JPS58105910A - Solid bath composition - Google Patents

Solid bath composition

Info

Publication number
JPS58105910A
JPS58105910A JP20414681A JP20414681A JPS58105910A JP S58105910 A JPS58105910 A JP S58105910A JP 20414681 A JP20414681 A JP 20414681A JP 20414681 A JP20414681 A JP 20414681A JP S58105910 A JPS58105910 A JP S58105910A
Authority
JP
Japan
Prior art keywords
bath
peg
bath agent
solid
bath composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP20414681A
Other languages
Japanese (ja)
Inventor
Tadashi Kato
正 加藤
Masao Takahashi
雅夫 高橋
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
MAI SUKINKEAA LAB KK
Original Assignee
MAI SUKINKEAA LAB KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by MAI SUKINKEAA LAB KK filed Critical MAI SUKINKEAA LAB KK
Priority to JP20414681A priority Critical patent/JPS58105910A/en
Publication of JPS58105910A publication Critical patent/JPS58105910A/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof
    • A61K8/66Enzymes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations

Abstract

PURPOSE:A solid bath composition, prepared by incorporating to a raw material and solidifying the resultant mixture stably and easily without deteriorating the component, and inhibiting the reaction and decomposition during the storage thereof without adversely affecting the human body, e.g. skin roughening. CONSTITUTION:A solid bath composition containing a raw material for the bath, particularly a foamable bath composition or bath composition containing an enzyme, and 30-70wt% polyethylene glycol (PEG). There is no fear in the composition of causing any reaction and decomposition during the storage thereof completely since the bath components, e.g. a foaming agent or enzyme, present in the raw material for the bath are wrapped separately in PEG and inhibited contact with the outside air. PEG having 950-3,700 average molecular weight or a mixture of PEG having various molecular weights may be preferably used after adjusting the average molecular weight of the mixture to said range, and the freezing point thereof is preferably 30-58 deg.C.

Description

【発明の詳細な説明】 本発明は固型浴剤組成物に関する。[Detailed description of the invention] The present invention relates to solid bath agent compositions.

一般に浴剤は粉末、顆粒、液体の形態で汎用せられてい
る。然しなから、粉末やaS浴剤の場合にはその製造の
際、所謂粉塵飛散の発生を避は得す、工業的不利なるを
免れなかつ九。他方液体浴剤の場合には粉塵飛散と云う
欠点は存しないが、重量が過大となると貴う欠点があり
、ま九粉末、顆粒、液体の何れも嵩高となるため、包装
段階、流通段階に於ける不便・不都合さは当業者の等し
く痛感するところであった。
Bath additives are generally available in powder, granule, and liquid forms. However, in the case of powders and aS bath additives, the production of so-called dust scattering is unavoidable, which is an unavoidable industrial disadvantage. On the other hand, liquid bath additives do not have the disadvantage of dust scattering, but they do have the disadvantage of being too heavy.Powders, granules, and liquids are all bulky, so they are difficult to handle at the packaging and distribution stages. Those skilled in the art are equally keenly aware of the inconvenience and inconvenience caused.

そζで、本発明者は斯かる従来の欠点を、固型浴剤を提
供することによシ解消すべく種々研究を重ねた結果、ポ
リエチレングリコール(以下PICGと称する。)を配
合すれば、浴剤成分を変質せしめることなく安定に、か
つ常温で容易に成型し得ると共に、得られ九固型浴剤は
肌アレ等何ら人体に悪影響を与えないと云う驚くべき事
実を見い出し、本発明な完成したものである・・ 従って、本発明は浴剤原料にポリエチレングリコールを
配合して成る固型浴剤組成物である。
Therefore, the present inventor has conducted various researches in order to solve these conventional drawbacks by providing a solid bath agent, and has found that if polyethylene glycol (hereinafter referred to as PICG) is blended, The inventors of the present invention have discovered the surprising fact that they can be stably and easily molded at room temperature without altering the bath additive components, and that the resulting solid bath additives do not have any adverse effects on the human body such as skin irritation. It has been completed... Therefore, the present invention is a solid bath agent composition comprising polyethylene glycol added to the bath agent raw materials.

本発明に於ける浴剤原料は、浴剤として使用可能なもの
であれば如何なるものでもよいが、特に発泡性浴剤組成
物、酵素含有浴剤組成物等の如く、大気中の水分によ〕
反応、分解し易い成分を含有する浴剤組成物の場合に最
龜効果的に実施される。
The bath agent raw materials in the present invention may be of any type as long as they can be used as bath agents, but in particular, materials that are sensitive to atmospheric moisture, such as foaming bath agent compositions and enzyme-containing bath agent compositions, may be used. ]
This is most effectively carried out in the case of bath agent compositions containing components that easily react and decompose.

