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JPH07173078A - Antipruritic composition - Google Patents

Antipruritic composition

Info

Publication number
JPH07173078A
JPH07173078A JP5321459A JP32145993A JPH07173078A JP H07173078 A JPH07173078 A JP H07173078A JP 5321459 A JP5321459 A JP 5321459A JP 32145993 A JP32145993 A JP 32145993A JP H07173078 A JPH07173078 A JP H07173078A
Authority
JP
Japan
Prior art keywords
antipruritic
weight
parts
composition
skin
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
Application number
JP5321459A
Other languages
Japanese (ja)
Other versions
JP4022675B2 (en
Inventor
Kimiko Sugita
喜美子 杉田
Shigeo Tanaka
重男 田中
Fumio Urushizaki
文男 漆崎
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.)
Taisho Pharmaceutical Co Ltd
Original Assignee
Taisho Pharmaceutical Co Ltd
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 Taisho Pharmaceutical Co Ltd filed Critical Taisho Pharmaceutical Co Ltd
Priority to JP32145993A priority Critical patent/JP4022675B2/en
Publication of JPH07173078A publication Critical patent/JPH07173078A/en
Application granted granted Critical
Publication of JP4022675B2 publication Critical patent/JP4022675B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

(57)【要約】 【目的】 速効かつ優れた鎮痒効果が得られる鎮痒剤組
成物を提供するものである。 【構成】 鎮痒成分と粒径0.01〜1.0mmのリン
酸水素カルシウムを含有し、適用時に手や指によって患
部に擦りつけることにより強力な鎮痒効果を発揮し、し
かも皮膚を損傷しないことを特徴とする鎮痒剤組成物で
ある。
(57) [Summary] [Object] To provide an antipruritic composition which is fast-acting and has an excellent antipruritic effect. [Structure] Contains an antipruritic component and calcium hydrogen phosphate having a particle size of 0.01 to 1.0 mm, and exerts a strong antipruritic effect by rubbing the affected area with a hand or a finger at the time of application, and does not damage the skin. An antipruritic composition characterized by the following:

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は鎮痒剤組成物、詳しくは
皮膚へ塗布すると速効かつ強力な鎮痒効果が得られる鎮
痒剤組成物に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an antipruritic composition, and more particularly to an antipruritic composition which, when applied to the skin, provides a rapid and strong antipruritic effect.

【0002】[0002]

【従来の技術】蚊などの虫に刺されると激しい痒みが生
じる。これに対応する従来の鎮痒剤薬としては、抗ヒス
タミン剤、局所麻酔剤および皮膚刺激剤を配合したクリ
ーム剤、液剤および水性ゲル剤が用いられている。
2. Description of the Related Art When it is bitten by insects such as mosquitoes, severe itching occurs. As conventional antipruritic drugs corresponding thereto, creams, liquids and aqueous gels containing antihistamines, local anesthetics and skin stimulants are used.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、これら
の薬物が鎮痒効果を発現するためには、薬物が皮膚を透
過して作用部位に到達しなければならず、作用発現まで
に時間がかかる。そのため実際にはほとんど鎮痒効果が
なく、痒みをがまんできず皮膚を掻き壊して、皮膚の状
態を悪化させてしまう。
However, in order for these drugs to exert an antipruritic effect, the drugs must penetrate the skin to reach the site of action, and it takes a long time to develop the action. Therefore, in practice, there is almost no antipruritic effect, and the itching cannot be covered and the skin is scratched and the skin condition is deteriorated.

【0004】[0004]

【課題を解決するための手段】本発明者らは、この欠点
を改善するため、粉粒体を含有する鎮痒剤組成物につい
て種々検討した結果、粉粒体の種類、大きさ、形および
かたさが鎮痒効果に大きく影響し、ある特定の粉粒体を
使用すると強力な鎮痒効果を発揮することを見いだし本
発明を完成した。
[Means for Solving the Problems] In order to remedy this drawback, the present inventors have conducted various studies on antipruritic compositions containing powders and granules, and as a result, the type, size, shape and hardness of the granules have been investigated. The present invention has been completed based on the finding that is strongly affected by the antipruritic effect, and that it exerts a strong antipruritic effect when a specific powder or granular material is used.

