JPS6324490B2 - - Google Patents
Info
- Publication number
- JPS6324490B2 JPS6324490B2 JP58180664A JP18066483A JPS6324490B2 JP S6324490 B2 JPS6324490 B2 JP S6324490B2 JP 58180664 A JP58180664 A JP 58180664A JP 18066483 A JP18066483 A JP 18066483A JP S6324490 B2 JPS6324490 B2 JP S6324490B2
- Authority
- JP
- Japan
- Prior art keywords
- activated carbon
- aloe
- oil
- treatment
- water
- 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.)
- Expired
Links
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 81
- 235000011399 aloe vera Nutrition 0.000 claims description 37
- 241001116389 Aloe Species 0.000 claims description 35
- 239000000203 mixture Substances 0.000 claims description 24
- 239000013040 bath agent Substances 0.000 claims description 16
- 238000011282 treatment Methods 0.000 description 37
- 238000010438 heat treatment Methods 0.000 description 32
- 238000000605 extraction Methods 0.000 description 18
- 239000007788 liquid Substances 0.000 description 17
- 239000003960 organic solvent Substances 0.000 description 13
- 239000000047 product Substances 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- 239000003921 oil Substances 0.000 description 11
- 235000019198 oils Nutrition 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
- 239000000049 pigment Substances 0.000 description 8
- 238000001914 filtration Methods 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- 239000000284 extract Substances 0.000 description 6
- 238000003860 storage Methods 0.000 description 6
- 239000003021 water soluble solvent Substances 0.000 description 6
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- 239000003610 charcoal Substances 0.000 description 5
- 239000013065 commercial product Substances 0.000 description 5
- 229910052938 sodium sulfate Inorganic materials 0.000 description 5
- 235000011152 sodium sulphate Nutrition 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 4
- 239000003205 fragrance Substances 0.000 description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 241000157282 Aesculus Species 0.000 description 3
- 235000003261 Artemisia vulgaris Nutrition 0.000 description 3
- 240000006891 Artemisia vulgaris Species 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- 206010013786 Dry skin Diseases 0.000 description 3
- 239000004166 Lanolin Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 3
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 3
- 238000003287 bathing Methods 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
- 239000003814 drug Substances 0.000 description 3
- 230000037336 dry skin Effects 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 239000000796 flavoring agent Substances 0.000 description 3
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- 235000010181 horse chestnut Nutrition 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 229940039717 lanolin Drugs 0.000 description 3
- 235000019388 lanolin Nutrition 0.000 description 3
- 229940057995 liquid paraffin Drugs 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 235000017550 sodium carbonate Nutrition 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- LRFVTYWOQMYALW-UHFFFAOYSA-N 9H-xanthine Chemical compound O=C1NC(=O)NC2=C1NC=N2 LRFVTYWOQMYALW-UHFFFAOYSA-N 0.000 description 2
- 235000002961 Aloe barbadensis Nutrition 0.000 description 2
- 244000144927 Aloe barbadensis Species 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 235000015701 Artemisia arbuscula Nutrition 0.000 description 2
- 235000002657 Artemisia tridentata Nutrition 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 241000723346 Cinnamomum camphora Species 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 244000184734 Pyrus japonica Species 0.000 description 2
- 235000005733 Raphanus sativus var niger Nutrition 0.000 description 2
- 240000001970 Raphanus sativus var. sativus Species 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 229940069521 aloe extract Drugs 0.000 description 2
- 235000021302 avocado oil Nutrition 0.000 description 2
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- 239000011230 binding agent Substances 0.000 description 2
- 239000010624 camphor oil Substances 0.000 description 2