因に1一般に発泡性浴剤は重炭酸す) IJウム、セス
キ炭酸ナトリウム等の塩基性無機化合物、酒石酸、クエ
ン酸等の酸性化合物及び芒硝、硼砂9食塩郷の混合組成
物であり、使用するにあたり、浴湯中で互に反応してC
O。
In general, effervescent bath additives are a mixture of basic inorganic compounds such as bicarbonate, sodium sesquicarbonate, acidic compounds such as tartaric acid and citric acid, and sodium chloride salts such as mirabilite and borax. , they react with each other in bath water and C
O.

ガスの気泡を発生させるものであるが、保存中大気中の
水分によシ自然に反応して発泡性を喪失すると云う欠点
を有するものであり九。
Although it generates gas bubbles, it has the disadvantage that it naturally reacts with moisture in the atmosphere during storage and loses its foaming properties.9.

そこで、従来は斯かる欠点を改善するために、芒硝、澱
粉等の吸湿剤を加えることが行なわれていたが、その効
果は実質上殆ど認められないものであった。
Therefore, conventionally, in order to improve such defects, moisture absorbing agents such as Glauber's salt and starch have been added, but the effects have been practically unrecognized.

また、酵素含有浴剤の場合も、当該酵素が吸湿性が強く
大気中では不安定であるため、気密性容器に入れると共
に、酵素の最も安定な pH域6〜8に保持するよう無
機塩を加えて安定性の維持を図ってい九が、未だ充分な
る効果が得られていないのが実情である。
In the case of enzyme-containing bath additives, the enzymes are highly hygroscopic and unstable in the atmosphere, so they should be placed in an airtight container and inorganic salts should be added to keep the enzymes in the most stable pH range of 6 to 8. In addition, although efforts have been made to maintain stability, the reality is that sufficient effects have not yet been obtained.

然るとき、本発明固型浴剤組成物に於ては、浴剤原料中
に発泡剤、酵素等が存在した場合、これら発泡剤、酵素
等はPKGKよって包み込まれた状態になっているため
、各浴剤成分は互に隔離され、かつ外気との接触が阻止
されているので、保存中の反応、分解の慣れを完全に払
拭し得るものである。
In this case, in the solid bath agent composition of the present invention, if foaming agents, enzymes, etc. are present in the bath agent raw materials, these foaming agents, enzymes, etc. are in a state of being encapsulated by PKGK. Since the bath agent components are isolated from each other and prevented from coming into contact with the outside air, reactions and decomposition during storage can be completely eliminated.

すなわち、本願発明は浴剤原料として発泡性浴剤組成物
、酵素含有浴剤組成物を用い九場合には、当該浴剤組成
物の上記の如き欠点を一挙に解消し得る優れた効果を与
えるものである。
That is, when the present invention uses a foaming bath agent composition or an enzyme-containing bath agent composition as a raw material for a bath agent, it provides an excellent effect that can eliminate the above-mentioned drawbacks of the bath agent composition at once. It is something.

本発明に用いられるPICGは平均分子量950〜37
00のもの、若しくは各種分子量のPIGを当該平均分
子量値となる如く適宜併用したものが好ましく、ま九そ
の凝固点は30〜58℃のものが好適である。
PICG used in the present invention has an average molecular weight of 950 to 37
00, or those in which PIG of various molecular weights are appropriately used in combination so as to obtain the average molecular weight value, and those having a freezing point of 30 to 58°C are preferable.

PIGの配合量は、浴剤成分、使用時に於ける浴剤の状
態によって異なるが、含有率が30〜70重量憾となる
如く配合するのが喪い結果を与える。
The amount of PIG to be blended varies depending on the bath additive components and the condition of the bath additive at the time of use, but blending in such a way that the content is 30 to 70% by weight will give the best results.

本発明固型浴剤組成物は、例えば上記の如き浴剤原料と
PEGとを乾燥状態にて混合した後加熱溶解し、盗いて
均一に攪拌して型に流し込み、冷却成型するか、若しく
は同化後型打ちするととくよって製造される。
The solid bath agent composition of the present invention can be prepared, for example, by mixing the above-mentioned bath agent raw materials and PEG in a dry state, heating and dissolving the mixture, stirring it uniformly, pouring it into a mold, cooling and molding it, or by assimilating it. It is manufactured by stamping and twisting.

次に、試験例を挙げて本発明の詳細な説明する。Next, the present invention will be explained in detail by giving test examples.

