JP2017123833A - 組成物 - Google Patents
組成物 Download PDFInfo
- Publication number
- JP2017123833A JP2017123833A JP2016031449A JP2016031449A JP2017123833A JP 2017123833 A JP2017123833 A JP 2017123833A JP 2016031449 A JP2016031449 A JP 2016031449A JP 2016031449 A JP2016031449 A JP 2016031449A JP 2017123833 A JP2017123833 A JP 2017123833A
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- JP
- Japan
- Prior art keywords
- acid
- extract
- compound
- derivatives
- salt
- 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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- 229940088594 vitamin Drugs 0.000 claims abstract description 19
- 229930003231 vitamin Natural products 0.000 claims abstract description 19
- 235000013343 vitamin Nutrition 0.000 claims abstract description 19
- 239000011782 vitamin Substances 0.000 claims abstract description 19
- 150000001413 amino acids Chemical class 0.000 claims abstract description 18
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- 238000007033 dehydrochlorination reaction Methods 0.000 abstract description 10
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- 150000003722 vitamin derivatives Chemical class 0.000 abstract description 6
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- 239000000284 extract Substances 0.000 description 46
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- 239000010452 phosphate Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
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Landscapes
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Cosmetics (AREA)
Abstract
Description
本発明は、アミノ酸又はビタミンの塩酸塩の脱塩酸処理物と、酸性化合物とを含有する組成物である。
本発明は、アミノ酸又はビタミンの塩酸塩の脱塩酸処理物を含有する組成物である。
アミノ酸の塩酸塩としては、例えば、リジン又はヒドロキシリジンの塩酸塩、システイン塩酸塩、オルニチン塩酸塩、アルギニン塩酸塩、グルコサミンの塩酸塩等が挙げられ、ビタミンの塩酸塩としては、チアミン塩酸塩、ピリドキシン塩酸塩等が挙げられる。
リジン塩酸塩100gを精製水900gに溶解した。この塩酸塩水溶液を強塩基性陰イオン交換樹脂カラムに通液し、脱塩酸処理を行った。この液を濃縮乾固し、リジン10gを得た。
グルコサミン塩酸塩100gを精製水900gに溶解した。この塩酸塩水溶液を強塩基性陰イオン交換樹脂カラムに通液し、脱塩酸処理を行った。この液を濃縮乾固し、グルコサミン72gを得た。
チアミン塩酸塩100gを精製水900gに溶解した。この塩酸塩水溶液を強塩基性陰イオン交換樹脂カラムに通液し、脱塩酸処理を行った。この液を濃縮乾固し、チアミン43gを得た。
ピリドキシン塩酸塩100gを精製水900gに溶解した。この塩酸塩水溶液を強塩基性陰イオン交換樹脂カラムに通液し、脱塩酸処理を行った。この液を濃縮乾固し、ピリドキシン6gを得た。
