JPS62283916A - Sanitary ware having staggered dissolution timing - Google Patents
Sanitary ware having staggered dissolution timingInfo
- Publication number
- JPS62283916A JPS62283916A JP61128324A JP12832486A JPS62283916A JP S62283916 A JPS62283916 A JP S62283916A JP 61128324 A JP61128324 A JP 61128324A JP 12832486 A JP12832486 A JP 12832486A JP S62283916 A JPS62283916 A JP S62283916A
- Authority
- JP
- Japan
- Prior art keywords
- components
- component
- water
- dissolution
- effect
- 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
- 238000004090 dissolution Methods 0.000 title claims abstract description 32
- 239000006185 dispersion Substances 0.000 claims abstract description 15
- 239000000049 pigment Substances 0.000 claims abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000004480 active ingredient Substances 0.000 claims description 20
- 239000003205 fragrance Substances 0.000 claims description 14
- 239000002775 capsule Substances 0.000 abstract description 38
- 239000000203 mixture Substances 0.000 abstract description 20
- 102000004190 Enzymes Human genes 0.000 abstract description 17
- 108090000790 Enzymes Proteins 0.000 abstract description 17
- 230000000694 effects Effects 0.000 abstract description 16
- 238000003287 bathing Methods 0.000 abstract description 11
- 229920003169 water-soluble polymer Polymers 0.000 abstract description 4
- 239000003463 adsorbent Substances 0.000 abstract description 3
- 239000002304 perfume Substances 0.000 abstract description 3
- 239000011782 vitamin Substances 0.000 abstract description 3
- 229940088594 vitamin Drugs 0.000 abstract description 3
- 229930003231 vitamin Natural products 0.000 abstract description 3
- 235000013343 vitamin Nutrition 0.000 abstract description 3
- 239000003814 drug Substances 0.000 abstract description 2
- 229940079593 drug Drugs 0.000 abstract description 2
- 150000003722 vitamin derivatives Chemical class 0.000 abstract description 2
- 239000000306 component Substances 0.000 abstract 13
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 238000013329 compounding Methods 0.000 abstract 1
- 230000002255 enzymatic effect Effects 0.000 abstract 1
- 230000001976 improved effect Effects 0.000 abstract 1
- 239000008187 granular material Substances 0.000 description 26
- 238000000034 method Methods 0.000 description 25
- 239000000654 additive Substances 0.000 description 7
- 235000019646 color tone Nutrition 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000001856 Ethyl cellulose Substances 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 235000010980 cellulose Nutrition 0.000 description 3
- 239000003599 detergent Substances 0.000 description 3
- 229920001249 ethyl cellulose Polymers 0.000 description 3
- 235000019325 ethyl cellulose Nutrition 0.000 description 3
- 230000001815 facial effect Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 235000002639 sodium chloride Nutrition 0.000 description 3
- 229920000945 Amylopectin Polymers 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- 229920002907 Guar gum Polymers 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 235000010418 carrageenan Nutrition 0.000 description 2
- 239000000679 carrageenan Substances 0.000 description 2
- 229920001525 carrageenan Polymers 0.000 description 2
- 229940113118 carrageenan Drugs 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 239000008273 gelatin Substances 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000011852 gelatine desserts Nutrition 0.000 description 2
- 239000000665 guar gum Substances 0.000 description 2
- 235000010417 guar gum Nutrition 0.000 description 2
- 229960002154 guar gum Drugs 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 2
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 150000004804 polysaccharides Chemical class 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 235000017550 sodium carbonate Nutrition 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- 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 2
- 241000196324 Embryophyta Species 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 101710180316 Protease 2 Proteins 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- -1 Sulfate ester Chemical class 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 239000013040 bath agent Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229960002900 methylcellulose Drugs 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 229960000292 pectin Drugs 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 229910000031 sodium sesquicarbonate Inorganic materials 0.000 description 1
- 235000018341 sodium sesquicarbonate Nutrition 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000003826 tablet Substances 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
- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Cosmetics (AREA)
Abstract
Description
【発明の詳細な説明】
３、発明の詳細な説明
（イ） 産業上の利用分野
本発明は、複数の有効成分、色素、香料等を含有するサ
ニタリー商品に関する。Detailed Description of the Invention 3. Detailed Description of the Invention (a) Field of Industrial Application The present invention relates to sanitary products containing a plurality of active ingredients, pigments, fragrances, and the like.