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- 230000000052 comparative effect Effects 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 239000010639 cypress oil Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000009499 grossing Methods 0.000 description 2
- 239000002198 insoluble material Substances 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 230000003020 moisturizing effect Effects 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
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- 239000007787 solid Substances 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- 239000000341 volatile oil Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- 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 description 1
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- 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 description 1
- 240000000073 Achillea millefolium Species 0.000 description 1
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- 229920001817 Agar Polymers 0.000 description 1
- 235000019489 Almond oil Nutrition 0.000 description 1
- AFHJQYHRLPMKHU-XXWVOBANSA-N Aloin Natural products O=C1c2c(O)cc(CO)cc2[C@H]([C@H]2[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O2)c2c1c(O)ccc2 AFHJQYHRLPMKHU-XXWVOBANSA-N 0.000 description 1
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- 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 description 1
- 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 description 1
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- 102000002322 Egg Proteins Human genes 0.000 description 1
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- QWDJLDTYWNBUKE-UHFFFAOYSA-L magnesium bicarbonate Chemical compound [Mg+2].OC([O-])=O.OC([O-])=O QWDJLDTYWNBUKE-UHFFFAOYSA-L 0.000 description 1
- 239000002370 magnesium bicarbonate Substances 0.000 description 1
- 235000014824 magnesium bicarbonate Nutrition 0.000 description 1
- 229910000022 magnesium bicarbonate Inorganic materials 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 235000014380 magnesium carbonate Nutrition 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 239000001525 mentha piperita l. herb oil Substances 0.000 description 1
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- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 229940056211 paraffin Drugs 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 235000019477 peppermint oil Nutrition 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- DPLVEEXVKBWGHE-UHFFFAOYSA-N potassium sulfide Chemical compound [S-2].[K+].[K+] DPLVEEXVKBWGHE-UHFFFAOYSA-N 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
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- ULYXRGMMWHJFHL-UHFFFAOYSA-N raunin Natural products C1=CC(=O)OC2=C3C4=C(C)C(=O)OC4COC3=CC=C21 ULYXRGMMWHJFHL-UHFFFAOYSA-N 0.000 description 1
- 239000010666 rose oil Substances 0.000 description 1
- 235000019719 rose oil Nutrition 0.000 description 1
- 235000013974 saffron Nutrition 0.000 description 1
- 239000004248 saffron Substances 0.000 description 1
- 235000019512 sardine Nutrition 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
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- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- 235000019830 sodium polyphosphate Nutrition 0.000 description 1
- 229910000031 sodium sesquicarbonate Inorganic materials 0.000 description 1
- 235000018341 sodium sesquicarbonate Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
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- 239000008107 starch Substances 0.000 description 1
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- 239000001384 succinic acid Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
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- BWMISRWJRUSYEX-SZKNIZGXSA-N terbinafine hydrochloride Chemical compound Cl.C1=CC=C2C(CN(C\C=C\C#CC(C)(C)C)C)=CC=CC2=C1 BWMISRWJRUSYEX-SZKNIZGXSA-N 0.000 description 1
- 201000004647 tinea pedis Diseases 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 235000001019 trigonella foenum-graecum Nutrition 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- WCTAGTRAWPDFQO-UHFFFAOYSA-K trisodium;hydrogen carbonate;carbonate Chemical compound [Na+].[Na+].[Na+].OC([O-])=O.[O-]C([O-])=O WCTAGTRAWPDFQO-UHFFFAOYSA-K 0.000 description 1
