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JPH0529003B2 - - Google Patents
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JPH0529003B2 - - Google Patents

Info

Publication number
JPH0529003B2
JPH0529003B2 JP12032585A JP12032585A JPH0529003B2 JP H0529003 B2 JPH0529003 B2 JP H0529003B2 JP 12032585 A JP12032585 A JP 12032585A JP 12032585 A JP12032585 A JP 12032585A JP H0529003 B2 JPH0529003 B2 JP H0529003B2
Authority
JP
Japan
Prior art keywords
cyclodextrin
carbon dioxide
bath
dioxide gas
present
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 - Lifetime
Application number
JP12032585A
Other languages
Japanese (ja)
Other versions
JPS61277610A (en
Inventor
Hidenori Yorozu
Yasuteru Eguchi
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP12032585A priority Critical patent/JPS61277610A/en
Publication of JPS61277610A publication Critical patent/JPS61277610A/en
Publication of JPH0529003B2 publication Critical patent/JPH0529003B2/ja
Granted 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/732Starch; Amylose; Amylopectin; Derivatives thereof
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/22Gas releasing

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は浴用剤、更に詳細には、炭酸ガスを吸
着させたシクロデキストリン若しくはシクロデキ
ストリン誘導体を含有する新規な浴用剤に関す
る。 〔従来の技術〕 温泉はその含有成分により種々の病気に効果を
示すことから広く国民に親しまれ、又、医療の手
段としても用いられている。温泉の有効成分とし
ては、食塩、芒硝、重曹などの塩類が良く知られ
ているが、炭酸ガス、硫化水素などのガス成分も
重要な役割を果たしている。しかし、これら温泉
有効ガス成分は気体であるため、温泉水から有効
ガス成分は揮散してしまい充分な効果を得られな
いことが多い。 そこで、従来よりこれら温泉有効ガス成分によ
る湯治効果を家庭での入浴中にも得るべく様々な
工夫がなされてきた。炭酸ガス(炭酸泉)の場
合、最も一般的なのは酸と炭酸塩の反応により、
浴水中で炭酸ガスを発生させ効率良く溶かそうと
いうものである。 〔発明が解決しようとする問題点〕 しかしながら、従来のこれらの方法において
は、湯のたき直しのたびに浴用剤の投入を続けて
いると、浴湯中の炭酸ガス以外の塩濃度が高くな
ることによつて肌のべとつきを感じたり、お湯の
味が悪くなる等の種々の問題点があつた。 〔問題点を解決するための手段〕 斯かる実状において、本発明者は、従来の炭酸
ガスによる湯治効果を家庭での入浴中に、しかも
快適に得られるようにすべく鋭意検討を重ねた結
果、高圧下で炭酸ガスとシクロデキストリンを接
触させることにより、炭酸ガスを吸着含有するシ
クロデキストリンが安定に得られ、これは、水と
接触することにより、吸着含有された炭酸ガスを
放出するという性質を有すること、及び炭酸ガス
をシクロデキストリンあるいはシクロデキストリ
ン誘導体に吸着させたものを浴用剤に配合するこ
とにより塩濃度を高めることなく優れた浴用効果
を有する浴用剤が得られることを見出し、本発明
を完成した。 すなわち、本発明は、炭酸ガスを吸着させたシ
クロデキストリン若しくはシクロデキストリン誘
導体を含有することを特徴とする浴用剤を提供す
るものである。 本発明で使用されるシクロデキストリンとして
は、α−シクロデキストリン、β−シクロデキス
トリン、γ−シクロデキストリンなどが挙げられ
る。又、シクロデキストリン誘導体としては、グ
ルコシル−α−シクロデキストリン、クルコシル
−β−シクロデキストリン、グルコシル−γ−シ
クロデキストリン、マルトシル−α−シクロデキ
ストリン、マルトトリオシル−α−シクロデキス
トリンなどの分枝シクロデキストリン;o−ジ−
メチル−β−シクロデキストリン、o−トリ−メ
チル−β−シクロデキストリンなどのメチル化シ
クロデキストリン;シクロデキストリンをエピク
ロルヒドリンで架橋した低重合ポリマーなどのシ
クロデキストリンポリマー;アシル化シクロデキ
ストリン;アルキル化シクロデキストリン;アミ
ノ化シクロデキストリンなどが挙げられる。就
中、α−シクロデキストリンが強い炭酸ガス吸着
能力を有しているようである。また、これらのシ
クロデキストリン又はシクロデキストリン誘導体
は、実質的に水分を含有しないものが好ましい。 炭酸ガスをシクロデキストリン又はシクロデキ
ストリン誘導体に吸着させるには、例えば炭酸ガ
スを1Kg/cm2以上、好ましくは5〜15Kg/cm2の圧
力下でシクロデキストリン又はシクロデキストリ
ン誘導体に接触させることにより行なわれる。当
該吸着工程の温度は、30℃以下、特に20℃以下が
好ましい。炭酸ガスの吸着量は、シクロデキスト
リン又はシクロデキストリン誘導体100gあたり
2g以上であることが好ましい。 本発明の浴用剤は、これを浴湯に加えたときの
浴湯の液性が弱酸性、より具体的には浴用剤の
0.01重量%水溶液のPHが4〜7、特に6〜6.7に
なるようにするものであることが好ましい。PHが
4より低いと肌への刺激性が強くなり、7を超え
ると本発明の効果が減少傾向となる。これは、本
発明の効果が、PHが酸性の場合には炭酸ガスは
CO2分子として存在して血流促進作用を示すが、
PHがアルカリ性側では炭酸ガスは大部分がCO2 2-
イオンあるいはHCO3 -イオンとして存在するた
め当該効果はあまり期待できないという原理に基
くものであるためである。 斯かる条件を具備するために、本発明の浴用剤
に0.01重量%水溶液のPHが4〜7になるようにコ
ハク酸、フマル酸等の有機酸又はこれらの塩;あ
るいはリン酸又はその塩等の酸性物質を適当量配
合することが好ましい。 本発明の浴用剤には必要に応じて、塩化ナトリ
ウム、炭酸水素ナトリウム、炭酸ナトリウム、ホ
ウ砂、ミヨウバン、硫酸ナトリウム、硫化カリウ
ム、セスキ炭酸ナトリウム、チオ硫酸ナトリウ
ム、リン酸ナトリウム、酸化カルシウム、硝酸カ
リウム、硝酸ナトリウム、塩化カリウム、炭酸カ
リウム、重質炭酸マグネシウム、塩化アンモニウ
ム、イオウなどの無機塩類の他、有機塩類、有機
酸、1価アルコール類、多価アルコール類、油脂
類、鉱物、生薬、保湿剤、色素、香料など通常浴
用剤に用いられる成分を添加することができる。 本発明の浴用剤は、錠剤、顆粒剤等の通常の浴
用剤の剤型として作用しうるが、これを通水性の
ある布、不織布などの繊維集合体、例えば袋体で
包んだ形にして使用に供することもできる。 〔本発明の効果〕 本発明の浴用剤は、浴湯に加えることにより放
出された炭酸ガスによる湯治効果、すなわち、血
行促進効果、肌のしつとり感等が非常に優れたも
のである。また、本発明浴用剤は、塩を使用する
必要がないので、これを湯のたき直しのたびに加
えても従来品の如き塩濃度の高まりがなく、使用
感の点でも優れたものである。更に本発明に用い