【0005】すなわち本発明は、鎮痒成分と粒径0.0
1〜1.0mmのリン酸水素カルシウムを含有すること
を特徴とする鎮痒剤組成物である。以下に本発明の成分
についてさらに詳細に説明する。
That is, in the present invention, the antipruritic component and the particle size are 0.0
The antipruritic composition is characterized by containing 1 to 1.0 mm of calcium hydrogen phosphate. The components of the present invention will be described in more detail below.

【0006】本発明に用いられるリン酸水素カルシウム
は、手、指等の塗布または塗擦で崩壊しないかたさを持
ち、角ばった形の粉粒体であり、その粒径は0.01〜
1.0mmであることが必要であり、特に好ましい粒径
は0.15〜0.5mmである。これより小さいと十分
な鎮痒効果が得られず、これより大きいと使用感が好ま
しくない。また、この粉粒体は適用時に手や指によって
患部に擦りつけても、皮膚を損傷してはならない。その
配合量は鎮痒剤組成物全体に対して0.5〜15重量%
が好ましく、特に好ましくは3〜10重量%である。
Calcium hydrogen phosphate used in the present invention is a powdery material in the shape of a square having a hardness that does not disintegrate by coating or rubbing with hands, fingers, etc.
It is necessary to be 1.0 mm, and a particularly preferable particle size is 0.15 to 0.5 mm. If it is smaller than this, a sufficient antipruritic effect cannot be obtained, and if it is larger than this, the usability is unfavorable. In addition, the powder or granular material should not damage the skin even if it is rubbed on the affected area with the hands or fingers at the time of application. Its content is 0.5 to 15% by weight based on the whole antipruritic composition.
Is preferable, and particularly preferably 3 to 10% by weight.

【0007】本発明に用いられる鎮痒成分としては、酢
酸ハイドロコーチゾン、酢酸デキサメタゾン、酢酸プレ
ドニゾロン等の各種ステロイド剤、インドメタシン、イ
ブプロフェン、ブフェキサマック等の非ステドイド系抗
炎症剤、塩酸ジブカイン、リドカイン、アミノ安息香酸
ナトリウム等の局所麻酔剤、塩酸ジフェンヒドラミン、
マレイン酸クロルフェニラミン、塩酸イソチペンジル等
の抗ヒスタミン剤、塩酸クロルヘキシジン、塩化デカリ
ニウム、イソプロピルメチルフェノール等の殺菌剤、ト
ウガラシチンキ、dl−メントール、dl−カンフル、
サリチル酸メチル等の皮膚刺激剤、その他アラントイ
ン、グリチルレチン酸、グリチルリチン酸ジカリウム等
の抗炎症作用を有する化合物、クロタミトン等の鎮痒作
用を持つ化合物があげられる。これらは単独または2種
以上を組み合わせて用いることができ、その配合量は鎮
痒剤組成物全体に対して0.01〜10重量%が好まし
い。
The antipruritic ingredients used in the present invention include various steroid agents such as hydrocortisone acetate, dexamethasone acetate, and prednisolone acetate, non-stedoid anti-inflammatory agents such as indomethacin, ibuprofen, bufexamac, dibucaine hydrochloride, lidocaine, amino. Local anesthetics such as sodium benzoate, diphenhydramine hydrochloride,
Chlorpheniramine maleate, antihistamines such as isothipendyl hydrochloride, chlorhexidine hydrochloride, decalinium chloride, bactericides such as isopropylmethylphenol, capsicum tincture, dl-menthol, dl-camphor,
Examples include skin irritants such as methyl salicylate, other compounds having anti-inflammatory action such as allantoin, glycyrrhetinic acid and dipotassium glycyrrhizinate, and compounds having antipruritic action such as crotamiton. These may be used alone or in combination of two or more, and the compounding amount thereof is preferably 0.01 to 10% by weight based on the whole antipruritic composition.