- 235000016788 valerian Nutrition 0.000 description 1
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- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Landscapes
- Cosmetics (AREA)
Description
この発明は、特定の処理をほどこしたアロエ分
画物を含有する浴用剤組成物に関する。
従来より、アロエやアロエエキスは、特に民間
的にひび、あかぎれ、やけど、切り傷、水虫等の
治療に用いられている。しかしながら、アロエエ
キスは特有のにおいを有し、その色が濃褐色であ
るうえ、変色しやすいアロイン等のアントラキノ
ン誘導体などを含んでおり、浴用剤組成物中に配
合した場合、におい、色、沈澱等が大きな問題と
なる。このため、配合量も少なめに制限され効果
を十分に発揮させることができなかつた。
この発明の目的は、ひび、あかびれ、荒れ性等
によるカサカサした肌に、入浴後、しつとりした
なめらかさを十分に与えることができ、しかもア
ロエエキス特有のにおいもなく、かつ系の保存安
定性が高く、着色、変色などの問題がない浴用剤
組成物を提供することである。
すなわち、この発明は、アロエ樹液を活性炭処
理して得られたアロエ分画物を含有する浴用剤組
成物を提供する。
以下、この発明を詳細に説明する。この発明に
用いるアロエ分画物は次に述べる原料と処理工程
により得られる。原料となるアロエとしてはアロ
エベラ、シヤボンアロエ、キダチアロエを好適な
ものとして挙げることができる。
これらにアロエの全草、葉部もしくはゼリー部
を圧搾、破砕、粉砕等して得られる樹液を好まし
く過して次の活性炭処理に供する。尚固型物が
混ざつた樹液をそのまま次の工程にまわしても差
支えない。その場合は後の適宜な段階で固型物を
除去する。
次に、このようにして得られるアロエ樹液に対
してバツチ法により活性炭処理を施す。この活性
炭処理により変色し易い有色成分が確実に除去さ
れ、無色乃至淡黄色で水可溶性の創傷治療等に生
理活性作用を有する物質が得られるものである。
これに対し、活性炭処理を行なわない場合には、
有色成分、水不溶性成分が良好に除去されず、本
発明の入浴剤成分としては適当でない。
このバツチ法による活性炭処理において使用す
る活性炭は獣炭、骨炭のような動物炭でも、ヤシ
殻炭等の植物炭でもよいが、吸着力が高く、安価
な植物炭がより好ましい。また、活性炭は粉末の
ものでも粒状のものでもよいが、粉末、特に100
〜400メツシユのものが好ましい。活性炭の使用
量は元のアロエ樹液の重量に対し0.1〜20%(重
量%、以下同じ)、より好ましくは1〜10%とす
ることが望ましい。バツチ法による活性炭処理に
際し、活性炭を加えた後、液を機械撹拌等の手段
で撹拌することが好ましいが、この場合撹拌時間
は15分〜3時間、特に30分〜1時間とすることが
好ましい。なえ、活性炭処理は低温又は室温下で
行なうこともでき、また後述する加熱処理と同時
に行なう場合には加熱下に行なう。
活性炭処理後は、その後更に他の処理を行なう
場合にはそのまま、好ましくは活性炭を除去した
ものについて所定の処理を施し、また活性炭処理
を最終段階として行なつた場合には過等の適宜
な分離手段により活性炭を除去し、その液を目
的分画物として採取する。
活性炭処理を行なうことによつて得られた目的
分画物は、処理液の状態で殆んど無色透明であ
る。この目的分画物は、変色し易い有色色素成分
や水不溶性成分が除去されたものであつて、創傷
治療作用などの優れた生理活性作用を有する。な
お、前記処理液は、目的分画物としてそのまま本
発明の入浴剤組成物に添加することもできるが、
加熱乾燥、噴霧乾燥、凍結乾燥等の適宜な乾燥法
を採用し、水分を留去して、さらさらした白色乃
至淡黄色の粉末状物質としたものを粒状もしくは
粉状の入浴剤組成物に添加することは、貯蔵安定
性等の点から更に好ましいことである。
更に又、上記活性炭処理に加えて加熱処理を行
なうと、より好適なアロエ分画物が得られる。こ
の加熱処理により、加熱や経時によつて変性する
物質(起炎性物質)が除去された安定性に勝れた
生理活性物質が得られる。また、加熱処理によ
り、アロエ樹液の粘稠性がなくなり、過工程が
極めて容易になるため操作性の点でも有利であ
る。
なお、加熱処理と活性炭処理とはどちらを先に
行なつてもよく、また同時に行なつてもよいが、
加熱処理を行なつた後に活性炭処理を施すか、或
いは加熱処理と活性炭処理とを同時に行なうよう
にすることが好ましい。
前記加熱処理は、常圧下又は減圧下において、
温度50〜90℃、より好ましくは60〜80℃である。
また、加熱時間は0.5〜3時間、より好ましくは
1〜2時間である。加熱温度が50℃よりも低い場
合、或いは加熱時間が30分よりも短かい場合は加
熱処理の効果が十分に発揮されず、不溶物を分離
する工程で上記不純成分を十分に除去し得ない場
合が生じる。また、加熱温度が90℃より高い場
合、或いは加熱時間が3時間よりも長い場合には
有効成分の変質や発酵、不溶物の分解可溶化とい
つた問題が生じる場合がある。
前記加熱処理を行なう場合、単にアロエ樹液を
上記処理条件において加熱するだけでもよいが、
この加熱処理を行なう際にアロエ樹液を同時に濃
縮したり(この場合、アロエ樹液は最初の樹液量
の10倍以下、より好ましくは2〜5倍程度の濃縮
液とすることが望ましい)、また水分をほぼ完全
に蒸発させても差支えない。
加熱処理後は、これを最終段階で行なつた場合
は水不溶物を過等の手段によつて除いたものを
目的分画物として採取し、加熱処理後活性炭処理
或いは後述する水可溶性有機溶媒による抽出処理
を行なう場合はそのまま又は水不溶物を除去した
ものを使用する。なお、加熱処理後に活性炭処理
を行なう場合、この加熱処理工程において樹液を
濃縮したような場合は、これに水を好ましくは最
初の樹液量の2〜10倍の濃縮液となるように加
え、これに活性炭を投入することが好ましい。
本発明に用いるアロエ分画物を得る場合、上述
した活性炭処理に加えて、或いは活性炭処理と加
熱処理とに加えて更に水可溶性有機溶媒による抽
出処理を行なうことができ、この有機溶媒による
抽出処理により樹脂類などやアルコール難溶性物
質を更に確実に除去することができる。
この抽出処理は、前記活性炭処理或いは加熱処
理の前もしくは後のいずれの段階で行なつてもよ
いが、特に上記三者の処理を行なう場合は加熱処
理後活性炭処理を行なう工程の前もしくは後、又
は加熱処理と活性炭処理とを同時に施す工程の前
もしくは抽出処理を行なうようにすることが好ま
しい。
なお、水可溶性有機溶媒による抽出処理を活性
炭処理或いは加熱処理に先立つて行なう場合は、
アロエ樹液に有機溶媒を加えて抽出を行ない、そ
の抽出液を採取し、有機溶媒を留去したもの又は
有機溶媒を留去したものに水を加えたものを次の
工程(活性炭処理工程、加熱処理工程)にまわす
ものである。
水可溶性有機溶媒による抽出処理を活性炭処理
の後に行なう場合は活性炭を除去することによつ
て得られる処理液、好ましくはその濃縮液又は乾
燥物に有機溶媒を加えて抽出するものであり、加
熱処理の後に行なう場合は加熱処理後の樹液、好
ましくはその濃縮液又は加熱乾燥物に有機溶媒を
加えて抽出し、抽出後は上述したように抽出液、
その濃縮液又は溶媒留去したものを採取するもの
である。なお、抽出処理を最終工程として行なつ
た場合には、得られた抽出液から溶媒を留去した
ものを目的分画物として採取することが好ましい
が、使用目的に応じては溶媒を留去せずに(特に
水可溶性溶媒としてエタノールやイソプロパノー
ルを用いた場合は)抽出液、或いはその濃縮液を
そのまま使用に供することもできる。
この抽出工程において、抽出に用いる有機溶媒
としてはエタノール、メタノール、イソプロパノ
ール、n―プロピルアルコール、n―ブチルアル
コール、tert―ブチルアルコール、ソルビトー
ル、アセトン等の水可溶性溶媒が使用され、抽出
処理は特にこれら水可溶性溶媒を20〜80%、より
好ましくは25〜40%濃度で含む水との混合溶媒と
することが好ましい。この場合、前記水可溶性溶
媒はその1種を単独で使用しても2種以上を併用
するようにしてもよい。また、有機溶媒(水可溶
性溶媒、特に水可溶性溶媒―水の混合溶媒)の使
用量は、有機溶媒中で抽出されるべき物質が0.1
〜30%、より望ましくは1〜10%濃度となるよう
な量とすることが好ましい。抽出条件としては、
温度0〜25℃で抽出時間1時間〜数日、より望ま
しくは3〜48時間の条件が好ましく採用される。
抽出処理後はその抽出液を採取する。この水可溶
性有機溶媒による抽出処理を行なつて得られる目
的分画物は樹脂類などやアルコール難溶性物質が
確実に除去されたものである。
而して、上記方法により得られた目的分画物
は、優れた組織賦活作用を有するものであり、ま
た変色し易い有色色素成分や水不溶性成分を含ま
ず、無色乃至淡黄色であり、特に加熱処理を行な
つたものは、熱変性、経時的変性による水不溶性
成分(起炎性物質)が確実に除去され、安定で変
色、変質するようなことがなく、また水可溶性有
機溶媒による抽出処理を行なつたものはアルコー
ル難溶性物質を含まないものであり、種々の製品
に配合してもその外観等を損なうことがなく、製
品の品質上で問題となるおそれもない。かつこの
生理活性物質は水溶性で水に殆んど任意の割合で
