶融性または熱可塑性材料で構成しなければならない。Welding can be carried out by heating, sonication, gluing, radio frequency or mechanical compression. When welding is performed by heating, ultrasonic waves or high frequency, at least the periphery of the upper layer and the lower layer must be made of a heat-meltable or thermoplastic material.
【0036】
本発明の物品はプラスチック材料製ケースに、または金属(例えば、アルミニ
ウム)製外表面及び該物品を1つ以上収容し得るプラスチック製内表面を有する
2層構造物に包装され得る。The articles of the present invention may be packaged in a case made of plastic material or in a two-layer structure having a metal (eg, aluminum) outer surface and a plastic inner surface that may contain one or more of the articles.
【0037】 下記実施例は本発明を説明するためのものである。[0037] The following examples serve to illustrate the invention.
【0038】
実施例1:カプセル化メークアップファンデーションを含む物品
a) カプリル酸/カプリン酸トリグリセリド19.5g、パルミチン酸エチ
ル−2−ヘキシル11g、オクタン酸ケトステアリル19.5g、水素添加ヤシ
油5g、フェノキシエタノール1.45g、オクチルメトキシシンナメート1g
、パルミチン酸アスコルビル0.2g、EDTA粉末0.05g、ジメチルジス
テアリルアンモニウムベントナイト0.3g、シリカ5g、マイカ4g、超微粉
タルク20moos 2g、ナイロン12 6g及び顔料25gの組成を有する
無水メークアップファンデーションを調製した。[0038]
Example 1: Article containing encapsulated make-up foundation
a) 19.5 g of caprylic / capric triglyceride, ethyl palmitate
Ru-2-hexyl 11 g, ketostearyl octanoate 19.5 g, hydrogenated palm
Oil 5g, phenoxyethanol 1.45g, octyl methoxycinnamate 1g
, 0.2 g of ascorbyl palmitate, 0.05 g of EDTA powder, dimethyldis
Tearyl ammonium bentonite 0.3g, silica 5g, mica 4g, ultrafine powder
It has the composition of 20 g of talc, 2 g of nylon, 126 g of nylon and 25 g of pigment.
An anhydrous makeup foundation was prepared.
【0039】
b) メークアップファンデーションのカプセル化
600ml容量のビーカーにおいて、豚ゼラチン5gを水130gに溶解し、
膨張させ、混合物を220rpmで撹拌しながら55℃とした(全操作中水浴を
用いて一定温度を維持した)。平均直径1,000μmのカプセルを得るように
撹拌を一定に維持した。次いで、無水メークアップファンデーション25mlを
添加し、55℃に予備加熱し、2分間乳化した。次いで、蒸留水90mlに溶解
させた0.5%ヘキサメタリン酸ナトリウム20mlを55℃に予備加熱した後
添加した。B) Encapsulation of make-up foundation In a beaker with a capacity of 600 ml, 5 g of pork gelatin was dissolved in 130 g of water,
It was allowed to expand and the mixture was brought to 55 ° C. with stirring at 220 rpm (water bath was used to maintain constant temperature during all operations). Agitation was kept constant so as to obtain capsules with an average diameter of 1,000 μm. Next, 25 ml of anhydrous make-up foundation was added, preheated to 55 ° C., and emulsified for 2 minutes. Then, 20 ml of 0.5% sodium hexametaphosphate dissolved in 90 ml of distilled water was preheated to 55 ° C. and then added.
【0040】
反応媒体のpHを4〜5の値に下げるために1N クエン酸を用いて調節した
。顕微鏡を使用して、コアセルベーションが起こったことを確認した。加熱を中
止し、反応媒体を撹拌しながら約1.5時間で室温に戻した。The pH of the reaction medium was adjusted with 1N citric acid in order to lower the value to 4-5. A microscope was used to confirm that coacervation had occurred. The heating was discontinued and the reaction medium was allowed to return to room temperature in about 1.5 hours with stirring.
【0041】
温度を氷を用いて約15℃に低下させ続けた後、1.5%グルタルアルデヒド
10mlを添加し、撹拌しながら2時間反応させた。この間は架橋時間に相当し
、カプセルは固化した。After the temperature was continuously lowered to about 15 ° C. using ice, 10 ml of 1.5% glutaraldehyde was added, and the mixture was reacted for 2 hours while stirring. During this period, the capsule was solidified corresponding to the crosslinking time.
