JPH09157161A - Treating agent for skin disease - Google Patents
Treating agent for skin diseaseInfo
- Publication number
- JPH09157161A JPH09157161A JP34676695A JP34676695A JPH09157161A JP H09157161 A JPH09157161 A JP H09157161A JP 34676695 A JP34676695 A JP 34676695A JP 34676695 A JP34676695 A JP 34676695A JP H09157161 A JPH09157161 A JP H09157161A
- Authority
- JP
- Japan
- Prior art keywords
- bufexamac
- crotamiton
- treating agent
- skin diseases
- component
- 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
Links
- 208000017520 skin disease Diseases 0.000 title claims abstract description 28
- MXJWRABVEGLYDG-UHFFFAOYSA-N bufexamac Chemical compound CCCCOC1=CC=C(CC(=O)NO)C=C1 MXJWRABVEGLYDG-UHFFFAOYSA-N 0.000 claims abstract description 28
- 229960000962 bufexamac Drugs 0.000 claims abstract description 28
- DNTGGZPQPQTDQF-XBXARRHUSA-N crotamiton Chemical compound C/C=C/C(=O)N(CC)C1=CC=CC=C1C DNTGGZPQPQTDQF-XBXARRHUSA-N 0.000 claims abstract description 24
- 229960003338 crotamiton Drugs 0.000 claims abstract description 24
- 239000003814 drug Substances 0.000 claims description 15
- 229940124597 therapeutic agent Drugs 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 abstract description 14
- 238000002360 preparation method Methods 0.000 abstract description 10
- 230000003110 anti-inflammatory effect Effects 0.000 abstract description 8
- 206010012438 Dermatitis atopic Diseases 0.000 abstract description 5
- 201000008937 atopic dermatitis Diseases 0.000 abstract description 5
- 239000000203 mixture Substances 0.000 abstract description 5
- 239000000739 antihistaminic agent Substances 0.000 abstract description 3
- IVHBBMHQKZBJEU-UHFFFAOYSA-N cinchocaine hydrochloride Chemical compound [Cl-].C1=CC=CC2=NC(OCCCC)=CC(C(=O)NCC[NH+](CC)CC)=C21 IVHBBMHQKZBJEU-UHFFFAOYSA-N 0.000 abstract description 3
- 229940045574 dibucaine hydrochloride Drugs 0.000 abstract description 3
- 239000003589 local anesthetic agent Substances 0.000 abstract description 3
- 229960000520 diphenhydramine Drugs 0.000 abstract description 2
- ZZVUWRFHKOJYTH-UHFFFAOYSA-N diphenhydramine Chemical compound C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 ZZVUWRFHKOJYTH-UHFFFAOYSA-N 0.000 abstract description 2
- GUGOEEXESWIERI-UHFFFAOYSA-N Terfenadine Chemical compound C1=CC(C(C)(C)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 GUGOEEXESWIERI-UHFFFAOYSA-N 0.000 abstract 1
- 230000000202 analgesic effect Effects 0.000 abstract 1
- 230000001387 anti-histamine Effects 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 12
- 230000001139 anti-pruritic effect Effects 0.000 description 10
- 208000003251 Pruritus Diseases 0.000 description 9
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000007803 itching Effects 0.000 description 6
- 239000002674 ointment Substances 0.000 description 5
- 230000003637 steroidlike Effects 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 230000002757 inflammatory effect Effects 0.000 description 4
- 208000024891 symptom Diseases 0.000 description 4
- LEACJMVNYZDSKR-UHFFFAOYSA-N 2-octyldodecan-1-ol Chemical compound CCCCCCCCCCC(CO)CCCCCCCC LEACJMVNYZDSKR-UHFFFAOYSA-N 0.000 description 3
- 206010015150 Erythema Diseases 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 241000700159 Rattus Species 0.000 description 3
- BTFJIXJJCSYFAL-UHFFFAOYSA-N arachidyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 3
- 235000010418 carrageenan Nutrition 0.000 description 3
- 229920001525 carrageenan Polymers 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-Menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 description 2
- 229940058015 1,3-butylene glycol Drugs 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 2
- 206010061218 Inflammation Diseases 0.000 description 2
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 2
- 206010030113 Oedema Diseases 0.000 description 2
- 206010033733 Papule Diseases 0.000 description 2