るシクロデキストリン及びその誘導体が水溶性で
あるため、湯がにごつたり、沈澱物が生じたりす
ることがない優れた浴用剤である。 次に、本発明浴用剤の浴用効果を下記方法によ
り評価した。結果を第1表に示す。 評価方法: 後記実施例1及び2、比較例1に示す浴用剤を
毎日1個宛浴湯に投入し、パネラー20名に5日間
常法に従つて使用してもらい、5日後に1個投入
後の浴用剤としての全体評価(総合的な使用感)、
あたたまり感、湯上りのさわやかさ及びさつぱり
感を調べた。
[Industrial Application Field] The present invention relates to a bath agent, and more particularly to a novel bath agent containing a cyclodextrin or a cyclodextrin derivative on which carbon dioxide gas has been adsorbed. [Prior Art] Hot springs are widely popular among the people because they are effective against various diseases depending on the ingredients they contain, and are also used as a means of medical treatment. Salts such as table salt, mirabilite, and baking soda are well known as active ingredients in hot springs, but gas components such as carbon dioxide and hydrogen sulfide also play an important role. However, since these hot spring effective gas components are gases, the effective gas components often volatilize from the hot spring water, making it impossible to obtain sufficient effects. Therefore, various efforts have been made to obtain the therapeutic effects of hot spring effective gas components even during bathing at home. In the case of carbon dioxide gas (carbonated springs), the most common reaction is between acid and carbonate,
The idea is to generate carbon dioxide gas in bath water to efficiently dissolve it. [Problems to be solved by the invention] However, in these conventional methods, if bath additives are continuously added every time the bath water is reheated, the concentration of salts other than carbon dioxide gas in the bath water increases. There were various problems such as the skin feeling sticky and the hot water tasting bad. [Means for Solving the Problems] Under these circumstances, the inventor of the present invention has made extensive studies to make it possible to comfortably obtain the conventional hot water treatment effect of carbon dioxide gas while taking a bath at home. By bringing carbon dioxide gas into contact with cyclodextrin under high pressure, cyclodextrin containing adsorbed carbon dioxide gas can be stably obtained, and this has the property of releasing the adsorbed carbon dioxide gas when it comes into contact with water. The present invention has been based on the discovery that a bath agent having excellent bathing effects can be obtained without increasing the salt concentration by incorporating carbon dioxide adsorbed into a cyclodextrin or cyclodextrin derivative into a bath agent. completed. That is, the present invention provides a bath agent characterized by containing cyclodextrin or a cyclodextrin derivative to which carbon dioxide gas has been adsorbed. Examples of the cyclodextrin used in the present invention include α-cyclodextrin, β-cyclodextrin, and γ-cyclodextrin. In addition, as cyclodextrin derivatives, branched cyclodextrin such as glucosyl-α-cyclodextrin, crucosyl-β-cyclodextrin, glucosyl-γ-cyclodextrin, maltosyl-α-cyclodextrin, maltotriosyl-α-cyclodextrin, etc. ;o-ji-
Methylated cyclodextrin such as methyl-β-cyclodextrin and o-tri-methyl-β-cyclodextrin; cyclodextrin polymers such as low polymerization polymers obtained by crosslinking cyclodextrin with epichlorohydrin; acylated cyclodextrin; alkylated cyclodextrin; Examples include aminated cyclodextrin. Among these, α-cyclodextrin seems to have a strong ability to adsorb carbon dioxide gas. Moreover, these cyclodextrins or cyclodextrin derivatives preferably contain substantially no water. Carbon dioxide gas can be adsorbed on cyclodextrin or cyclodextrin derivatives by, for example, bringing carbon dioxide gas into contact with cyclodextrin or cyclodextrin derivatives under a pressure of 1 kg/cm 2 or more, preferably 5 to 15 kg/cm 2 . . The temperature in the adsorption step is preferably 30°C or lower, particularly 20°C or lower. The amount of carbon dioxide gas adsorbed is preferably 2 g or more per 100 g of cyclodextrin or cyclodextrin derivative. The bath additive of the present invention has a weakly acidic liquid property when added to the bath water, and more specifically, the bath additive has a weak acidity.