α) 肌アレ試験 PICGを30唾、70s各々含有する本発明浴剤試料
につき、家庭婦人50人(25〜50才)をパネラ−と
して、連続各IO回使川波の官能評価によシ肌アレ試験
を行ったところ、何ら肌アレの影響は認められなかった
α) Skin irritation test For the bath salt samples of the present invention containing PICG for 30 s and 70 s, 50 household women (aged 25 to 50 years old) were used as a panel to evaluate skin irritation using Kawanami's sensory evaluation for each consecutive IO test. When tested, no skin irritation was observed.

伐)発泡性試験 各試料100fを相対ル度85嘔、温度20℃の環境中
に48時間放置後、水温40℃、500COの水中に投
入して、発生するCO,ガス量及びガス発生持続時間を
測定した。
Foaming test) 100 f of each sample was left in an environment with a relative degree of 85 °C and a temperature of 20 °C for 48 hours, and then put into water with a temperature of 40 °C and 500 CO to measure the amount of CO generated, the amount of gas, and the duration of gas generation. was measured.

この結果を第1表に示す。The results are shown in Table 1.

第1表 試料の説明 比較品1は後記実施例1の成分中PIGを除いて得九粉
末浴剤組成物、本発明品1〜5は後記実施例1の成分中
PKGt−fi該含有率にして得た固型浴剤組成物であ
る。岡、使用し九PIGの平均分子量は表中括弧内に表
記した。
Table 1 Description of samples Comparative product 1 is a powdered bath agent composition obtained by excluding PIG in the components of Example 1 described later, and products 1 to 5 of the present invention are obtained by excluding the PKGt-fi content in the components of Example 1 described later. This is the solid bath agent composition obtained. The average molecular weight of the nine PIGs used is shown in parentheses in the table.

上記表から明らかな如く、本発明浴剤組成物は従来浴剤
に比し、顕著な発泡効果を有するものである。
As is clear from the above table, the bath additive composition of the present invention has a remarkable foaming effect compared to conventional bath additives.

(3)  酵素活性試験 各試料を相対湿度85鳴、温度20℃の環境中に保存し
、一定時間ごとに試料を水500114に溶解してその
酵素活性残存率を測定し九。この結果を第2表に示す。
(3) Enzyme activity test Each sample was stored in an environment with a relative humidity of 85°C and a temperature of 20°C, and the remaining rate of enzyme activity was measured by dissolving the sample in water 500114 at regular intervals.9. The results are shown in Table 2.

第2表 罎 邊Y 比較品2は後記実施例3の成分中PIGを除いて得た粉
末浴剤組成物、本発明品6〜8は後記実施例3の成分中
PICGを当該含有率にして得九固型浴剤組成物である
。tL pmGは平均分子量4,000のものを使用し
た。
Table 2 Comparative product 2 is a powder bath agent composition obtained by excluding PIG from the components of Example 3 described later, and products 6 to 8 of the present invention are obtained by excluding PICG from the components of Example 3 described later. This is a solid bath agent composition. The tL pmG used had an average molecular weight of 4,000.

上記表から明らかな如く、本発明浴剤組成物は従来浴剤
に比し顕著な酵素活性の安定性を有する本のである。
As is clear from the above table, the bath additive composition of the present invention has remarkable stability in enzyme activity compared to conventional bath additives.

以下実施例を挙げて本発明を更に説明する。The present invention will be further explained below with reference to Examples.

実施例1゜ 重炭酸ナトリウム20t1重酒石酸ナトリウム201.
PEG(3,700)31f%芒硝20t1硼砂5t’
s食塩2 f %香料1.Of。
Example 1 Sodium bicarbonate 20t1 Sodium bitartrate 201.
PEG (3,700) 31f% mirabilite 20t1 borax 5t'
s Salt 2 f % Flavoring 1. Of.

フロレツセン(着色料)1.Ofを乾燥状態にて混合す
る。次いで加熱溶解せしめ先後、攪拌して均一にする。
Floretssen (coloring agent) 1. Mix Of in a dry state. The mixture is then heated and dissolved, and then stirred to make it uniform.

60℃で粘稠な液体となる。斯くして得られた浴剤組成
物の均一性を失なわしめないよう攪拌しながら冷却し、
42℃で型に流し込み、冷却成型するか、固化後常温で
型打ちして発泡性固型浴剤組成物を得る。
It becomes a viscous liquid at 60°C. Cool the bath agent composition obtained in this way while stirring so as not to lose its uniformity.
A foamable solid bath composition is obtained by pouring into a mold at 42° C. and cooling and molding, or after solidifying, molding at room temperature.

