JPH03109312A - Capsule for cosmetic application and method of its production - Google Patents
Capsule for cosmetic application and method of its productionInfo
- Publication number
- JPH03109312A JPH03109312A JP2241052A JP24105290A JPH03109312A JP H03109312 A JPH03109312 A JP H03109312A JP 2241052 A JP2241052 A JP 2241052A JP 24105290 A JP24105290 A JP 24105290A JP H03109312 A JPH03109312 A JP H03109312A
- Authority
- JP
- Japan
- Prior art keywords
- capsule
- weight
- alginate
- aqueous solution
- oil
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000002775 capsule Substances 0.000 title claims abstract description 104
- 239000002537 cosmetic Substances 0.000 title claims abstract description 40
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- 238000000034 method Methods 0.000 title description 10
- 239000000126 substance Substances 0.000 claims abstract description 60
- 239000007864 aqueous solution Substances 0.000 claims abstract description 35
- 239000007788 liquid Substances 0.000 claims abstract description 33
- 239000011162 core material Substances 0.000 claims abstract description 32
- -1 alkali metal alginate salt Chemical class 0.000 claims abstract description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 20
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims abstract description 14
- 238000005406 washing Methods 0.000 claims abstract description 6
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims abstract description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 16
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 claims description 16
- 229940072056 alginate Drugs 0.000 claims description 15
- 235000010443 alginic acid Nutrition 0.000 claims description 15
- 229920000615 alginic acid Polymers 0.000 claims description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 12
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 claims description 9
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical class O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 claims description 9
- 235000010413 sodium alginate Nutrition 0.000 claims description 9
- 239000000661 sodium alginate Substances 0.000 claims description 9
- 229940005550 sodium alginate Drugs 0.000 claims description 9
- 235000011187 glycerol Nutrition 0.000 claims description 8
- 239000004166 Lanolin Substances 0.000 claims description 7
- 229910052782 aluminium Inorganic materials 0.000 claims description 7
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 claims description 7
- 235000010407 ammonium alginate Nutrition 0.000 claims description 7
- 239000000728 ammonium alginate Substances 0.000 claims description 7
- KPGABFJTMYCRHJ-YZOKENDUSA-N ammonium alginate Chemical compound [NH4+].[NH4+].O1[C@@H](C([O-])=O)[C@@H](OC)[C@H](O)[C@H](O)[C@@H]1O[C@@H]1[C@@H](C([O-])=O)O[C@@H](O)[C@@H](O)[C@H]1O KPGABFJTMYCRHJ-YZOKENDUSA-N 0.000 claims description 7
- 229940039717 lanolin Drugs 0.000 claims description 7
- 235000019388 lanolin Nutrition 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 claims description 6
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 claims description 6
- 235000010408 potassium alginate Nutrition 0.000 claims description 6
- 239000000737 potassium alginate Substances 0.000 claims description 6
- MZYRDLHIWXQJCQ-YZOKENDUSA-L potassium alginate Chemical compound [K+].[K+].O1[C@@H](C([O-])=O)[C@@H](OC)[C@H](O)[C@H](O)[C@@H]1O[C@@H]1[C@@H](C([O-])=O)O[C@@H](O)[C@@H](O)[C@H]1O MZYRDLHIWXQJCQ-YZOKENDUSA-L 0.000 claims description 6
- 229940032094 squalane Drugs 0.000 claims description 6
- 235000008524 evening primrose extract Nutrition 0.000 claims description 5
- 239000010475 evening primrose oil Substances 0.000 claims description 5
- 229940089020 evening primrose oil Drugs 0.000 claims description 5
- DUXYWXYOBMKGIN-UHFFFAOYSA-N trimyristin Chemical compound CCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCC DUXYWXYOBMKGIN-UHFFFAOYSA-N 0.000 claims description 5
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims description 4
- YYGNTYWPHWGJRM-UHFFFAOYSA-N (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC=C(C)C YYGNTYWPHWGJRM-UHFFFAOYSA-N 0.000 claims description 4
- 102000008186 Collagen Human genes 0.000 claims description 4
- 108010035532 Collagen Proteins 0.000 claims description 4
- BHEOSNUKNHRBNM-UHFFFAOYSA-N Tetramethylsqualene Natural products CC(=C)C(C)CCC(=C)C(C)CCC(C)=CCCC=C(C)CCC(C)C(=C)CCC(C)C(C)=C BHEOSNUKNHRBNM-UHFFFAOYSA-N 0.000 claims description 4
- 229920001436 collagen Polymers 0.000 claims description 4
- DWMMZQMXUWUJME-UHFFFAOYSA-N hexadecyl octanoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)CCCCCCC DWMMZQMXUWUJME-UHFFFAOYSA-N 0.000 claims description 4
- 239000003921 oil Substances 0.000 claims description 4
- 235000019198 oils Nutrition 0.000 claims description 4
- 239000004006 olive oil Substances 0.000 claims description 4
- 235000008390 olive oil Nutrition 0.000 claims description 4
- 229940031439 squalene Drugs 0.000 claims description 4
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 claims description 4
- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical group CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 claims description 3
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 claims description 3
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 3
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 claims description 3
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 claims description 3
- 241000772415 Neovison vison Species 0.000 claims description 3
- 239000002202 Polyethylene glycol Substances 0.000 claims description 3
- 235000021302 avocado oil Nutrition 0.000 claims description 3
- 239000008163 avocado oil Substances 0.000 claims description 3
- 239000004359 castor oil Substances 0.000 claims description 3
- 235000019438 castor oil Nutrition 0.000 claims description 3
- 229940086555 cyclomethicone Drugs 0.000 claims description 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
- 239000000194 fatty acid Substances 0.000 claims description 3
- 229930195729 fatty acid Natural products 0.000 claims description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 3
- 229920002674 hyaluronan Polymers 0.000 claims description 3
- 229960003160 hyaluronic acid Drugs 0.000 claims description 3
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims description 3
- 229920001223 polyethylene glycol Polymers 0.000 claims description 3
- 239000000600 sorbitol Substances 0.000 claims description 3
- 229940042585 tocopherol acetate Drugs 0.000 claims description 3
- 229940058015 1,3-butylene glycol Drugs 0.000 claims description 2
- LEEDMQGKBNGPDN-UHFFFAOYSA-N 2-methylnonadecane Chemical compound CCCCCCCCCCCCCCCCCC(C)C LEEDMQGKBNGPDN-UHFFFAOYSA-N 0.000 claims description 2
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 claims description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims description 2
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 2
- 235000019437 butane-1,3-diol Nutrition 0.000 claims description 2
- 235000012343 cottonseed oil Nutrition 0.000 claims description 2
- 239000002385 cottonseed oil Substances 0.000 claims description 2
- 235000019441 ethanol Nutrition 0.000 claims description 2
- 150000004665 fatty acids Chemical class 0.000 claims description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims description 2
