JP2021195324A - External composition - Google Patents
External composition Download PDFInfo
- Publication number
- JP2021195324A JP2021195324A JP2020101676A JP2020101676A JP2021195324A JP 2021195324 A JP2021195324 A JP 2021195324A JP 2020101676 A JP2020101676 A JP 2020101676A JP 2020101676 A JP2020101676 A JP 2020101676A JP 2021195324 A JP2021195324 A JP 2021195324A
- Authority
- JP
- Japan
- Prior art keywords
- component
- shaving
- external composition
- weight
- skin inflammation
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 72
- 201000004624 Dermatitis Diseases 0.000 claims abstract description 45
- 150000003839 salts Chemical class 0.000 claims abstract description 25
- NNJVILVZKWQKPM-UHFFFAOYSA-N Lidocaine Chemical compound CCN(CC)CC(=O)NC1=C(C)C=CC=C1C NNJVILVZKWQKPM-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229960004194 lidocaine Drugs 0.000 claims abstract description 15
- JDLSRXWHEBFHNC-UHFFFAOYSA-N Ufenamate Chemical compound CCCCOC(=O)C1=CC=CC=C1NC1=CC=CC(C(F)(F)F)=C1 JDLSRXWHEBFHNC-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229950010121 ufenamate Drugs 0.000 claims abstract description 10
- MPDGHEJMBKOTSU-YKLVYJNSSA-N 18beta-glycyrrhetic acid Chemical compound C([C@H]1C2=CC(=O)[C@H]34)[C@@](C)(C(O)=O)CC[C@]1(C)CC[C@@]2(C)[C@]4(C)CC[C@@H]1[C@]3(C)CC[C@H](O)C1(C)C MPDGHEJMBKOTSU-YKLVYJNSSA-N 0.000 claims description 35
- MPDGHEJMBKOTSU-UHFFFAOYSA-N Glycyrrhetinsaeure Natural products C12C(=O)C=C3C4CC(C)(C(O)=O)CCC4(C)CCC3(C)C1(C)CCC1C2(C)CCC(O)C1(C)C MPDGHEJMBKOTSU-UHFFFAOYSA-N 0.000 claims description 13
- 229960003720 enoxolone Drugs 0.000 claims description 13
- 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 claims description 12
- 206010061218 Inflammation Diseases 0.000 claims description 11
- 239000003242 anti bacterial agent Substances 0.000 claims description 11
- 230000004054 inflammatory process Effects 0.000 claims description 11
- 239000011732 tocopherol Substances 0.000 claims description 11
- 229930003799 tocopherol Natural products 0.000 claims description 11
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- 229960001295 tocopherol Drugs 0.000 claims description 10
- 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 claims description 10
- 230000000844 anti-bacterial effect Effects 0.000 claims description 8
- 239000003899 bactericide agent Substances 0.000 claims description 8
- 210000001015 abdomen Anatomy 0.000 claims description 5
- 210000003905 vulva Anatomy 0.000 claims description 5
- 208000003251 Pruritus Diseases 0.000 claims description 4
- 210000000436 anus Anatomy 0.000 claims description 4
- 230000007803 itching Effects 0.000 claims description 4
- ZZVUWRFHKOJYTH-UHFFFAOYSA-N diphenhydramine Chemical compound C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 ZZVUWRFHKOJYTH-UHFFFAOYSA-N 0.000 claims 1
- 230000000694 effects Effects 0.000 description 31
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- -1 butyl flufenamic acid Chemical compound 0.000 description 16
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- 239000002202 Polyethylene glycol Substances 0.000 description 8
- 229920001223 polyethylene glycol Polymers 0.000 description 8
- 229940042585 tocopherol acetate Drugs 0.000 description 7
- 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 6
- 230000000052 comparative effect Effects 0.000 description 6
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 5
- 229940079593 drug Drugs 0.000 description 5
- 150000003611 tocopherol derivatives Chemical class 0.000 description 5
- IJALWSVNUBBQRA-UHFFFAOYSA-N 4-Isopropyl-3-methylphenol Chemical compound CC(C)C1=CC=C(O)C=C1C IJALWSVNUBBQRA-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000006071 cream Substances 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 150000002148 esters Chemical group 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- NFIDBGJMFKNGGQ-UHFFFAOYSA-N isopropylmethylphenol Natural products CC(C)CC1=CC=CC=C1O NFIDBGJMFKNGGQ-UHFFFAOYSA-N 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000001993 wax Substances 0.000 description 4
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000004166 Lanolin Substances 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 3
- 235000019388 lanolin Nutrition 0.000 description 3
- 229940039717 lanolin Drugs 0.000 description 3
- 239000003589 local anesthetic agent Substances 0.000 description 3
- 230000007721 medicinal effect Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 125000001453 quaternary ammonium group Chemical group 0.000 description 3
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 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 2
- FDCJDKXCCYFOCV-UHFFFAOYSA-N 1-hexadecoxyhexadecane Chemical compound CCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCC FDCJDKXCCYFOCV-UHFFFAOYSA-N 0.000 description 2
- ASKIVFGGGGIGKH-UHFFFAOYSA-N 2,3-dihydroxypropyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(O)CO ASKIVFGGGGIGKH-UHFFFAOYSA-N 0.000 description 2
- FLPJVCMIKUWSDR-UHFFFAOYSA-N 2-(4-formylphenoxy)acetamide Chemical compound NC(=O)COC1=CC=C(C=O)C=C1 FLPJVCMIKUWSDR-UHFFFAOYSA-N 0.000 description 2
- LVYLCBNXHHHPSB-UHFFFAOYSA-N 2-hydroxyethyl salicylate Chemical compound OCCOC(=O)C1=CC=CC=C1O LVYLCBNXHHHPSB-UHFFFAOYSA-N 0.000 description 2
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 2
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N Alanine Chemical compound CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 description 2
- 241000723346 Cinnamomum camphora Species 0.000 description 2
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 208000010201 Exanthema Diseases 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000000739 antihistaminic agent Substances 0.000 description 2
- 230000003796 beauty Effects 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- KVYGGMBOZFWZBQ-UHFFFAOYSA-N benzyl nicotinate Chemical compound C=1C=CN=CC=1C(=O)OCC1=CC=CC=C1 KVYGGMBOZFWZBQ-UHFFFAOYSA-N 0.000 description 2
- FUWUEFKEXZQKKA-UHFFFAOYSA-N beta-thujaplicin Chemical compound CC(C)C=1C=CC=C(O)C(=O)C=1 FUWUEFKEXZQKKA-UHFFFAOYSA-N 0.000 description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 2
- 229930008380 camphor Natural products 0.000 description 2
- 229960000846 camphor Drugs 0.000 description 2
- YKPUWZUDDOIDPM-SOFGYWHQSA-N capsaicin Chemical compound COC1=CC(CNC(=O)CCCC\C=C\C(C)C)=CC=C1O YKPUWZUDDOIDPM-SOFGYWHQSA-N 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
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- 229940074979 cetyl palmitate Drugs 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
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- 239000002537 cosmetic Substances 0.000 description 2
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
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- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
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Abstract
Description
本発明は、剃毛後における皮膚の炎症の改善に用いられる外用組成物に関する。 The present invention relates to an external composition used for improving skin inflammation after shaving.
