JP7621628B2 - 皮膚外用剤及びスクリーニング方法 - Google Patents
皮膚外用剤及びスクリーニング方法 Download PDFInfo
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- JP7621628B2 JP7621628B2 JP2018208491A JP2018208491A JP7621628B2 JP 7621628 B2 JP7621628 B2 JP 7621628B2 JP 2018208491 A JP2018208491 A JP 2018208491A JP 2018208491 A JP2018208491 A JP 2018208491A JP 7621628 B2 JP7621628 B2 JP 7621628B2
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Description
また、本発明は、肌荒れ改善用、鎮痒用、鎮痛用又は敏感肌用の皮膚外用剤の有効成分をスクリーニングする方法であって、培養液中で表皮細胞を培養する第1の工程と、前記培養液中に内分泌系のストレスホルモンを添加して培養する第2の工程と、前記培養液中に内分泌系のストレスホルモン及び有効成分を添加して培養する第3の工程と、第2の工程及び第3の工程でそれぞれ培養した表皮細胞における神経成長因子の遺伝子発現量を測定し、比較する工程と、内分泌系のストレスホルモンにより誘導された神経成長因子生成抑制効果を有する有効成分を選択する第4の工程を含む方法である。
本発明は、(A)米の抽出物溶液を蛋白分解酵素で処理して得られる加水分解物溶液と、(B)米糠抽出物溶液を蛋白分解酵素で処理して得られる加水分解物溶液との混合物溶液を有することを特徴とする。
(1)米の加水分解物溶液の調製
精白米175gを、0.25N水酸化ナトリウム水溶液700gに、室温で18時間浸漬した。不溶物を濾過で除き、濾液に対して蛋白分解酵素であるアクチナーゼ及びパパインをそれぞれ130mg添加して酵素分解処理を行った。酵素処理は各酵素の至適pHにて、40℃2時間保持することによって行った。ここに得られた酵素処理液を濾過して、淡黄色透明の米抽出物加水分解物溶液1360gを得た(固形分濃度1.12%)。
(2)米糠の加水分解物溶液の調製
米糠500gに0.1M乳酸水溶液1500gを加え、撹拌して米糠と乳酸水溶液を十分混合した後、室温に1日静置した。次に不溶物を濾過で除き、濾液をパパインで処理した。酵素処理は酵素を1.2mg使用し、酵素の至適pHに於いて、80℃1時間保持することによって行った。処理により生じた不溶物を濾別し、濾液をフィチン酸でpH6.5として淡黄色透明の米糠抽出物加水分解溶液720gを得た(固形分濃度3.63%)。
(3)混合物溶液の調製
上述の通り調製した米加水分解物溶液及び米糠加水分解溶液を、米加水分解物溶液:米糠加水分解物溶液=6:4の混合比で混合し、淡黄色透明の混合物溶液を得た(固形分濃度1.92%)。
製造例1の調製方法(3)において、米加水分解物溶液:米糠加水分解物溶液=5:5の混合比で混合する他は、製造例1の調製方法と同様にして、淡黄色透明の混合物溶液を得た(固形分濃度1.95%)。
正常ヒト表皮細胞を増殖添加剤含有HuMediaKG2[クラボウ社製]にて6×104個/mLに調製し、24穴プレートに1mLを播種して、5%CO2、飽和水蒸気下、37℃で培養した。培養1日後、製造例1の抽出物とコルチゾール(ナカライテスク社製)40μMを培養液に添加して試験区を設定し、当該培養液で表皮細胞を培養した。ここで、製造例1の抽出物は、培養液全量に対して溶液として終濃度が3%となるように添加した。また、比較対照として、製造例1の抽出物に代えて、PBS(-)溶液のみを培養液(培養液全量に対するPBS(-)の終濃度を3%に調整したもの)に添加した対照区と、PBS(-)溶液とコルチゾール40μMを培養液に添加したコントロール区を設定した。