- 229920003063 hydroxymethyl cellulose Polymers 0.000 claims description 2
- 229940031574 hydroxymethyl cellulose Drugs 0.000 claims description 2
- 239000001863 hydroxypropyl cellulose Substances 0.000 claims description 2
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 claims description 2
- 229940119170 jojoba wax Drugs 0.000 claims description 2
- 229940057995 liquid paraffin Drugs 0.000 claims description 2
- 235000013772 propylene glycol Nutrition 0.000 claims description 2
- 239000012266 salt solution Substances 0.000 claims description 2
- 239000010497 wheat germ oil Substances 0.000 claims description 2
- VYGQUTWHTHXGQB-FFHKNEKCSA-N Retinol Palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C VYGQUTWHTHXGQB-FFHKNEKCSA-N 0.000 claims 2
- 235000019172 retinyl palmitate Nutrition 0.000 claims 1
- 239000011769 retinyl palmitate Substances 0.000 claims 1
- 229940108325 retinyl palmitate Drugs 0.000 claims 1
- 238000000576 coating method Methods 0.000 abstract description 34
- 239000000463 material Substances 0.000 abstract description 34
- 239000011248 coating agent Substances 0.000 abstract description 33
- 230000000694 effects Effects 0.000 abstract description 6
- 229910052783 alkali metal Inorganic materials 0.000 abstract description 5
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 9
- 239000004745 nonwoven fabric Substances 0.000 description 7
- 238000002156 mixing Methods 0.000 description 6
- 230000003020 moisturizing effect Effects 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000005538 encapsulation Methods 0.000 description 5
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 3
- 108010010803 Gelatin Proteins 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 229920000159 gelatin Polymers 0.000 description 3
- 239000008273 gelatin Substances 0.000 description 3
- 235000019322 gelatine Nutrition 0.000 description 3
- 235000011852 gelatine desserts Nutrition 0.000 description 3
- 229920000831 ionic polymer Polymers 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 230000010349 pulsation Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000000110 cooling liquid Substances 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- DOKHEARVIDLSFF-UHFFFAOYSA-N prop-1-en-1-ol Chemical group CC=CO DOKHEARVIDLSFF-UHFFFAOYSA-N 0.000 description 2
- 239000001944 prunus armeniaca kernel oil Substances 0.000 description 2
- 229960003471 retinol Drugs 0.000 description 2
- 235000020944 retinol Nutrition 0.000 description 2
- 239000011607 retinol Substances 0.000 description 2
- 239000011257 shell material Substances 0.000 description 2
- 239000007901 soft capsule Substances 0.000 description 2
- ZSLUVFAKFWKJRC-IGMARMGPSA-N 232Th Chemical compound [232Th] ZSLUVFAKFWKJRC-IGMARMGPSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229910052776 Thorium Inorganic materials 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000010410 calcium alginate Nutrition 0.000 description 1
- 239000000648 calcium alginate Substances 0.000 description 1
- 229960002681 calcium alginate Drugs 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- OKHHGHGGPDJQHR-YMOPUZKJSA-L calcium;(2s,3s,4s,5s,6r)-6-[(2r,3s,4r,5s,6r)-2-carboxy-6-[(2r,3s,4r,5s,6r)-2-carboxylato-4,5,6-trihydroxyoxan-3-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate Chemical compound [Ca+2].O[C@@H]1[C@H](O)[C@H](O)O[C@@H](C([O-])=O)[C@H]1O[C@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@H](O2)C([O-])=O)O)[C@H](C(O)=O)O1 OKHHGHGGPDJQHR-YMOPUZKJSA-L 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Substances OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000007902 hard capsule Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 210000001161 mammalian embryo Anatomy 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000002244 precipitate Substances 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
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
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
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/733—Alginic acid; Salts thereof
-
- 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
- A61K8/11—Encapsulated compositions
-
- 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/26—Aluminium; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
- A61K2800/805—Corresponding aspects not provided for by any of codes A61K2800/81 - A61K2800/95
Abstract
Description
【発明の詳細な説明】
発明の技術分野
本発明は、アルギン酸アルミニウムを皮膜材として用い
て皮膜強度および水不溶性を調節し、該被膜内に皮膚に
有益な親油性物質を内蔵させたカプセル表面に親水性物
質を添加させて成る化粧料用カプセルおよびその製造方
法に関する。DETAILED DESCRIPTION OF THE INVENTION Technical Field of the Invention The present invention is directed to the use of aluminum alginate as a coating material to adjust the coating strength and water insolubility, and to coat the capsule surface with a lipophilic substance beneficial to the skin incorporated within the coating. The present invention relates to a cosmetic capsule containing a hydrophilic substance and a method for producing the same.
従来の技術
現在、−船釣に市販されているカプセルには、種々の形
態があるが、硬質カプセル、軟質カプセル等以外に継ぎ
目がないカプセルなどがある。軟質カプセルは皮膜材が
ゼラチン等からなっており、皮膜が厚く堅いため、カプ
セルを手で容易に破裂させることが難しく、カプセルを
破裂させるのに特別な器具が必要である。BACKGROUND OF THE INVENTION At present, there are various types of capsules commercially available for boat fishing, including hard capsules, soft capsules, and seamless capsules. The coating material of soft capsules is made of gelatin or the like, and because the coating is thick and hard, it is difficult to easily rupture the capsule by hand, and a special instrument is required to rupture the capsule.
また継ぎ目がないカプセルは、カプセルの皮膜材と芯材
とをそれぞれ2重ノズルで移送させて2重ノズルの端で
皮膜物質と芯材物質のジェット流を起こし、このジェッ
ト流の先端で表面張力によって皮膜材が芯材を取り巻い
た液滴を形成し、次いでこの液滴を硬化液や冷却液に滴
下して形成される。このカプセルは、液中硬化被覆法を
応用した2重ノズル滴下方式によって形成されたカプセ
ルであって、製法の原理上粒子が球形になり、流動性と
充填性が優れていることが知られている。In addition, seamless capsules are made by transporting the shell material and core material of the capsule through double nozzles, creating a jet flow of the film material and core material at the end of the double nozzle, and at the tip of this jet flow, surface tension The coating material forms droplets surrounding the core material, and the droplets are then dropped into a curing liquid or a cooling liquid. These capsules are formed by a double nozzle dropping method that applies an in-liquid curing coating method, and it is known that due to the principle of the manufacturing process, the particles are spherical and have excellent fluidity and filling properties. There is.
このような継ぎ目のないカプセルの製造では、皮膜材と
してアルギン酸ナトリウムを用い、得られた液滴を塩化
カルシウム水溶液に滴下して硬化させる方法が広く使用
されてきた。しかしながら、アルギン酸ナトリウムを塩
化カルシウムで硬化させたカプセルは皮膜強度が高すぎ
るため、化粧品として使用する際に容易に破裂すること
が困難であるという問題があった。また、ゼラチン水溶
液の液滴を冷却液に滴下し硬化させることにより得られ
た皮膜材を用いた継ぎ目のないカプセルカプセルを化粧
品に応用した場合、カプセルの外状が親水性物質である
ため、ゼラチン皮膜が溶かされてしまう。In the production of such seamless capsules, a method has been widely used in which sodium alginate is used as a coating material, and the resulting droplets are dropped into an aqueous calcium chloride solution and cured. However, capsules made by hardening sodium alginate with calcium chloride have too high a film strength, so there is a problem in that they are difficult to burst when used as cosmetics. In addition, when a seamless capsule using a film material obtained by dropping droplets of an aqueous gelatin solution into a cooling liquid and curing it is applied to cosmetics, gelatin The film will be dissolved.