【0042】
カプセル同士がくっつくのを避けるために微細シリカを1へら添加した。媒体
をデカントした後、濾過し、蒸留水で濯いだ。カプセルを0.5%の保存剤を含
有する水中において保持した。Fine silica was added to the spatula to avoid capsules sticking together. After decanting the medium, it was filtered and rinsed with distilled water. The capsules were kept in water containing 0.5% preservative.
【0043】
c) カプセル化メークアップファンデーションを含有する物品の製造
上記方法に従って作成したカプセル4gを、ポリエステル繊維30重量%及び
ビスコース繊維70重量%を含む混合物を主成分とする外側不織層をも含む透過
性層の不織ポリエステルからなる内側サブ層に堆積させた。次いで、この層に、
ポリエチレンフィルムからなる内側サブ層と不織天然セルロースからなる外側サ
ブ層を含む不透過性層を全面的に合わせた。C) Manufacture of Articles Containing Encapsulated Make-up Foundation 4 g of capsules prepared according to the above method are treated with an outer non-woven layer based on a mixture containing 30% by weight of polyester fibers and 70% by weight of viscose fibers. Was also deposited on the inner sublayer consisting of the nonwoven polyester of the permeable layer. Then on this layer,
An impermeable layer comprising an inner sub-layer made of polyethylene film and an outer sub-layer made of non-woven natural cellulose was overlaid together.
【0044】
次いで、2つの層の周囲の間を超音波で溶着した。こうして、単に折り曲げ、
押圧することによりカプセルが活性化され、その後透過性層を介してメークアッ
プファンデーションが移行して該メークアップファンデーションが皮膚に接触す
る本発明の製品が得られた。Then, ultrasonic welding was performed between the periphery of the two layers. So just fold,
The product of the invention was obtained in which the capsules were activated by pressing and then the make-up foundation migrated through the permeable layer and the make-up foundation contacted the skin.
【0045】
実施例2〜4は、各種化粧品組成物を含有する本発明の物品に関する。これら
の物品は実施例1に記載の方法により製造したが、局所組成物の種類の点でのみ
実施例1の物品とは異なる。Examples 2-4 relate to articles of the invention containing various cosmetic compositions. These articles were made by the method described in Example 1, but differed from the articles of Example 1 only in the type of topical composition.
【0046】
実施例2:局所カプセル化メークアップファンデーションを含有する製品
PEG−8−密蝋8%、流動パラフィン10%、プロピレングリコールジペル
ラゴネート(PGDP)8%、セチルアルコール1.5%、イソステアリン酸イ
ソステアリル2%、ステアリン酸2%、微粉砕顔料6%及び100mlまでの水
の組成を有する典型的な色合いのベースを調製した。[0046]
Example 2: Product containing topical encapsulated makeup foundation
PEG-8-8% beeswax, liquid paraffin 10%, propylene glycol dipel
Lagonate (PGDP) 8%, cetyl alcohol 1.5%, isostearic acid
Sostearyl 2%, stearic acid 2%, finely divided pigment 6% and water up to 100 ml
A typical shade base having the following composition was prepared.
【0047】
実施例3:カプセル化水中油型エマルション組成物を含有する物品
流動パラフィン25%、ステアリルアルコール(2EO)3.4%、ステアリ
ルアルコール(21EO)1.6%、トリエタノールアミン0.25%、カルボ
ポールETD 2020(アクリルポリマー;Goodrich Corp.か
ら市販されている)0.25%、フェノキシ−2−エタノール0.4%、プロピ
レングリコール4%、100mlまでの水の組成を有する水中油型エマルション
を調製した。[0047]
Example 3: Article containing encapsulated oil-in-water emulsion composition
Liquid paraffin 25%, stearyl alcohol (2EO) 3.4%, steari
Alcohol (21EO) 1.6%, triethanolamine 0.25%, carbo
Paul ETD 2020 (acrylic polymer; Goodrich Corp.
Commercially available) 0.25%, phenoxy-2-ethanol 0.4%, propylene
Oil-in-water emulsion with a composition of 4% ren glycol and water up to 100 ml.
Was prepared.