溶解するものであり、即ち浴中で充分な分散性を
有し本発明浴剤の肌への効果であるしつとりした
なめらかさの付与を保証する。しかも、この分画
物は安全性も高く、皮膚に適用しても刺激性がな
いものである。
この発明の浴用剤組成物は、上述したアロエ分
画物を単品で使用しても良いが、更に後述する常
用成分を含んでいてもよい。後述する常用成分を
含む浴用剤の場合には、全組成物中のアロエ分画
物の配合量は、通常0.1〜99%好ましくは0.1ない
し95重量%、さらに好ましくは0.1ないし30重量
%である。
この発明の浴用剤組成物は、通常、アロエ分画
物の浴中濃度が0.1ないし30ppmになる量使用さ
れる。0.1ppm未満の使用量ではカサカサした肌
にしつとりしたなめらかさを与える効果が不十分
になる。0.1ppmないし30ppmにおいては入浴後
のしつとりしたなめらかさの向上が認められたが
30ppmを超えるとほとんど性能の向上が認められ
ず、また、若干アロエ特有のにおいが認められ
た。
この発明の浴用剤組成物態様である、上記アロ
エ分画物の他に更に常用成分を含む浴用剤は以下
に記載の成分の1種又は2種以上を1〜99.9%好
ましくは5〜99.9%より好ましくは70〜99.9%含
むものである。すなわち、無機塩類としては、例
えば、塩化ナトリウム、ヨウ化カリウム、塩化ア
ンモニウム、硫酸アルミニウム、硫化カリウム、
硫酸カリウム、炭酸水素ナトリウム、炭酸ナトリ
ウム、セスキ炭酸ナトリウム、炭酸マグネシウ
ム、重炭酸マグネシウム、ホウ砂、ホウ酸、無水
ケイ酸、メタケイ酸、ポリリン酸ナトリウム、リ
ン酸水素カルシウム、リン酸ナトリウム、イオ
ウ、湯の花等を挙げることができる。これら無機
塩類の浴剤中の量は1〜99.9%、好ましくは5〜
99.9%である。また、油分としては、オリーブ
油、大豆油、アーモンド油、落下生油、ヒマシ
油、ヤシ油、パーム油、タートル油、ヌカ油、ア
ボカド油、ミンク油、卵黄油、牛脂、ラノリン、
スクワレン、流動パラフイン、ワセリン、パラフ
イン等を挙げることができる。これら油分の浴剤
中の量は0〜10%、好ましくは0.1〜1%である。
精油類としては、例えば、ハツカ油、ジヤスミ
ン、人造ジヤ香、カンフアー、シヨウ脳油、ヒノ
キ油、トウヒ油、リユウ油、テレビン油、ケイ皮
油、ベルガモツト油、ミカン油、シヨウブ油、パ
イン油、ラベンダー油、ベイ油、オレンジ油、シ
ンナモン油、スギ油、丁字油、ヒバ油、バラ油、
ユーカリ油、レモン油等を挙げることができる。
これら精油類は浴剤中に0〜10%好ましくは0.1
〜1%の範囲で用いられる。
本発明の浴用剤組成物には、前記成分の他、必
要に応じ、さらに生薬や粘結剤、その他の成分を
添加することもできる。それらの具体例を以下に
示す。
生薬:
ソウジユツ、ビヤクジユツ、カノコソウ、ケイ
ガイ、コウボク、センキユウ、トウヒ、ニンジ
ン、ケイヒ、シヤクヤク、ハツカ葉、オウゴン、
ブクリヨウ、シヨウブ、マツブサ、ビヤクシ、サ
フラン、オウバク、ウイキヨウ、チンピ、ガン
ピ、カミツレ、ダイコン、ヤナギ、クスノキ、ニ
ワトコ、ソクズ、ナギナタコウジユ、ヤツデ、セ
キシヨウ、ヨモギ、オトギリソウ、ユズ、ダイダ
イ、モモ、サイカチ、ビワ、スイカズラ、ヨロイ
グサ、ボダイジユ、トチノキ、ノコギリソウ、ホ
ツプ、ローズマリー、カバノキ、マツ、ヤレンズ
ラ、ランタナ、カンゾウ、キツソウコン、マロニ
エ等。
粘結剤:
カゼイン、カルボキシメチルセルロース、ナト
リウム塩、ペクチン、デンプン、メチルセルロー
ス、エチルセルロース、アルギン酸ナトリウム、
ポリビニルアルコール、ポリビニルピロリドン、
ポリビニルメチルエーテル、カラヤゴム、ローカ
ストビーンガム、トラガカントガム、カラゲナ
ン、カーボボール、アカシヤガム、カンテン等。
医薬品、医薬部外品及び化粧品用タール系色素
(キサンチン系等)、界面活性剤(アニオン系、カ
チオン系、両性及びノニオン系)、アスコルビン
酸又はその塩、明ばん類、香料、殺菌剤、還元剤
等。又水性入浴剤として上記各種成分を含合する
組成物を水性溶媒でバランスさせることもでき
る。
次に、この発明の実施例及び比較例を示し、こ
の発明の効果を具体的に説明する。各例の説明に
先立ち、アロエ分画物の具体的調製方法並びにな
めらか感付与性能及び保存安定性の試験法につい
て説明する。なお、各例で用いた組成物は、紙管
中に45℃で7日間保存した後のものである。
アロエ分画物の調製
製造例 1
キダチアロエ葉部10Kgにミキサーにて破砕し、
綿布による過、更に紙による自然過を行な
い、黄緑色のやや不透明な樹液7.5Kgを得た。次
にこの樹液を常温300mmHg減下で3.7Kgになるま
で濃縮した。これに300gの粉末活性炭を加え、
常温で約30分間撹拌した後、紙を用いて吸引
過し、次いで水で活性炭を洗いその洗浄液を液
に加えた。この液を浴温40℃でアスピレータ減
圧下に濃縮し、さらに真空乾燥を行ない、白色粉
末170gを得た。
製造例 2
キダチアロエ葉部10Kgをミキサーにて破砕し、
綿布による過、更に紙による自然過を行な
い、黄緑色のやや不透明な樹液7.5Kgを得た。次
にこの樹液を300mmHg減圧下で70℃、30分間加
熱し、3.7Kgの濃縮樹液を得た。これに300gの粉
末活性炭を加え、室温で約30分間撹拌した後、
紙を用いて吸引過し、次いで水で活性炭を洗い
その洗浄液を液に加えた。この液を浴温40℃
でアスピレータ減圧下に濃縮し、さらに真空乾燥
を行ない、白色粉末172gを得た。
製造例 3
キダチアロエ葉部10Kgをフードスライサー、パ
ルパー、フイニシヤーの順に処理し、緑色の樹液
7.7Kgを得た。この樹液に粉末活性炭700gを加
え、室温で約30分間撹拌した後にフイルタープレ
ス機にて過した。この液を浴温40℃に加熱し
ながらアスピレータ減圧下に約1/5量になるまで
濃縮して1.6Kgの濃縮物を得た。
これにエタノール0.8を加え、30分間撹拌し、
室温で約1日間静置した後、析出した白色沈澱物
を紙を用いて吸引過し、液を得た。これを
浴温40℃でアスピレータ減圧下に濃縮し、更に真
空乾燥を行なつて白黄色粉末116gを得た。
〔比較製造例 1〕
キダチアロエ葉部10Kgをミキサーにて破砕し、
綿布による過、更に紙による自然過を行な
い、黄緑色のやや不透明な樹液7.5Kgを得た。こ
の樹液を凍結乾燥し、奥褐色の粉末210gを得た。
試験法1 (なめらか感付与性能)
肌がカサカサしているパネラー5名の左右の前
腕部の一方を、後述する市販の浴用剤組成物を
100ppm含む42℃の浴湯に、他方をこの発明の浴
用剤組成物を100ppm含む42℃の浴湯に10分間浸
漬した後タオルドライし、タオルドライ10分後の
肌のなめらか感を一対比較により下記基準で評価
した。
評価基準
◎…市販品に比べて非常に優れた効果がある
〇…市販品に比べてかなり優れた効果がある
△…市販品に比べてやや優れた効果がある
×…市販品に比べて同等又はそれ以下の効果しか
ない
試験法2 (保存安定性)
浴用剤組成物の香り及び色調に関する保存安定
性については、市販品との一対比較により、下記
基準で評価した。
評価基準
◎…市販品よりも変化が認められない
〇…市販品と同等の変化が認められるが商品価値
上問題となる程度ではない。
△…市販品に比べ変化がやや認められる
×…市販品に比べ変化が著しく認められる
なお、使用した市販品の分析による成分組成は
次の通りである。
硫酸ナトリウム 58%(重量)
炭酸水素ナトリウム 40%
流動パラフイン 0.5%
ウラニン色素 0.3%
香 料 1.2%
試験例
第1表に示す組成を有する浴用剤組成物を調調
製し、そのなめらか感付与性能及び保存安定性を
試験した。結果を同表に示す。なお、表中、組成
は重量%で示されている。
The present invention relates to a bath agent composition containing an aloe fraction subjected to a specific treatment. Traditionally, aloe vera and aloe extracts have been used, especially in folk medicine, to treat cracks, chaps, burns, cuts, athlete's foot, and the like. However, aloe extract has a unique odor, is dark brown in color, and contains anthraquinone derivatives such as aloin, which are easily discolored. etc. become a big problem. For this reason, the blending amount was also limited to a small amount, and the effect could not be fully exhibited. The purpose of this invention is to provide enough moisture and smoothness to dry skin due to cracks, rashes, roughness, etc. after bathing, without the odor peculiar to aloe extract, and with a storage-stable system. To provide a bath agent composition which has high properties and