したがって、このような継ぎ目のないカプセルを化粧品
に応用する場合には、カプセルを破裂して使用するため
カプセルが破裂する皮膜強度が適当に調節されており、
カプセルの外状として親水性物質を添加する際にカプセ
ル皮膜が親水性物質によって溶かされずかつカプセル形
態が変形しないカプセルでなければならない。Therefore, when applying such a seamless capsule to cosmetics, the capsule is used after being ruptured, so the strength of the film at which the capsule ruptures must be appropriately adjusted.
When a hydrophilic substance is added to the outer surface of the capsule, the capsule film must not be dissolved by the hydrophilic substance and the capsule form must not be deformed.
一方、特に皮膚に活性のある物質として親油性物質を挙
げることができ、現在、化粧品製造において親油性物質
が多用されている。ところが、これら親油性物質は空気
と接触するに従って酸化される物質が多く、化粧品の安
定性に問題が生じるため化粧料に多量に配合することが
難しく、物質によっては全く配合できなかった。On the other hand, lipophilic substances can be mentioned as substances that are particularly active on the skin, and lipophilic substances are currently widely used in the production of cosmetics. However, many of these lipophilic substances are oxidized when they come into contact with air, which poses problems in the stability of cosmetics, making it difficult to incorporate large amounts into cosmetics, and some substances cannot be incorporated at all.
発明の目的
本発明はこのような従来技術にともなう問題点を解決し
ようとするものであって、皮膚に活性を与えることがで
き、化粧品の配合性および安全性が優れた親油性物質か
らなる芯材と、適切な皮膜強度を有した継ぎ目のない球
形の水不溶性皮膜材とからなるカプセルの外状に皮膚に
補湿力を与える親水性物質を添加させて成る化粧料用カ
プセルおよびその製造方法を提供することを目的として
いる。OBJECT OF THE INVENTION The present invention aims to solve the problems associated with the prior art, and provides a core made of a lipophilic substance that is able to impart activity to the skin and has excellent blendability and safety in cosmetics. and a seamless spherical water-insoluble film material having appropriate film strength, and a capsule for cosmetics comprising a hydrophilic substance that imparts moisturizing power to the skin added to the outer surface of the capsule, and a method for producing the same. is intended to provide.
発明の概要
本発明に係る化粧料用カプセルは、芯材である親油性物
質を濃度0.5重量%〜3重量96のアルギン酸アルカ
リ塩水溶液で取り巻いた液滴を、濃度0.2重量96〜
10重量96のアルミニウム塩水溶液で硬化させて水洗
した後、その表面に親水性物質を添加したことを特徴と
している。Summary of the Invention The cosmetic capsule according to the present invention comprises liquid droplets in which a lipophilic substance as a core material is surrounded by an alginate alkali salt aqueous solution having a concentration of 0.2% by weight to 3% by weight.
It is characterized in that it is cured with an aqueous aluminum salt solution of 10% by weight and 96%, washed with water, and then a hydrophilic substance is added to its surface.
本発明に係る化粧料用カプセルの製造方法は、濃度0.
5重量96〜3重量96のアルギン酸アルカリ塩水溶液
と親油性物質とを2重ノズルに通過させることにより、
上記アルギン酸アルカリ塩水溶液が上記親油性物質を取
り巻くようにしだ液滴を調製し、該液滴をアルミニウム
イオン水溶液で硬化させてカプセルを形成した後、該カ
プセルをイオン交換水で水洗し、次いでカプセル表面に
親水性物質を添加することを特徴としている。The method for producing capsules for cosmetics according to the present invention has a concentration of 0.
By passing an alginate alkali salt aqueous solution of 5 96 to 3 96 by weight and a lipophilic substance through a double nozzle,
A droplet is prepared so that the alginate aqueous solution surrounds the lipophilic substance, the droplet is hardened with an aqueous aluminum ion solution to form a capsule, the capsule is washed with ion-exchanged water, and then the capsule is It is characterized by adding a hydrophilic substance to the surface.
本発明に係る化粧料用カプセルおよびその製造方法によ
れば、親油性物質からなる芯材を適切な皮膜強度を有し
た継ぎ目がない球形の水不溶性皮膜材で被覆し、かつカ
プセルの外状に皮膚に補湿力を与える親水性物質を添加
させた化粧料用カプセルを提供することができる。According to the cosmetic capsule and the manufacturing method thereof according to the present invention, a core material made of a lipophilic substance is covered with a seamless spherical water-insoluble film material having an appropriate film strength, and the outer shape of the capsule is It is possible to provide a capsule for cosmetics to which a hydrophilic substance that provides moisturizing power to the skin is added.
発明の詳細な説明
本発明に係る化粧料用カプセルは、簡単には、アルギン
酸アルカリ金属塩またはアルギン酸アンモニウム塩の水
溶液と親油性物質を2重ノズルの先端へ移送させ、アル
ギン酸アルカリ金属塩またはアルギン酸アンモニウム塩
水溶液が親油性物質を取り巻くようにした液滴を調製し
、この液滴を多価金属イオン水溶液の硬化液に滴下して
硬化させるカプセル化工程と、硬化液を分離除去し、カ
プセル表面に残存された硬化液と副生成物をイオン交換
水で水洗した後、カプセル表面に親水性物質を添加させ
る外状添加工程とを含む製造方法により製造される。Detailed Description of the Invention The capsule for cosmetics according to the present invention can be easily produced by transferring an aqueous solution of an alkali metal salt of alginate or ammonium alginate and a lipophilic substance to the tip of a double nozzle. An encapsulation process involves preparing droplets in which a salt aqueous solution surrounds a lipophilic substance, dropping these droplets onto a hardening solution of a polyvalent metal ion aqueous solution, and hardening the solution. After washing the remaining hardening liquid and by-products with ion-exchanged water, the capsule is manufactured by a manufacturing method including an external addition step of adding a hydrophilic substance to the surface of the capsule.
このような化粧料用カプセルの製造をさらに具体的に説
明すると、カプセルの皮膜物質であるアルギン酸金属塩
、アルギン酸アンモニウム塩などの0.5〜3重量96
水溶液と芯材物質である親油性物質とは、それぞれ貯蔵
タンクに連結された定量ポンプを介して2重ノズルに移
送される。この際、ポンプによって移送される液体の脈
動を減少させるためにポンプとノズルとの間にテンブナ
−が設けられる。ここでテンブナ−はポンプによる脈動
を吸収できる衝繋吸収空気層を形成させて移送される液
体の脈動を減少させることができる。To explain the production of such cosmetic capsules in more detail, the capsule coating material, such as alginate metal salt, alginate ammonium salt, etc., has a weight of 0.5 to 3.