（ロ） 従来の技術
たとえば、サニタリー商品の一つである入浴剤は、液状
、粉状、顆粒状或は打錠を問わず、有効成分、色素、香
料等の全ての組成成分を、単に均一に混合、あるいは乳
化混合することによって組成しており、入浴剤の使用時
においては、これらの組成成分は、全て同時若しくはほ
ぼ同時に溶解し、その効能を発揮するものである。(b) Conventional technology For example, bath additives, which are one of the sanitary products, are made by simply uniformly distributing all the active ingredients, pigments, fragrances, etc., regardless of whether they are in liquid, powder, granule or tablet form. When the bath agent is used, all of these components are dissolved at the same time or almost at the same time, and exhibit their effectiveness.
（ハ） 発明が解決しようとする問題点・しかし、入浴
剤の組成成分の効能に着目した場合、各組成成分は、そ
れぞれ独自の効能、効用を有するものであり、これら組
成成分を全部同時に溶解させ全効能を同時に発揮させる
よりも、各組成成分の発揮時間に時差を設けたほうが、
より人体に有効な入浴効果をもたらすことができる場合
もある。(c) Problems to be solved by the invention - However, when focusing on the efficacy of the components of bath salts, each component has its own efficacy and efficacy, and it is difficult to dissolve all of these components at the same time. It is better to create a time difference in the time each component exerts its effects than to exert all its effects at the same time.
In some cases, it may be possible to bring about a bathing effect that is more effective for the human body.
また、従来の入浴剤の組成成分は、浴湯に投入と同時に
完全に溶解し、浴湯の色を単一色からなる所望の色に変
えるのみであり、入浴者の視覚をたのしませるという面
で充分ではない。In addition, the components of conventional bath additives completely dissolve as soon as they are added to the bath water, and only change the color of the bath water to a desired color consisting of a single color, which is said to be visually pleasing to the bather. not enough in terms of
以上のことは、入浴剤以外のサニタリー商品。The above are sanitary products other than bath additives.
例えば、洗顔剤、洗濯用洗剤等においても同様である。For example, the same applies to facial cleansers, laundry detergents, and the like.
本発明は、上記問題点を解決することができるサニタリ
ー商品を提供することを目的とする。An object of the present invention is to provide a sanitary product that can solve the above problems.
（ニ） 問題点を解決するための手段
本発明は、有効成分、色素、香料等、複数の組成成分を
含有し、かつそれら組成成分の浴湯又は水等への分散・
溶解速度を相互に異ならせたことを特徴とする時差溶解
性のサニタリー商品に係るものである。(d) Means for Solving the Problems The present invention contains a plurality of compositional components such as active ingredients, pigments, fragrances, etc., and the dispersion and dispersion of these compositional components in bath water, water, etc.
This invention relates to sanitary products with staggered dissolution characterized by mutually different dissolution rates.
本発明において、分散・溶解速度を相互に相違させる方
法としては、水溶性カプセルを用いる方法や、組成成分
を水溶性高分子組成物に配合する方法、あるいは多孔性
吸着物に吸着させる方法などの技術がある。In the present invention, methods for making the dispersion and dissolution rates different from each other include a method using water-soluble capsules, a method of blending the constituent components into a water-soluble polymer composition, a method of adsorbing the components to a porous adsorbent, etc. There is technology.
ここに、水溶性カプセルを用いた分散・溶解速度の相違
方法とは、カラギーナン、メチルセルロース、ペクチン
、アルギン酸、アミロペクチン、グアガム、エチルセル
ロース、ヒドロキシエチルセルロース、ｈルボキシメチ
ルセルＯ−ス等の多糖類や、セルロース誘導体の他、ゼ
ラチンやポリビニルアルコール等組成による水溶性のカ
プセルによって、サニタリー製品の全であるいはその一
部の組成成分を被包することによって行なうものである
。Here, the different methods of dispersion and dissolution rate using water-soluble capsules include polysaccharides such as carrageenan, methylcellulose, pectin, alginic acid, amylopectin, guar gum, ethylcellulose, hydroxyethylcellulose, h-ruboxymethylcellulose, This is done by encapsulating all or some of the components of the sanitary product in a water-soluble capsule made of gelatin, polyvinyl alcohol, etc. in addition to cellulose derivatives.