is free from problems such as coloring and discoloration. That is, the present invention provides a bath agent composition containing an aloe fraction obtained by treating aloe sap with activated carbon. This invention will be explained in detail below. The aloe fraction used in this invention can be obtained using the following raw materials and processing steps. Suitable examples of aloe that can be used as raw materials include aloe vera, syabone aloe, and kidachi aloe. The sap obtained by squeezing, crushing, crushing, etc. the whole plant, leaf or jelly part of aloe is preferably passed through these and subjected to the next activated carbon treatment. In addition, the sap mixed with solid matter may be passed on to the next process as it is. In that case, the solid matter is removed at an appropriate later stage. Next, the aloe sap thus obtained is treated with activated carbon by a batch method. This activated carbon treatment reliably removes colored components that are easily discolored, resulting in a colorless to pale yellow, water-soluble substance that has physiologically active effects for wound treatment and the like.
On the other hand, if activated carbon treatment is not performed,
Colored components and water-insoluble components are not removed well, and this is not suitable as a bath agent component of the present invention. The activated carbon used in this batch method activated carbon treatment may be animal charcoal, such as animal charcoal or bone charcoal, or vegetable charcoal, such as coconut shell charcoal, but vegetable charcoal, which has high adsorption power and is inexpensive, is more preferable. Activated carbon may be powdered or granular, but powder, especially 100%
~400 mesh is preferred. The amount of activated carbon to be used is preferably 0.1 to 20% (weight %, same hereinafter), more preferably 1 to 10%, based on the weight of the original aloe sap. When treating activated carbon by the batch method, it is preferable to stir the liquid by means such as mechanical stirring after adding the activated carbon, but in this case, the stirring time is preferably 15 minutes to 3 hours, particularly 30 minutes to 1 hour. . Yes, the activated carbon treatment can be carried out at low temperature or room temperature, and when carried out simultaneously with the heat treatment described below, it is carried out under heating. After activated carbon treatment, if other treatments are to be carried out after that, the activated carbon can be removed as is, preferably after the activated carbon has been removed, and then subjected to the prescribed treatment, or if activated carbon treatment is carried out as the final step, it can be separated as appropriate. Activated carbon is removed by a means, and the resulting liquid is collected as a target fraction. The target fraction obtained by the activated carbon treatment is almost colorless and transparent in the form of a treatment liquid. This target fraction has colored pigment components that easily change color and water-insoluble components removed, and has excellent physiologically active effects such as wound healing effects. Note that the treatment liquid can be added as it is to the bath additive composition of the present invention as a target fraction, but
Adopt an appropriate drying method such as heat drying, spray drying, freeze drying, etc. to distill off the moisture, and add the free white to pale yellow powder to a granular or powdered bath additive composition. It is more preferable to do so in terms of storage stability and the like. Furthermore, a more suitable aloe fraction can be obtained by carrying out a heat treatment in addition to the above activated carbon treatment. By this heat treatment, a physiologically active substance with excellent stability is obtained from which substances that are denatured by heating or aging (inflammatory substances) are removed. Furthermore, the heat treatment eliminates the viscosity of the aloe sap, making over-processing extremely easy, which is advantageous in terms of operability. Note that either the heat treatment or the activated carbon treatment may be performed first, or they may be performed at the same time.
