JP2010001239A - 外用組成物 - Google Patents
外用組成物 Download PDFInfo
- Publication number
- JP2010001239A JP2010001239A JP2008160946A JP2008160946A JP2010001239A JP 2010001239 A JP2010001239 A JP 2010001239A JP 2008160946 A JP2008160946 A JP 2008160946A JP 2008160946 A JP2008160946 A JP 2008160946A JP 2010001239 A JP2010001239 A JP 2010001239A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- hair
- poe
- ether
- composition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 9
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- 125000003277 amino group Chemical group 0.000 claims description 6
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- C07D277/04—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
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- A61Q19/00—Preparations for care of the skin
- A61Q19/08—Anti-ageing preparations
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- A—HUMAN NECESSITIES
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Abstract
【解決手段】本発明に係る外用組成物は、(化1)で示される2‐チオチアゾリジン‐4‐カルボン酸又はその誘導体或いは(化2)で示される2‐メチルチアゾリジン‐2,4‐ジカルボン酸又はその誘導体或いはそれらの塩から選ばれる1種又は2種以上を含有することを特徴とする。
【選択図】なし
Description
(処方例1)
2‐チオチアゾリジン‐4‐カルボン酸又は2‐メチルチアゾリジン‐2,4‐ジカルボン酸或いはこれらの合計として 1.0質量%
アスコルビン酸 1.0質量%
グリセリン 2.0質量%
1,3−ブチレングリコール 2.0質量%
トリメチルグリシン 3.0質量%
1,2−ペンタンジオール 3.0質量%
ポリオキシエチレンメチルグルコシド 3.5質量%
キサンタンガム 0.3質量%
クエン酸 0.02質量%
クエン酸Na 0.2質量%
メチルパラベン 0.15質量%
精製水 残部
なお、処方例1において、2‐チオチアゾリジン‐4‐カルボン酸又は2‐メチルチアゾリジン‐2,4‐ジカルボン酸或いはこれらの合計を1.0質量%とするのは、例示であり、0.01〜10質量%の範囲で、変更しても良い。また、2‐チオチアゾリジン‐4‐カルボン酸の誘導体、2‐メチルチアゾリジン‐2,4‐ジカルボン酸の誘導体を用いても良い。