- VYGQUTWHTHXGQB-FFHKNEKCSA-N Retinol Palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C VYGQUTWHTHXGQB-FFHKNEKCSA-N 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- 206010042674 Swelling Diseases 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
- 229940125715 antihistaminic agent Drugs 0.000 description 2
- 239000003908 antipruritic agent Substances 0.000 description 2
- 235000019437 butane-1,3-diol Nutrition 0.000 description 2
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 239000002552 dosage form Substances 0.000 description 2
- 230000003628 erosive effect Effects 0.000 description 2
- 231100000321 erythema Toxicity 0.000 description 2
- 230000004054 inflammatory process Effects 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 229960003517 isothipendyl Drugs 0.000 description 2
- OQJBSDFFQWMKBQ-UHFFFAOYSA-N isothipendyl Chemical compound C1=CN=C2N(CC(C)N(C)C)C3=CC=CC=C3SC2=C1 OQJBSDFFQWMKBQ-UHFFFAOYSA-N 0.000 description 2
- 210000003141 lower extremity Anatomy 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- 230000001823 pruritic effect Effects 0.000 description 2
- 239000008213 purified water Substances 0.000 description 2
- 150000003431 steroids Chemical class 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- -1 thecaine Chemical compound 0.000 description 2
- 229940088594 vitamin Drugs 0.000 description 2
- 239000011782 vitamin Substances 0.000 description 2
- 229930003231 vitamin Natural products 0.000 description 2
- 235000013343 vitamin Nutrition 0.000 description 2
- 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 1
- CRBBOOXGHMTWOC-NPDDRXJXSA-N 1,4-Anhydro-6-O-dodecanoyl-2,3-bis-O-(2-hydroxyethyl)-D-glucitol Chemical compound CCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](OCCO)[C@H]1OCCO CRBBOOXGHMTWOC-NPDDRXJXSA-N 0.000 description 1
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 description 1
- FDCJDKXCCYFOCV-UHFFFAOYSA-N 1-hexadecoxyhexadecane Chemical compound CCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCC FDCJDKXCCYFOCV-UHFFFAOYSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- CIVCELMLGDGMKZ-UHFFFAOYSA-N 2,4-dichloro-6-methylpyridine-3-carboxylic acid Chemical compound CC1=CC(Cl)=C(C(O)=O)C(Cl)=N1 CIVCELMLGDGMKZ-UHFFFAOYSA-N 0.000 description 1
- HBTAOSGHCXUEKI-UHFFFAOYSA-N 4-chloro-n,n-dimethyl-3-nitrobenzenesulfonamide Chemical compound CN(C)S(=O)(=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 HBTAOSGHCXUEKI-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 206010003645 Atopy Diseases 0.000 description 1
- 206010006784 Burning sensation Diseases 0.000 description 1
- DBAKFASWICGISY-BTJKTKAUSA-N Chlorpheniramine maleate Chemical compound OC(=O)\C=C/C(O)=O.C=1C=CC=NC=1C(CCN(C)C)C1=CC=C(Cl)C=C1 DBAKFASWICGISY-BTJKTKAUSA-N 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 1
- 206010048768 Dermatosis Diseases 0.000 description 1
- 206010013786 Dry skin Diseases 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 208000006877 Insect Bites and Stings Diseases 0.000 description 1
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 description 1
- NNJVILVZKWQKPM-UHFFFAOYSA-N Lidocaine Chemical compound CCN(CC)CC(=O)NC1=C(C)C=CC=C1C NNJVILVZKWQKPM-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241000700157 Rattus norvegicus Species 0.000 description 1
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
- MSCCTZZBYHQMQJ-AZAGJHQNSA-N Tocopheryl nicotinate Chemical compound C([C@@](OC1=C(C)C=2C)(C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)CC1=C(C)C=2OC(=O)C1=CC=CN=C1 MSCCTZZBYHQMQJ-AZAGJHQNSA-N 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
- 230000002411 adverse Effects 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 229960000686 benzalkonium chloride Drugs 0.000 description 1
- 229960001950 benzethonium chloride Drugs 0.000 description 1
- UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 1
- BLFLLBZGZJTVJG-UHFFFAOYSA-N benzocaine Chemical compound CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- 229960001948 caffeine Drugs 0.000 description 1
- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 description 1