近年の美容に対する意識の高まりから、体毛の除去処理が幅広い層において行われている。体毛を除去処理する方法としては、通常、脱毛、剃毛及び除毛であり、脱毛に関しては、専門機関(医療機関及び美容サロン)が専門の機器を用いて行うことも広く浸透している。 Due to the growing awareness of beauty in recent years, hair removal treatment is being performed in a wide range of people. The methods for removing body hair are usually hair removal, shaving, and hair removal, and it is also widespread that specialized institutions (medical institutions and beauty salons) use specialized equipment for hair removal.
一方で、未だ最も多くの比率を占める処理方法が、自己処理による剃毛である。自己処理でも家電製品、毛抜き、除毛用化粧料等を用いて脱毛や除毛が行われることもあるものの、剃毛の手軽さは他の方法を圧倒している。更に、デリケートゾーン(下腹部、外陰部、肛門部)の自己処理には実質的に剃毛しか手段がないのが実情である。 On the other hand, the treatment method that still accounts for the largest proportion is shaving by self-treatment. Even with self-treatment, hair removal and hair removal may be performed using home appliances, tweezers, hair removal cosmetics, etc., but the ease of shaving overwhelms other methods. Furthermore, the fact is that the only means for self-treatment of the delicate zone (lower abdomen, vulva, anus) is practically shaving.
剃毛時、皮膚は、剃毛治具の刃が接触したり、刃のガード材等の保護具による摩擦に晒されたりといった接触刺激を受けるため、剃毛後に炎症を起こしやすい。更に、剃毛後の体毛の先端には角があるとともに、すぐに伸びることで周りの皮膚をさらに傷つきやすくすることも、炎症の原因となる。一般に腕や足等の皮膚では、剃毛による皮膚の炎症は比較的少ない(非特許文献1)が、特に陰部の皮膚は、他の部位の皮膚より薄く過敏である上に、体毛が他の部位よりも太く、剃毛治具のハンドリングが困難で刺激を与えやすく、且つ、剃毛後は下着で圧迫され常に蒸れた過酷な環境に晒されることから、剃毛による炎症リスクは極端に高い。このため、自己処理での剃毛によるトラブルは後を絶たない。 During shaving, the skin is susceptible to contact stimuli such as contact with the blade of the shaving jig and exposure to friction by a protective device such as a guard material for the blade, so that the skin is liable to become inflamed after shaving. In addition, the tips of the hair after shaving have horns, and the hair grows quickly to make the surrounding skin more vulnerable, which also causes inflammation. Generally, for skin such as arms and legs, skin inflammation due to shaving is relatively small (Non-Patent Document 1), but skin in the pubic area is thinner and more sensitive than skin in other parts, and body hair is other. The risk of inflammation due to shaving is extremely high because it is thicker than the site, it is difficult to handle the shaving jig and it is easy to irritate, and after shaving it is pressed by underwear and constantly exposed to the harsh environment of steam. .. For this reason, troubles caused by shaving by self-treatment are endless.
本発明は、剃毛後における皮膚の炎症の改善に用いられる外用組成物を提供することを目的とする。 It is an object of the present invention to provide an external composition used for improving skin inflammation after shaving.
本発明者らは、鋭意検討した結果、ウフェナマートとリドカイン類とを配合した外用組成物が、剃毛後における皮膚の炎症の改善に優れた効果を示すことを見出した。本発明は、この知見に基づいて、更に検討を重ねることにより完成したものである。 As a result of diligent studies, the present inventors have found that an external composition containing ufenamate and lidocaines has an excellent effect on improving skin inflammation after shaving. The present invention has been completed by further studies based on this finding.
即ち、本発明は、下記に掲げる態様の発明を提供する。
項1. (A)ウフェナマート及び(B)リドカイン及び/又はその塩を含み、剃毛後における皮膚の炎症の改善に用いられる、外用組成物。
項2. 下腹部、外陰部、及び/又は肛門部における皮膚の炎症に適用される、項1に記載の外用組成物。
項3. 痒みを伴わない炎症に適用される、項1又は2に記載の外用組成物。
項4. (C)グリチルレチン酸、グリチルレチン酸の誘導体、及び/又はそれらの塩、(D)ジフェンヒドラミン及び/又はその塩、(E)トコフェロール及び/又はその誘導体、並びに/若しくは(F)抗菌又は殺菌剤を更に含有する、項1〜3のいずれかに記載の外用組成物。
That is, the present invention provides the inventions of the following aspects.
Item 1. An external composition containing (A) ufenamate and (B) lidocaine and / or a salt thereof, which is used for improving skin inflammation after shaving.
Item 2. Item 2. The external composition according to Item 1, which is applied to skin inflammation in the lower abdomen, vulva, and / or anus.
Item 3. Item 2. The external composition according to Item 1 or 2, which is applied to inflammation without itching.
Item 4. Further (C) glycyrrhetinic acid, a derivative of glycyrrhetinic acid and / or a salt thereof, (D) diphenhydramine and / or a salt thereof, (E) tocopherol and / or a derivative thereof, and / or (F) an antibacterial or bactericidal agent. Item 8. The external composition according to any one of Items 1 to 3.
本発明によれば、剃毛後における皮膚の炎症の改善に用いられる外用組成物が提供される。 According to the present invention, there is provided an external composition used for improving skin inflammation after shaving.
本発明の外用組成物は、(A)ウフェナマート(以下において、「(A)成分」とも記載する)並びに(B)リドカイン及び/又はその塩(以下において、「(B)成分」又は「リドカイン類」とも記載する)を含有し、剃毛後における皮膚の炎症の改善に用いられることを特徴とする。また、本発明の外用組成物は、更に、(C)グリチルレチン酸、グリチルレチン酸の誘導体、及び/又はそれらの塩(以下において、「(C)成分」又は「グリチルレチン酸類」とも記載する)、(D)ジフェンヒドラミン及び/又はその塩(以下において、「(D)成分」又は「ジフェンヒドラミン類」とも記載する)、(E)トコフェロール及び/又はその誘導体(以下において、「(E)成分」又は「トコフェロール類」とも記載する)並びに/若しくは(F)第四級アンモニウム系抗菌剤(以下において、「(F)成分」とも記載する)を含有していてもよい。剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、本発明の外用組成物は、(A)成分、(B)成分、(C)成分、(D)成分、(E)成分、及び(F)成分を含むことが好ましい。以下、本発明の外用組成物について詳述する。 The composition for external use of the present invention comprises (A) ufenamate (hereinafter, also referred to as "(A) component") and (B) lidocaine and / or a salt thereof (hereinafter, "(B) component" or "lidocaine". ”), And is characterized by being used for improving skin inflammation after shaving. Further, the external composition of the present invention further comprises (C) glycyrrhetinic acid, a derivative of glycyrrhetinic acid, and / or a salt thereof (hereinafter, also referred to as "component (C)" or "glycyrrhetinic acid"), ( D) Diphenhydramine and / or a salt thereof (hereinafter, also referred to as "(D) component" or "diphenhydramines"), (E) tocopherol and / or a derivative thereof (hereinafter, "(E) component" or "tocopherol". It may also contain (also referred to as “class”) and / or (F) a quaternary ammonium-based antibacterial agent (hereinafter, also referred to as “(F) component”). From the viewpoint of further improving the effect of improving skin inflammation after shaving, the external composition of the present invention comprises (A) component, (B) component, (C) component, (D) component, and (E) component. , And (F) component are preferably contained. Hereinafter, the external composition of the present invention will be described in detail.