2‐チオチアゾリジン‐4‐カルボン酸含有の外用組成物及び2‐メチルチアゾリジン‐2,4‐ジカルボン酸含有の外用組成物について、化粧品としての実用レベルでのラジカル消去能を有しているか否かの確認を行った。本検討において実用レベルのラジカル消去能とはラジカル消去率50%以上の時を指す。ラジカル消去能の確認は次のようにして行った。DPPH(1,1‐diphenyl‐2‐picrylhydrazyl)をエタノールにより溶解し、1mM溶液濃度に調製した。さらに、被験化合物は、水に溶解し0.5又は1.0w/v%溶液濃度に調製し、被験化合物溶液とした。被験化合物溶液1mLに、エタノールを5mL及びDPPH溶液0.27mL加え混合した。その後、20分間室温に放置し、試験溶液とした。別に水1mLにエタノールを5mLおよびDPPH溶液0.27mL加え混合した。その後、20分間室温に放置し、空試験溶液とした。試験溶液、空試験溶液につき、波長520nmにおける吸光度AT、ABを測定した。被験化合物のDPPHラジカル消去率は、次式(数1)により算出し、DPPHラジカル消去能を判定した。表1からわかるように、2‐チオチアゾリジン‐4‐カルボン酸含有の外用組成物及び2‐メチルチアゾリジン‐2,4‐ジカルボン酸含有の外用組成物ともに、1.0w/v%時では充分実用レベルのラジカル消去能を示した。また、2‐チオチアゾリジン‐4‐カルボン酸含有の外用組成物は0.5w/v%時にも実用レベルのラジカル消去能を示した。
2‐チオチアゾリジン‐4‐カルボン酸含有の外用組成物及び2‐メチルチアゾリジン‐2,4‐ジカルボン酸含有の外用組成物について、化粧品としての実用レベルでの過酸化水素消去能を有しているか否かの確認を行った。本検討において実用レベルの過酸化水素消去能とは過酸化水素消去率50%以上の時を指す。過酸化水素消去能の確認は次のようにして行った。フェノール、4‐アミノアンチピリンをそれぞれ1M Tris緩衝液(pH8.0)に溶かし、それぞれ40mM、8mM溶液濃度に調製した。また、ペルオキシダーゼを1M Tris緩衝液(pH8.0)に溶かし、約3125U/mL溶液濃度に調製した。さらに上記のように調製したフェノール溶液、4‐アミノアンチピリン溶液、ペルオキシダーゼ溶液をそれぞれ1mL、及び1M Tris緩衝液(pH8.0)7mLを混合し発色溶液とした。ジエチレントリアミン5酢酸をリン酸緩衝液PBS(−)に溶かし、0.5mM溶液濃度に調製した。さらに、被験化合物は、水に溶解し0.5又は1.0w/v%溶液濃度に調製し、被験化合物溶液とした。被験化合物溶液0.4mLと1mMの過酸化水素溶液0.4mLを混合し、37℃で10分間加温した後、発色溶液0.4mLを加え、さらに37℃で10分間加温した。別に、空試験として被験化合物溶液の代わりにジエチレントリアミン5酢酸溶液0.4mLで同様の操作を行った。また、試薬ブランクとして過酸化水素溶液の代わりに水0.4mLで同様の操作を行った。試験溶液、空試験溶液、試薬ブランク溶液につき、波長510nmにおける吸光度AT、AB、ARを測定した。被験化合物の過酸化水素消去率は、次式(数2)により算出し、過酸化水素消去能を判定した。表2からわかるように、2‐チオチアゾリジン‐4‐カルボン酸含有の外用組成物及び2‐メチルチアゾリジン‐2,4‐ジカルボン酸含有の外用組成物ともに、1.0w/v%時では充分実用レベルの過酸化水素消去能を示した。また、2‐メチルチアゾリジン‐2,4‐ジカルボン酸含有の外用組成物は0.5w/v%時にも実用レベルの過酸化水素消去能を示した。
2‐チオチアゾリジン‐4‐カルボン酸含有の外用組成物及び2‐メチルチアゾリジン‐2,4‐ジカルボン酸含有の外用組成物について、化粧品としての実用レベルでのチロシナーゼ活性阻害能を有しているか否かの確認を行った。本検討において実用レベルのチロシナーゼ活性阻害能とはチロシナーゼ活性阻害率50%以上の時を指す。チロシナーゼ活性阻害能の確認は次のようにして行った。チロシナーゼ、チロシンをそれぞれ0.67Mリン酸緩衝液(pH6.8)により溶解し、それぞれ50U/mL、0.03w/v%の溶液濃度に調製した。さらに、被験化合物は、水に溶解し0.5w/v%溶液濃度に調製し、被験化合物溶液とした。被験化合物溶液1.2mLに、チロシン溶液、およびチロシナーゼ溶液をそれぞれ1.2mL加え混合した。その後、30分間30℃で加温し、試験溶液とした。別に水1.2mLにチロシン溶液、およびチロシナーゼ溶液をそれぞれ1.2mL加え混合した。その後、30分間30℃で加温し、空試験溶液とした。試験溶液、空試験溶液につき、波長475nmにおける吸光度AT、ABを測定した。被験化合物のチロシナーゼ活性阻害率は、次式(数3)により算出しし、チロシナーゼ阻害能を判定した。表3からわかるように、2‐チオチアゾリジン‐4‐カルボン酸含有の外用組成物及び2‐メチルチアゾリジン‐2,4‐ジカルボン酸含有の外用組成物ともに、0.5w/v%時に充分実用レベルのチロシナーゼ活性阻害能を示した。