【0048】
実施例4:油中水型エマルション組成物を含有する物品
カプリル酸/カプリン酸トリグリセリド19.5%、ポリプロポキシステアリ
ルアルコール7.5%、PEG−30ジポリヒドロキシステアレート4%、流動
パラフィン5%、Parsol MCS(2−エチルヘキシルメトキシシンナメ
ート;Givaudanから市販されている)1%、Oxynex LM(酸化
防止剤;Merckから市販されている)0.2%、フェノキシエタノール1%
、NaCl 1%、100mlまでの水の組成を有する油中水型エマルションを
調製した。[0048]
Example 4: Article containing a water-in-oil emulsion composition
Caprylic acid / capric acid triglyceride 19.5%, polypropoxy stealy
7.5% alcohol, 4% PEG-30 dipolyhydroxystearate, flow
Paraffin 5%, Parsol MCS (2-ethylhexyl methoxycinnamate
1%, commercially available from Givaudan), Oxynex LM (oxidized)
Inhibitor; commercially available from Merck) 0.2%, phenoxyethanol 1%
, NaCl 1%, water-in-oil emulsion with composition of water up to 100 ml
Prepared.
【図1】
医薬品または化粧品局所組成物を含有するカプセルを数個含む本発明の物品の
部分切取り斜視図である。FIG. 1 is a partial cutaway perspective view of an article of the present invention containing several capsules containing a pharmaceutical or cosmetic topical composition.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) A61K 7/021 A61K 7/021 7/48 7/48 7/50 7/50 9/06 9/06 9/08 9/08 9/48 9/48 B65D 83/00 B65D 83/00 D (81)指定国 EP(AT,BE,CH,CY, DE,DK,ES,FI,FR,GB,GR,IE,I T,LU,MC,NL,PT,SE),OA(BF,BJ ,CF,CG,CI,CM,GA,GN,GW,ML, MR,NE,SN,TD,TG),AP(GH,GM,K E,LS,MW,MZ,SD,SL,SZ,TZ,UG ,ZW),EA(AM,AZ,BY,KG,KZ,MD, RU,TJ,TM),AE,AG,AL,AM,AT, AU,AZ,BA,BB,BG,BR,BY,BZ,C A,CH,CN,CR,CU,CZ,DE,DK,DM ,DZ,EE,ES,FI,GB,GD,GE,GH, GM,HR,HU,ID,IL,IN,IS,JP,K E,KG,KP,KR,KZ,LC,LK,LR,LS ,LT,LU,LV,MA,MD,MG,MK,MN, MW,MX,MZ,NO,NZ,PL,PT,RO,R U,SD,SE,SG,SI,SK,SL,TJ,TM ,TR,TT,TZ,UA,UG,US,UZ,VN, YU,ZA,ZW (72)発明者 カルクビ,サミラ フランス国、エフ−76800・サン・エチエ ンヌ・ドユ・ルブレイ、リユ・デ・フイ ヌ・ランド、5 (72)発明者 フオルテール,サビヌ フランス国、エフ−14360・トルービル− シユール−メール、リユ・ドウ・ラ・カ ベ、57 Fターム(参考) 3E014 AA07 4C076 AA06 AA09 AA11 AA53 AA58 BB24 BB31 CC10 CC18 FF68 4C083 AA082 AA122 AC022 AC072 AC122 AC172 AC182 AC242 AC342 AC352 AC392 AC422 AC532 AC542 AC692 AD072 AD092 AD642 BB21 CC02 CC05 CC11 CC12 CC22 CC23 DD14 DD22 DD23 DD32 DD33 DD41 DD47 EE03 EE05 EE09─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 7 Identification code FI theme code (reference) A61K 7/021 A61K 7/021 7/48 7/48 7/50 7/50 9/06 9/06 9 / 08 9/08 9/48 9/48 B65D 83/00 B65D 83/00 D (81) Designated countries EP (AT, BE, CH, CY, DE, DK, ES, FI, FR, GB, GR, IE , IT, LU, MC, NL, PT, SE), OA (BF, BJ, CF, CG, CI, CM, GA, GN, GW, ML, MR, NE, SN, TD, TG), AP ( GH, GM, K E, LS, MW, MZ, SD, SL, SZ, TZ, UG, ZW), EA (AM, AZ, BY, KG, KZ, MD, RU, TJ, TM), AE, AG , AL, AM, AT, AU, AZ, BA, B, BG, BR, BY, BZ, CA, CH, CN, CR, CU, CZ, DE, DK, DM, DZ, EE, ES, FI, GB, GD, GE, GH, GM, HR, HU , ID, IL, IN, IS, JP, KE, KG, KP, KR, KZ, LC, LK, LR, LS, LT, LU, LV, MA, MD, MG, MK, MN, MW, MX, MZ, NO, NZ, PL, PT, RO, RU, SD, SE, SG, SI, SK, SL, TJ, TM, TR, TT, TZ, UA, UG, US, UZ, VN, YU, ZA , ZW (72) Inventor Kalkby, Samira France, F-76800 Saint-Etienne Dou Le Bray, Lieu de Fine Land, 5 (72) Inventor Fortale, Sabine France, F-14360・ Trouville-Churle-Mer, Lieu-de-la- Cover, 57 F term (reference) 3E014 AA07 4C076 AA06 AA09 AA11 AA53 AA58 BB24 BB31 CC10 CC18 FF68 4C083 AA082 AA122 AC022 AC072 AC122 AC172 AC182 AC242 AC342 AC352 AC392 AC22 AC21 AC22 AC22 AC22 AC22 AC22 AC22 AC052 DD23 DD32 DD33 DD41 DD47 EE03 EE05 EE09