- 229960000846 camphor Drugs 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 229960001927 cetylpyridinium chloride Drugs 0.000 description 1
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 1
- 229960003291 chlorphenamine Drugs 0.000 description 1
- SOYKEARSMXGVTM-UHFFFAOYSA-N chlorphenamine Chemical compound C=1C=CC=NC=1C(CCN(C)C)C1=CC=C(Cl)C=C1 SOYKEARSMXGVTM-UHFFFAOYSA-N 0.000 description 1
- 229940046978 chlorpheniramine maleate Drugs 0.000 description 1
- 229960001747 cinchocaine Drugs 0.000 description 1
- PUFQVTATUTYEAL-UHFFFAOYSA-N cinchocaine Chemical compound C1=CC=CC2=NC(OCCCC)=CC(C(=O)NCCN(CC)CC)=C21 PUFQVTATUTYEAL-UHFFFAOYSA-N 0.000 description 1
- 229940000425 combination drug Drugs 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 1
- 229940031578 diisopropyl adipate Drugs 0.000 description 1
- 229960000525 diphenhydramine hydrochloride Drugs 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000037336 dry skin Effects 0.000 description 1
- 235000006694 eating habits Nutrition 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229960004194 lidocaine Drugs 0.000 description 1
- 229960004393 lidocaine hydrochloride Drugs 0.000 description 1
- YECIFGHRMFEPJK-UHFFFAOYSA-N lidocaine hydrochloride monohydrate Chemical compound O.[Cl-].CC[NH+](CC)CC(=O)NC1=C(C)C=CC=C1C YECIFGHRMFEPJK-UHFFFAOYSA-N 0.000 description 1
- 229960005015 local anesthetics Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 235000005152 nicotinamide Nutrition 0.000 description 1
- 239000011570 nicotinamide Substances 0.000 description 1
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 description 1
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- ZUFQODAHGAHPFQ-UHFFFAOYSA-N pyridoxine hydrochloride Chemical compound Cl.CC1=NC=C(CO)C(CO)=C1O ZUFQODAHGAHPFQ-UHFFFAOYSA-N 0.000 description 1
- 229960004172 pyridoxine hydrochloride Drugs 0.000 description 1
- 235000019171 pyridoxine hydrochloride Nutrition 0.000 description 1
- 239000011764 pyridoxine hydrochloride Substances 0.000 description 1
- 235000020944 retinol Nutrition 0.000 description 1
- 239000011607 retinol Substances 0.000 description 1
- 229960003471 retinol Drugs 0.000 description 1
- 235000019172 retinyl palmitate Nutrition 0.000 description 1
- 239000011769 retinyl palmitate Substances 0.000 description 1
- 229940108325 retinyl palmitate Drugs 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 229940083466 soybean lecithin Drugs 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 229940042585 tocopherol acetate Drugs 0.000 description 1
- 229950009883 tocopheryl nicotinate Drugs 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
Landscapes
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、皮膚疾患治療剤に
関し、更に詳述すると、ブフェキサマックの抗炎症作用
を増強するとともに、優れた鎮痒効果を付与した皮膚疾
患治療剤に関する。TECHNICAL FIELD The present invention relates to a therapeutic agent for skin diseases, and more specifically to a therapeutic agent for skin diseases which enhances the anti-inflammatory action of bufexamac and imparts an excellent antipruritic effect.
【0002】[0002]
【従来の技術及び発明が解決しようとする課題】食生活
の欧米化、生活環境の変化、ストレスの増大等に伴い、
さまざまな皮膚疾患、特にアトピー素因に基づくアトピ
ー性皮膚炎になる人が増加の一途を辿っている。これら
の皮膚疾患に対しては、一般にステロイド系及び/又は
非ステロイド系の外用剤による治療がおこなわれてい
る。2. Description of the Related Art With the westernization of eating habits, changes in living environment, increased stress, etc.,
An increasing number of people have various skin diseases, especially atopic dermatitis due to atopic diathesis. These skin diseases are generally treated with steroidal and / or non-steroidal external preparations.
【0003】しかしながら、ステロイド系の外用剤は副
作用が強く、連用すると逆に皮膚状態を悪化させる場合
もあった。また、非ステロイド系外用剤は副作用は弱い
が有効性が低く、ステロイド系外用剤の補助として使用
されているにすぎない。However, the external preparations of steroid type have strong side effects, and if they are used continuously, they may adversely affect the skin condition. In addition, non-steroidal external preparations have weak side effects but low efficacy and are only used as an adjunct to steroidal external preparations.