(A)ウフェナマート
本発明の外用組成物は、(A)成分としてウフェナマートを含有する。ウフェナマートは、フルフェナム酸ブチルとも呼ばれ、脂溶性の非ステロイド性抗炎症薬として公知の薬剤である。(A)成分は、単独では剃毛後における皮膚の炎症を改善する効果があまりないが、本発明の外用組成物は、剃毛後における皮膚の炎症に対する優れた改善効果を発揮することが可能である。
(A) Ufenamart The external composition of the present invention contains Ufenamart as a component (A). Ufenamate, also called butyl flufenamic acid, is a known drug as a fat-soluble non-steroidal anti-inflammatory drug. The component (A) alone does not have much effect of improving skin inflammation after shaving, but the external composition of the present invention can exert an excellent effect of improving skin inflammation after shaving. Is.
本発明の外用組成物において、(A)成分の含有量については、発揮させるべき薬効等に応じて適宜設定されるが、例えば1〜20重量%が挙げられる。剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、本発明の外用組成物における(A)成分の含有量として、好ましくは3〜6重量%、更に好ましくは4.5〜5.5重量%が挙げられる。 In the external composition of the present invention, the content of the component (A) is appropriately set according to the medicinal effect to be exerted, and examples thereof include 1 to 20% by weight. From the viewpoint of further improving the effect of improving skin inflammation after shaving, the content of the component (A) in the external composition of the present invention is preferably 3 to 6% by weight, more preferably 4.5 to 5%. .5% by weight is mentioned.
(B)リドカイン類
本発明の外用組成物は、(B)成分として、リドカイン及び/又はその塩を含有する。リドカインは、キシロカインとも称され、局所麻酔効果を有することが知られている公知の薬剤である。(B)成分は局所麻酔剤であって、それ自体は炎症を改善するものではないが、(A)成分と組み合わされることによって、剃毛後における皮膚の炎症に対する改善効果を飛躍的に向上させる。
(B) Lidocaines The external composition of the present invention contains lidocaine and / or a salt thereof as the component (B). Lidocaine, also referred to as xylocaine, is a known drug known to have a local anesthetic effect. The component (B) is a local anesthetic and does not improve inflammation by itself, but when combined with the component (A), it dramatically improves the effect of improving skin inflammation after shaving. ..
リドカインの塩としては、薬学的に許容されるものである限り特に制限されないが、具体的には、塩酸塩等の無機酸塩が挙げられる。 The salt of lidocaine is not particularly limited as long as it is pharmaceutically acceptable, and specific examples thereof include inorganic acid salts such as hydrochloride.
本発明の外用組成物において、リドカイン及びその塩の中から1種を選択して単独で使用してもよく、また2種以上を組み合わせて使用してもよい。リドカイン及びその塩の中でも、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、好ましくはリドカインが挙げられる。 In the external composition of the present invention, one kind may be selected from lidocaine and a salt thereof and used alone, or two or more kinds may be used in combination. Among lidocaine and its salts, lidocaine is preferably mentioned from the viewpoint of further improving the effect of improving skin inflammation after shaving.
本発明の外用組成物における(B)成分の含有量については、付与すべき薬効等に応じて適宜設定すればよいが、例えば、(B)成分の総量で、0.1〜5重量%、好ましくは0.2〜2重量%、より好ましくは0.5〜1.5重量%が挙げられる。 The content of the component (B) in the external composition of the present invention may be appropriately set according to the medicinal effect to be imparted, and for example, the total amount of the component (B) is 0.1 to 5% by weight. It is preferably 0.2 to 2% by weight, more preferably 0.5 to 1.5% by weight.
本発明の外用組成物において、(A)成分に対する(B)成分の比率については、(A)成分及び(B)成分の各含有量に応じて定まるが、例えば、(A)成分1重量部当たり、(B)成分の総量として、例えば0.01〜1.5重量部、好ましくは0.05〜1重量部、より好ましくは0.1〜0.5重量部が挙げられる。 In the external composition of the present invention, the ratio of the component (B) to the component (A) is determined according to the contents of the component (A) and the component (B), and is, for example, 1 part by weight of the component (A). The total amount of the component (B) is, for example, 0.01 to 1.5 parts by weight, preferably 0.05 to 1 part by weight, and more preferably 0.1 to 0.5 parts by weight.
(C)グリチルレチン酸類
本発明の外用組成物は、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、(C)成分として、グリチルレチン酸、その誘導体、及び/又はそれらの塩を含有することができる。
(C) Glycyrrhetinic acid The external composition of the present invention contains glycyrrhetinic acid, a derivative thereof, and / or a salt thereof as the component (C) from the viewpoint of further improving the effect of improving skin inflammation after shaving. Can be contained.
グリチルレチン酸は、抗炎症作用や抗アレルギー作用等を有することが知られている公知の薬剤である。 Glycyrrhetinic acid is a known drug known to have an anti-inflammatory action, an antiallergic action and the like.
グリチルレチン酸の誘導体としては、薬学的に許容されることを限度として特に制限されないが、具体的には、グリチルレチン酸ピリドキシン、グリチルレチン酸ステアリル、グリチルレチン酸グリセリル、グリチルレチン酸モノグルクロニド等が挙げられる。これらのグリチルレチン酸の誘導体は、1種単独で使用してもよく、また2種以上を組み合わせて使用してもよい。 The derivative of glycyrrhetinic acid is not particularly limited as long as it is pharmaceutically acceptable, and specific examples thereof include pyridoxine glycyrrhetinate, stearyl glycyrrhetinate, glyceryl glycyrrhetinate, and monoglucuronide glycyrrhetinate. These derivatives of glycyrrhetinic acid may be used alone or in combination of two or more.
グリチルレチン酸及び/又はその誘導体の塩としては、薬学的に許容されるものである限り特に制限されないが、具体的には、ナトリウム塩、カリウム塩等のアルカリ金属塩;アンモニウム塩等が挙げられる。これらの塩は、1種単独で使用してもよく、また2種以上を組み合わせて使用してもよい。 The salt of glycyrrhetinic acid and / or a derivative thereof is not particularly limited as long as it is pharmaceutically acceptable, and specific examples thereof include alkali metal salts such as sodium salt and potassium salt; ammonium salts and the like. These salts may be used alone or in combination of two or more.