また、水溶性高分子に配合することによる分散、溶解速
度の相違方法とは、ポリビニルアルコール、エチルセル
ロース、とドロキシエチルセルロース、ヒドロキシプロ
ピルセルロース、カルボキシメチルセルロースなどの水
溶性高分子組成物中に、サニタリー製品の全てのあるい
は一部の組成成分を練り込み、乾燥し、成型することに
よって行なうものである。In addition, the difference in dispersion and dissolution rate by blending with water-soluble polymers refers to the differences in dispersion and dissolution rates when blended with water-soluble polymers such as polyvinyl alcohol, ethyl cellulose, droxyethyl cellulose, hydroxypropyl cellulose, carboxymethyl cellulose, etc. in sanitary products. This is done by kneading all or some of the ingredients, drying, and molding.
また、多孔性吸着物に吸着させることによる分散溶解速
度の相違方法とは、塩化ナトリウム、硫酸ナトリウム、
炭酸水素ナトリウム、炭酸ナトリウムなどの多孔性結晶
体′に、サニタリー製品の全て又は一部の組成成分を吸
着させることによって行うものである。In addition, the different methods of dispersion dissolution rate by adsorption to porous adsorbents include sodium chloride, sodium sulfate,
This is done by adsorbing all or some of the components of the sanitary product onto a porous crystal such as sodium hydrogen carbonate or sodium carbonate.
また、造粒化によって、分散・溶解速度を相互に相違さ
せることもできる。Furthermore, by granulation, the dispersion and dissolution rates can be made different.
本発明によるサニタリー商品の分散・溶解速度は以上の
方法を組合わせることによっても異ならせることができ
る。The dispersion/dissolution rate of sanitary products according to the present invention can also be varied by combining the above methods.
（ホ） 作用・効果
以上説明した構成により、本発明は、以下の効果を奏す
る。(e) Actions and Effects With the configuration described above, the present invention provides the following effects.
■溶解速度を組成成分ごとに異ならせることができるの
で、効能、効果作用を多段的に行わせることができる。(2) Since the dissolution rate can be varied for each component, efficacy and effects can be achieved in multiple stages.
例えば、入浴剤や洗顔剤の場合、第１の有効成分によっ
て皮膚をなめらかにし、次に酵素成分を拡開した皮膚面
に作用させ、その侵、生薬を作用させる等、サニタリー
製品を使用した効果を最大に上げることができる。For example, in the case of bath salts and facial cleansers, the first active ingredient smooths the skin, then the enzyme component acts on the expanded skin surface, and the effects of using sanitary products include the action of crude drugs. can be maximized.
■洗濯用洗剤や入浴剤として用いた場合、組成成分の色
調を多層化することにより、使用時色調が多段的に変化
し、消費者の視覚を楽しませることができる。■When used as a laundry detergent or bath additive, by layering the color tones of the constituent ingredients, the color tone changes in multiple stages during use, making it possible for consumers to enjoy their visual sense.
■入浴剤として用いた場合、組成層の温度溶解性を調節
することにより入浴温度の変化（上昇）で色調、香り、
有効成分が多段的に溶解し、入浴を楽しむことができ、
又有効成分溶解と、入浴温度の調節が可能であり、従っ
て効能効果をより助長することができ、入浴温度をも知
ることができる。■When used as a bath additive, by adjusting the temperature solubility of the composition layer, changes in bathing temperature (increase) can change the color tone, fragrance, etc.
The active ingredients are dissolved in multiple stages, allowing you to enjoy bathing.
In addition, it is possible to dissolve the active ingredients and adjust the bathing temperature, so the efficacy can be further enhanced and the bathing temperature can also be determined.
■ビタミン、酵素などの不安定成分をカプセルなどの方
法で、各々を多層化することにより、これらの成分の長
期的安定を図ることができ、従って商品の長期的効能、
・効果を呈することができる。■ By layering unstable ingredients such as vitamins and enzymes in capsules or other methods, it is possible to stabilize these ingredients over the long term, thereby increasing the long-term efficacy of the product.
・Can exhibit effects.