It is preferable to perform the activated carbon treatment after the heat treatment, or to perform the heat treatment and the activated carbon treatment at the same time. The heat treatment is performed under normal pressure or reduced pressure,
The temperature is 50-90°C, more preferably 60-80°C.
Moreover, the heating time is 0.5 to 3 hours, more preferably 1 to 2 hours. If the heating temperature is lower than 50°C or the heating time is shorter than 30 minutes, the effect of the heat treatment will not be sufficiently exhibited, and the above impurity components will not be sufficiently removed in the process of separating insoluble materials. A situation may arise. Furthermore, if the heating temperature is higher than 90° C. or if the heating time is longer than 3 hours, problems such as deterioration and fermentation of the active ingredients and decomposition and solubilization of insoluble materials may occur. When performing the heat treatment, the aloe sap may be simply heated under the above treatment conditions, but
When performing this heat treatment, the aloe sap may be concentrated at the same time (in this case, it is desirable that the aloe sap be a concentrated liquid of 10 times or less, more preferably 2 to 5 times the initial amount of sap), or There is no problem even if it is almost completely evaporated. After the heat treatment, if this is done at the final stage, water-insoluble matter is removed by filtration or other means, and the target fraction is collected, and after the heat treatment, it is treated with activated carbon or treated with a water-soluble organic solvent as described below. When performing an extraction treatment, use it as it is or after removing water-insoluble matter. In addition, when performing activated carbon treatment after heat treatment, if the sap is concentrated during this heat treatment process, add water to this so that the concentrated liquid is preferably 2 to 10 times the initial amount of sap. It is preferable to add activated carbon. When obtaining the aloe fraction used in the present invention, in addition to the above-mentioned activated carbon treatment, or in addition to the activated carbon treatment and heat treatment, an extraction treatment with a water-soluble organic solvent can be performed. This allows resins and poorly soluble substances to be removed more reliably. This extraction treatment may be performed at any stage before or after the activated carbon treatment or heat treatment, but especially when performing the above three treatments, it may be performed before or after the activated carbon treatment after the heat treatment, Alternatively, it is preferable to perform an extraction treatment or before a step of simultaneously applying heat treatment and activated carbon treatment. In addition, when performing extraction treatment with a water-soluble organic solvent prior to activated carbon treatment or heat treatment,
Extraction is performed by adding an organic solvent to the aloe sap, and the extract is collected and the organic solvent is distilled off, or the organic solvent is distilled off and water is added to it for the next process (activated carbon treatment process, heating). processing process). When extraction treatment with a water-soluble organic solvent is performed after activated carbon treatment, extraction is performed by adding an organic solvent to the treated liquid obtained by removing activated carbon, preferably the concentrated liquid or dried product, and heat treatment. In the case of extraction after heating, an organic solvent is added to the sap after heat treatment, preferably its concentrated liquid or heat-dried product, and after extraction, the extract liquid,
The concentrated liquid or the one after the solvent has been distilled off is collected. In addition, when extraction treatment is performed as the final step, it is preferable to distill off the solvent from the obtained extract and collect it as the desired fraction, but depending on the purpose of use, distilling off the solvent may be necessary. Alternatively, the extract or its concentrate can be used as is (particularly when ethanol or isopropanol is used as the water-soluble solvent). In this extraction process, water-soluble solvents such as ethanol, methanol, isopropanol, n-propyl alcohol, n-butyl alcohol, tert-butyl alcohol, sorbitol, and acetone are used as organic solvents for extraction, and the extraction process is particularly performed using these solvents. It is preferable to use a mixed solvent with water containing a water-soluble solvent in a concentration of 20 to 80%, more preferably 25 to 40%. In this case, the water-soluble solvent may be used alone or in combination of two or more. In addition, the amount of organic solvent (water-soluble solvent, especially mixed solvent of water-soluble solvent and water) used should be 0.1
It is preferred that the amount is such that the concentration is ~30%, more preferably 1-10%. The extraction conditions are:
Conditions of a temperature of 0 to 25° C. and an extraction time of 1 hour to several days, more preferably 3 to 48 hours are preferably employed.
After the extraction process, the extract is collected. The target fraction obtained by performing this extraction treatment with a water-soluble organic solvent is one in which resins and poorly alcohol-soluble substances are reliably removed. Therefore, the target fraction obtained by the above method has an excellent tissue activating effect, does not contain colored pigment components that easily change color, and does not contain water-insoluble components, and is colorless to pale yellow. Heat-treated products reliably remove water-insoluble components (flame-causing substances) due to heat denaturation and denaturation over time, are stable, do not discolor or change in quality, and are easily extracted with water-soluble organic solvents. The treated products do not contain substances that are poorly soluble in alcohol, so even if they are blended into various products, their appearance etc. will not be impaired, and there is no risk of problems with the quality of the products. In addition, this physiologically active substance is water-soluble and dissolves in water at almost any ratio, that is, it has sufficient dispersibility in the bath and provides the moisturizing effect that the bath agent of the present invention has on the skin. Guarantees smoothness. Furthermore, this fraction is highly safe and does not cause irritation when applied to the skin. The bath agent composition of the present invention may use the above-mentioned aloe fraction alone, but may also contain the commonly used ingredients described below. In the case of bath preparations containing commonly used ingredients as described below, the amount of the aloe fraction in the total composition is usually 0.1 to 99%, preferably 0.1 to 95% by weight, and more preferably 0.1 to 30% by weight. . The bath composition of the present invention is usually used in an amount such that the aloe fraction has a concentration in the bath of 0.1 to 30 ppm. If the amount used is less than 0.1 ppm, the effect of moisturizing and smoothing dry skin will be insufficient. At 0.1ppm to 30ppm, an improvement in moist and smooth skin after bathing was observed.