本発明の外用組成物は、(C)成分として、グリチルレチン酸、グリチルレチン酸の塩、グリチルレチン酸の誘導体、グリチルレチン酸の誘導体の塩の中から、1種を選択して使用してもよく、2種以上を組み合わせて使用してもよい。 The external composition of the present invention may be used by selecting one from glycyrrhetinic acid, a salt of glycyrrhetinic acid, a derivative of glycyrrhetinic acid, and a salt of a derivative of glycyrrhetinic acid as the component (C). You may use a combination of seeds or more.
これらの(C)成分の中でも、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、好ましくは、グリチルレチン酸が挙げられる。 Among these components (C), glycyrrhetinic acid is preferably mentioned from the viewpoint of further improving the effect of improving skin inflammation after shaving.
本発明の外用組成物において、(C)成分の含有量については、特に制限されず、付与すべき薬効等に応じて適宜設定すればよいが、例えば、(C)成分の総量で、0.05〜5重量%が挙げられ、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、好ましくは0.1〜1重量%、更に好ましくは0.2〜0.5重量%が挙げられる。 In the external composition of the present invention, the content of the component (C) is not particularly limited and may be appropriately set according to the medicinal effect to be imparted. For example, the total amount of the component (C) is 0. 05 to 5% by weight, preferably 0.1 to 1% by weight, more preferably 0.2 to 0.5% by weight, from the viewpoint of further improving the effect of improving skin inflammation after shaving. Can be mentioned.
本発明の外用組成物において、(A)成分に対する(C)成分の比率については、(A)成分及び(C)成分の各含有量に応じて定まるが、例えば、(A)成分1重量部当たり、(C)成分の総量が0.01〜0.9重量部が挙げられる。剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、(A)成分1重量部当たり、(C)成分の総量が、好ましくは0.03〜0.5重量部、更に好ましくは0.05〜0.1重量部が挙げられる。 In the external composition of the present invention, the ratio of the component (C) to the component (A) is determined according to the contents of the component (A) and the component (C), and is, for example, 1 part by weight of the component (A). The total amount of the component (C) is 0.01 to 0.9 parts by weight. From the viewpoint of further improving the effect of improving skin inflammation after shaving, the total amount of the component (C) per 1 part by weight of the component (A) is preferably 0.03 to 0.5 part by weight, more preferably. Examples include 0.05 to 0.1 parts by weight.
(D)ジフェンヒドラミン類
本発明の外用組成物は、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、(D)成分としてジフェンヒドラミン及び/又はその塩を含有することができる。ジフェンヒドラミンは、抗ヒスタミン作用があることが知られている公知の薬剤である。(D)成分は、単独では剃毛後における皮膚の炎症を改善する効果がほとんどないが(A)成分及び(B)成分と組み合わされることで、剃毛後における皮膚の炎症の改善効果を顕著に向上させることが可能である。
(D) Diphenhydramines The external composition of the present invention can contain diphenhydramine and / or a salt thereof as the component (D) from the viewpoint of further improving the effect of improving skin inflammation after shaving. Diphenhydramine is a known drug known to have antihistamine activity. The component (D) has almost no effect of improving skin inflammation after shaving by itself, but when combined with the components (A) and (B), the effect of improving skin inflammation after shaving is remarkable. It is possible to improve to.
ジフェンヒドラミンの塩としては、薬学的に許容されるものである限り特に制限されないが、具体的には、塩酸塩、クエン酸塩、コハク酸塩、酒石酸塩、フマル酸塩、マレイン酸塩、サリチル酸塩、ジフェニルジスルホン酸塩、タンニン酸塩、ラウリル硫酸塩、硫酸塩等の酸付加塩が挙げられる。これらの塩は、1種単独で使用してもよく、また2種以上を組み合わせて使用してもよい。 The salt of diphenhydramine is not particularly limited as long as it is pharmaceutically acceptable, but specifically, hydrochloride, citrate, succinate, tartrate, fumarate, maleate, salicylate. , Diphenyldisulfonate, tannate, lauryl sulfate, sulfate and other acid addition salts. These salts may be used alone or in combination of two or more.
本発明の外用組成物は、(D)成分として、ジフェンヒドラミン及びその塩の中から、1種を選択して使用してもよく、2種以上を組み合わせて使用してもよい。 The external composition of the present invention may be used by selecting one of diphenhydramine and a salt thereof as the component (D), or may be used in combination of two or more.
これらの(D)成分の中でも、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、好ましくはジフェンヒドラミンが挙げられる。 Among these components (D), diphenhydramine is preferably mentioned from the viewpoint of further improving the effect of improving skin inflammation after shaving.
本発明の外用組成物において、(D)成分の含有量については、特に制限されないが、例えば、(D)成分の総量で、0.1〜5重量%が挙げられる。剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、本発明の外用組成物における(D)成分の含有量として、好ましくは0.3〜2重量%、更に好ましくは0.5〜1.5重量%が挙げられる。 In the external composition of the present invention, the content of the component (D) is not particularly limited, and for example, the total amount of the component (D) may be 0.1 to 5% by weight. From the viewpoint of further improving the effect of improving skin inflammation after shaving, the content of the component (D) in the external composition of the present invention is preferably 0.3 to 2% by weight, more preferably 0.5. ~ 1.5% by weight is mentioned.
本発明の外用組成物において、(A)成分に対する(D)成分の比率については、(A)成分及び(D)成分の各含有量に応じて定まるが、例えば、(A)成分1重量部当たり、(D)成分の総量が0.01〜1.2重量部が挙げられる。剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、(A)成分1重量部当たり、(D)成分の総量が、好ましくは0.05〜0.8重量部、更に好ましくは0.1〜0.5重量部が挙げられる。 In the external composition of the present invention, the ratio of the component (D) to the component (A) is determined according to the contents of the component (A) and the component (D), and is, for example, 1 part by weight of the component (A). The total amount of the component (D) is 0.01 to 1.2 parts by weight. From the viewpoint of further improving the effect of improving skin inflammation after shaving, the total amount of the component (D) per 1 part by weight of the component (A) is preferably 0.05 to 0.8 parts by weight, more preferably. 0.1 to 0.5 parts by weight may be mentioned.
(E)トコフェロール類
本発明の外用組成物は、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、(E)成分としてトコフェロール及び/又はその誘導体をさらに含有することができる。
(E) Tocopherols The external composition of the present invention can further contain tocopherol and / or a derivative thereof as the component (E) from the viewpoint of further improving the effect of improving skin inflammation after shaving.
トコフェロールは、ビタミンEとして知られる公知の化合物である。トコフェロールは、d体、l体、dl体のいずれであってもよいが、好ましくはdl体が挙げられる。また、トコフェロールは、α体、β体、γ体、δ体のいずれであってもよいが、好ましくはα体が挙げられる。 Tocopherol is a known compound known as Vitamin E. The tocopherol may be any of d-form, l-form, and dl-form, but dl-form is preferable. Further, the tocopherol may be any of α-form, β-form, γ-form, and δ-form, but α-form is preferable.