[成分] 部
製造例1の化合物 3.0
コラーゲン 5.0
クエン酸 0.1
甘味料(スクロース) 0.01
アスコルビン酸 0.01
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の化合物に代えて、製造例2の化合物3.0部を用いるほかは、処方例1と同様にして飲料を得た。
処方例1に含まれる製造例1の化合物に代えて、製造例3の化合物3.0部を用いるほかは、処方例1と同様にして飲料を得た。
処方例1に含まれる製造例1の化合物に代えて、製造例4の化合物3.0部を用いるほかは、処方例1と同様にして飲料を得た。
[成分] 部
製造例1の化合物 2.0
製造例2の化合物 2.0
製造例3の化合物 2.0
製造例4の化合物 2.0
アスコルビン酸 5.0
脂肪酸エステル 10.0
乳酸カルシウム 20.0
乳糖 30.0
上記重量部の各成分を混合した後、加圧成形し、錠剤とした。
[A成分] 部
オリーブ油 1.0
ポリオキシエチレン(5.5)セチルアルコール 5.0
ブチルパラベン 0.1
[B成分]
製造例1の化合物 2.0
アスコルビン酸 2.0
エタノール 5.0
グリセリン 5.0
1,3−ブチレングリコール 5.0
ピロ亜硫酸ナトリウム 2.0
クエン酸 適量
クエン酸三ナトリウム 0.4
水酸化カリウム 適量
精製水 全量が100部となる量
[C成分]
香料 適量
A成分及びB成分をそれぞれ80℃以上に加温後、A成分にB成分を加えて攪拌し、さらにヒスコトロン(5000rpm)で2分間ホモジナイズを行った。これを50℃まで冷却した後、C成分を加えて攪拌混合し、さらに30℃以下まで冷却して化粧水を得た。
処方例1のB成分に含まれる製造例1の化合物に代えて、製造例2の化合物1.0部を用いるほかは、処方例1と同様にして化粧水を得た。
処方例1のB成分に含まれる製造例1の化合物に代えて、製造例3の化合物1.0部を用いるほかは、処方例1と同様にして化粧水を得た。
処方例1のB成分に含まれる製造例1の化合物に代えて、製造例4の化合物1.0部を用いるほかは、処方例1と同様にして化粧水を得た。
[A成分] 部
流動パラフィン 6.0
ヘキサラン 4.0
ホホバ油 1.0
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
大豆レシチン 1.5
乳酸菌発酵米 2.0
[B成分]
製造例1の化合物 2.0
アスコルビン酸 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
クエン酸ナトリウム 0.1
精製水 全量が100部となる量
[C成分]
香料 適量
上記のA成分とB成分をそれぞれ80℃以上に加熱した後、攪拌混合した。これを50℃まで冷却した後、C成分を加えてさらに攪拌混合して乳液を得た。
処方例5のB成分中、アスコルビン酸に代えて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5のB成分中、アスコルビン酸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5のB成分中、アスコルビン酸に代えてコウジ酸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5のB成分中、アスコルビン酸に代えて3−O−エチルアスコルビン酸2.0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5のB成分中、アスコルビン酸に代えてサリチル酸0.3部を用いるほかは処方例5と同様にして乳液を得た。
[A成分] 部
スクワラン 3.0
ベヘニルアルコール 3.0
ヘキサラン 4.0
ホホバ油 1.0
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
グリセリン脂肪酸エステル 1.0
大豆レシチン 1.5
[B成分]
製造例2の化合物 0.5
製造例4の化合物 0・5
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
グリチルリチン酸ジカリウム 0.1
グリセリン 3.0
1,3−ブチレングリコール 2.0
ピロ亜硫酸ナトリウム 0.01
精製水 全量が100部となる量
[成分] 部
製造例1の化合物 1.0
製造例3の化合物 1.0
エタノール 10.0
グリセリン 3.0
1、3−ブチレングリコール 2.0
メチルパラベン 0.2
クエン酸 0.1
クエン酸ナトリウム 0.3
カルボキシビニルポリマー 0.1
カテキン 0.1
キサンタンガム 0.1
香料 適量
水酸化カリウム 適量
精製水 全量が100部となる量
上記の成分を混合してローションを得た。
本発明の製造例1〜4に係る化合物の安全性を皮膚一次刺激抑制試験により評価した。
[試験方法]
被験者5名(20〜60歳の男女)に対してそれぞれの上腕内側部に被験部を設け、洗浄後に初期値として各被験者の被験部の紅斑量を紅斑量測定装置(メグザメーターMexameter(登録商標) MX18、Courage+Khazaka社製)により測定した。その後、被験部に製造例1〜4の化合物(終濃度が2.0%)を含有した水溶液を4時間閉塞パッチした。閉塞パッチ終了後、被験部を水洗し、3時間後に、各被験者の被験部の紅斑量を上記測定装置により測定し、初期値から処理直後の値を差し引いた値について一次刺激抑制量として5名の被験者の平均値を算出した。また、コントロールとして製造例1〜4の代わりに、精製水を用いて上記と同様の操作を行った。さらに、比較対象として、製造例1〜4の化合物の脱塩酸塩処理前のものをそれぞれ比較例1〜4として使用し、同様の試験を行った。
[表1]
本発明に係る化合物と酸性化合物を含有する併用組成物に関し、着色の経時性変化の目視試験により、評価した。
[試験方法]
以下の混合物を調製し(pH6.5)、4℃、20℃及び40℃の温度条件の下、1週間毎に4週間、着色を目視により確認した。なお、以下の「部」とは、重量%を示すものとする。
(混合物)
[1]製造例1の化合物(1)、製造例2の化合物(2)、製造例3の化合物(3)又は製造例4の化合物(4):1.0部
[2]酸性化合物:アスコルビン酸(A)、アスコルビン酸グルコシド(B)、3−O−エチルアスコルビン酸(C):2.0部
[3]1,3−ブチレングリコール:5.0部
[4]防腐剤(メチルパラベン):0.2部
[5]精製水:82部
[表2−1(A)]
[試験方法]
以下の混合物を調製し(pH6.5)、4℃、20℃及び40℃の温度条件の下、1週間毎に4週間、着色を目視により確認した。なお、以下の「部」とは、重量%を示すものとする。
(混合物)
[1]製造例1の化合物(1)、製造例2の化合物(2)、製造例3の化合物(3)又は製造例4の化合物(4):1.0部
[2]酸性化合物:アスコルビン酸(A)、アスコルビン酸グルコシド(B)又は3−O−エチルアスコルビン酸(C):2.0部
[3]ピロ亜硫酸ナトリウム:0.2部
[4]クエン酸:適量
[5]クエン酸ナトリウム:0.4部
[6]1,3−ブチレングリコール:5.0部
[7]防腐剤(メチルパラベン):0.2部
[8]精製水:全量を100部とする
[表2−2(A)]
本試験例3においては、下記の本発明試料(1)〜(7)及び比較試料(1)及び(2)について、使用感を評価した。なお、以下の「部」とは、重量%を示すものとする。
(1)本発明試料1
[成分] 部
エタノール 2.0
グリセリン 5.0
メチルパラベン 0.1
製造例1の化合物 2.0
アスコルビン酸グルコシド 2.0
クエン酸ナトリウム 0.6
精製水 全量が100部となる量
(2)本発明試料2
上記本発明試料1において製造例1の化合物に代えて、製造例2の化合物2.0部を配合したエッセンス。
(3)本発明試料3
上記本発明試料1において製造例1の化合物に代えて、製造例3の化合物2.0部を配合したエッセンス。
(4)本発明試料4.
上記本発明試料1において製造例1の化合物に代えて、製造例4の化合物2.0部を配合したエッセンス。
(5)本発明試料5
上記本発明試料1においてアスコルビン酸グルコシドに代えてアスコルビン酸2.0部を配合したエッセンス。
(6)本発明試料6
上記本発明試料1においてアスコルビン酸グルコシドに代えて3−O−エチルアスコルビン酸2.0部を配合したエッセンス。
(7)本発明試料7
上記本発明試料1においてアスコルビン酸グルコシドに代えてアルブチン3.0部を配合したエッセンス。
(8)比較試料1
上記本発明試料1の組成において製造例1の化合物を含まないエッセンス。
[試験方法]
無作為に抽出した年齢25〜60歳の男女21名を被験者として、7グループに分け、各グループの被験者に本発明試料1〜7のいずれか1つと、比較試料1とを、それぞれ左右の頬部に、本発明例又は比較例の乳液を1日2回(朝、晩)、1ヵ月間塗布してもらった時の使用感を評価した。使用感は、手に取った感触(イ)、塗布時の伸び(ロ)、塗布時のなめらかさ(ハ)、及び塗布後の感触(ニ)に基づいて、5:非常に良い、4:良い、3:普通、2:やや悪い、1:悪い、という5段階評価によって、それぞれ行い、本発明試料については各グループの被験者による評価値の合計を示し、比較試料については各グループの被験者による評価値の合計を平均した値を示した。
[表3]
Claims (2)
- アミノ酸又はビタミンの塩酸塩の脱塩酸処理物を含有する組成物。
- アミノ酸又はビタミンの塩酸塩の脱塩酸処理物と、酸性化合物とを含有する組成物。
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