【0008】さらに本発明の鎮痒剤組成物には、上記成
分の他に外用剤に一般に用いられる添加物を配合するこ
とができる。この様な成分の例としては、ポリオキシエ
チレン硬化ヒマシ油等の界面活性剤、エタノール、イソ
プロピルアルコール等のアルコール類、プロピレングリ
コール、ジプロピレングリコール、ポリプロピレングリ
コール、ブチレングリコール、エチレングリコール、ポ
リエチレングリコール、グリセリン等の多価アルコール
類、カルボキシビニルポリマー等のゲル化剤、アンモニ
ア水、ジイソパノールアミン等の中和剤、リン酸塩、ク
エン酸塩、亜リン酸塩、酢酸塩等のpH調節剤、ジブチ
ルヒドロキシトルエン、ブチルヒドロキシアニソールな
どの抗酸化剤、パラオキシ安息香酸メチル、パラオキシ
安息香酸プロピルなどの防腐剤、香料、水等が含まれ
る。
Further, the antipruritic composition of the present invention may contain, in addition to the above components, additives generally used for external preparations. Examples of such components include surfactants such as polyoxyethylene hydrogenated castor oil, alcohols such as ethanol and isopropyl alcohol, propylene glycol, dipropylene glycol, polypropylene glycol, butylene glycol, ethylene glycol, polyethylene glycol, glycerin. Polyhydric alcohols such as, gelling agents such as carboxyvinyl polymers, ammonia water, neutralizing agents such as diisopropanolamine, pH adjusting agents such as phosphates, citrates, phosphites, acetates, etc. Antioxidants such as dibutylhydroxytoluene and butylhydroxyanisole, preservatives such as methyl paraoxybenzoate and propyl paraoxybenzoate, perfumes and water are included.

【0009】また、本発明の鎮痒剤組成物はクリーム
剤、ゲル剤、液剤等の各種の外用剤とすることができ
る。
The antipruritic composition of the present invention can be used in various external preparations such as creams, gels and liquids.

【0010】[0010]

【発明の効果】本発明の鎮痒剤組成物は、特定の粒径、
かたさおよび形の粉粒体を含有し、適用時に手や指によ
って患部に擦りつけることにより強力な鎮痒効果を発揮
し、しかも皮膚を損傷することがない。
The antipruritic composition of the present invention has a specific particle size,
It contains hard and shaped powders, and exerts a strong antipruritic effect by rubbing it on the affected area with hands or fingers at the time of application, and does not damage the skin.

【0011】[0011]

【実施例】以下に実施例を挙げて更に詳細に説明する。EXAMPLES The present invention will be described in more detail below with reference to examples.

【0012】実施例1 エタノール41.4重量部とポリオキシエチレン硬化ヒ
マシ油2重量部の混合液に、塩酸ジブカイン0.3重量
部、ジフェンヒドラミン1重量部、dl−メントール
3.5重量部およびdl−カンフル2重量部を加え溶解
した。これを水27.3重量部にカルボキシビニルポリ
マー1.5重量部を分散させた液に加えて攪拌混合し、
ジイソプロパノールアミン1.0重量部を水10重量部
で希釈した液を徐々に加えて中和した。その後、平均粒
子径0.25mmのリン酸水素カルシウム10重量部を
加え、鎮痒剤組成物を得た。
EXAMPLE 1 0.34 parts by weight of dibucaine hydrochloride, 1 part by weight of diphenhydramine, 3.5 parts by weight of dl-menthol and dl were added to a mixed solution of 41.4 parts by weight of ethanol and 2 parts by weight of polyoxyethylene hydrogenated castor oil. -2 parts by weight of camphor was added and dissolved. This was added to a liquid in which 1.5 parts by weight of carboxyvinyl polymer was dispersed in 27.3 parts by weight of water, and the mixture was stirred and mixed,
A solution prepared by diluting 1.0 part by weight of diisopropanolamine with 10 parts by weight of water was gradually added to neutralize. Then, 10 parts by weight of calcium hydrogen phosphate having an average particle diameter of 0.25 mm was added to obtain an antipruritic composition.