2‐チオチアゾリジン‐4‐カルボン酸含有の外用組成物及び2‐メチルチアゾリジン‐2,4‐ジカルボン酸含有の外用組成物について、化粧品としての実用レベルでの毛髪ウェーブ・カーリング能を有しているか否かの確認を行った。毛髪ウェーブ・カーリング能の確認は次のようにして行った。被験化合物は、水に溶解しアンモニアによりpH=9.0に調製した後に被験化合物濃度を5.0%に調製した溶液を被験化合物溶液とした。洗浄した人毛で毛束(25cm、0.5g/1束)を所定数準備し、その毛束を、ガラス製ロッド(直径6mm)に均一に巻きつけた。各毛髪束を、被験化合物溶液もしくは比較例として水に漬けた状態で、50℃の恒温水槽に15分間放置した。次に、被験化合物溶液もしくは水から取り出した毛束を1分間水洗し、よく水分を切った後、2%過酸化水素溶液に漬けた状態で、室温に10分間放置する。その後、上記と同様の2%過酸化水素溶液への浸漬及び室温放置操作を更に1回繰り返した後に1分間水洗し、毛髪束をロッドからていねいに取り外し、その毛髪束のカールの状態を観察し、目視で毛髪ウェーブ効果の判定をした。
判定基準:
◎:強いカールがかかっている
○:穏やかなカールがかかっている
×:カールがほとんどかかっていない
含硫化合物はしばしばその不快な強い刺激臭が問題となる。そのことから、本発明に使用される2‐チオチアゾリジン‐4‐カルボン酸又は2‐メチルチアゾリジン‐2,4‐ジカルボン酸の臭いに関して官能試験を行った。臭いの官能試験は次のようにして行った。被験化合物をそれぞれ0.5g量り、無作為に選出したモニター男女14人(男9人、女5人)により、嗅覚による官能試験を行った。評価は5段階評価とし、14人の平均点を示した。表5からわかるように、本発明に使用される2−チオチアゾリジン‐4‐カルボン酸又は2‐メチルチアゾリジン‐2,4‐ジカルボン酸は臭いの問題がない。
評価基準:
5:強く刺激臭を感じ、使用に問題がある。
4:刺激臭を感じ、使用に問題がある。
3:わずかに刺激臭を感じるが、使用に差し支えない。
2:刺激臭をほとんど感じず、使用に問題がない。
1:刺激臭を全く感じず、使用に問題がない。
2‐チオチアゾリジン‐4‐カルボン酸含有の外用組成物及び2‐メチルチアゾリジン‐2,4‐ジカルボン酸含有の外用組成物について、化粧品としての実用レベルでの安定性を有しているか否かの確認を行った。被験化合物は、水に溶解し5.0w/v%溶液濃度に調製し、被験化合物溶液とした。被験化合物と同様にラジカル消去能、過酸化水素消去能、チロシナーゼ活性阻害能を持ち、化粧品等へ配合されるL‐システインを比較化合物として同様に水に溶解し5.0w/v%溶液濃度に調製し、比較化合物溶液とした。用意した各溶液を、室温で1週間静置した後に、各溶液の状態を目視で観察し、安定性を判定した。
判定基準:
○:安定性が良く化粧品に適用できる
△:やや安定性に欠けるため制限付きで適用できる
×:安定性が悪く化粧品に適用できない
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Cited By (10)
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JP2013014540A (ja) * | 2011-07-04 | 2013-01-24 | Mandom Corp | 保湿化粧料 |
WO2013081146A1 (ja) * | 2011-11-30 | 2013-06-06 | 味の素株式会社 | シワ防止化粧料 |
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CN115279893A (zh) * | 2020-03-16 | 2022-11-01 | 味之素株式会社 | 动物细胞的培养方法 |
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