（へ） 実施例
［実施例１］
本実施例は、サニタリー製品が入浴剤である場合の組成
成分である有効成分、酵素、色素、香料等の分解・溶解
速度を相違させるための具体的方法を示す。(f) Example [Example 1] This example describes a specific method for differentiating the decomposition/dissolution rate of active ingredients, enzymes, pigments, fragrances, etc., which are the composition components when the sanitary product is a bath additive. shows.
ａ） 第１図に示す形態は、炭酸水素ナトリウム、塩化
ナトリウム、炭酸ナトリウム、硫酸ナトリウム、セスキ
炭酸ナトリウム、ホウ砂、硫化カワウム、など無機塩類
に、各種植物成分を配合した粉末有効成分１中に、顆粒
化した蛋白分解酵素２、カラギーナン、メチルセルロ−
ス
ルギン酸、アミロペクチン、グアガム、エチルセルロー
ス、ヒドロキシエチルセルロース、ヒドロキシプロピル
セルロース、カルボキシメチルセルロース等の多糖類や
、セルロース誘導体の他、ゼラチンやポリビニルアルコ
ール等組成による水溶性の香料カプセル３、同色素カプ
セル４、及び同色素カプセル５を混合したものである。a) The form shown in Figure 1 is a powdered active ingredient 1 containing inorganic salts such as sodium bicarbonate, sodium chloride, sodium carbonate, sodium sulfate, sodium sesquicarbonate, borax, and sulfate, and various plant ingredients. , granulated protease 2, carrageenan, methylcellulose
In addition to polysaccharides such as sulginic acid, amylopectin, guar gum, ethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, and carboxymethyl cellulose, and cellulose derivatives, water-soluble fragrance capsules 3 and pigment capsules 4 with compositions such as gelatin and polyvinyl alcohol are used. This is a mixture of dye capsules 5.
ここに、各組成成分の配合及び溶解時間の一例を示すと
、第１表の如くなる。Table 1 shows an example of the composition and dissolution time of each component.
ト の ｆ−Ｃ４
第１表から明らかなように、入浴剤の各組成成分は相互
に分散・溶解温度を異にするので、浴湯内に投入される
と、まず粉体有効成分１が溶解し、ついで酵素顆粒２、
色素カプセル４、色素カプセル５、香料カプセル３の順
に時差を保持しながら溶解することになる。f-C4 As is clear from Table 1, each component of a bath additive has a different dispersion/dissolution temperature. Then, enzyme granules 2,
The dye capsule 4, the dye capsule 5, and the fragrance capsule 3 are dissolved in this order while maintaining the time difference.
このように、溶解速度を組成成分毎に異ならせることに
よって、それらの効能、効果を多段的に行わせることが
でき、最適の入浴効果をあげることができる。In this way, by varying the dissolution rate for each component, the efficacy and effect of each component can be achieved in multiple stages, and the optimal bathing effect can be achieved.
また、組成成分の色調を多層化することにより、使用時
色調が多段的に変化し、入浴者の視覚を楽しませること
ができる。Furthermore, by layering the color tones of the composition components, the color tone changes in multiple stages during use, making it possible to enjoy the visual sense of bathers.
また、組成層の温度溶解性を調節することにより入浴温
度の変化（上昇〉で色調、香り、有効成分が多段的に溶
解し、入浴を楽しむことができ、又有効成分溶解と、入
浴ｔＡ度の調節が可能であり、従って効能、効果をより
助長することができ、入浴温度を知ることができる。In addition, by adjusting the temperature solubility of the composition layer, the color tone, scent, and active ingredients will dissolve in multiple stages as the bathing temperature changes (increase), allowing you to enjoy bathing. It is possible to adjust the bathing temperature, therefore, the efficacy and effect can be further enhanced, and the bathing temperature can be known.
ｂ） 第２図に示す方法は、粉体有効成分１０中に、酵
素カプセル１１、着色顆粒１２、着色顆粒１３及び＠香
顆粒１４を混合したものである。b) In the method shown in FIG. 2, enzyme capsules 11, colored granules 12, colored granules 13 and @flavor granules 14 are mixed in powdered active ingredient 10.