【0004】本発明は上記事情に鑑みなされたもので、
種々の皮膚疾患に対する効果が高く、副作用の少ない皮
膚疾患治療剤を提供することを目的とする。[0004] The present invention has been made in view of the above circumstances,
It is an object of the present invention to provide a therapeutic agent for skin diseases that is highly effective against various skin diseases and has few side effects.
【0005】[0005]
【課題を解決するための手段及び発明の実施の形態】本
発明者らは、上記従来技術の欠点に鑑み、皮膚疾患患者
の皮膚症状を改善し、副作用の少ない皮膚疾患治療剤を
得るべく鋭意研究を重ねた結果、非ステロイド系抗炎症
剤であるブフェキサマックにクロタミトンを併用するこ
とにより、ブフェキサマックの皮膚からの吸収性が改善
され、ブフェキサマックの抗炎症作用が増強されるた
め、皮膚疾患による紅斑、腫脹、丘疹、びらん、痂皮及
び鱗屑といった症状が改善されるとともに、クロタミト
ンの鎮痒作用により皮膚疾患特有のそう痒感が相乗的に
改善され、かつ、ステロイド系外用剤特有の局部の発
赤、灼熱感及びつっぱり感等の副作用の無い皮膚疾患治
療剤が得られることを知見し、本発明をなすに至った。Means for Solving the Problems and Modes for Carrying Out the Invention In view of the above-mentioned drawbacks of the prior art, the present inventors have eagerly aimed to improve the skin symptoms of patients with skin diseases and obtain a therapeutic agent for skin diseases with few side effects. As a result of repeated studies, the combined use of crotamiton with bufexamac, a nonsteroidal anti-inflammatory drug, improves the skin absorbability of bufexamac and enhances the anti-inflammatory effect of bufexamac. , Symptoms such as erythema, swelling, papules, erosion, crust and scale due to skin diseases are improved, and pruriticity peculiar to skin diseases is synergistically improved by the antipruritic effect of crotamiton, and it is unique to steroid external preparations. It was found that a therapeutic agent for skin diseases free of side effects such as local redness, burning sensation and tightness can be obtained, and the present invention has been completed.
【0006】以下、本発明につき更に詳しく説明する
と、本発明の皮膚疾患治療剤は、ブフェキサマックとク
ロタミトンとを併用したものである。The present invention will be described in more detail below. The therapeutic agent for skin diseases of the present invention is a combination of bufexamac and crotamiton.
【0007】ここで、本発明におけるブフェキサマック
の配合量は製剤中2.0〜10重量%、好ましくは2.
5〜5重量%である。2.0重量%未満ではその効果は
発揮されず、10重量%を超える配合量では、有効性面
で意味が無いばかりか、製品の製造工程上好ましくない
場合が生じる。また、クロタミトンの配合量はブフェキ
サマックの2倍重量以上の配合、好ましくは2倍重量以
上5倍重量未満、配合量として製剤中2〜30重量%、
好ましくは5〜20重量%である。クロタミトンの配合
がブフェキサマックの2倍重量未満では、クロタミトン
の経皮吸収促進作用が発現されないばかりか、鎮痒作用
も発現されないため、その効果は低くなる場合がある。
一方、5倍重量以上配合すると、製剤の安定性上問題が
生じる場合がある。The blending amount of bufexamac in the present invention is 2.0 to 10% by weight, preferably 2.
5 to 5% by weight. If it is less than 2.0% by weight, the effect is not exhibited, and if it is more than 10% by weight, it is meaningless in terms of effectiveness and may not be preferable in the production process of the product. In addition, the amount of crotamiton compounded is 2 times or more by weight of bufexamac, preferably 2 times or more and less than 5 times by weight, 2 to 30% by weight of the formulation in the formulation
Preferably it is 5 to 20% by weight. If the content of crotamiton is less than twice the weight of bufexamac, not only the transdermal absorption promoting action of crotamiton is not exhibited but also the antipruritic action is not exhibited, so that the effect may be reduced.
On the other hand, if it is blended in an amount of 5 times the weight or more, problems may occur in the stability of the preparation.