添加3時間後の試験区の細胞をTrizol試薬(Invitrogen社製)0.5mLで回収した。回収した細胞に対してクロロホルム(和光純薬工業社製)100μL添加して撹拌混合し遠心分離機(TOMY社製/MX-160)で12,500rpm、4℃の条件下で15分間遠心分離した後、水層のみを200μL分取した。回収した水層にイソプロパノール(和光純薬工業社製)500μLを添加して撹拌混合し、12,500rpm、4℃の条件下で15分間遠心分離してtotal RNAの沈殿物を得た。total RNAに75%エタノールを1mL添加して撹拌して洗浄し、12,500rpm、4℃条件下で15分間遠心分離して沈殿を回収した。回収したtotal RNAを所定のキット(PrimeScript RT reagent Kit with gDNA Eraser (Perfect Real Time)[タカラバイオ社製]を用いて逆転写反応し、cDNAを合成した。合成したcDNAをサンプルとして、Thermal Cycler Dice(登録商標)Real Time System Single[タカラバイオ社製]、及びSYBR(登録商標)Premix Ex TaqTM II(Tli RNaseH Plus)[タカラバイオ社製]を用いて、各種遺伝子の発現と、内部標準物質G3PDH遺伝子の発現の検出を行った。ここで、G3PDH(glyceraldehyde-3-phosphate dehydrogenase)は、ハウスキーピング遺伝子(多くの組織や細胞中に共通して一定量発現する遺伝子であって、常に発現され,細胞の維持,増殖に不可欠な遺伝子である)の一つであり、発現量が常に一定とされていることから、PCRの実験では内部標準として用いられるものである。試験結果は、G3PDH遺伝子の発現量を一定とした場合の、それぞれの試験区での各遺伝子の発現量を比較した。本試験系においては、対照区での遺伝子発現量を100としたときの試験区及びコントロール区でのそれぞれの遺伝子の発現量の相対値を求めた。
[成分] 部
ホホバ油 1.0
ポリオキシエチレン(5.5)セチルアルコール 5.0
メチルパラベン 0.1
製造例1の混合物溶液 2.0
グリセリン 5.0
1,3-ブチレングリコール 5.0
クエン酸ナトリウム 0.2
精製水 全量が100部となる量
処方例1に含まれる製造例1の混合物溶液に代えて、製造例2の混合物溶液2.0部を用いるほかは、処方例1と同様にして化粧水を得た。
[成分] 部
スクワラン 5.0
ヘキサラン 3.0
ホホバ油 1.0
ツバキ油 1.5
ポリオキシエチレン(20)ソルビタンモノステアレート 1.0
親油型ステアリン酸グリセリル 1.0
水添大豆レシチン 1.5
製造例1の混合物溶液 3.0
L-アスコルビン酸-2-グルコシド 2.0
水酸化カリウム 0.5
グリセリン 3.0
1,3-ブチレングリコール 2.0
カルボキシメチルセルロース 0.3
キサンタンガム 0.2
ヒアルロン酸ナトリウム 0.01
精製水 全量が100部となる量
処方例3の成分中、L-アスコルビン酸-2-グルコシド2.0部及び水酸化カリウム0.5部に代えてアルブチン3.0部を用いるほかは処方例5と同様にして乳液を得た。
処方例3の成分中、L-アスコルビン酸-2-グルコシド2.0部及び水酸化カリウム0.5部に代えてニコチン酸アミド5.0部を用いるほかは処方例3と同様にして乳液を得た。
処方例3の成分中、L-アスコルビン酸-2-グルコシド2.0部及び水酸化カリウム0.5部に代えてトラネキサム酸2.0部を用いるほかは処方例3と同様にして乳液を得た。
処方例3の成分中、L-アスコルビン酸-2-グルコシド2.0部及び水酸化カリウム0.5部に代えてトラネキサム酸セチルエステル塩酸塩2.0部を用いるほかは処方例3と同様にして乳液を得た。
[成分] 部