It is preferable that the pH of the 0.01% by weight aqueous solution is 4 to 7, particularly 6 to 6.7. When the pH is lower than 4, the irritation to the skin becomes strong, and when it exceeds 7, the effect of the present invention tends to decrease. This means that the effect of the present invention is that when the pH is acidic, carbon dioxide gas is
Exists as CO 2 molecules and exhibits a blood flow promoting effect,
When the pH is alkaline, carbon dioxide gas is mostly CO 2 2-
This is because it is based on the principle that since it exists as an ion or HCO 3 - ion, the effect cannot be expected much. In order to meet such conditions, organic acids such as succinic acid and fumaric acid, or salts thereof; or phosphoric acid or salts thereof, etc. are added to the bath agent of the present invention so that the pH of the 0.01% aqueous solution is 4 to 7. It is preferable to blend an appropriate amount of an acidic substance. The bath agent of the present invention may optionally contain sodium chloride, sodium hydrogen carbonate, sodium carbonate, borax, alum, sodium sulfate, potassium sulfide, sodium sesquicarbonate, sodium thiosulfate, sodium phosphate, calcium oxide, potassium nitrate, In addition to inorganic salts such as sodium nitrate, potassium chloride, potassium carbonate, heavy magnesium carbonate, ammonium chloride, and sulfur, organic salts, organic acids, monohydric alcohols, polyhydric alcohols, oils and fats, minerals, herbal medicines, and humectants. Ingredients commonly used in bath preparations, such as dyes, fragrances, etc., can be added. The bath additive of the present invention can act as a tablet, granule, or other conventional bath additive formulation, but it can be wrapped in a fiber aggregate such as a water-permeable cloth or nonwoven fabric, such as a bag. It can also be put to use. [Effects of the Present Invention] The bath additive of the present invention has excellent hot water treatment effects due to the carbon dioxide gas released when added to bath water, ie, blood circulation promoting effect, skin moisturizing feeling, etc. In addition, the bath preparation of the present invention does not require the use of salt, so even if it is added every time hot water is reheated, the salt concentration does not increase as with conventional products, and it is also excellent in terms of feeling of use. . Furthermore, since the cyclodextrin and its derivatives used in the present invention are water-soluble, it is an excellent bathing agent that does not cause the water to become cloudy or to form precipitates. Next, the bath effect of the bath agent of the present invention was evaluated by the following method. The results are shown in Table 1. Evaluation method: One bath additive shown in Examples 1 and 2 and Comparative Example 1 described later was added to bath water every day, and 20 panelists were asked to use it according to the usual method for 5 days, and after 5 days, one was added. Overall evaluation as a bath additive (overall feeling of use),
The feeling of warmth, refreshing feeling after bathing, and refreshing feeling were investigated.