The aqueous solution and the lipophilic substance as the core material are transferred to the dual nozzle through metering pumps connected to storage tanks, respectively. At this time, a tensioner is provided between the pump and the nozzle to reduce pulsation of the liquid transferred by the pump. Here, the tenbunner can reduce the pulsation of the liquid being transferred by forming an impingement-absorbing air layer that can absorb the pulsation caused by the pump.
皮膜形成物質としては、イオン性高分子、すなわちアル
ギン酸ナトリウム、アルギン酸カリウム、アルギン酸ア
ンモニウム、ポリアクリル酸、カルボキシメチルセルロ
ース、エチレン−マレイン酸無水物共重合体、メチルビ
ニルエーテル−マレイン酸無水物共重合体、プロピレン
−マレ不ン酸無水物共重合体、ビニルアセテート−マレ
イン酸共重合体等を挙げることができる。しかしながら
、アルギン酸アルカリ塩を除いた上記陰イオン性高分子
物質などは、カプセルを形成することが困難で、皮膜形
成時間が長く、また皮膜強度が低いために製造工程中に
破壊され易く、したがって、化粧品用カプセルの被膜材
として適当ではない。Film-forming substances include ionic polymers such as sodium alginate, potassium alginate, ammonium alginate, polyacrylic acid, carboxymethylcellulose, ethylene-maleic anhydride copolymer, methyl vinyl ether-maleic anhydride copolymer, propylene Examples include -maleic anhydride copolymers, vinyl acetate-maleic acid copolymers, and the like. However, with the above-mentioned anionic polymeric substances other than alginate alkali salts, it is difficult to form capsules, the film formation time is long, and the film strength is low, so that they are easily destroyed during the manufacturing process. It is not suitable as a coating material for cosmetic capsules.
本発明で用いられる皮膜形成物質としては、アルギン酸
ナトリウム、アルギン酸カリウム、アルギン酸アンモニ
ウムから選択される少なくとも1種を挙げることができ
る。The film-forming substance used in the present invention includes at least one selected from sodium alginate, potassium alginate, and ammonium alginate.
本発明で芯材として使用できる親油性物質としては、流
動パラフィン、流動イソパラフィン、スクアラン、トリ
ミリスチン酸グリセリン、セチルオクタノエート、トリ
(カプリル、カプリン酸)グリセリン、メチルポリシロ
キサン、シクロメチコン、液状ラノリン、ラノリン脂肪
酸イソプロピル、イソプロピルミリステート、イソプロ
ピルパルミテート、ブチルステアレート、アプリコート
カネルオイル、コムギの胚種油等がある。Lipophilic substances that can be used as core materials in the present invention include liquid paraffin, liquid isoparaffin, squalane, glyceryl trimyristate, cetyl octanoate, tri(caprylic, capric) glycerin, methylpolysiloxane, cyclomethicone, liquid lanolin. , lanolin fatty acid isopropyl, isopropyl myristate, isopropyl palmitate, butyl stearate, apricot kernel oil, wheat germ oil, etc.
また、月見草油、スクアレン、酢酸トコフェロール、バ
ルミチン酸レチノール、アボカド油、綿実油、ミンク油
、ヒマシ油、オリーブ油、ホホバ油等は皮膚に活性を与
える物質であるが、酸化されやすい物質であるため、現
在の化粧品には多くの、量を配合することが困難であっ
たが、本発明では、上記物質をカプセル化することによ
り酸化防止効果をきたし、製品の安定性を増進させて皮
膚に効果の多い化粧料を提供することができる。In addition, substances such as evening primrose oil, squalene, tocopherol acetate, retinol balmitate, avocado oil, cottonseed oil, mink oil, castor oil, olive oil, and jojoba oil are active on the skin, but they are easily oxidized, so However, in the present invention, by encapsulating the above-mentioned substances, it has been difficult to incorporate them in large amounts into cosmetics, which has an antioxidant effect, improves the stability of the product, and has many effects on the skin. Cosmetics can be provided.
本発明では、このような芯部性物質を1種以上、好まし
くは2種以上用いることが望ましい。In the present invention, it is desirable to use one or more types, preferably two or more types of such core substances.
本発明で被膜材として用いられるアルギン酸ナトリウム
、アルギン酸カリウム、アルギン酸アンモニウムなどの
水溶液は、濃度が0.5〜3重量%の範囲である。この
濃度が、0.5重量%未満であるとカプセル皮膜材が薄
く成りすぎ、カプセル形成が困難となる。また3重量%
を超えると、アルギン酸アルカリ金属水溶液の粘度が高
(なり、皮膜材の移送が困難となる。また、2重ノズル
より流出する芯材と皮膜材との流量比により、゛カプセ
ル皮膜の厚さが変化するため、このような条件もカプセ
ル形成に影響を及ぼす。カプセル形成に好ましい芯材の
流量は3.5〜7.2g/分であり、好ましい皮膜材の
流量は4.2〜6.5g/分であり、このような芯材と
皮膜材との流量比は110.8〜1/1.4の範囲であ
る。このような条件下ではカプセル形成が良好で、皮膜
の厚さも程よく調節できる。すなわち芯材と皮膜材との
流量比が、110.8を超える、即ち被膜剤の流量が0
.8未満となると皮膜の形成が不良となり、カプセル化
が難しく、皮膜が薄く成りすぎる傾向があり、1/1.
4未満であると、皮膜が厚くなるので破裂性の面で問題
があり、カプセル化される親油性物質の量が相対的に少
なくなるためカプセル効率が低下する。The aqueous solution of sodium alginate, potassium alginate, ammonium alginate, etc. used as a coating material in the present invention has a concentration in the range of 0.5 to 3% by weight. When this concentration is less than 0.5% by weight, the capsule coating material becomes too thin, making it difficult to form capsules. Also 3% by weight
If the alkali metal alginate aqueous solution has a high viscosity, it becomes difficult to transfer the coating material.Also, depending on the flow rate ratio of the core material and coating material flowing out from the double nozzle, the thickness of the capsule coating will increase. These conditions also affect capsule formation, as the core material flow rate is 3.5 to 7.2 g/min and the preferred coating material flow rate is 4.2 to 6.5 g/min for capsule formation. /min, and the flow rate ratio between the core material and the coating material is in the range of 110.8 to 1/1.4.Under these conditions, capsule formation is good and the coating thickness can be adjusted appropriately. That is, the flow rate ratio of the core material and the coating material exceeds 110.8, that is, the flow rate of the coating material is 0.
.. If it is less than 8, the film formation will be poor, encapsulation will be difficult, and the film will tend to be too thin.
When it is less than 4, the film becomes thick, which causes problems in terms of rupture, and the amount of encapsulated lipophilic substance becomes relatively small, resulting in a decrease in encapsulation efficiency.