この場合、溶解は粉体有効成分１０→着５顆粒１４→着
色顆粒１２→着色顆粒１３→醇素カプセル１１の順序で
行われる。In this case, the dissolution is carried out in the order of powder active ingredient 10 → colored granules 14 → colored granules 12 → colored granules 13 → sulfur capsules 11.
なお、各組成成分の内容は、はぼ方法ａ）の場合と同様
である。Note that the contents of each composition component are the same as in the case of Habo method a).
Ｃ） 第３図に示す方法は、有効成分カプセル２、０と
、色素カプセル２１と、色素カプセル２２と、香料カプ
セル２３とを混合したちのである。C) The method shown in FIG. 3 involves mixing active ingredient capsules 2,0, dye capsules 21, dye capsules 22, and fragrance capsules 23.
この場合、溶解は有効成分カプセル２０→占料カブはル
２３→邑素カプセル２１→色素力プロル２２、の順序で
行われる。In this case, the dissolution is carried out in the order of active ingredient capsule 20 -> Sanryu Kaburu 23 -> Eupso Capsule 21 -> Pigment Power Prol 22.
なお、各組成成分の内容は、はぼ方法ａ）の場合と同様
である。Note that the contents of each composition component are the same as in the case of Habo method a).
〔１） 第４図に示す方法は、有効成分顆粒３０と、酵
素顆粒３１と、着色顆粒３２と、υ色顆粒３３と、着香
顆粒３４とを混合したものである。[1] In the method shown in FIG. 4, active ingredient granules 30, enzyme granules 31, colored granules 32, υ-colored granules 33, and flavored granules 34 are mixed.
この場合、溶解は、有効成分顆粒３０−４着香顆粒３４
→肴邑顆粒３２→着色顆粒３３→酵素顆粒３１の順序で
行われる。In this case, dissolution includes active ingredient granules 30-4 flavoring granules 34
This is carried out in the following order: → Soybean granules 32 → Colored granules 33 → Enzyme granules 31.
なお、各組成成分の内容は、はぼ方法ａ）の場合と同様
である。Note that the contents of each composition component are the same as in the case of Habo method a).
ｅ） 第５図に示す方法は、香料カプセル４０を核とし
てその外周に色素カプセル４１、有効成分カプセル４２
、及び酵素カプセル４３を多層にカプセル化したもので
ある。e) The method shown in FIG. 5 uses a fragrance capsule 40 as a core and a pigment capsule 41 and an active ingredient capsule 42 around the core.
, and an enzyme capsule 43 are encapsulated in multiple layers.
この場合、溶解は酵素カプセル４３→有効成分カプセル
４２→色素カプセル４１→香料カプセル４ ’Ｃの順序
で行われる。In this case, dissolution is performed in the order of enzyme capsule 43 → active ingredient capsule 42 → dye capsule 41 → fragrance capsule 4'C.
なお、各組成成分の内容は、はぼ方法ａ）の場合と同様
である。Note that the contents of each composition component are the same as in the case of Habo method a).
ｆ） 第６図に示す方法は、粉体有効成分カプセル５０
中に、酵素カプセル５１、色素カプセル５２、色素カプ
セル５３、及び香料カプセル５４を混合したものである
。f) The method shown in FIG.
Inside, an enzyme capsule 51, a pigment capsule 52, a pigment capsule 53, and a fragrance capsule 54 are mixed.
この場合、溶解は有効成分カプセル５０→酵素力プセル
５１→香料カプセル５４→色素カプセル５２→色素カプ
セル５３の順序で行われる。In this case, dissolution is performed in the order of active ingredient capsule 50 → enzyme capsule 51 → perfume capsule 54 → dye capsule 52 → dye capsule 53.
なお、各組成成分の内容は、はぼ方法ａ）の場合と同様
である。Note that the contents of each composition component are the same as in the case of Habo method a).
［実施例２］
本実施例は、サニタリー製品が顆粒状洗顔剤である場合
の組成成分である基剤、酵素、香料等の分解・溶解速度
を相違させるための具体的方法を示す。[Example 2] This example shows a specific method for varying the decomposition/dissolution rates of the base, enzyme, fragrance, etc., which are the composition components when the sanitary product is a granular facial cleanser.