トコフェロールの誘導体としては、薬学的に許容されることを限度として特に制限されないが、例えば、酢酸、ニコチン酸、コハク酸等のカルボン酸とのエステル体、リン酸とのジエステル体等が挙げられる。これらのトコフェロールの誘導体の中でも、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、好ましくはカルボン酸とのエステル体、更に好ましくは酢酸トコフェロールが挙げられる。 The derivative of tocopherol is not particularly limited as long as it is pharmaceutically acceptable, and examples thereof include an ester form with a carboxylic acid such as acetic acid, nicotinic acid, and succinic acid, and a diester form with phosphoric acid. Among these tocopherol derivatives, an ester form with a carboxylic acid is preferable, and tocopherol acetate is more preferable, from the viewpoint of further improving the effect of improving skin inflammation after shaving.
また、トコフェロールの誘導体は、d体、l体、dl体のいずれであってもよいが、好ましくはdl体が挙げられる。更に、トコフェロールの誘導体は、α体、β体、γ体、δ体のいずれであってもよいが、好ましくはα体が挙げられる。 The derivative of tocopherol may be d-form, l-form, or dl-form, but dl-form is preferable. Further, the derivative of tocopherol may be any of α-form, β-form, γ-form, and δ-form, but α-form is preferable.
本発明の外用組成物において、(E)成分として、トコフェロール及びその誘導体の中から1種を選択して単独で使用してもよく、また2種以上を組み合わせて使用してもよい。(E)成分の中でも、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、好ましくはトコフェロールの誘導体、より好ましくはトコフェロールのカルボン酸とのエステル体、更に好ましくは酢酸トコフェロール、特に好ましくは酢酸d−α−トコフェロール、酢酸l−α−トコフェロール、酢酸dl−α−トコフェロールが挙げられる。 In the external composition of the present invention, as the component (E), one of tocopherol and its derivative may be selected and used alone, or two or more thereof may be used in combination. Among the components (E), from the viewpoint of further improving the effect of improving skin inflammation after shaving, a derivative of tocopherol, more preferably an ester of tocopherol with a carboxylic acid, still more preferably tocopherol acetate, particularly. Preferred examples thereof include d-α-tocopherol acetate, l-α-tocopherol acetate and dl-α-tocopherol acetate.
本発明の外用組成物が(E)成分を含む場合における(E)成分の含有量については、特に制限されないが、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、(E)成分の総量として、例えば0.05〜2重量%、好ましくは0.1〜1.3重量%、更に好ましくは0.3〜0.8重量%が挙げられる。 The content of the component (E) when the external composition of the present invention contains the component (E) is not particularly limited, but from the viewpoint of further improving the effect of improving skin inflammation after shaving, (E). ) The total amount of the components is, for example, 0.05 to 2% by weight, preferably 0.1 to 1.3% by weight, and more preferably 0.3 to 0.8% by weight.
また、本発明の外用組成物が(E)成分を含む場合において、(A)成分に対する(E)成分の比率については、各成分の前記含有量の範囲に基づいて定まるが、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、(A)成分1重量部当たり、(E)成分の総量として0.01〜1重量部、好ましくは0.03〜0.5重量部、更に好ましくは0.05〜0.3重量部が挙げられる。 Further, when the external composition of the present invention contains the component (E), the ratio of the component (E) to the component (A) is determined based on the range of the content of each component, but after shaving. From the viewpoint of further improving the effect of improving skin inflammation, the total amount of the component (E) is 0.01 to 1 part by weight, preferably 0.03 to 0.5 part by weight, per 1 part by weight of the component (A). More preferably, 0.05 to 0.3 parts by weight is mentioned.
(F)抗菌又は殺菌剤
本発明の外用組成物は、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、(F)成分として抗菌又は殺菌剤をさらに含有することができる。
(F) Antibacterial or bactericidal agent The external composition of the present invention may further contain an antibacterial or bactericidal agent as the component (F) from the viewpoint of further improving the effect of improving skin inflammation after shaving.
抗菌又は殺菌剤としては、薬学的又は香粧学的に許容されることを限度として特に限定されない。例えば、第四級アンモニウム系抗菌剤、イソプロピルメチルフェノール、ヒノキチオール、塩酸クロルヘキシジン、グルコン酸クロルヘキシジン、トリクロサン、塩化リゾチーム、スルファジン等が挙げられる。第四級アンモニウム系抗菌剤としては、具体的には、塩化セチルピリジニウム、塩化ベンゼトニウム、塩化ベンザルコニウム、塩化デカリニウム、塩化アルキルジメチルアンモニウム、塩化アルキルトリメチルアンモニウム、塩化メチルベンゼトニウム、塩化ラウロイルコラミノホルミルメチルピリジニウム等が挙げられる。 The antibacterial or bactericidal agent is not particularly limited as long as it is pharmaceutically or cosmetically acceptable. Examples thereof include quaternary ammonium antibacterial agents, isopropylmethylphenol, hinokitiol, chlorhexidine hydrochloride, chlorhexidine gluconate, triclosan, lysozyme chloride, sulfadine and the like. Specific examples of the quaternary ammonium antibacterial agent include cetylpyridinium chloride, benzethonium chloride, benzalkonium chloride, decalinium chloride, alkyldimethylammonium chloride, alkyltrimethylammonium chloride, methylbenzethonium chloride, and lauroylcolaminoformylmethyl chloride. Examples include pyridinium.
これらの抗菌又は殺菌剤は、1種単独で使用してもよく、また2種以上を組み合わせて使用してもよい。 These antibacterial or bactericidal agents may be used alone or in combination of two or more.
これらの抗菌又は殺菌剤の中でも、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、好ましくは、イソプロピルメチルフェノールが挙げられる。 Among these antibacterial or bactericidal agents, isopropylmethylphenol is preferable from the viewpoint of further improving the effect of improving skin inflammation after shaving.
本発明の外用組成物が(F)成分を含む場合における(F)成分の含有量については、使用する抗菌又は殺菌剤の種類等に応じて適宜設定すればよいが、例えば、0.01〜1重量%が挙げられる。剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、(C)成分の含有量として、好ましくは0.03〜0.5重量%、更に好ましくは0.05〜0.3重量%が挙げられる。 When the external composition of the present invention contains the component (F), the content of the component (F) may be appropriately set according to the type of antibacterial or bactericidal agent used, and is, for example, 0.01 to. 1% by weight is mentioned. From the viewpoint of further improving the effect of improving skin inflammation after shaving, the content of the component (C) is preferably 0.03 to 0.5% by weight, more preferably 0.05 to 0.3% by weight. %.