【0008】本発明の皮膚疾患治療剤には、種々の皮膚
疾患に対する有効性を高めるためにブフェキサマックと
クロタミトンのほか、抗ヒスタミン剤、局所麻酔剤、殺
菌剤及びビタミン剤など種々の有効成分を配合できる。
配合できる抗ヒスタミン剤としては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、ジフェンヒドラミン塩基、クロルフェニラミン塩
基などが0.1〜2重量%配合できる。局所麻酔剤とし
ては、塩酸ジブカイン、塩酸イソチペンジル、塩酸リド
カイン、テーカイン、ジブカイン、リドカイン、パラア
ミノ安息香酸エチルなどが0.1〜2重量%配合でき
る。殺菌剤としては、塩化ベンザルコニウム、塩化ベン
ゼトニウム、セチルピリジニウムクロライド、ビオゾー
ル、フェノールなどが0.05〜1重量%配合できる。
また、ビタミン剤としてはトコフェロール、酢酸トコフ
ェロール、ニコチン酸トコフェロール、ニコチン酸アミ
ド、塩酸ピリドキシン、レチノール、パルミチン酸レチ
ノールなどが0.05〜3重量%配合できる。そのほ
か、本発明の皮膚疾患治療剤には清涼化剤としてメント
ール及び/又はカンフル等を0.1〜5重量%配合でき
る。The agent for treating skin diseases of the present invention contains various active ingredients such as antihistamines, local anesthetics, fungicides and vitamins in addition to bufexamac and crotamiton in order to enhance the effectiveness against various skin diseases. it can.
As antihistamines that can be blended, 0.1 to 2% by weight of diphenhydramine hydrochloride, chlorpheniramine maleate, isothipendyl hydrochloride, diphenhydramine base, chlorpheniramine base and the like can be blended. As the local anesthetic, 0.1-2% by weight of dibucaine hydrochloride, isothipendyl hydrochloride, lidocaine hydrochloride, thecaine, dibucaine, lidocaine, ethyl paraaminobenzoate, etc. can be blended. As the bactericide, 0.05 to 1% by weight of benzalkonium chloride, benzethonium chloride, cetylpyridinium chloride, biozole, phenol or the like can be added.
As the vitamin preparation, tocopherol, tocopherol acetate, tocopherol nicotinate, nicotinic acid amide, pyridoxine hydrochloride, retinol, retinol palmitate, etc. can be added in an amount of 0.05 to 3% by weight. In addition, 0.1 to 5% by weight of menthol and / or camphor and the like can be added as a cooling agent to the therapeutic agent for skin diseases of the present invention.
【0009】本発明の皮膚疾患治療剤の剤形は任意であ
り、溶液系、乳液系、クリーム系、軟膏系、及びゲル製
剤系等、どのような剤形でもよく、このような剤形を与
える公知の賦形剤などの成分を配合することができる。The dosage form of the therapeutic agent for skin diseases of the present invention is arbitrary, and any dosage form such as solution type, emulsion type, cream type, ointment type and gel type may be used. Ingredients such as known excipients to be given can be blended.
【0010】本発明のブフェキサマックとクロタミトン
を配合した皮膚疾患治療剤は、疾患のある皮膚に適用し
たときに、クロタミトンがブフェキサマック経皮吸収を
促進することにより、ブフェキサマックの抗炎症効果が
増強されるとともに、クロタミトンの鎮痒作用により、
皮膚疾患に特有の紅斑、丘疹、腫脹、びらん、痂皮、鱗
屑及びそう痒といった症状を軽減する作用が強く、ステ
ロイド系外用剤のような副作用が発現しない皮膚疾患治
療剤を得ることができるが、この場合、本発明の皮膚疾
患治療剤は1日1〜3回程度患部に塗布すると共に、1
回の投与量(塗布量)はブフェキサマックが10〜50
mg、クロタミトンが20〜150mgとすることがで
きる。The therapeutic agent for skin diseases containing bufexamac and crotamiton of the present invention, when applied to diseased skin, crotamiton promotes percutaneous absorption of bufexamac so that bufexamac has anti-inflammatory properties. As the effect is enhanced, the antipruritic effect of crotamiton,
Although it is possible to obtain a therapeutic agent for skin diseases, which has a strong effect of reducing symptoms such as erythema, papules, swelling, erosion, crust, scales and pruritus, which are peculiar to skin diseases, and which does not cause side effects like external steroidal agents. In this case, the therapeutic agent for skin diseases of the present invention is applied to the affected area about 1 to 3 times a day, and
Bufexamac is 10 to 50 times
mg and crotamiton can be 20 to 150 mg.