〔実施例〕〔Example〕

次に実施例を挙げて本発明を説明する。 実施例 1 α−シクロデキストリン(日本食品化工)1Kg
をとり炭酸ガスを8Kg/cm2の圧をかけて吸着させ
た。炭酸ガスの吸着量は40.4gであつた。この炭
酸ガスを吸着させたα−シクロデキストリン80部
に、硫酸ナトリウム10部、コハク酸−ナトリウム
5部、色素微量、香料0.5部、デキストリン4.5部
を加え、1錠50gの錠剤とした。この錠剤をアル
ミピロー包装し、浴用剤とした。 実施例 2 α−シクロデキストリン(日本食品化工)1Kg
をとり炭酸ガスを10Kg/cm2の圧をかけて吸着させ
た。炭酸ガスの吸着量は42.0gであつた。この炭
酸ガスを吸着させたα−シクロデキストリン98部
に、塩化ナトリウム2部、色素微量、香料微量を
加え1錠50gの浴用剤とした。 比較例 1 実施例1において、炭酸ガスを吸着させないα
−シクロデキストリンを用い、同様の配合で浴用
剤を製した。
Next, the present invention will be explained with reference to Examples. Example 1 α-Cyclodextrin (Nihon Shokuhin Kako) 1Kg
was taken and carbon dioxide gas was adsorbed by applying a pressure of 8 kg/cm 2 . The amount of carbon dioxide gas adsorbed was 40.4 g. 10 parts of sodium sulfate, 5 parts of sodium succinate, a trace amount of dye, 0.5 part of fragrance, and 4.5 parts of dextrin were added to 80 parts of α-cyclodextrin on which carbon dioxide gas had been adsorbed, and each tablet weighing 50 g was prepared. The tablets were packaged in an aluminum pillow and used as a bath preparation. Example 2 α-Cyclodextrin (Nihon Shokuhin Kako) 1Kg
was taken and carbon dioxide gas was adsorbed by applying a pressure of 10 kg/cm 2 . The amount of carbon dioxide adsorbed was 42.0g. To 98 parts of α-cyclodextrin on which carbon dioxide gas had been adsorbed, 2 parts of sodium chloride, a trace amount of a coloring matter, and a trace amount of a fragrance were added to prepare a bath agent weighing 50 g per tablet. Comparative example 1 In Example 1, α that does not adsorb carbon dioxide gas
- Bath preparations were prepared using cyclodextrin and the same formulation.

【特許請求の範囲】[Claims]

1 経皮吸収性薬物を含有した常温で感圧接着性
を有する薬物含有基材層と、体温によつて蒸発揮
散する薬物を含有した担持体とを積層したことを
特徴とする外用医薬部材。
1. An external pharmaceutical member comprising a drug-containing base layer containing a transdermal absorbable drug and having pressure-sensitive adhesive properties at room temperature, and a carrier containing a drug that evaporates and evaporates with body temperature.

JP12032585A 1985-06-03 1985-06-03 Bathing agent Granted JPS61277610A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12032585A JPS61277610A (en) 1985-06-03 1985-06-03 Bathing agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12032585A JPS61277610A (en) 1985-06-03 1985-06-03 Bathing agent

Publications (2)

Publication Number Publication Date
JPS61277610A JPS61277610A (en) 1986-12-08
JPH0529003B2 true JPH0529003B2 (en) 1993-04-28

Family

ID=14783458

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12032585A Granted JPS61277610A (en) 1985-06-03 1985-06-03 Bathing agent

Country Status (1)

Country Link
JP (1) JPS61277610A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63246319A (en) * 1987-04-01 1988-10-13 Kao Corp Bathing agent
JPH0236115A (en) * 1988-07-23 1990-02-06 San Paruko Kk Bathing agent
US6444619B1 (en) * 2000-09-28 2002-09-03 Rohm And Haas Company Delivery system for cyclopropenes

Also Published As

Publication number Publication date
JPS61277610A (en) 1986-12-08

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