カプセル化工程では、2重ノズルの先端にアルギン酸ア
ルカリ金属塩、アルギン酸アンモニウム塩などの水溶液
と親油性物質とが同時に移送され、芯材である親油性物
質を皮膜材であるアルギン酸塩水溶液が取り巻く液滴が
形成される。この液滴は、アルミニウムイオン水溶液に
滴下されると、アルギン酸陰イオンとアルミニウム陽イ
オンとの間のイオン結合によって硬化され、カプセルを
形成する。ここで硬化液としては、塩化アルミニウム、
硫酸アルミニウムの水溶液を用いる。硬化液のアルミニ
ウムイオン濃度は0.2〜10重量%の範囲となること
が好ましい。アルミニウムイオンの濃度が0.2重量9
6未満であると、硬化速度が遅く皮膜の強度が弱くなり
、濃度が10重量96を超えると硬化速度が早く、皮膜
強度にも別に影響を与えないものの、多価金属塩の消耗
量が大きくなる。カプセルを硬化させる工程中では、カ
プセルの芯材が親油性物質であり比重か低いため、カプ
セルは硬化液の表面に浮き上がる。したがうて、硬化中
には硬化液を緩やかに攪拌しカプセルの皮膜を一様に硬
化させることが好ましい。このような硬化工程では、硬
化時間は通常30〜40分である。In the encapsulation process, an aqueous solution such as alkali metal alginate or ammonium alginate and a lipophilic substance are simultaneously transferred to the tip of a double nozzle, and the core material, the lipophilic substance, is surrounded by the alginate aqueous solution, which is the coating material. Droplets are formed. When this droplet is dropped into an aqueous aluminum ion solution, it is hardened by ionic bonding between alginate anions and aluminum cations, forming a capsule. Here, the curing liquid includes aluminum chloride,
An aqueous solution of aluminum sulfate is used. The aluminum ion concentration of the curing liquid is preferably in the range of 0.2 to 10% by weight. The concentration of aluminum ions is 0.2 weight 9
If the concentration is less than 6, the curing speed will be slow and the strength of the film will be weak; if the concentration exceeds 10% by weight, the curing speed will be fast and the film strength will not be affected, but the amount of polyvalent metal salt consumed will be large. Become. During the process of curing the capsules, the core material of the capsules is a lipophilic substance and has a low specific gravity, so the capsules float to the surface of the curing liquid. Therefore, during curing, it is preferable to gently stir the curing liquid to uniformly cure the capsule film. In such a curing process, the curing time is typically 30 to 40 minutes.
本発明では、このようなカプセル化工程が終了した後、
ろ過工程としてカプセルと硬化液をろ過して硬化液を除
去する。ろ過されたカプセルの皮膜表面には硬化液であ
る多価金属水溶液と副生物が存在するため、がイオン交
換水で水洗して除去する。In the present invention, after such an encapsulation step is completed,
In the filtration step, the capsules and the hardening liquid are filtered to remove the hardening liquid. Since the polyvalent metal aqueous solution and by-products, which are the hardening liquid, are present on the membrane surface of the filtered capsules, they are removed by washing with ion-exchanged water.
さらに、本発明では、上記のカプセルを化粧品に用いる
とき皮膚に補湿力を与えるために、補湿力を有する水溶
性高分子物質、親水性物質などをカプセル表面に添加さ
せる。Further, in the present invention, in order to impart moisturizing power to the skin when the capsule is used in cosmetics, a water-soluble polymeric substance, a hydrophilic substance, etc. having a moisturizing power is added to the surface of the capsule.
このようなカプセル表面に添加される親水性物質等は外
状と言い、この外状の量は最終化粧品全体量の6〜30
重量%であることが好ましい。外状として用いられる親
水性物質としては、ヒアルトン酸、コラーゲン、グリセ
リン、1.3−ブチレングリコール、プロピレングリコ
ール、エタノール、オクタドデカノール、ソルビトール
、ポリエチレングリコール、ヒドロキシプロピルセルロ
ース、ヒドロキシメチルセルロース等がある。水溶性高
分子物質の中でイオン性高分子等を用いる場合には、皮
膜材の多価金属イオンとイオン性高分子物質とが互いに
結合してカプセルが凝集するようになるので、比較的少
量用いることが好ましい。Hydrophilic substances, etc. added to the capsule surface are called external substances, and the amount of external substances is 6 to 30% of the total amount of the final cosmetic product.
Preferably, it is % by weight. Hydrophilic substances used as the external material include hyaltonic acid, collagen, glycerin, 1,3-butylene glycol, propylene glycol, ethanol, octadecanol, sorbitol, polyethylene glycol, hydroxypropylcellulose, hydroxymethylcellulose, and the like. When using ionic polymers among the water-soluble polymer substances, the polyvalent metal ions of the coating material and the ionic polymer substances bond with each other and the capsules aggregate, so a relatively small amount of It is preferable to use
本発明では、このような水溶性高分子物質を少なくとも
一種、好ましくは二種以上混合して用いることが好まし
い。In the present invention, it is preferable to use at least one type of such water-soluble polymeric substances, preferably a mixture of two or more types.
本発明に係る化粧料用カプセルの使用方法としては、化
粧料用カプセル1〜2gを不織布に包み手で破裂させ、
カプセルの被膜を不織布に付着させ、液状成分を不織布
から皮膚に塗布する方法を挙げることができる。この際
用いる不織布としてはセルロース、ポリエステル、ポリ
プロピレン、ポリエチレン、ナイロン、ビスコースレー
ヨン等の諸費からなるものか好ましく、不織布には孔か
多数形成されていることか好ましい。A method for using the cosmetic capsules according to the present invention is to wrap 1 to 2 g of cosmetic capsules in a nonwoven fabric and rupture them by hand.
A method may be mentioned in which a capsule film is attached to a nonwoven fabric and a liquid component is applied to the skin from the nonwoven fabric. The nonwoven fabric used in this case is preferably one made of various materials such as cellulose, polyester, polypropylene, polyethylene, nylon, viscose rayon, etc. It is preferable that the nonwoven fabric has a large number of holes.
このように本願発明の化粧料用カプセルを不織布を用い
て使用すれば皮膚に有用な親油性物質と補湿力を有する
親水性物質とを皮膚に供給することができるのみならず
不織布による皮膚のマツサージ効果も得ることができる
。In this way, when the capsule for cosmetics of the present invention is used with a non-woven fabric, it is possible not only to supply the skin with a lipophilic substance useful for the skin and a hydrophilic substance with a moisturizing ability, but also to improve the ability of the non-woven fabric to moisturize the skin. You can also get a pine surge effect.
発明の効果
本発明に係る化粧料用カプセルおよびその製造方法によ
れば、皮膚に活性を与えることができ、化粧品の配合性
および安全性が優れた親油性物質からなる芯材と、適切
な皮膜強度を有した継ぎ目のない球形の水不溶性皮膜材
とからなるカプセルの外状に皮膚に補湿力を与える親水
性物質を添加させて成る化粧料用カプセルおよびその製
造方法を効率よく提供することができる。Effects of the Invention According to the capsule for cosmetics and the manufacturing method thereof according to the present invention, a core material made of a lipophilic substance that can give activity to the skin and is excellent in blendability and safety in cosmetics, and an appropriate film. To efficiently provide a capsule for cosmetics comprising a strong, seamless spherical water-insoluble film material and a hydrophilic substance imparting moisturizing power to the skin added to the outer surface of the capsule, and a method for producing the same. I can do it.
以下本発明を実施例により説明するが、本発明はこれら
実施例に限定されるものではない。EXAMPLES The present invention will be explained below with reference to Examples, but the present invention is not limited to these Examples.