Claims (18)
て、(i)前記局所組成物透過性の上層及び(ii)前記局所組成物不透過性の
繊維材料からなる下層を含み、前記した2つの層は全面的に重なり合っており且
つ前記局所組成物を含有しているカプセルが少なくとも1つ配置されるスペース
を規定するようにその周囲を溶着することにより互いに維持されていることを特
徴とする前記物品。1. An article for applying a cosmetic or pharmaceutical topical composition comprising: (i) a top layer permeable to the topical composition and (ii) a bottom layer composed of a fibrous material impermeable to the topical composition. Including the two layers described above being entirely overlapped and maintained together by welding around their perimeters to define a space in which at least one capsule containing the topical composition is placed. The article as described above.
に記載の物品。2. Article according to claim 1, characterized in that the upper layer is made of fibrous material.
る請求の範囲第1項または第2項に記載の物品。3. An article according to claim 1, wherein each of the lower layer and the upper layer is made of a non-woven fiber material.
を含む多層構造からなることを特徴とする請求の範囲第1項〜第3項のいずれか
1項に記載の物品。4. The structure according to claim 1, wherein the lower layer has a multi-layer structure including an inner impermeable sub-layer and an outer sub-layer made of a fibrous material. Goods.
ンのフィルムからなることを特徴とする請求の範囲第4項に記載の物品。5. Article according to claim 4, characterized in that the inner impermeable sublayer consists of a film of polymeric material, preferably polyethylene.
囲第4項または第5項に記載の物品。6. Article according to claim 4 or 5, characterized in that the outer sublayer is made of cellulose.
あることを特徴とする請求の範囲第1項〜第6項のいずれか1項に記載の物品。7. Article according to any one of claims 1 to 6, characterized in that the topical composition is in liquid, paste, semi-paste or gel form.
囲第1項〜第7項のいずれか1項に記載の物品。8. Article according to any one of claims 1 to 7, characterized in that the topical composition is a cosmetic composition.
組成物であることを特徴とする請求の範囲第1項〜第7項のいずれか1項に記載
の物品。9. Article according to any one of claims 1 to 7, characterized in that the topical composition is a pharmaceutical composition, in particular a dermatological or ophthalmic pharmaceutical composition.
は皮膚衛生またはクレンジング製品であることを特徴とする請求の範囲第8項に
記載の物品。10. Article according to claim 8, characterized in that the cosmetic composition is a make-up product, a skin care product or a skin hygiene or cleansing product.
ことを特徴とする請求の範囲第10項に記載の物品。11. Article according to claim 10, characterized in that the make-up product is a make-up foundation.
とを特徴とする請求の範囲第10項に記載の物品。12. Article according to claim 10, characterized in that the skin hygiene or cleansing product is a make-up remover.
むことを特徴とする請求の範囲第1項〜第12項のいずれか1項に記載の物品。13. Article according to any one of claims 1 to 12, characterized in that it comprises two or more capsules having an average diameter of 0.5 to 5 mm.