実施例2゜ 重炭酸ナトリウム25t1重酒石酸ナトリクム25F、
PEG(3,700)44F、芒硝3F、硼砂2t、食
塩0.5F、香料0.4t。
Example 2 Sodium bicarbonate 25t1 Sodium bitartrate 25F,
PEG (3,700) 44F, Glauber's Salt 3F, borax 2t, salt 0.5F, fragrance 0.4t.

フロレツセン(着色料)0.1fを組成分として、実施
例1と同様にして発泡性向型浴剤組成物を得る。
A foaming bath agent composition is obtained in the same manner as in Example 1 except that 0.1 f of floretscen (coloring agent) is used as a component.

実施例3゜ 蛋白質分解酵素1.Of、重酒石酸ナトリウム20f1
重炭酸ナトリウム20t1 PKG(3,700)30F%硼砂5F、芒硝20t1
食塩2fs 香料1.Of、フロレツセン(着色料)i
、orを組成分として、実施例1と同様にして酵素含有
固型浴剤組成物を得る。            。
Example 3゜Proteolytic enzyme 1. Of, sodium bitartrate 20f1
Sodium bicarbonate 20t1 PKG (3,700) 30F% borax 5F, Glauber's salt 20t1
Salt 2fs Flavoring 1. Of, floretssen (coloring agent) i
An enzyme-containing solid bath composition was obtained in the same manner as in Example 1 using , or as the ingredients. .

以上that's all

Claims (1)

【特許請求の範囲】 L 浴剤原料にポリエチレングリプールを配合して成る
固型浴剤組成物。 2 浴剤原料が発泡性浴剤組成物である特許請求の範囲
第1項記載の固型浴剤組成物。 五 浴剤原料が酵素含有浴剤組成物である特許請求の範
囲第1項記載の固型浴剤組成物。
[Scope of Claims] L A solid bath agent composition comprising polyethylene glycol added to bath agent raw materials. 2. The solid bath agent composition according to claim 1, wherein the bath agent raw material is a foaming bath agent composition. 5. The solid bath agent composition according to claim 1, wherein the bath agent raw material is an enzyme-containing bath agent composition.
JP20414681A 1981-12-17 1981-12-17 Solid bath composition Pending JPS58105910A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20414681A JPS58105910A (en) 1981-12-17 1981-12-17 Solid bath composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20414681A JPS58105910A (en) 1981-12-17 1981-12-17 Solid bath composition

Publications (1)

Publication Number Publication Date
JPS58105910A true JPS58105910A (en) 1983-06-24

Family

ID=16485593

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20414681A Pending JPS58105910A (en) 1981-12-17 1981-12-17 Solid bath composition

Country Status (1)

Country Link
JP (1) JPS58105910A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6087213A (en) * 1983-10-17 1985-05-16 Tadao Shiraishi Preparation of enzyme-containing bathing agent
JPS60166607A (en) * 1984-02-08 1985-08-29 Hara Sogyo Kk Bath additive
JPH02142721A (en) * 1988-11-22 1990-05-31 Shiseido Co Ltd Preparation of solid bathing agent
US5035091A (en) * 1988-12-30 1991-07-30 Kabushiki Kaisha Daimon Automatically operated opening and closing roof
JP2005336060A (en) * 2004-05-24 2005-12-08 Kimi Kasei Kk Granular bathing agent composition
WO2013180048A1 (en) 2012-05-28 2013-12-05 株式会社ホットアルバム炭酸泉タブレット Method for producing tablet, and tablet

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6087213A (en) * 1983-10-17 1985-05-16 Tadao Shiraishi Preparation of enzyme-containing bathing agent
JPS6324972B2 (en) * 1983-10-17 1988-05-23 Tadao Shiraishi
JPS60166607A (en) * 1984-02-08 1985-08-29 Hara Sogyo Kk Bath additive
JPS6328409B2 (en) * 1984-02-08 1988-06-08 Hara Herusu Kogyo Kk
JPH01303149A (en) * 1984-02-08 1989-12-07 Hara Herusu Kogyo Kk Health bath
JPH0365987B2 (en) * 1984-02-08 1991-10-15
JPH02142721A (en) * 1988-11-22 1990-05-31 Shiseido Co Ltd Preparation of solid bathing agent
US5035091A (en) * 1988-12-30 1991-07-30 Kabushiki Kaisha Daimon Automatically operated opening and closing roof
JP2005336060A (en) * 2004-05-24 2005-12-08 Kimi Kasei Kk Granular bathing agent composition
WO2013180048A1 (en) 2012-05-28 2013-12-05 株式会社ホットアルバム炭酸泉タブレット Method for producing tablet, and tablet
KR20150018808A (en) 2012-05-28 2015-02-24 가부시키가이샤 홋토아루바무 탄산센 타부렛토 Method for producing tablet, and tablet

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