【0011】[0011]
【実施例】以下、実施例と比較例を示し、本発明を具体
的に説明するが、本発明は下記実施例に制限されるもの
ではない。EXAMPLES The present invention will be described below in detail with reference to examples and comparative examples, but the present invention is not limited to the following examples.
【0012】〔実施例1,2、比較例1,2〕表1に示
す処方について、70℃に加熱したAの油相部を、同じ
く70℃に加熱したBの水相部に加えて乳化し、クリー
ムを作成し、以下の試験を行った。[Examples 1 and 2, Comparative Examples 1 and 2] With respect to the formulations shown in Table 1, the oil phase part of A heated to 70 ° C. was added to the water phase part of B similarly heated to 70 ° C. to emulsify. Then, a cream was prepared and the following tests were conducted.
【0013】[0013]
【表1】 [Table 1]
【0014】<抗炎症試験:カラゲニン足浮腫抑制試験
>体重110〜130gのWistar系ラットを1群
10匹として用いた。ラットの右後肢の足容積をボリュ
ーム・ディファレンシャル・メーター(volume
differential meter)で測定し、各
群の平均足容積がほぼ一定となるように群分けした。起
炎剤注射2時間及び1時間前の2回、右後足蹠部に試料
を塗擦し、塗擦部位を粘着包帯で被覆保護した。起炎剤
として1%カラゲニン懸濁液0.1mlを同足蹠皮下に
注射した。起炎剤注射後、1時間毎に5時間まで経時的
に右後肢容積を測定し、起炎剤注射前の足容積から下記
の式に基づいて浮腫率と抑制率を算出した。<Anti-inflammatory Test: Carrageenin Paw Edema Inhibition Test> Wistar rats weighing 110 to 130 g were used as one group consisting of 10 rats. The volume of the right hind limb of the rat is measured by a volume differential meter (volume).
The measurement was made by using a differential meter), and the animals were divided into groups so that the average foot volume of each group was almost constant. The sample was rubbed twice on the right hind footpad 2 hours and 1 hour before the injection of the inflammatory agent, and the rubbed site was covered and protected with an adhesive bandage. 0.1 ml of a 1% carrageenin suspension as an inflammatory agent was subcutaneously injected into the footpad. The volume of the right hind limb was measured hourly for up to 5 hours after injection of the inflammatory agent, and the edema rate and the inhibition rate were calculated from the paw volume before injection of the inflammatory agent based on the following formula.
【0015】[0015]
【数1】 (Equation 1)
【0016】試験結果を表2に示す。この結果から、ブ
フェキサマック、クロタミトン単味ではラットのカラゲ
ニン起炎による浮腫を抑制する作用は弱く、ブフェキサ
マックにクロタミトンを配合した場合のみ抑制作用、即
ち抗炎症作用が強くなることが認められた。この増強作
用は、ブフェキサマックとクロタミトンを組み合わせた
ことにより、ブフェキサマックの経皮吸収性が改善され
たためと考えられる。The test results are shown in Table 2. From these results, it was confirmed that bufexamac and crotamiton alone have a weak effect of suppressing edema due to carrageenin inflammation in rats, and that the effect of suppressing caffeine only when bufexamac is combined with crotamiton is strong. It was This potentiating effect is considered to be because the transdermal absorbability of bufexamac was improved by combining bufexamac and crotamiton.
【0017】[0017]
【表2】 [Table 2]
【0018】<鎮痒試験>健常人5名を選定し、起痒剤
として新しく擦りおろしたヤマイモを用いて試験した。
即ち、起痒剤塗擦30分前に試料約0.2gを直径約4
cmの範囲に2回に分けて塗布した。30分後、試料を
アルコール綿で良く拭き取り、皮膚を乾燥させた後、起
痒剤として新しく擦りおろしたヤマイモ0.5gを塗擦
し、起痒した。起痒した直後より、痒みの程度を表3の
基準に従って20秒毎に痒みが消出するまで評点し、そ
の総合点を結果とした。なお、試験の最初に比較対照と
して、無処置で同様の起痒剤を塗擦した時、非常に強い
痒みを感じることを確認してから、試験を開始した。こ
こで、結果は20秒毎に評点を与え、0点になるまで評
点し、これを累積したもので、コントロールは約10分
後に0点になり、その総合点(累積点)は75点程度で
あった。本試験を5回繰り返し、この平均を試験結果と
した。<Antipruritic test> Five healthy persons were selected and tested using freshly grated yam as an itching agent.