本発明の外用組成物が(F)成分を含む場合において、(A)成分と(F)成分の比率は、前述するこれらの両成分の各含有量に応じて定まるが、例えば、(A)成分1重量部当たり、(F)成分が0.001〜0.5重量部、好ましくは0.005〜0.1重量部、更に好ましくは0.01〜0.05重量部が挙げられる。 When the external composition of the present invention contains the component (F), the ratio of the component (A) to the component (F) is determined according to the contents of both of these components described above, and is determined by, for example, (A). Examples of the component (F) are 0.001 to 0.5 parts by weight, preferably 0.005 to 0.1 parts by weight, and more preferably 0.01 to 0.05 parts by weight per 1 part by weight of the component.
その他の成分
本発明の外用組成物は、前述する成分の他に、必要に応じて、他の薬理成分を含んでもよい。このような薬理成分としては、例えば、抗ヒスタミン剤(マレイン酸クロルフェニラミン等)、局所麻酔剤(ジブカイン、プロカイン、テトラカイン、ブピバカイン、メピバカイン、クロロプロカイン、プロパラカイン、メプリルカイン又はこれらの塩)、安息香酸アルキルエステル(例えばアミノ安息香酸エチル、塩酸パラブチルアミノ安息香酸ジエチルアミノエチル)、オルソカイン、オキセサゼイン、オキシポリエントキシデカン、ロートエキス、ペルカミンパーゼ、テシットデシチン等)、抗炎症剤(アラントイン、サリチル酸、サリチル酸グリコール、サリチル酸メチル、インドメタシン、フェルビナク、ジクロフェナクナトリウム、ロキソプロフェンナトリウム等)、鎮痒剤(クロタミトン、チアントール等)、皮膚保護剤(コロジオン、ヒマシ油等)、血行促進成分(ノニル酸ワニリルアミド、ニコチン酸ベンジルエステル、カプサイシン、トウガラシエキス等)、清涼化剤(メントール、カンフル等)、ビタミン類(ビタミンA,B,C,D等)、ムコ多糖類(コンドロイチン硫酸ナトリウム、ヒアルロン酸等)等が挙げられる。
Other Ingredients The external composition of the present invention may contain other pharmacological components in addition to the above-mentioned components, if necessary. Examples of such pharmacological components include antihistamines (chlorpheniramine maleate, etc.), local anesthetics (dibucaine, procaine, tetracaine, bupivacaine, mepivacaine, chloroprocaine, proparacaine, meprilcaine or salts thereof), alkyl benzoate. Esters (eg ethyl aminobenzoate, diethylaminoethyl parabutylaminobenzoate), orthokine, oxesazein, oxypolyentoxydecane, funnel extract, percaminpase, tesitdecitin, etc.), anti-inflammatory agents (alantin, salicylic acid, glycol salicylate, methyl salicylate, etc.) Indomethacin, fervinac, diclofenac sodium, loxoprofen sodium, etc.), antipruritic agents (crotamiton, thiantoll, etc.), skin protectants (corodion, castor oil, etc.), blood circulation promoting components (nonyl acid vanillylamide, nicotinic acid benzyl ester, capsaicin, peppermint extract, etc.) ), Cooling agents (menthol, camphor, etc.), vitamins (vitamins A, B, C, D, etc.), mucopolysaccharides (sodium chondroitin sulfate, hyaluronic acid, etc.) and the like.
前述する成分の他に、必要に応じて、皮膚外用剤等に通常使用される他の基剤や添加剤を含んでもよい。このような基材や添加剤としては、薬学的に許容されることを限度として特に制限されないが、例えば、水、低級アルコール(例えば、イソプロパノール)、多価アルコール(グリセリン、プロピレングリコール、ジプロピレングリコール、1,3−ブチレングリコール等)等の水性基剤;油類(オリーブ油、サフラワー油、大豆油、つばき油、とうもろこし油、なたね油、ひまわり油、綿実油、落花生油、ラード、スクワラン、魚油等)、鉱物油(流動パラフィン、パラフィン、ゲル化炭化水素、ワセリン等)、ワックス類・ロウ類(ミツロウ、カルナウバロウ、キャンデリラロウ、セレシン、ライスワックス、マイクロクリスタリンワックス等)、エステル油(ミリスチン酸イソプロピル、アジピン酸イソプロピル、セバシン酸ジエチル、セバシン酸イソプロピル、パルミチン酸イソプロピル、パルミチン酸セチル、オレイン酸エチル等)、脂肪酸アルキルエステル、脂肪酸(ステアリン酸、オレイン酸、パルミチン酸、ベヘン酸、リノール酸、ラノリン等)、脂肪酸エステル(パルミチン酸セチル、パルミチン酸イソプロピル、ミリスチン酸イソプロピル、リノール酸エチル等)、高級アルコール(ステアリルアルコール、セタノール、ベヘニルアルコール、ミリスチルアルコール、オレイルアルコール、ヘキサデシルアルコール、ラノリンアルコール等)、コレステロール、トリ2−エチルヘキサン酸グリセリル、2−エチルヘキサン酸セチル、シリコーンオイル(ジメチルポリシロキサン、環状シリコーン等)等の油性基剤;POE(10〜50モル)フィトステロールエーテル、POE(10〜50モル)ジヒドロコレステロールエーテル、POE(10〜50モル)2−オクチルドデシルエーテル、POE(10〜50モル)デシルテトラデシルエーテル、POE(10〜50モル)オレイルエーテル、POE(2〜50モル)セチルエーテル(セトマクロゴール1000等)、POE(5〜50モル)ベヘニルエーテル、POE(5〜30モル)ポリオキシプロピレン(5〜30モル)2−デシルテトラデシルエーテル、POE(10〜50モル)ポリオキシプロピレン(2〜30モル)セチルエーテルなどのポリオキシエチレンアルキルエーテル、これらのリン酸・リン酸塩(POEセチルエーテルリン酸ナトリウムなど)、POE(20〜60モル)ソルビタンモノオレート、POE(10〜60モル)ソルビタンモノイソステアレート、POE(10〜80モル)グリセリルモノイソステアレート、POE(10〜30モル)グリセリルモノステアレート、POE(20〜100モル)・ポリオキシプロピレン変性シリコーン、POE・アルキル変性シリコーン、モノラウリン酸ポリエチレングリコール、モノパルミチン酸ポリエチレングリコール、モノステアリン酸ポリエチレングリコール、ジラウリン酸ポリエチレングリコール、ジパルミチン酸ポリエチレングリコール、ジステアリン酸ポリエチレングリコール、ジオレイン酸ポリエチレングリコール、ジリシノレイン酸ポリエチレングリコール、ポリオキシエチレン硬化ヒマシ油(5〜100)、ポリソルベート(20〜85)、グリセリン脂肪酸エステル(モノステアリン酸グリセリン等)、水素添加大豆リン脂質、水素添加ラノリンアルコール等の界面活性剤;清涼化剤(メントール、カンフル、ボルネオール、ハッカ水、ハッカ油等)、防腐剤(メチルパラベン、プロピルパラベン、安息香酸、安息香酸ナトリウム、ソルビン酸等)、着香剤(シトラール、1,8−シオネール、シトロネラール、ファルネソール等)、着色剤(タール色素(褐色201号、青色201号、黄色4号、黄色403号等)、カカオ色素、クロロフィル、酸化アルミニウム等)、粘稠剤(カルボキシビニルポリマー、ヒプロメロース、ポリビニルピロリドン、アルギン酸ナトリウム、エチルセルロース、ヒドロキシエチルセルロース、カルボキシメチルセルロースナトリウム、キサンタンガム、カラギーナン等)、pH調整剤(リン酸、塩酸、クエン酸、クエン酸ナトリウム、コハク酸、酒石酸、水酸化ナトリウム、水酸化カリウム、トリエタノールアミン、トリイソプロパノールアミン等)、湿潤剤(dl−ピロリドンカルボン酸ナトリウム液、D−ソルビトール液、マクロゴール等)、安定化剤(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、エデト酸ナトリウム、メタリン酸ナトリウム、L−アルギニン、L−アスパラギン酸、DL−アラニン、グリシン、エリソルビン酸ナトリウム、没食子酸プロピル、亜硫酸ナトリウム、二酸化硫黄、クロロゲン酸、カテキン、ローズマリー抽出物等)、酸化防止剤、紫外線吸収剤、キレート剤、粘着剤、緩衝剤、溶解補助剤、可溶化剤、保存剤等の添加剤が挙げられる。 