JPS5843365B2 - Hydrophilic poultice - Google Patents
Hydrophilic poulticeInfo
- Publication number
- JPS5843365B2 JPS5843365B2 JP9032778A JP9032778A JPS5843365B2 JP S5843365 B2 JPS5843365 B2 JP S5843365B2 JP 9032778 A JP9032778 A JP 9032778A JP 9032778 A JP9032778 A JP 9032778A JP S5843365 B2 JPS5843365 B2 JP S5843365B2
- Authority
- JP
- Japan
- Prior art keywords
- poultice
- magnesium aluminate
- hydrophilic
- poultices
- aluminate metasilicate
- 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
- WMGSQTMJHBYJMQ-UHFFFAOYSA-N aluminum;magnesium;silicate Chemical compound [Mg+2].[Al+3].[O-][Si]([O-])([O-])[O-] WMGSQTMJHBYJMQ-UHFFFAOYSA-N 0.000 claims description 13
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 239000000203 mixture Substances 0.000 description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 8
- -1 cationic aluminum compounds Chemical class 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 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 4
- 239000005995 Aluminium silicate Substances 0.000 description 4
- 241000723346 Cinnamomum camphora Species 0.000 description 4
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 4
- 108010010803 Gelatin Proteins 0.000 description 4
- 235000012211 aluminium silicate Nutrition 0.000 description 4
- 229960000846 camphor Drugs 0.000 description 4
- 229930008380 camphor Natural products 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 229920000159 gelatin Polymers 0.000 description 4
- 239000008273 gelatin Substances 0.000 description 4
- 235000019322 gelatine Nutrition 0.000 description 4
- 235000011852 gelatine desserts Nutrition 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical group O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
- 229960001047 methyl salicylate Drugs 0.000 description 4
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 4
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 4
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 3
- 238000007792 addition Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 229940041616 menthol Drugs 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 150000001639 boron compounds Chemical class 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 239000000679 carrageenan Substances 0.000 description 2
- 235000010418 carrageenan Nutrition 0.000 description 2
- 229920001525 carrageenan Polymers 0.000 description 2
- 229940113118 carrageenan Drugs 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 230000002496 gastric effect Effects 0.000 description 2
- 239000003349 gelling agent Substances 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 229910052751 metal Chemical class 0.000 description 2
- 239000002184 metal Chemical class 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 239000011505 plaster Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 230000035900 sweating Effects 0.000 description 2
- 238000011282 treatment Methods 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
- 208000034656 Contusions Diseases 0.000 description 1
- 229920002085 Dialdehyde starch Polymers 0.000 description 1
- 206010020601 Hyperchlorhydria Diseases 0.000 description 1
- 208000008930 Low Back Pain Diseases 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- 241000277269 Oncorhynchus masou Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 208000010040 Sprains and Strains Diseases 0.000 description 1
- 208000007107 Stomach Ulcer Diseases 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 230000001760 anti-analgesic effect Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000035597 cooling sensation Effects 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 239000007933 dermal patch Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 201000005917 gastric ulcer Diseases 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 241000411851 herbal medicine Species 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 201000009240 nasopharyngitis Diseases 0.000 description 1
- 208000004296 neuralgia Diseases 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229910009112 xH2O Inorganic materials 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
Landscapes
- Medicinal Preparation (AREA)
Description
【発明の詳細な説明】
本発明は消炎、鎮痛等の治療に用いる外用皮膚貼布薬で
ある親水性パップ剤、ことにその基剤の改良に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a hydrophilic poultice, which is an external skin patch used for anti-inflammatory and analgesic treatments, and particularly to improvements in its base.
パップ剤は、腰痛、神経痛、リウマチ、肩こり、打身、
捻挫等の治療のために古くから使用されている製剤であ
る。Poultices can be used to treat lower back pain, neuralgia, rheumatism, stiff shoulders, bruises,
This is a preparation that has been used for a long time to treat sprains and other conditions.
パップ剤は膏基剤中に有効成分であるサリチル酸メチル
、カンフル、メントール等の生薬を混合してなる。Poultices are made by mixing herbal medicines such as active ingredients methyl salicylate, camphor, and menthol in a plaster base.
このようなパップ剤の組成、製造等については多数の文
献中に開示されている。The composition, production, etc. of such poultices are disclosed in numerous documents.
しかしながら、これらの従来の市販ないしは文献公知の
パップ剤では、たとえば長期間保存した場合に見られる
湿潤剤、薬効成分、水等の分離の如き保存に係わる欠点
、および特に夏期および発汗時におけるパップ剤自体の
軟化、皮膚へのパップ剤の残り、長期間貼布した際のパ
ップ剤の固化等の使用に係わる欠点がある。However, these conventional poultices commercially available or known in the literature have disadvantages related to storage, such as separation of humectants, medicinal ingredients, water, etc., which occur when stored for a long period of time, and the disadvantages of poultices especially in summer and during sweating. There are disadvantages related to use, such as softening of the poultice itself, residual poultices on the skin, and solidification of poultices when applied for a long period of time.