That is, about 30 minutes before rubbing the pruritic agent, about 0.2 g of the sample had a diameter of about 4
It was applied twice in a range of cm. After 30 minutes, the sample was thoroughly wiped with alcohol cotton to dry the skin, and then 0.5 g of freshly grated yam as an itch was applied and itched. Immediately after itching, the degree of itching was evaluated according to the criteria in Table 3 every 20 seconds until the itching disappeared, and the total score was taken as the result. As a comparative control, the test was started at the beginning of the test after it was confirmed that very strong itching was felt when the same pruritic agent was rubbed without treatment. Here, the result is given every 20 seconds, and is scored until it reaches 0, and this is accumulated. The control becomes 0 after 10 minutes, and the total score (cumulative score) is about 75. Met. This test was repeated 5 times, and this average was used as the test result.
【0019】[0019]
【表3】 試験結果を表4に示した。ブフェキサマック単味製剤で
は鎮痒効果は全くないが、クロタミトンとの配合剤であ
る本発明品では高い鎮痒作用が確認された。[Table 3] The test results are shown in Table 4. Although the bufexamac plain preparation had no antipruritic effect at all, the antipruritic effect was confirmed to be high in the product of the present invention which is a combination drug with crotamiton.
【0020】[0020]
【表4】 [Table 4]
【0021】以上の抗炎症試験、鎮痒試験の結果より、
ブフェキサマックとクロタミトンを組み合わせて配合す
ることにより、アトピー性皮膚炎等の皮膚疾患に特有で
ある炎症とそう痒といった症状に有用な治療剤となるこ
とがわかった。From the results of the above anti-inflammatory test and antipruritic test,
It was found that the combination of bufexamac and crotamiton is a useful therapeutic agent for symptoms such as inflammation and pruritus that are peculiar to skin diseases such as atopic dermatitis.
【0022】 〔実施例3〕 乳液 A(油相部) ブフェキサマック 2.5 重量% クロタミトン 7.5 モノステアリン酸ソルビタン 3.0 POE(20)モノステアリン酸ソルビタン 4.0 オクチルドデカノール 1.0 アジピン酸ジイソプロピル 1.0 大豆レシチン 1.0 B(水相部) 10.0 1,3−ブチレングリコール 0.2 メチルパラベン 0.2 カルボキシビニルポリマー 0.2 水酸化カリウム 適量 精製水 残量 合計 100.0 重量% 60℃に加熱したAの油相部を同じく60℃に加熱した
Bの水相部に加え乳化冷却後、水酸化カリウムで中和
し、乳液を得る。本発明品は乳液として患部が広い場合
に使用される。Example 3 Emulsion A (oil phase portion) Bufexamac 2.5 wt% crotamiton 7.5 sorbitan monostearate 3.0 POE (20) sorbitan monostearate 4.0 octyldodecanol 1. 0 diisopropyl adipate 1.0 soybean lecithin 1.0 B (water phase part) 10.0 1,3-butylene glycol 0.2 methylparaben 0.2 carboxyvinyl polymer 0.2 potassium hydroxide proper amount purified water residual amount total 100 0.0 wt% The oil phase portion of A heated to 60 ° C. is added to the water phase portion of B similarly heated to 60 ° C., the mixture is emulsified and cooled, and then neutralized with potassium hydroxide to obtain an emulsion. The product of the present invention is used as an emulsion when the affected area is wide.
【0023】 〔実施例4〕 油性軟膏 ブフェキサマック 5.0 重量% クロタミトン 15.0 オクチルドデカノール 5.0 モノステアリン酸グリセリン 2.0 プラスチベース 残量 合計 100.0 重量% ブフェキサマック、クロタミトン、オクチルドデカノー
ル及びモノステアリン酸グリセリンを60℃で加熱溶解
し、プラスチベースと練合して、油性軟膏を調製する。
本発明品はアトピー性皮膚炎、乾燥性皮膚症など皮膚の
乾燥が著しい場合に使用される。Example 4 Oil Ointment Bufexamac 5.0 wt% Crotamiton 15.0 Octyldodecanol 5.0 Glycerin monostearate 2.0 Plastibase Total residual amount 100.0 wt% Bufexamac, crotamiton, Octyldodecanol and glycerin monostearate are dissolved by heating at 60 ° C. and kneaded with plastibase to prepare an oily ointment.
The product of the present invention is used when the skin is extremely dry such as atopic dermatitis and dry skin disease.