本実施例に係るサニタリー製品は、第７図に示す方法を
有するものであり、基剤顆粒６０と、酵素顆粒６１と、
着香顆粒６２と、ビタミン８２Ｂ粒６３とを混合したも
のである。The sanitary product according to this example has the method shown in FIG. 7, and includes base granules 60, enzyme granules 61,
This is a mixture of flavoring granules 62 and vitamin 82B granules 63.
かかるサニタリー製品の組成及び溶解速度を以下の第２
表に示す。The composition and dissolution rate of such sanitary products are as follows:
Shown in the table.
ＬＯ囚の
本実施例２においても上・記実施例１と同様な溶解速度
の相違に基づく効果が認められた。In this Example 2 of the LO prisoner, the same effect as in Example 1 above based on the difference in dissolution rate was observed.
［実施例３〕
本実施例は、サニタリー製品が酵素配合の洗濯用洗剤で
ある場合の組成成分である基剤、酵素、色素、香料等の
分散・溶解速度を相違さぼるための具体的方法を示す。[Example 3] This example describes a specific method for improving the dispersion/dissolution rate of the base, enzyme, pigment, fragrance, etc., which are the composition components when the sanitary product is an enzyme-containing laundry detergent. show.
本実施例に係るサニタリー製品は、第８図に示す方法を
有するものであり、基剤顆粒７ｏと、酵素顆粒７１と、
着香顆粒７２と、着色顆粒７３とを混合したものである
。The sanitary product according to this example has the method shown in FIG. 8, and includes base granules 7o, enzyme granules 71,
This is a mixture of flavored granules 72 and colored granules 73.
かかるサニタリー製品の組成及び溶解速度を以下の第３
表に示す。The composition and dissolution rate of such sanitary products are determined in the third section below.
Shown in the table.
処方
益赳！拉 粒径０直鎖アル
キルベンゼンスルホン酸ナトリウム高級アルコールＥＯ
付加物硫酸エステルナトリトリポリリン酸ナトリウム
ゼオライト
ケイ酸ナトリウム
硫酸ナトリウム
セッケン
カルボキシメチルセルロース
ポリエチレングリコール（分子量６０００ ）旺久！拉
粒径蛋白質分解酵素（１
０万単位／９）
１五随狡 粒径１色皿粒
粒径第３表
□ □
、７〜１．３ｍｍ
１７．０％
ラム ５．５
２０．０
６．３
１２．０ ９０％ 即溶解３３．７
３．２
０、２
２．１
１．５〜１．８ｍｍ
８．０％ ２０〜２５秒後溶解
３、０〜３．３ｍｍ １．０ ５〜８秒後
溶解２．０〜２．５ｍｍ １．０ １０〜
１５秒後溶解本実施例においても、上記実施例１．２と
同様・な溶解速度の相違に基づく効果が認められた。Prescription benefit! Particle size 0 linear alkylbenzene sulfonate sodium higher alcohol EO
Adducts Sulfate ester Sodium tripolyphosphate Zeolite Sodium silicate Sodium sulfate Sodium carboxymethyl cellulose Polyethylene glycol (molecular weight 6000) Oku! Particle size proteolytic enzyme (1
00,000 units/9) 150000 grain size 1 color dish grain
Particle size Table 3 □ □, 7-1.3mm 17.0% Ram 5.5 20.0 6.3 12.0 90% Instant dissolution 33.7 3.2 0, 2 2.1 1.5- 1.8mm 8.0% Dissolved after 20-25 seconds 3, 0-3.3mm 1.0 Dissolved after 5-8 seconds 2.0-2.5mm 1.0 10-
Dissolution after 15 seconds In this example as well, the same effect as in Example 1.2 based on the difference in dissolution rate was observed.