【0013】実施例2 塩酸イソチベンジル0.75重量部、塩酸ジブカイン
0.3重量部、塩化デカリニウム0.1重量部、アンモ
ニア水1.5重量部、dl−メントール1重量部および
dl−カンフル2重量部をエタノール35重量部に溶解
し、カルボキシビニルポリマー0.4重量部を水48.
95重量部に混合分散させた液に加えて攪拌混合した。
これに平均粒子径0.25mmのリン酸水素カルシウム
10重量部を加え、鎮痒剤組成物を得た。
Example 2 0.75 parts by weight of isothibenzyl hydrochloride, 0.3 parts by weight of dibucaine hydrochloride, 0.1 part by weight of decarinium chloride, 1.5 parts by weight of aqueous ammonia, 1 part by weight of dl-menthol and 2 of dl-camphor. Parts by weight are dissolved in 35 parts by weight of ethanol, and 0.4 parts by weight of carboxyvinyl polymer is added to 48.
It was added to the liquid mixed and dispersed in 95 parts by weight and stirred and mixed.
10 parts by weight of calcium hydrogen phosphate having an average particle diameter of 0.25 mm was added thereto to obtain an antipruritic composition.

【0014】比較例1、2 実施例1および2からリン酸水素カルシウムを取り除い
て調製した鎮痒剤組成物を各々比較例1、2とした。
Comparative Examples 1 and 2 The antipruritic compositions prepared by removing calcium hydrogen phosphate from Examples 1 and 2 were designated as Comparative Examples 1 and 2, respectively.

【0015】試験例1 健康な成人女性5名を被験者とし、前腕の経表皮水分喪
失量(以下TWLと略記する)をエバポリメーターEP
−10(Servo Med社製)を用いて測定した。実施例1
および比較例1を各々2分間塗布した後、塗布部を水で
洗浄した。塗布前と塗布60分後のTWLを各々測定し
た結果を図1に示す。
Test Example 1 Five healthy adult women were used as test subjects, and the transepidermal water loss of the forearm (hereinafter abbreviated as TWL) was evaluated by an evaporation meter EP.
It was measured using -10 (manufactured by Servo Med). Example 1
After applying each of Comparative Examples 1 and 2 for 2 minutes, the applied part was washed with water. The results of measuring the TWL before coating and after 60 minutes after coating are shown in FIG.

【0016】この結果、実施例1および比較例1のTW
Lは同程度であり、本発明のリン酸水素カルシウムの粉
粒体を含有した鎮痒剤組成物が皮膚を損傷しないことを
確認した。
As a result, the TW of Example 1 and Comparative Example 1
L was similar, and it was confirmed that the antipruritic composition containing the powdery particles of calcium hydrogen phosphate of the present invention does not damage the skin.

【0017】試験例2 健康な成人男性5名を被験者とし、手の甲に直径5mm
程度の穴を開けたゴム手袋を着用し、蚊(ヒトスジシマ
カ雌成虫)の入ったケージに手を差し込み、蚊1匹に吸
血させた。吸血後に手をケージから抜き手袋を外し、痒
みがスコア3になったら、実施例1、2および比較例
1、2の鎮痒剤組成物を30μl取り、約2分間患部を
マッサージするように塗布した。適用後、一定時間毎に
痒みの程度を自己判定した。痒みの判定基準を表1に、
結果を表2に示す。
Test Example 2 Five healthy adult men were used as subjects, and the back of the hand had a diameter of 5 mm.
Wearing rubber gloves with a hole, a hand was put into a cage containing a mosquito (adult Aedes albopictus female adult) and one mosquito sucked blood. After blood-sucking, the hands were removed from the cage, the gloves were removed, and when the itch became score 3, 30 μl of the antipruritic composition of Examples 1 and 2 and Comparative Examples 1 and 2 was applied and massaged onto the affected area for about 2 minutes. . After application, the degree of itching was self-determined at regular intervals. Table 1 shows the criteria for itching.
The results are shown in Table 2.