In addition to the above-mentioned components, other bases and additives usually used for external skin preparations and the like may be contained, if necessary. Such base materials and additives are not particularly limited as long as they are pharmaceutically acceptable, but for example, water, lower alcohols (for example, isopropanol), polyhydric alcohols (glycerin, propylene glycol, dipropylene glycol). , 1,3-butylene glycol, etc.); oils (olive oil, saflower oil, soybean oil, camellia oil, corn oil, rapeseed oil, sunflower oil, cottonseed oil, peanut oil, lard, squalane, fish oil, etc.) , Mineral oil (liquid paraffin, paraffin, gelled hydrocarbon, vaseline, etc.), waxes / waxes (mitsurou, carnauba wax, candelilla wax, selecin, rice wax, microcrystallin wax, etc.), ester oil (isopropyl myristate, etc.) Isopropyl adipate, diethyl sebacate, isopropyl sebacate, isopropyl palmitate, cetyl palmitate, ethyl oleate, etc.), fatty acid alkyl esters, fatty acids (stearic acid, oleic acid, palmitic acid, behenic acid, linoleic acid, lanolin, etc.) , Fatty acid esters (cetyl palmitate, isopropyl palmitate, isopropyl myristate, ethyl linoleate, etc.), higher alcohols (stearyl alcohol, cetanol, behenyl alcohol, myristyl alcohol, oleyl alcohol, hexadecyl alcohol, lanolin alcohol, etc.), cholesterol, tri Oily bases such as glyceryl 2-ethylhexanate, cetyl 2-ethylhexanate, silicone oil (dimethylpolysiloxane, cyclic silicone, etc.); POE (10-50 mol) phytosterol ether, POE (10-50 mol) dihydrocholesterol Ether, POE (10-50 mol) 2-octyldodecyl ether, POE (10-50 mol) decyltetradecyl ether, POE (10-50 mol) oleyl ether, POE (2-50 mol) cetyl ether (set macrogol) 1000 etc.), POE (5-50 mol) behenyl ether, POE (5-30 mol) polyoxypropylene (5-30 mol) 2-decyltetradecyl ether, POE (10-50 mol) polyoxypropylene (2-) 30 mol) Polyoxyethylene alkyl ethers such as cetyl ethers, their phosphates and phosphates (POE cetyl ether sodium phosphate, etc.), POE (20-60 mol) sorbitan monoolates, POE (10-60 mol) ) Solbitan monoisostearate, POE (10-80 mol) glyceryl monoisostearate, POE (10-30 mol) glyceryl monostearate, POE (20-100 mol) / polyoxypropylene-modified silicone, POE / alkyl-modified Silicone, Monolaurate Polyethylene Glycol, Monopalmitate Polyethylene Glycol, Monostearate Polyethylene Glycol, Dilaurate Polyethylene Glycol, Dipalmitate Polyethylene Glycol, Distearate Polyethylene Glycol, Dioleate Polyethylene Glycol, Diricinoleate Polyethylene Glycol, Polyoxyethylene Cure Surfactants such as castor oil (5-100), polysorbate (20-85), glycerin fatty acid esters (glycerin monostearate, etc.), hydrogenated soybean phospholipids, hydrogenated lanolin alcohol; refreshing agents (menthol, camphor, etc.) Borneol, peppermint water, peppermint oil, etc.), preservatives (methylparaben, propylparaben, benzoic acid, sodium benzoate, sorbic acid, etc.), flavoring agents (citral, 1,8-sionel, citronellal, farnesol, etc.), colorants (Tar pigments (brown 201, blue 201, yellow 4, yellow 403, etc.), cocoa pigments, chlorophyll, aluminum oxide, etc.), viscous agents (carboxyvinyl polymer, hypromellose, polyvinylpyrrolidone, sodium alginate, ethyl cellulose, etc.) Hydroxyethyl cellulose, sodium carboxymethyl cellulose, xanthan gum, carrageenan, etc.), pH adjusters (phosphate, hydrochloric acid, citric acid, sodium citrate, succinic acid, tartrate acid, sodium hydroxide, potassium hydroxide, triethanolamine, triisopropanolamine, etc. ), Wetting agent (dl-pyrrolidone sodium carboxylate solution, D-sorbitol solution, macrogol, etc.), stabilizer (dibutylhydroxytoluene, butylhydroxyanisole, sodium edetate, sodium metaphosphate, L-arginine, L-asparagine) Acids, DL-alanine, glycine, sodium erythorbate, propyl gallate, sodium sulfite, sulfur dioxide, chlorogenic acid, catechin, rosemary extract, etc.), antioxidants, UV absorbers, chelating agents, adhesives, buffers , Additives such as solubilizers, solubilizers, preservatives and the like.
性状・製剤形態等
本発明の外用組成物の性状としては特に限定されず、水性液状組成物、水性ゲル状組成物、油性ゲル状組成物、乳化組成物等が挙げられる。この中でも、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、好ましくは乳化組成物が挙げられる。乳化組成物の乳化状態については、水中油型又は油中水型のいずれであってもよいが、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点から、好ましくは水中油型が挙げられる。
Properties, formulation form, etc. The properties of the external composition of the present invention are not particularly limited, and examples thereof include an aqueous liquid composition, an aqueous gel composition, an oil gel composition, and an emulsified composition. Among these, an emulsified composition is preferable from the viewpoint of further improving the effect of improving skin inflammation after shaving. The emulsified state of the emulsified composition may be either an oil-in-water type or a water-in-oil type, but the oil-in-water type is preferable from the viewpoint of further improving the effect of improving skin inflammation after shaving. Can be mentioned.