実施例1
イオン交換水98.2gにアルギン酸ナトリウム1.8
gを攪拌しながら加えてアルギン酸ナトリウム水溶液を
調製し、皮膜材貯蔵タンクに貯蔵した。カプセルの芯材
物質は、ヒマシ油20重量部、スクアラン23重量部、
液状ラノリン13重量部、シクロメチコン27.5重量
部、酢酸トコフロール12重量部、月見草油4重量部、
ノくルミチン酸レチノール0.5重量部を混合して調製
し、芯材貯蔵タンクに貯蔵した。このような芯材と皮膜
材とをポンプにて2重ノズルに移送したが、この際、皮
膜相流量は4.3g/分、芯材流量は5.2g/分であ
った。ノズル端に形成されだ液滴を硫酸アルミニウム4
重量%水溶液に攪拌しながら滴下し、35分間硬化させ
ることにより、カプセルの平均粒径が4mmであるカプ
セルを製造した。Example 1 1.8 g of sodium alginate in 98.2 g of ion-exchanged water
g was added with stirring to prepare an aqueous sodium alginate solution, which was stored in a coating material storage tank. The core material of the capsule is 20 parts by weight of castor oil, 23 parts by weight of squalane,
13 parts by weight of liquid lanolin, 27.5 parts by weight of cyclomethicone, 12 parts by weight of tocoflor acetate, 4 parts by weight of evening primrose oil,
It was prepared by mixing 0.5 parts by weight of retinol rumitate and stored in a core material storage tank. The core material and film material were transferred to a double nozzle using a pump, and at this time, the flow rate of the film phase was 4.3 g/min and the flow rate of the core material was 5.2 g/min. Droplets formed at the end of the nozzle are washed with aluminum sulfate 4
Capsules having an average particle size of 4 mm were manufactured by dropping the mixture into a wt % aqueous solution with stirring and curing for 35 minutes.
次いで、硬化されたカプセルを濾過して硬化液を除去し
、イオン交換水で水洗した。The cured capsules were then filtered to remove the cured liquid and washed with ion-exchanged water.
このときカプセルが水洗されて排出される液を50g採
取し、BaC1飽和水溶液を滴下させて白い沈澱物が析
出されな(なるまで水洗した。次に水洗されたカプセル
に外状を添加した。カプセル外状はグリセリン32重量
部、プロピレングリコール13重量部、オクタデカノー
ル7重量部、エタノール4重量部、コラーゲン4重量部
、ヒアルロン酸3重量部、ヒドロキシプロピレンセルロ
ース0.5重量部、イオン交換水36.5重量部を混合
して調製し、この外状を添加させて化粧料用カプセルを
製造した。At this time, 50 g of the liquid discharged after the capsules were washed with water was collected, and a BaCl saturated aqueous solution was added dropwise thereto.The capsules were washed with water until no white precipitate was deposited.Next, the outer shell was added to the washed capsules. External composition: 32 parts by weight of glycerin, 13 parts by weight of propylene glycol, 7 parts by weight of octadecanol, 4 parts by weight of ethanol, 4 parts by weight of collagen, 3 parts by weight of hyaluronic acid, 0.5 parts by weight of hydroxypropylene cellulose, 36 parts by weight of ion-exchanged water. A cosmetic capsule was prepared by mixing 0.5 parts by weight and adding this outer form.
実施例2
アルギン酸ナトリウム2.5重量%水溶液と硬化液とし
て塩化アルミニウム7重量%水溶液を調製した。カプセ
ルの芯材物質としては、トリ(カプリル、カプリン酸)
グリセリン22重量部、スクアラン26重量部、アボカ
ド油25重量部、オリーブ油18重量部、月見草油5重
量部、スクアレン4重量部を混合して使用した。これら
の芯材と皮膜材とを2重ノズルに移送して液滴を形成さ
せ、塩化アルミニウム水溶液において硬化させカプセル
を製造した。Example 2 A 2.5% by weight aqueous solution of sodium alginate and a 7% by weight aqueous solution of aluminum chloride as a curing liquid were prepared. The core material of the capsule is tri (caprylic, capric acid).
A mixture of 22 parts by weight of glycerin, 26 parts by weight of squalane, 25 parts by weight of avocado oil, 18 parts by weight of olive oil, 5 parts by weight of evening primrose oil, and 4 parts by weight of squalene was used. These core materials and coating materials were transferred to a double nozzle to form droplets, and the droplets were cured in an aqueous aluminum chloride solution to produce capsules.
この際、皮膜材の流量は6.3g/分、芯材の流量は6
.9g/分とし、1〜3.5市の大きさのカプセルが製
造できた。次に実施例1の方法で濾過、水洗したあと実
施例1と同様の外状を添加して化粧料用カプセルを製造
した。At this time, the flow rate of the coating material was 6.3 g/min, and the flow rate of the core material was 6.3 g/min.
.. At a rate of 9 g/min, capsules with a size of 1 to 3.5 cities could be produced. Next, after filtration and washing with water in the same manner as in Example 1, the same external form as in Example 1 was added to produce cosmetic capsules.
実施例3
皮膜材としてアルギン酸カルシウム2.2重量%水溶液
を調製し皮膜材貯蔵タンクに貯蔵した。Example 3 A 2.2% by weight aqueous solution of calcium alginate was prepared as a coating material and stored in a coating material storage tank.
硬化液として塩化アルミニウム2重量%水溶液を調製し
て硬化槽に貯蔵した。カプセルの芯材物質は、液体ラノ
リン27重量部、スクアラン22重量部、酢酸トコフェ
ノール14重量部、セチルオクタノエート10重量部、
ブチルステアレート12重量部、イソプロピレンパルミ
テート8重量部、ミンク油7重量部を混合して調製し使
用した。A 2% by weight aqueous solution of aluminum chloride was prepared as a curing solution and stored in a curing tank. The core material of the capsule is 27 parts by weight of liquid lanolin, 22 parts by weight of squalane, 14 parts by weight of tocopherol acetate, 10 parts by weight of cetyl octanoate,
It was prepared and used by mixing 12 parts by weight of butyl stearate, 8 parts by weight of isopropylene palmitate, and 7 parts by weight of mink oil.
芯材物質と皮膜材とを2重ノズルを介して実施例1と同
様の条件で流し、得られだ液滴を硬化液である塩化アル
ミニウム水溶液で硬化した後、濾過、水洗の工程を経て
カプセルを製造した。The core material material and the coating material are flowed through a double nozzle under the same conditions as in Example 1, and the resulting droplets are cured with an aqueous aluminum chloride solution, which is a curing liquid, and then filtered and washed with water to form capsules. was manufactured.
次に外状液としてグリセリン13重量部、ヒドロキシエ
チルセルロース0.7重量部、オクタドデカノール9重
量部、1.3−″j−チレングリコール12重量部、エ
タノール5重量部、イオン交換水60.3重量部を混合
して調製し用いた。外状添加工程では、はカプセル10
0gに外状20gを混合して化粧品用カプセルを製造し
た。Next, as an external liquid, 13 parts by weight of glycerin, 0.7 parts by weight of hydroxyethyl cellulose, 9 parts by weight of octadodecanol, 12 parts by weight of 1.3-''j-ethylene glycol, 5 parts by weight of ethanol, and 60.3 parts by weight of ion-exchanged water. It was prepared and used by mixing parts by weight.In the external addition step, 10 capsules were mixed.
Cosmetic capsules were prepared by mixing 0 g of the outer layer with 20 g of the outer layer.
実施例4
皮膜材としてアルギン酸カリウム2.5重量%水溶液を
用い、硬化液として硫酸アルミニウム1.596tf!
L水溶液を用いて実施例1と同じ芯材物質を用い、実施
例1と同じ条件で平均粒径4mmのカプセルを製造した
。Example 4 A 2.5% by weight aqueous solution of potassium alginate was used as the coating material, and 1.596 tf of aluminum sulfate was used as the curing liquid!
Capsules with an average particle size of 4 mm were manufactured using the L aqueous solution and the same core material as in Example 1 under the same conditions as in Example 1.
実施例5
アルギン酸アンモニウム2.5重量%水溶液を調製して
皮膜材貯蔵タンクに貯蔵した。硬化液として硫酸アルミ
ニウム3重ff196水溶液を用い、芯材物質としては
、トリミリスチン酸グリセリン25重量部、セチルオク
タノエート21重量部、ラノリン脂肪酸イソプロピル1
9重量部、スクアラン12重量部、コムギの胚種油8重
量部、アプリコートカネルオイル7重量部、スクアレン
4重量部、オリーブ油3重量部、月見草油1重量部を混
合して用いた。アルギン酸カリウム水溶液を6.2g重
分速度とし、上記の芯材物質は3.8g重分で2重ノズ
ルに移送してこの中ノズル端で液滴を形成するようにし
た。液滴を硬化液である硫酸アルミニウム水溶液に落と
して30分間硬化させることにより、平均粒径が3.5
mmであるカプセルを製造した。Example 5 A 2.5% by weight aqueous solution of ammonium alginate was prepared and stored in a coating material storage tank. A triple aluminum sulfate FF196 aqueous solution was used as the curing liquid, and the core materials were 25 parts by weight of glycerin trimyristate, 21 parts by weight of cetyl octanoate, and 1 part by weight of isopropyl lanolin fatty acid.
A mixture of 9 parts by weight, 12 parts by weight of squalane, 8 parts by weight of wheat embryo seed oil, 7 parts by weight of apricot kernel oil, 4 parts by weight of squalene, 3 parts by weight of olive oil, and 1 part by weight of evening primrose oil was used. The potassium alginate aqueous solution was set at a rate of 6.2 g, and the core material was transferred to a double nozzle at a rate of 3.8 g to form droplets at the end of the middle nozzle. By dropping the droplets into an aluminum sulfate aqueous solution, which is a curing liquid, and curing them for 30 minutes, the average particle size was reduced to 3.5.
Capsules of mm were manufactured.
硬化されたカプセルをろ過して硬化液を除去し、イオン
交換水で水洗した後再度ろ過した。次いでろ過されたカ
プセルに外状液を添加した。外状としては、グリセリン
12重量部、エタノール7重量部、プロピレングリコー
ル8重量部、ソルビトールポリエチレングリコール8重
量部、オクタドデカノール2重量部、ヒドロキシプロピ
レンセルロース1重量部、ヒアルロン酸3重量部、コラ
ーゲン2重量部、イオン交換水57重量部を混合して用
いた。外状添加工程ではカプセル100gに外状液30
gの割合で混合して外状を添加し化粧料用カプセルを製
造した。The hardened capsules were filtered to remove the hardening liquid, washed with ion-exchanged water, and then filtered again. The external liquid was then added to the filtered capsules. Externally, 12 parts by weight of glycerin, 7 parts by weight of ethanol, 8 parts by weight of propylene glycol, 8 parts by weight of sorbitol polyethylene glycol, 2 parts by weight of octadodecanol, 1 part by weight of hydroxypropylene cellulose, 3 parts by weight of hyaluronic acid, 2 parts by weight of collagen. parts by weight and 57 parts by weight of ion-exchanged water were used. In the external liquid addition process, 30 external liquid is added to 100 g of capsules.
Cosmetic capsules were manufactured by mixing the ingredients in a proportion of 1.5 g and adding an outer layer.
(皮膜強度の比較試験)
実施例1と同様の方法でアルギン酸すトリウム水溶液が
親油性物質を取り巻く液滴を硫酸アルミニウム水溶液に
滴下して硬化させて製造した本発明のカプセルと、液滴
を塩化カルシウム水溶液に滴下して硬化させたカプセル
とを皮膜強度で比較した。皮膜強度はレオメータ(Rh
eometer)で測定した。(Comparative test of film strength) Capsules of the present invention were produced by dropping and curing droplets of an aqueous solution of thorium alginate surrounding a lipophilic substance into an aqueous solution of aluminum sulfate in the same manner as in Example 1; The film strength was compared with capsules that were cured by dropping them into a calcium aqueous solution. Film strength is measured using a rheometer (Rh
eometer).
具体的には、底面が円板形態を有するロッドを2cm/
seeの速度で下降させてカプセルを一定速度で徐々に
押すようにした。Specifically, a rod whose bottom surface has a disk shape is 2 cm/
The capsule was gradually pushed at a constant speed by descending at a speed of .
すると、カプセルを押すロッドは力を受け、この力が計
測器に表示される。この際、カプセルが破壊されたとき
の力を測定して皮膜強度とした。The rod pushing the capsule will then experience a force, and this force will be displayed on the instrument. At this time, the force when the capsule was broken was measured and determined as the film strength.
得られた結果を表1に示すが、下記の表1は上記の試料
をそれぞれ25個ずつ測定して平均して得た値である。The obtained results are shown in Table 1. Table 1 below is the average value obtained by measuring 25 of each of the above samples.
表 1
表1に示されるように、塩化カルシウム水溶液を用いて
硬化したカプセルの皮膜の強度は159.8g重であっ
て、皮膜強度が高すぎるため手でカプセルを容易に破裂
することが困難である。しかしながら、本発明のカプセ
ルの皮膜の強度は18.02重であって手で破裂するこ
とが容易で化粧用として有利な皮膜の強度を有する。Table 1 As shown in Table 1, the strength of the capsule film hardened using an aqueous calcium chloride solution was 159.8 g, and the film strength was so high that it was difficult to easily rupture the capsule by hand. be. However, the capsule of the present invention has a film strength of 18.02 times, which is easy to burst by hand, and has a film strength that is advantageous for cosmetic use.
Claims (1)
量%のアルギン酸アルカリ塩水溶液で取り巻いた液滴を
、濃度0.2重量%〜10重量%のアルミニウム塩水溶
液で硬化させて水洗した後、その表面に親水性物質を添
加したことを特徴とする化粧料用カプセル。(2)上記
アルギン酸アルカリ塩が、アルギン酸ナトリウム、アル
ギン酸カリウム、アルギン酸アンモニウムからなる群か
ら選択される少なくとも一種であることを特徴とする請
求項第1項に記載の化粧料用カプセル。 (3)上記アルミニウム塩が、塩化アルミニウム、硫酸
アルミニウムからなる群から選択される少なくとも一種
であることを特徴とする請求項第1項に記載の化粧料用
カプセル。(4)上記親油性物質が、流動パラフィン、
流動イソパラフィン、スクアラン、トリミリスチン酸グ
リセリン、セチルオクタノエート、トリ(カプリル、カ
プリン酸)グリセリン、メチルポリシロキサン、シクロ
メチコン、液状ラノリン、ラノリン脂肪酸イソプロピル
、イソプロピルミリステート、イソプロピルパルミテー
ト、ブチルステアレート、アプリコトカネルオイル、コ
ムギの胚種油、月見草油、スクアレン、酢酸トコフェロ
ール、パルミチン酸レチノール、アボカド油、綿実油、
ミンク油、ヒマシ油、オリーブ油、ホホバ油からなる群
から選択される2種以上を混合して使用することを特徴
とする請求項第1項に記載の化粧料用カプセル。 (5)上記親水性物質が、ヒアルロン酸、コラーゲン、
グリセリン、1,3−ブチレングリコール、プロピレン
グリコール、エタノール、オクタドデカノール、ソルビ
トール、ポリエチレングリコール、ヒドロキシプロピル
セルロース、ヒドロキシエチルセルロース、ヒドロキシ
メチルプロピルセルロース、ヒドロキシメチルセルロー
スからなる群から選択される2種以上の混合物であるこ
とを特徴とする請求項第1項に記載の化粧料用カプセル
。 (6)濃度0.5重量%〜3重量%のアルギン酸アルカ
リ塩水溶液と親油性物質とを2重ノズルに通過させるこ
とにより、上記アルギン酸アルカリ塩水溶液が上記親油
性物質を取り巻くようにした液滴を調製し、該液滴をア
ルミニウムイオン水溶液で硬化させてカプセルを形成し
た後、該カプセルをイオン交換水で水洗し、次いでカプ
セル表面に親水性物質を添加することを特徴とする化粧
料用カプセルの製造方法。[Scope of Claims] (1) Droplets surrounding a lipophilic substance as a core material with an aqueous alginate salt aqueous solution having a concentration of 0.5% to 3% by weight are A cosmetic capsule characterized in that a hydrophilic substance is added to the surface of the capsule after hardening with an aqueous aluminum salt solution and washing with water. (2) The cosmetic capsule according to claim 1, wherein the alginate alkali salt is at least one selected from the group consisting of sodium alginate, potassium alginate, and ammonium alginate. (3) The cosmetic capsule according to claim 1, wherein the aluminum salt is at least one selected from the group consisting of aluminum chloride and aluminum sulfate. (4) The lipophilic substance is liquid paraffin,
Liquid isoparaffin, squalane, glyceryl trimyristate, cetyl octanoate, tri(caprylic, capric) glycerin, methylpolysiloxane, cyclomethicone, liquid lanolin, isopropyl lanolin fatty acid, isopropyl myristate, isopropyl palmitate, butyl stearate, Apricotcannel oil, wheat germ oil, evening primrose oil, squalene, tocopherol acetate, retinol palmitate, avocado oil, cottonseed oil,
The capsule for cosmetics according to claim 1, characterized in that two or more selected from the group consisting of mink oil, castor oil, olive oil, and jojoba oil are used in combination. (5) The hydrophilic substance is hyaluronic acid, collagen,
A mixture of two or more selected from the group consisting of glycerin, 1,3-butylene glycol, propylene glycol, ethanol, octadecanol, sorbitol, polyethylene glycol, hydroxypropylcellulose, hydroxyethylcellulose, hydroxymethylpropylcellulose, and hydroxymethylcellulose. The capsule for cosmetics according to claim 1, characterized in that: (6) Droplets are formed by passing an aqueous alginate salt aqueous solution having a concentration of 0.5% to 3% by weight and a lipophilic substance through a double nozzle so that the alginate aqueous solution surrounds the lipophilic substance. A capsule for cosmetics, characterized in that the droplets are hardened with an aluminum ion aqueous solution to form a capsule, the capsule is washed with ion-exchanged water, and then a hydrophilic substance is added to the capsule surface. manufacturing method.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019890013184A KR920002279B1 (en) | 1989-09-12 | 1989-09-12 | Cosmetic capsule |
KR13,184 | 1989-09-12 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03109312A true JPH03109312A (en) | 1991-05-09 |
JPH0714853B2 JPH0714853B2 (en) | 1995-02-22 |
Family
ID=19289859
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2241052A Expired - Lifetime JPH0714853B2 (en) | 1989-09-12 | 1990-09-11 | Cosmetic capsule and method for producing the same |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPH0714853B2 (en) |
KR (1) | KR920002279B1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03287511A (en) * | 1990-04-03 | 1991-12-18 | Sunstar Inc | Cosmetic and using thereof |
JP2000007558A (en) * | 1998-06-17 | 2000-01-11 | Morishita Jintan Kk | Capsule preparation excellent in long-term preservation stability |
WO2014207829A1 (en) * | 2013-06-25 | 2014-12-31 | 三粧化研株式会社 | Method for producing soft capsule type external preparation, softening liquid, and soft capsule type external preparation |
JP2016124801A (en) * | 2014-12-26 | 2016-07-11 | ポーラ化成工業株式会社 | Capsule body and production method thereof |
CN115252439A (en) * | 2022-08-03 | 2022-11-01 | 中国药科大学 | Smearing type skin care product composition containing millimeter capsules and preparation method thereof |
-
1989
- 1989-09-12 KR KR1019890013184A patent/KR920002279B1/en not_active IP Right Cessation
-
1990
- 1990-09-11 JP JP2241052A patent/JPH0714853B2/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03287511A (en) * | 1990-04-03 | 1991-12-18 | Sunstar Inc | Cosmetic and using thereof |
JP2000007558A (en) * | 1998-06-17 | 2000-01-11 | Morishita Jintan Kk | Capsule preparation excellent in long-term preservation stability |
WO2014207829A1 (en) * | 2013-06-25 | 2014-12-31 | 三粧化研株式会社 | Method for producing soft capsule type external preparation, softening liquid, and soft capsule type external preparation |
US9642813B2 (en) | 2013-06-25 | 2017-05-09 | Sansho Kaken Kabushiki Kaisha | Method for producing soft capsule type external preparation, softening liquid, and soft capsule type external preparation |
JP2016124801A (en) * | 2014-12-26 | 2016-07-11 | ポーラ化成工業株式会社 | Capsule body and production method thereof |
CN115252439A (en) * | 2022-08-03 | 2022-11-01 | 中国药科大学 | Smearing type skin care product composition containing millimeter capsules and preparation method thereof |
CN115252439B (en) * | 2022-08-03 | 2023-12-19 | 中国药科大学 | Smearing type skin care product composition containing millimeter capsules and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
KR910005840A (en) | 1991-04-27 |
JPH0714853B2 (en) | 1995-02-22 |
KR920002279B1 (en) | 1992-03-21 |
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