When the concentration exceeded 30 ppm, almost no improvement in performance was observed, and a slight odor peculiar to aloe was observed. The bath agent which is an embodiment of the bath agent composition of the present invention and further contains commonly used ingredients in addition to the aloe fraction described above contains one or more of the following components in an amount of 1 to 99.9%, preferably 5 to 99.9%. More preferably, it contains 70 to 99.9%. That is, examples of inorganic salts include sodium chloride, potassium iodide, ammonium chloride, aluminum sulfate, potassium sulfide,
Potassium sulfate, sodium bicarbonate, sodium carbonate, sodium sesquicarbonate, magnesium carbonate, magnesium bicarbonate, borax, boric acid, silicic anhydride, metasilicic acid, sodium polyphosphate, calcium hydrogen phosphate, sodium phosphate, sulfur, yunohana etc. can be mentioned. The amount of these inorganic salts in the bath agent is 1 to 99.9%, preferably 5 to 99.9%.
It is 99.9%. In addition, oils include olive oil, soybean oil, almond oil, fallen raw oil, castor oil, coconut oil, palm oil, turtle oil, bran oil, avocado oil, mink oil, egg yolk oil, beef tallow, lanolin,
Examples include squalene, liquid paraffin, petrolatum, paraffin, and the like. The amount of these oils in the bath agent is 0 to 10%, preferably 0.1 to 1%. Examples of essential oils include peppermint oil, diasmine, artificial dia incense, camphor, camphor oil, cypress oil, spruce oil, rhubarb oil, turpentine oil, cinnamon bark oil, bergamot oil, tangerine oil, camphor oil, pine oil, and lavender. oil, bay oil, orange oil, cinnamon oil, cedar oil, clove oil, cypress oil, rose oil,
Examples include eucalyptus oil and lemon oil.
These essential oils should be contained in the bath agent in an amount of 0 to 10%, preferably 0.1%.
It is used in the range of ~1%. In addition to the above-mentioned components, crude drugs, binders, and other components may be added to the bath composition of the present invention, if necessary. Specific examples thereof are shown below. Herbal medicines: Soujiyutsu, Japanese yakiniku, Valerian, Keigai, Kouboku, Senkiyu, Spruce, Carrot, Keihi, Keihi, Citrus leaf, Scutellariae,
Japanese sagebrush, Japanese sagebrush, Japanese sardine, Japanese beaver, saffron, Japanese oak, fenugreek, chimpi, gampi, chamomile, radish, willow, camphor tree, elderberry, Japanese radish, Japanese koji, Japanese japonica, Japanese red herring, mugwort, hypericum, yuzu, Japanese radish, peach, cypress, Loquat, honeysuckle, nightweed, horse chestnut, horse chestnut, yarrow, hops, rosemary, birch, pine, japonica, lantana, daylily, yellowtail, horse chestnut, etc. Binder: casein, carboxymethylcellulose, sodium salt, pectin, starch, methylcellulose, ethylcellulose, sodium alginate,
polyvinyl alcohol, polyvinylpyrrolidone,
Polyvinyl methyl ether, karaya gum, locust bean gum, tragacanth gum, carrageenan, carbobol, acacia gum, agar, etc. Tar-based pigments (xanthine, etc.) for pharmaceuticals, quasi-drugs, and cosmetics, surfactants (anionic, cationic, amphoteric, and nonionic), ascorbic acid or its salts, alums, fragrances, bactericides, reduction agents etc. Further, as an aqueous bath additive, a composition containing the above-mentioned various components can be balanced with an aqueous solvent. Next, Examples and Comparative Examples of the present invention will be shown to specifically explain the effects of the present invention. Prior to explaining each example, a specific method for preparing an aloe fraction and a test method for smooth feeling imparting performance and storage stability will be explained. The compositions used in each example were stored in paper tubes at 45°C for 7 days. Preparation example of aloe fraction 1 10 kg of aloe leaves are crushed in a mixer,
After filtration with cotton cloth and natural filtration with paper, 7.5 kg of slightly opaque yellow-green sap was obtained. Next, this sap was concentrated to 3.7 kg at room temperature and under a 300 mmHg reduction. Add 300g of powdered activated carbon to this,
After stirring at room temperature for about 30 minutes, the mixture was suctioned and filtered using paper, and then the activated carbon was washed with water and the washing liquid was added to the liquid. This liquid was concentrated under reduced pressure with an aspirator at a bath temperature of 40°C, and further vacuum-dried to obtain 170 g of white powder. Production example 2 Crush 10 kg of Kidachi aloe leaves with a mixer,
After filtration with cotton cloth and natural filtration with paper, 7.5 kg of slightly opaque yellow-green sap was obtained. Next, this sap was heated at 70° C. for 30 minutes under a reduced pressure of 300 mmHg to obtain 3.7 kg of concentrated sap. After adding 300g of powdered activated carbon to this and stirring at room temperature for about 30 minutes,
It was filtered by suction using paper, and then the activated carbon was washed with water and the washing solution was added to the solution. Pour this solution into a bath at a temperature of 40℃.
The mixture was concentrated under reduced pressure using an aspirator and further dried in vacuo to obtain 172 g of white powder. Production example 3 10 kg of Kidachi aloe leaves are processed in the order of food slicer, pulper, and finisher to produce green sap.