とする請求の範囲第1項〜第13項のいずれか1項に記載の物品。14. Article according to any one of claims 1 to 13, characterized in that the capsule comprises an envelope consisting of a hydrophilic colloid.
の範囲第14項に記載の物品。15. Article according to claim 14, characterized in that the capsule envelope consists of gelatin.
の製造方法であって、局所組成物を含有しているカプセルの1つ以上を上層及び
下層のいずれかの内側表面上に堆積させ、他層を全面的に重ね合わせ、2つの層
をその周囲で互いに溶着させることを含むことを特徴とする前記方法。16. A method for producing an article according to any one of claims 1 to 15, wherein one or more capsules containing a topical composition are used as an upper layer or a lower layer. Depositing on the inner surface of the same and overlaying the other layers blanketly and welding the two layers together at their periphery.
り実施することを特徴とする請求の範囲第16項に記載の方法。17. Method according to claim 16, characterized in that the welding is carried out by heating, sonication, gluing, radio frequency or mechanical compression.
項〜第15項のいずれか1項に記載の物品の使用。18. A first claim for the application of a topical cosmetic composition to the skin.
Item 16. Use of the article according to any one of items 15 to 15.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9908952A FR2795928B1 (en) | 1999-07-09 | 1999-07-09 | ARTICLE FOR THE APPLICATION OF A TOPICAL COMPOSITION AND ITS PREPARATION METHOD |
| FR99/08952 | 1999-07-09 | ||
| US50246400A | 2000-02-11 | 2000-02-11 | |
| US09/502,464 | 2000-02-11 | ||
| PCT/FR2000/001953 WO2001003538A1 (en) | 1999-07-09 | 2000-07-06 | Article for applying a topical composition and method for preparing same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2003520063A true JP2003520063A (en) | 2003-07-02 |
Family
ID=26235028
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001508838A Withdrawn JP2003520063A (en) | 1999-07-09 | 2000-07-06 | Article for applying topical composition and method for producing the same |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1199956A1 (en) |
| JP (1) | JP2003520063A (en) |
| KR (1) | KR20020096039A (en) |
| AU (1) | AU6294800A (en) |
| WO (1) | WO2001003538A1 (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007503417A (en) * | 2003-08-27 | 2007-02-22 | バイヤースドルフ・アクチエンゲゼルシヤフト | Spherical cosmetic formulation for topical application |
| JP2008533252A (en) * | 2005-03-15 | 2008-08-21 | エスシーエス・スキン・ケア・システムズ・ゲーエムベーハー | Products for targeted release of active substances |
| WO2011019169A3 (en) * | 2009-08-08 | 2011-06-30 | Kim Yong Jin | Wrinkle-removing tape |
| CN102469868A (en) * | 2009-08-08 | 2012-05-23 | 金龙辰 | anti wrinkle tape |
| CN102469868B (en) * | 2009-08-08 | 2015-09-16 | 金龙辰 | Wrinkle-removing tape |
| US9144289B2 (en) | 2009-08-08 | 2015-09-29 | Yong Jin Kim | Wrinkle-removing tape |
| JP2014129312A (en) * | 2012-12-30 | 2014-07-10 | Shinshu Univ | Base material for sheet-like pack and sheet-like pack |
| KR20170070484A (en) * | 2015-12-14 | 2017-06-22 | 주식회사 코스메카코리아 | A method of manufacturing cosmetic puff using membrane film and Cosmetic puff manufactured by this method |
| KR101875423B1 (en) * | 2015-12-14 | 2018-08-02 | 주식회사 코스메카코리아 | A method of manufacturing cosmetic puff using membrane film and Cosmetic puff manufactured by this method |
| KR101927047B1 (en) | 2017-01-20 | 2018-12-10 | (주)아모레퍼시픽 | Cosmetic tools capable of make up conveniently |
| KR101947708B1 (en) | 2018-07-09 | 2019-02-13 | (주)아모레퍼시픽 | Cosmetic tools capable of make up conveniently |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1199956A1 (en) | 2002-05-02 |
| KR20020096039A (en) | 2002-12-28 |
| WO2001003538A1 (en) | 2001-01-18 |
| AU6294800A (en) | 2001-01-30 |
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| A300 | Application deemed to be withdrawn because no request for examination was validly filed |
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