現在までに、このような欠点、とりわけ高温時の軟化を
防止する目的でアルカリ土類金属および2価以上の金属
塩、エポキシ化合物、ホウ酸およびホウ素化合物、また
ホルマリン、ジアルデヒド澱粉等の各種アルデヒド化合
物およびケトン類を添加することが行なわれてきた。To date, in order to prevent such drawbacks, especially softening at high temperatures, alkaline earth metals and metal salts of divalent or higher valence, epoxy compounds, boric acid and boron compounds, and various aldehydes such as formalin and dialdehyde starch have been used. Additions of compounds and ketones have been used.
しかしながら、2価以上の金属塩の添加は他のゲル化剤
と反応して凝集現象の発生を招き、かえってパップ剤か
らの水分等の分離が増長される傾向を呈する。However, the addition of divalent or higher-valent metal salts reacts with other gelling agents, leading to the occurrence of agglomeration, which tends to increase the separation of water, etc. from the poultice.
またエポキシ化合物、ホウ素化合物、アルデヒド類およ
びケトン類を添加することは、パップ剤が人の皮膚に直
接貼付して使用される商品であることから安全性上の問
題を招く。Furthermore, the addition of epoxy compounds, boron compounds, aldehydes, and ketones poses safety problems since poultices are products that are applied directly to human skin.
本発明の目的は、このような欠点を招くことなく、前記
の問題点を解消して、パップ剤の商品価値の向上をめざ
すことにある。An object of the present invention is to solve the above-mentioned problems without causing such drawbacks, and to improve the commercial value of poultices.
すなわち、本発明は、親−水性パップ剤用基剤中にメタ
ケイ酸アルミン酸マグネシウムを添加したことを特徴と
する親水性パップ剤にある。That is, the present invention resides in a hydrophilic poultice agent characterized in that magnesium aluminate metasilicate is added to a base for a hydrophilic poultice agent.
すなわち発明者らはメタケイ酸アルミン酸マグネシウム
の添加により、従来不可避とされていた前述の問題点に
ついて大きな改善をなし得ることを研究の結果確認した
のである。That is, the inventors have confirmed through research that the above-mentioned problems, which were conventionally considered unavoidable, can be greatly improved by adding magnesium aluminate metasilicate.
本発明によって使用するメタケイ酸アルミン酸マグネシ
ウムはAl2O3・Mg0・2 S 102・xH2O
で表わされ、一般に胃酸過多症、胃カタル、胃潰瘍等の
治療用の薬物として、また錠剤、散剤、顆粒剤、カプセ
ル剤等の製剤工程における賦形剤、流動促進剤、成形剤
、吸着粉末化剤として広く使用されており、人間に対し
て全く安全な医薬品である。The magnesium aluminate metasilicate used according to the invention is Al2O3.Mg0.2 S 102.xH2O
It is generally used as a drug for the treatment of gastric hyperacidity, gastric catarrh, gastric ulcer, etc., and as an excipient, glidant, molding agent, and adsorbent powder in the formulation process of tablets, powders, granules, capsules, etc. It is widely used as a chemical agent and is completely safe for humans.
またこの化合物はアルミニウムがアルミン酸の形で構成
されていることからミョウバンや硫酸アルミニウム等の
カチオン系のアルミニウム化合物とはその性質において
明確に区別される。Furthermore, since this compound is composed of aluminum in the form of aluminic acid, it is clearly distinguished from cationic aluminum compounds such as alum and aluminum sulfate in terms of its properties.
本発明によるパップ剤を構成する膏基剤のメタケイ酸ア
ルミン酸マグネシウム以外の組成については従来のもの
と同様であり、粉末剤成分としてはカオリンが最も良好
であり、湿潤剤としてはグリセリン、ポリエチレングリ
コール等の多価アルコール、粘着ゲル化剤としてはポリ
アクリル酸ナトリウム、ゼラチン、カラギーナン、カル
ボキシメチルセルロース等が使用できる。The composition of the plaster base constituting the poultice of the present invention other than magnesium aluminate metasilicate is the same as that of conventional ones, and the best powder component is kaolin, and the wetting agents are glycerin and polyethylene glycol. As the adhesive gelling agent, sodium polyacrylate, gelatin, carrageenan, carboxymethyl cellulose, etc. can be used.
好適には、メタケイ酸アルミン酸マグネシウムは全体重
量比の0.3ないし1.5%の範囲で添加するのがよい
。Preferably, magnesium aluminate metasilicate is added in an amount of 0.3 to 1.5% of the total weight ratio.