スクワラン 3.0
セチルアルコール 1.0
モノステアリン酸ポリエチレングリコール 0.2
ジプロピレングリコール 1.0
イソオクタン酸セチル 1.0
ジメチルポリシクロキサン 1.0
製造例1の混合物溶液 2.0
乳酸菌発酵米 2.0
海藻抽出物 1.0
ラフィノース 2.0
1,3-ブチレングリコール 2.0
L-アスコルビン酸-2-グルコシド 2.0
水酸化カリウム 0.5
アセチル化ヒアルロン酸ナトリウム 0.2
グァーガム 3.0
セラミド 1.0
精製水 全量が100部となる量
[成分] 部
オリーブ油 5.0
ホホバ油 5.0
スクワラン 5.0
ベヘニルアルコール 2.0
パルミチン酸 2.5
製造例1の混合物溶液 2.0
乳酸菌発酵米 2.0
水素添加レシチン 0.5
カルボキシビニルポリマー 0.3
アルギン酸ナトリウム 0.2
海藻抽出物 2.0
メチルパラベン 0.15
エチルパラベン 0.03
精製水 全量が100部となる量
[成分] 部
ポリオキシエチレンソルビタンモノステアレート 1.5
セチルアルコール 3.0
モノステアリン酸グリセリル 1.0
スクワラン 5.0
オリーブ油 5.0
ジプロピレングリコール 3.0
製造例2の混合物溶液 2.0
ゲンチアナ抽出物 1.0
甘草抽出物 2.0
クエン酸 0.2
メチルパラベン 0.2
精製水 全量が100部となる量
[成分] 部
ステアリン酸 2.4
モノステアリン酸プロピレングリコール 2.0
セトステアリルアルコール 0.2
液状ラノリン 2.0
流動パラフィン 3.0
ミリスチン酸イソプロピル 8.5
プロピルパラベン 0.05
製造例1の混合物溶液 5.0
カルボキシメチルセルロースナトリウム 0.2
ベントナイト 0.5
プロピレングリコール 4.0
トリエタノールアミン 1.1
メチルパラベン 0.1
酸化チタン 8.0
タルク 4.0
着色顔料 適量
精製水 全量が100部となる量
[成分] 部
N-ラウロイルメチルアラニンナトリウム 25.0
ヤシ油脂肪酸カリウム液(40%) 26.0
ヤシ油脂肪酸ジエタノールアミド 3.0
メチルパラベン 0.1
製造例1の混合物溶液 5.0
1,3-ブチレングリコール 2.0
精製水 全量が100部となる量
[成分] 部
N-ヤシ油脂肪酸メチルタウリンナトリウム 10.0
ポリオキシエチレン(3)アルキルエーテル硫酸ナトリウム 20.0
ラウリルジメチルアミノ酢酸ベタイン 10.0
ヤシ油脂肪酸ジエタノールアミド 4.0
メチルパラベン 0.1
クエン酸 0.1
製造例1の混合物溶液 2.0
1,3-ブチレングリコール 2.0
精製水 全量が100部となる量
[成分] 部
ポリオキシエチレン(10)硬化ヒマシ油 1.0
塩化ジステアリルジメチルアンモニウム 1.5
塩化ステアリルトリメチルアンモニウム 2.0
2-エチルヘキサン酸グリセリル 1.0
セタノール 3.0
ステアリルアルコール 1.0
メチルパラベン 0.1
製造例2の混合物溶液 2.0
1,3-ブチレングリコール 5.0
精製水 全量が100部となる量
Claims (1)
- (A)米の抽出物溶液を蛋白分解酵素で処理して得られる加水分解物溶液と、(B)米糠の抽出物溶液を蛋白分解酵素で処理して得られる加水分解物溶液との混合物溶液を有効成分とするストレスに起因する神経成長因子生成の抑制剤。
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| JP2006117542A (ja) | 2004-10-19 | 2006-05-11 | Pias Arise Kk | 神経成長因子産生抑制剤、並びにその神経成長因子産生抑制剤を配合した皮膚外用剤、化粧料、医薬部外品、痒み予防及び治療剤、及びアトピー性皮膚炎治療剤 |
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