【0024】 〔実施例5〕 ゲル軟膏 ブフェキサマック 2.0 重量% クロタミトン 10.0 l−メントール 3.0 塩酸ジブカイン 0.5 POE(20)セチルエーテル 3.0 エタノール 35.0 1,3−ブチレングリコール 25.0 カルボキシビニルポリマー 1.5 ヒドロキシプロピルセルロース 0.1 精製水 残量 水酸化ナトリウム 0.2 合計 100.0 重量% それぞれを溶解した後、水酸化ナトリウムで中和して、
ゲル軟膏を調製する。本発明品は虫刺され等の痒みに対
する速効性が要求される皮膚疾患に使用される。Example 5 Gel Ointment Bufexamac 2.0 wt% crotamiton 10.0 l-menthol 3.0 dibucaine hydrochloride 0.5 POE (20) cetyl ether 3.0 ethanol 35.0 1,3- Butylene glycol 25.0 Carboxyvinyl polymer 1.5 Hydroxypropyl cellulose 0.1 Purified water Remaining amount of sodium hydroxide 0.2 Total 100.0 wt% After dissolving each of them, neutralizing with sodium hydroxide,
Prepare a gel ointment. The product of the present invention is used for skin diseases that require rapid action against itching such as insect bites.
【0025】[0025]
【発明の効果】本発明によれば、ブフェキサマック及び
クロタミトンを併用したことにより、ブフェキサマック
の抗炎症作用が増強されるとともに、鎮痒作用が付与さ
れるため、アトピー性皮膚炎、乾燥性皮膚症等の抗炎症
作用と鎮痒作用が要求される皮膚疾患の治療剤として最
適の薬剤を提供することができる。INDUSTRIAL APPLICABILITY According to the present invention, the combined use of bufexamac and crotamiton enhances the anti-inflammatory effect of bufexamac and imparts an antipruritic effect, thus atopic dermatitis and dryness. It is possible to provide an optimal drug as a therapeutic agent for a skin disease requiring anti-inflammatory action and antipruritic action such as dermatosis.
Claims (1)
有することを特徴とする皮膚疾患治療剤。1. A therapeutic agent for skin diseases, which comprises bufexamac and crotamiton.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP34676695A JPH09157161A (en) | 1995-12-13 | 1995-12-13 | Treating agent for skin disease |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP34676695A JPH09157161A (en) | 1995-12-13 | 1995-12-13 | Treating agent for skin disease |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH09157161A true JPH09157161A (en) | 1997-06-17 |
Family
ID=18385679
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP34676695A Pending JPH09157161A (en) | 1995-12-13 | 1995-12-13 | Treating agent for skin disease |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH09157161A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7109246B1 (en) | 1998-05-22 | 2006-09-19 | Hewlett Healthcare Ltd | Pharmaceutical compositions comprising an amphoteric surfactant an alkoxylated cetyl alcohol and a polar drug |
JP2010064995A (en) * | 2008-09-12 | 2010-03-25 | Nikko Chemical Co Ltd | Anti-inflammatory analgesic composition for external application |
JP2016000721A (en) * | 2014-05-22 | 2016-01-07 | ライオン株式会社 | External preparation composition and anti-inflammatory action enhancer |
JP2016003207A (en) * | 2014-06-17 | 2016-01-12 | ロート製薬株式会社 | External composition |
JP2017075129A (en) * | 2015-10-16 | 2017-04-20 | 株式会社マンダム | TRPV1 activity inhibitor |
-
1995
- 1995-12-13 JP JP34676695A patent/JPH09157161A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7109246B1 (en) | 1998-05-22 | 2006-09-19 | Hewlett Healthcare Ltd | Pharmaceutical compositions comprising an amphoteric surfactant an alkoxylated cetyl alcohol and a polar drug |
JP2010064995A (en) * | 2008-09-12 | 2010-03-25 | Nikko Chemical Co Ltd | Anti-inflammatory analgesic composition for external application |
JP2016000721A (en) * | 2014-05-22 | 2016-01-07 | ライオン株式会社 | External preparation composition and anti-inflammatory action enhancer |
JP2016003207A (en) * | 2014-06-17 | 2016-01-12 | ロート製薬株式会社 | External composition |
JP2017075129A (en) * | 2015-10-16 | 2017-04-20 | 株式会社マンダム | TRPV1 activity inhibitor |
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