中でも商品価値を考慮した場合に有効な処方例としては
後述の具体例が挙げられる。Among them, the specific examples described below are effective prescription examples when commercial value is taken into consideration.
以下に本発明の好適な実施例について詳述するが、本発
明はこれらに限定されない。Preferred embodiments of the present invention will be described in detail below, but the present invention is not limited thereto.
実施例 1
カオリン10部、メタケイ酸アルミン酸マグネシウム(
イノシリンUFL2)0.3部、ポリアクリル酸ナトリ
ウム3部、カルボキシメチルセルロース0.5部を混合
機内に入れ、これにグリセリン28.5部を徐々に加へ
てペースト状になるまで充分混合する。Example 1 10 parts of kaolin, magnesium aluminate metasilicate (
Put 0.3 parts of inocillin UFL2), 3 parts of sodium polyacrylate, and 0.5 parts of carboxymethyl cellulose into a mixer, gradually add 28.5 parts of glycerin, and mix thoroughly until it becomes paste-like.
別にゼラチン4.5部を水50部で膨潤させ、50ない
し60℃で溶解し、これを前記ペーストに加へて均一に
混合する。Separately, 4.5 parts of gelatin is swollen with 50 parts of water, dissolved at 50 to 60°C, and added to the paste and mixed uniformly.
これを35°Cないし40℃となるまで冷却し、その後
ソルビタン脂肪酸エステル0.9部、薬効成分を入れ、
全体が均一になるまで混合する。This was cooled to 35°C to 40°C, and then 0.9 parts of sorbitan fatty acid ester and medicinal ingredients were added.
Mix until everything is homogeneous.
薬効成分はサリチル酸メチル1部、カンフル1部、l−
メントール0.5部である。The medicinal ingredients are 1 part methyl salicylate, 1 part camphor, l-
It is 0.5 part of menthol.
次にこのパップ剤を展延機で不織布に一定の厚みで展延
し表面をポリエチレンフィルムで覆い、−の面積に切断
してパップ剤製剤とした。Next, this poultice was spread on a nonwoven fabric to a certain thickness using a spreading machine, the surface was covered with a polyethylene film, and the product was cut into a - area to obtain a poultice preparation.
このようにして得られたパップ剤製剤では、高温域にお
いておよび発汗時においてもパップ剤の軟化が起らず、
長時間貼布しておいた場合にも冷感、密着性、柔軟性を
失なわず、固化および分離現象もみられなかった。In the poultice preparation thus obtained, the poultice does not soften even in high temperature ranges and during sweating.
Even when it was applied for a long time, it did not lose its cooling sensation, adhesion, or flexibility, and no solidification or separation phenomena were observed.
本発明によるメタケイ酸アルミン酸マグネシウムの添加
による効果を明確にするため、上記組成のうちメタケイ
酸アルミン酸マグネシウムを除いて調製したパップ剤、
および現在市販されている2種のパップ剤について比較
テストを実施した。In order to clarify the effect of adding magnesium aluminate metasilicate according to the present invention, a poultice prepared by excluding magnesium aluminate metasilicate from the above composition,
A comparative test was conducted on two types of poultices currently on the market.
比較のための虐待条件として、35℃および45℃に各
々調節(±2°C)した恒温器に袋ごと各パップ剤を入
れ、1日(24時間)毎に取出し、薬体温度が室温に戻
らないうちに不織布等からの滲出、べた付きの有無、ポ
リエチレンフィルムを剥離した時フィルムへのパップ剤
の付着があるか否か、パップ剤を皮膚へ強く押しつけた
のちはなした時に皮膚へのパップ剤の残留があるか否か
、の4項目について評価を行なった。As an abuse condition for comparison, each bag of poultice was placed in a constant temperature chamber adjusted to 35°C and 45°C (±2°C), and taken out every day (24 hours) until the temperature of the drug reached room temperature. Check whether there is any oozing or stickiness from the non-woven fabric before it returns, whether the poultice sticks to the polyethylene film when it is peeled off, and whether the poultice sticks to the skin when the poultice is strongly pressed against the skin and then removed. Evaluation was performed on four items: whether or not there was any residual poultice.
35°Cにおける結果を第1表に、45℃における結果
を第2表に示した。The results at 35°C are shown in Table 1, and the results at 45°C are shown in Table 2.
サンプルIは本発明によるメタケイ酸アルミン酸マグネ
シウムを含むパップ剤、サンプル■およびlは市販の異
なる2種類のパップ剤、サンプル■はサンプルIのパッ
プ剤と同じ組成のうちメタケイ酸アルミン酸マグネシウ
ムを除外して調製したパップ剤を示す。Sample I is a poultice containing magnesium aluminate metasilicate according to the present invention, Samples ■ and l are two different commercially available poultices, and Sample ■ is the same composition as the poultice of Sample I but excludes magnesium aluminate metasilicate. This figure shows a poultice prepared as follows.