【0018】[0018]

【表1】 [Table 1]

【0019】[0019]

【表2】 [Table 2]

【0020】この結果より、本発明の鎮痒剤が痒みを速
やかに取り除くことを確認した。
From these results, it was confirmed that the antipruritic agent of the present invention quickly removes itch.

【図面の簡単な説明】[Brief description of drawings]

前腕の経表皮水分喪失量(TWL)の測定結果を示すも
のである。
It shows the measurement results of transepidermal water loss (TWL) of the forearm.

【図1】図1は、実施例1および比較例1で得た組成物
を前腕に塗布洗浄後のエバポリメーターEP−10によ
る経表皮水分喪失量の測定結果である。
FIG. 1 shows the results of measurement of transepidermal water loss using an evaporation meter EP-10 after the compositions obtained in Example 1 and Comparative Example 1 were applied and washed on the forearm.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】鎮痒成分および粒径0.01〜1.0mm
のリン酸水素カルシウムを含有することを特徴とする鎮
痒剤組成物。
1. An antipruritic component and a particle size of 0.01 to 1.0 mm
2. An antipruritic composition comprising the calcium hydrogen phosphate according to claim 1.
JP32145993A 1993-12-21 1993-12-21 Antipruritic composition Expired - Fee Related JP4022675B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32145993A JP4022675B2 (en) 1993-12-21 1993-12-21 Antipruritic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32145993A JP4022675B2 (en) 1993-12-21 1993-12-21 Antipruritic composition

Publications (2)

Publication Number Publication Date
JPH07173078A true JPH07173078A (en) 1995-07-11
JP4022675B2 JP4022675B2 (en) 2007-12-19

Family

ID=18132808

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32145993A Expired - Fee Related JP4022675B2 (en) 1993-12-21 1993-12-21 Antipruritic composition

Country Status (1)

Country Link
JP (1) JP4022675B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2775594A1 (en) * 1998-03-06 1999-09-10 Oreal USE OF A COMPOUND INHIBITING THE ACTIVITY OF A SODIUM CHANNEL OR A CALCIUM CHANNEL IN A TOPICAL USE COMPOSITION
JP2005047908A (en) * 2003-07-16 2005-02-24 Taisho Pharmaceut Co Ltd Anti-inflammatory analgesic composition for external use
WO2008038807A1 (en) * 2006-09-29 2008-04-03 Kobayashi Pharmaceutical Co., Ltd. External composition for skin
WO2021204568A1 (en) * 2020-04-07 2021-10-14 Universität Basel A topical composition for treatment of pruritus

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2775594A1 (en) * 1998-03-06 1999-09-10 Oreal USE OF A COMPOUND INHIBITING THE ACTIVITY OF A SODIUM CHANNEL OR A CALCIUM CHANNEL IN A TOPICAL USE COMPOSITION
WO1999044579A3 (en) * 1998-03-06 2000-01-06 Oreal Use of a compound inhibiting the activity of a sodium channel and a calcium channel in a composition for topical use
JP2005047908A (en) * 2003-07-16 2005-02-24 Taisho Pharmaceut Co Ltd Anti-inflammatory analgesic composition for external use
WO2008038807A1 (en) * 2006-09-29 2008-04-03 Kobayashi Pharmaceutical Co., Ltd. External composition for skin
JP2008088100A (en) * 2006-09-29 2008-04-17 Kobayashi Pharmaceut Co Ltd Skin external composition
WO2021204568A1 (en) * 2020-04-07 2021-10-14 Universität Basel A topical composition for treatment of pruritus

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Publication number Publication date
JP4022675B2 (en) 2007-12-19

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