本発明の外用組成物の製剤形態については特に制限されず、例えば、ローション剤、乳液剤、軟膏剤、クリーム剤等が挙げられる。この中でも、剃毛後における皮膚の炎症の改善効果をより一層向上させる観点及び塗布容易性の観点から、好ましくは、乳液剤、クリーム剤が挙げられる。 The pharmaceutical form of the external composition of the present invention is not particularly limited, and examples thereof include lotions, emulsions, ointments, and creams. Among these, emulsions and creams are preferable from the viewpoint of further improving the effect of improving skin inflammation after shaving and the ease of application.
本発明の外用組成物としては、具体的には、医薬品、医薬部外品、化粧品等が挙げられる。これらの製剤形態の中でも、好ましくは医薬品が挙げられる。 Specific examples of the external composition of the present invention include pharmaceuticals, quasi-drugs, cosmetics and the like. Among these pharmaceutical forms, pharmaceutical products are preferable.
用途
本発明の外用組成物は、剃毛後における皮膚の炎症の改善に用いられる。適用される炎症部位としては、体毛を剃毛した部位であれば特に限定されないが、本発明の外用組成物は、特に、デリケートゾーンといわれる、下腹部(Vゾーン)、外陰部(Iゾーン)、臀部、及び/又は肛門部(Oゾーン)における皮膚の炎症に好ましく適用される。
Uses The external composition of the present invention is used for improving skin inflammation after shaving. The site of inflammation to which the skin is applied is not particularly limited as long as it is a site where the body hair is shaved, but the external composition of the present invention is particularly limited to the lower abdomen (V zone) and the vulva (I zone), which are called delicate zones. , Buttocks, and / or skin inflammation in the anus (O zone).
皮膚の炎症の態様としては特に限定されないが、痛み(ヒリヒリ感)、かぶれ、赤いぶつぶつ等が挙げられる。また、本発明においては、好ましくは、痒みを伴わない炎症に対して適用することができる。 The mode of skin inflammation is not particularly limited, and examples thereof include pain (tingling sensation), rash, and red lumps. Further, in the present invention, it can be preferably applied to inflammation without itching.
本発明の外用組成物は、剃毛後の皮膚炎が生じている皮膚に、1日に1〜6回塗布することで適用することができる。また、本発明の外用組成物は、剃毛後における皮膚の炎症の改善効果をより効果的に得るために、例えば5日以上、好ましくは1週間以上塗布することが好ましい。 The external composition of the present invention can be applied to the skin having dermatitis after shaving by applying it 1 to 6 times a day. In addition, the external composition of the present invention is preferably applied, for example, for 5 days or more, preferably 1 week or more, in order to more effectively obtain the effect of improving skin inflammation after shaving.
以下、本発明を実施例により具体的に説明するが、本発明はこれらの実施例に限定されるものではない。 Hereinafter, the present invention will be specifically described with reference to Examples, but the present invention is not limited to these Examples.
試験例
表1に示す組成の外用組成物を、水中油型の乳化組成物(クリーム剤)として調製した。週に1回以上の剃毛によるカミソリ負けで、下腹部(Vゾーン)及び外陰部(Iゾーン)に、かぶれ、赤み、ヒリヒリ感の炎症(いずれも痒みを伴わないもの)を有する被験者(N=15)に対し、調製した外用組成物を患部に1週間(1日3回)塗布させた。1週間後、炎症の改善に関する満足度を5段階のVAS(満足・やや満足・どちらでもない・やや不満・不満)にて評価し、15名中「満足」と回答した被験者の割合(%)を「有効率」として求めた。なお、まず、比較例1、2及び実施例2について試験し、その後、試験前と同程度に剃毛による症状がぶり返した後に、比較例3〜5及び実施例2について試験した。結果を表1に示す。
The external composition having the composition shown in Test Example Table 1 was prepared as an oil-in-water emulsified composition (cream preparation). Subjects with rash, redness, and tingling inflammation (all without itching) in the lower abdomen (V zone) and vulva (I zone) due to razor loss due to shaving at least once a week (N) = 15), the prepared external composition was applied to the affected area for one week (three times a day). One week later, the degree of satisfaction with the improvement of inflammation was evaluated on a 5-point VAS (satisfied / slightly satisfied / neither / slightly dissatisfied / dissatisfied), and the percentage of subjects who answered "satisfied" out of 15 subjects (%). Was calculated as the "effective rate". First, Comparative Examples 1 and 2 and Example 2 were tested, and then Comparative Examples 3 to 5 and Example 2 were tested after the symptoms due to shaving returned to the same extent as before the test. The results are shown in Table 1.
表1に示されるとおり、有効成分としてウフェナマートのみを含む比較例1の外用組成物で満足と回答した被験者は少数であり、有効成分としてリドカインのみを含む比較例2の場合にいたってはわずかであったが、ウフェナマートとリドカインとを含む実施例1の外用組成物では、半数を超える被験者が満足と回答するほど炎症を改善する高い効果が認められた。また、ジフェンヒドラミン、グリチルレチン酸、酢酸トコフェロール、及びイソプロピルメチルフェノールを含む比較例3の外用組成物でも満足と回答した被験者はわずかであり、さらにウフェナマート又はリドカインを配合した比較例4及び5の外用組成物でも、満足と回答した被験者は半数にも満たなかった。一方で、ウフェナマート及びリドカインをジフェンヒドラミン、グリチルレチン酸、酢酸トコフェロール、及びイソプロピルメチルフェノールと共に含む実施例2の外用組成物では、ほとんどの被験者が満足と回答するほどに、炎症を改善する一層高い効果が認められた。 As shown in Table 1, a small number of subjects answered that they were satisfied with the external composition of Comparative Example 1 containing only ufenamate as an active ingredient, and only a small number of subjects in Comparative Example 2 containing only lidocaine as an active ingredient. However, the external composition of Example 1 containing ufenamate and lidocaine was found to be highly effective in improving inflammation so that more than half of the subjects answered that they were satisfied. In addition, few subjects answered that they were satisfied with the external composition of Comparative Example 3 containing diphenhydramine, glycyrrhetinic acid, tocopherol acetate, and isopropylmethylphenol, and the external compositions of Comparative Examples 4 and 5 containing ufenamate or lidocaine. However, less than half of the subjects answered that they were satisfied. On the other hand, the external composition of Example 2 containing ufenamate and lidocaine together with diphenhydramine, glycyrrhetinic acid, tocopherol acetate, and isopropylmethylphenol was found to be more effective in improving inflammation so that most subjects answered that they were satisfied. Was done.
[処方例]
表2に示す処方の外用組成物を、水中油型の乳化組成物(クリーム剤)として調製した。いずれの外用組成物も、剃毛後における皮膚の炎症に対して優れた改善効果を示した。
[Prescription example]
The external composition of the formulation shown in Table 2 was prepared as an oil-in-water emulsified composition (cream preparation). Both external compositions showed excellent ameliorating effects on skin inflammation after shaving.
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Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20240716 |