表中、−は全く無し、士は微量有り、+は少量有り、升
は多量有り、柑はかなり多量有り、の意味である。In the table, - means not at all, shi means a small amount, + means a small amount, masu means a large amount, and kan means a considerably large amount.
これらの表から明らかなように、本発明のパップ剤は他
、と比較して非常に優れた物性を示した。As is clear from these tables, the poultice of the present invention exhibited very superior physical properties compared to others.
実施例 2
実施例1と同様にして、サリチル酸メチル1.0優、l
j−メ7 ト−/110.5 %、カンフル1.0覧カ
オリン9.0 %、メタケイ酸アルミン酸マグネシウム
0.8 %、ポリアクリル酸ナトリウム4.0%、カラ
ギーナン0.5 %、ゼラチン4.0%、グリセリン3
0.0%、ソルビタン脂肪酸エステル0.8φおよび常
水適量でなる組成からパップ剤を調製した。Example 2 In the same manner as in Example 1, 1.0 or more l of methyl salicylate was added.
J-Me7 To/110.5%, camphor 1.0 kaolin 9.0%, magnesium aluminate metasilicate 0.8%, sodium polyacrylate 4.0%, carrageenan 0.5%, gelatin 4 .0%, glycerin 3
A poultice was prepared from a composition consisting of 0.0% sorbitan fatty acid ester, 0.8φ of sorbitan fatty acid ester, and an appropriate amount of ordinary water.
この場合にも、実施例1のパップ剤と同様な結果を示し
た。In this case as well, similar results to those of the poultice of Example 1 were shown.
実施例 3
実施例1と同様にして、サリチル酸メチル1.0俤、l
−メントール0.5係、カンフル1.0俤、カオリン8
.0条、メタケイ酸アルミン酸マグネシウム1.20/
)、ポリアクリル酸ナトリウム3.0φ、ゼラチン3.
5俤、グリセリン30.0 %、ソルビタン脂肪酸エス
テル0.9%および常水適量の組成からパップ剤を調製
した。Example 3 In the same manner as in Example 1, 1.0 k, l of methyl salicylate
-0.5 parts of menthol, 1.0 parts of camphor, 8 parts of kaolin
.. Article 0, magnesium aluminate metasilicate 1.20/
), sodium polyacrylate 3.0φ, gelatin 3.
A poultice was prepared from the following composition: 5 tons, 30.0% glycerin, 0.9% sorbitan fatty acid ester, and an appropriate amount of ordinary water.
この場合にも、実施例1のパップ剤と同様、良好な結果
を示した。In this case as well, similar to the poultice of Example 1, good results were shown.
以上本発明をその具体例について詳述したが、本発明は
この特定の実施例に限定されるものではなく、本発明の
精神を逸脱しないで幾多の変化変形がなし得ることはも
ちろんである。Although the present invention has been described above in detail with reference to specific examples, the present invention is not limited to these specific examples, and it goes without saying that many changes and modifications can be made without departing from the spirit of the invention.
Claims (1)
グネシウムを添加したことを特徴とする親水性パップ剤
。1. A hydrophilic poultice agent characterized in that magnesium aluminate metasilicate is added to a base for a hydrophilic poultice agent.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9032778A JPS5843365B2 (en) | 1978-07-26 | 1978-07-26 | Hydrophilic poultice |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9032778A JPS5843365B2 (en) | 1978-07-26 | 1978-07-26 | Hydrophilic poultice |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5517354A JPS5517354A (en) | 1980-02-06 |
| JPS5843365B2 true JPS5843365B2 (en) | 1983-09-27 |
Family
ID=13995421
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9032778A Expired JPS5843365B2 (en) | 1978-07-26 | 1978-07-26 | Hydrophilic poultice |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5843365B2 (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5721318A (en) * | 1980-07-14 | 1982-02-04 | Nitto Electric Ind Co Ltd | Plaster |
| EP0510210A4 (en) * | 1990-11-09 | 1992-11-25 | Teikoku Seiyaku Co., Ltd. | Procaterol-containing plaster |
| JP4978040B2 (en) * | 2006-03-31 | 2012-07-18 | ニチバン株式会社 | Topically applied transdermal absorption tape |
| CA2826003C (en) * | 2011-02-02 | 2019-01-08 | Yasuaki Okada | Blonanserin-containing patch preparation |
| KR101857316B1 (en) | 2011-02-02 | 2018-05-11 | 닛토덴코 가부시키가이샤 | Patch and patch preparation |
| EP2671593B1 (en) * | 2011-02-02 | 2017-06-07 | Nitto Denko Corporation | Patch preparation |
| JPWO2025041654A1 (en) * | 2023-08-24 | 2025-02-27 |
-
1978
- 1978-07-26 JP JP9032778A patent/JPS5843365B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5517354A (en) | 1980-02-06 |
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