Obtained 7.7Kg. 700 g of powdered activated carbon was added to this sap, stirred at room temperature for about 30 minutes, and then passed through a filter press. This liquid was concentrated to about 1/5 volume under reduced pressure using an aspirator while heating to a bath temperature of 40°C to obtain 1.6 kg of concentrate. Add 0.8 ethanol to this, stir for 30 minutes,
After standing at room temperature for about 1 day, the precipitated white precipitate was suctioned and filtered using paper to obtain a liquid. This was concentrated under reduced pressure using an aspirator at a bath temperature of 40°C, and further vacuum-dried to obtain 116 g of a white-yellow powder. [Comparative production example 1] Crush 10 kg of Kidachi aloe leaves with a mixer,
After filtration with cotton cloth and natural filtration with paper, 7.5 kg of slightly opaque yellow-green sap was obtained. This sap was freeze-dried to obtain 210 g of deep brown powder. Test method 1 (Smooth feeling imparting performance) One of the left and right forearms of five panelists with dry skin was treated with a commercially available bath additive composition described below.
The other was immersed in bath water at 42°C containing 100 ppm of the bath agent composition of this invention for 10 minutes, then towel-dried, and the smoothness of the skin was compared after 10 minutes of towel-drying. Evaluation was made using the following criteria. Evaluation criteria: ◎...Very superior effect compared to commercial products 〇...Very superior effect compared to commercial products △...Slightly superior effect compared to commercial products ×...Equivalent to commercial products Test method 2 which is less effective or less effective (Storage stability) The storage stability of the bath agent composition in terms of fragrance and color tone was evaluated using the following criteria by pairwise comparison with commercially available products. Evaluation criteria ◎...No change observed compared to the commercial product 〇...Change equivalent to the commercial product observed, but not to the extent that it poses a problem in terms of commercial value. △...A slight change is observed compared to the commercial product ×...A significant change is observed compared to the commercial product The component composition of the commercial product used was as follows. Sodium sulfate 58% (weight) Sodium hydrogen carbonate 40% Liquid paraffin 0.5% Uranine pigment 0.3% Fragrance 1.2% Test example A bath agent composition having the composition shown in Table 1 was prepared, and its smoothing performance and storage were evaluated. Stability was tested. The results are shown in the same table. In addition, in the table, the composition is shown in weight%.
【表】【table】
【表】
下記の組成(重量%)を有する浴用剤組成物を
調製し、試験したところ市販品に比べ優れた保存
安定性と入浴後のへのなめらかさ付与効果を示し
た。
実施例13 (顆粒状)
炭酸水素ナトリウム 50
硫酸ナトリウム 46.5
アロエ分画物(製造例1) 1
ラノリン 0.5
ラウニン色素 0.5
香 料 1.5
計100
実施例14 (粉末状)
炭酸水素ナトリウム 50
炭酸ナトリウム 3
硫酸ナトリウム 43.5
アロエ分画物(製造例2) 1
流動パラフイン 0.5
ウラニン色素 0.5
香 料 1.5
計100
実施例15 (液状)
プロピレングリコール 50
エタノール 20
硫酸ナトリウム 5
アロエ分画物(製造例3) 1
ラノリン 0.5
アボガド油 0.5
ウラニン色素 0.5
香 料 1.5
純 水 21
計100
実施例16 (発泡錠)
硫酸ナトリウム 8
炭酸水素ナトリウム 30
炭酸ナトリウム 19
アロエ分画物(製造例1) 1
クエン酸 20
酒石酸 10
こはく酸 10
ウラニン色素 0.5
香 料 1.5
計100[Table] A bath agent composition having the following composition (wt%) was prepared and tested, and it showed superior storage stability and smoothness after bathing compared to commercially available products. Example 13 (granular) Sodium hydrogen carbonate 50 Sodium sulfate 46.5 Aloe fraction (Production example 1) 1 Lanolin 0.5 Raunin pigment 0.5 Flavor 1.5 Total 100 Example 14 (Powder) Sodium hydrogen carbonate 50 Sodium carbonate 3 Sodium sulfate 43.5 Aloe fraction (Production example 2) 1 Liquid paraffin 0.5 Uranine pigment 0.5 Flavor 1.5 Total 100 Example 15 (liquid) Propylene glycol 50 Ethanol 20 Sodium sulfate 5 Aloe fraction (Production example 3) 1 Lanolin 0.5 Avocado oil 0.5 Uranine pigment 0.5 Flavor 1.5 Pure water 21 total 100 Example 16 (Effervescent tablet) Sodium sulfate 8 Sodium hydrogen carbonate 30 Sodium carbonate 19 Aloe fraction (Production example 1) 1 Citric acid 20 Tartaric acid 10 Succinic acid 10 Uranine pigment 0.5 Fragrance 1.5 total 100
Claims (1)
分画物を含有する浴用剤組成物。1. A bath agent composition containing an aloe fraction obtained by treating aloe sap with activated carbon.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58180664A JPS6072812A (en) | 1983-09-30 | 1983-09-30 | Bath agent composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58180664A JPS6072812A (en) | 1983-09-30 | 1983-09-30 | Bath agent composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6072812A JPS6072812A (en) | 1985-04-24 |
JPS6324490B2 true JPS6324490B2 (en) | 1988-05-20 |
Family
ID=16087150
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58180664A Granted JPS6072812A (en) | 1983-09-30 | 1983-09-30 | Bath agent composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6072812A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61286317A (en) * | 1985-06-13 | 1986-12-16 | Osaka Chem Lab | Bathing agent |
JPS6256410A (en) * | 1985-09-06 | 1987-03-12 | Soken:Kk | Production of cosmetic and bathing agent from aloe, mugwort and adlay |
JPH0663285U (en) * | 1993-02-09 | 1994-09-06 | 有限会社橋谷鉄工所 | Temporary placement device for manual power tools |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5815918A (en) * | 1981-07-21 | 1983-01-29 | Lion Corp | Preparation of physiologically active substance from aloe |
-
1983
- 1983-09-30 JP JP58180664A patent/JPS6072812A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5815918A (en) * | 1981-07-21 | 1983-01-29 | Lion Corp | Preparation of physiologically active substance from aloe |
Also Published As
Publication number | Publication date |
---|---|
JPS6072812A (en) | 1985-04-24 |
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