第１図〜第６図は、本発明の実施例１におけ（分散・溶
解速度の相違方法を示す説明図、第７し及び第８図は、
実施例２及び３における分散・ン；解速度の相違方法を
示す説明図である。
（１）：粉末有効成分
（２）：蛋自分解醇素
（３）二香料カプセル
（４）（５）：色素カプセル
特許出願人 白 石 忠 主
伐 理 人 松 尾 憲 −部落７図
第８図Figures 1 to 6 are explanatory diagrams showing different methods of dispersion and dissolution rates in Example 1 of the present invention, and Figures 7 and 8 are
FIG. 6 is an explanatory diagram showing a method for differentiating the dispersion and solution speed in Examples 2 and 3; (1): Powder active ingredient (2): Protein self-dissolving substance (3) Two-scented capsule (4) (5): Pigment capsule Patent applicant Tadashi Shiraishi Chief Director Ken Matsuo - Buraku 7 Figure 8
Claims (1)
、かつそれら含有成分の浴湯又は水等への分散・溶解速
度を相互に異ならせたことを特徴とする時差溶解性のサ
ニタリー商品。1) Staggered solubility sanitary products that contain multiple components such as active ingredients, pigments, and fragrances, and are characterized by having different dispersion and dissolution rates of these components in bath water, water, etc. merchandise.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61128324A JPH0714863B2 (en) | 1986-06-02 | 1986-06-02 | Staggered bath salts |
| JP12174090A JPH03128314A (en) | 1986-06-02 | 1990-05-10 | Bathing agent containing encapsulated material and dissolving with time-lag |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61128324A JPH0714863B2 (en) | 1986-06-02 | 1986-06-02 | Staggered bath salts |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12174090A Division JPH03128314A (en) | 1986-06-02 | 1990-05-10 | Bathing agent containing encapsulated material and dissolving with time-lag |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62283916A true JPS62283916A (en) | 1987-12-09 |
| JPH0714863B2 JPH0714863B2 (en) | 1995-02-22 |
Family
ID=14981960
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61128324A Expired - Fee Related JPH0714863B2 (en) | 1986-06-02 | 1986-06-02 | Staggered bath salts |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0714863B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20180020358A (en) * | 2016-08-17 | 2018-02-28 | 김민수 | A method for manufacturing a multiple-use bath preparation using natural ingredients, and the bath preparation manufactured the method |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4933905A (en) * | 1972-07-28 | 1974-03-28 | ||
| JPS5846019A (en) * | 1981-09-14 | 1983-03-17 | Kanebo Ltd | Nifedipine preparation with prolonged action |
| JPS5982311A (en) * | 1982-11-04 | 1984-05-12 | Shionogi & Co Ltd | Sustained release preparation of cephalexin |
| JPS5983952U (en) * | 1982-11-26 | 1984-06-06 | ア−ス製薬株式会社 | Solid cleaning agent for flush toilets |
| JPS601128A (en) * | 1983-06-15 | 1985-01-07 | Shionogi & Co Ltd | Long-acting cefaclor preparation |
| JPS604120A (en) * | 1983-06-22 | 1985-01-10 | Shionogi & Co Ltd | Pharmaceutical preparation of pinacidil of long acting type |
| JPS6293222A (en) * | 1985-10-21 | 1987-04-28 | Sunstar Inc | Formable bathing agent |
| JPS62223111A (en) * | 1986-03-26 | 1987-10-01 | Tsumura Juntendo Inc | Bathing agent composition |
-
1986
- 1986-06-02 JP JP61128324A patent/JPH0714863B2/en not_active Expired - Fee Related
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4933905A (en) * | 1972-07-28 | 1974-03-28 | ||
| JPS5846019A (en) * | 1981-09-14 | 1983-03-17 | Kanebo Ltd | Nifedipine preparation with prolonged action |
| JPS5982311A (en) * | 1982-11-04 | 1984-05-12 | Shionogi & Co Ltd | Sustained release preparation of cephalexin |
| JPS5983952U (en) * | 1982-11-26 | 1984-06-06 | ア−ス製薬株式会社 | Solid cleaning agent for flush toilets |
| JPS601128A (en) * | 1983-06-15 | 1985-01-07 | Shionogi & Co Ltd | Long-acting cefaclor preparation |
| JPS604120A (en) * | 1983-06-22 | 1985-01-10 | Shionogi & Co Ltd | Pharmaceutical preparation of pinacidil of long acting type |
| JPS6293222A (en) * | 1985-10-21 | 1987-04-28 | Sunstar Inc | Formable bathing agent |
| JPS62223111A (en) * | 1986-03-26 | 1987-10-01 | Tsumura Juntendo Inc | Bathing agent composition |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20180020358A (en) * | 2016-08-17 | 2018-02-28 | 김민수 | A method for manufacturing a multiple-use bath preparation using natural ingredients, and the bath preparation manufactured the method |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0714863B2 (en) | 1995-02-22 |
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|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |