JP5050350B2 - コラーゲン産生増強剤とその製造方法並びに用途 - Google Patents
コラーゲン産生増強剤とその製造方法並びに用途 Download PDFInfo
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- JP5050350B2 JP5050350B2 JP2005514562A JP2005514562A JP5050350B2 JP 5050350 B2 JP5050350 B2 JP 5050350B2 JP 2005514562 A JP2005514562 A JP 2005514562A JP 2005514562 A JP2005514562 A JP 2005514562A JP 5050350 B2 JP5050350 B2 JP 5050350B2
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- collagen production
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- fatty acids
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Description
<ローヤルゼリー由来のコラーゲン産生増強成分の分離と同定>
室温下、ブラジル産生ローヤルゼリー1gを精製水10mlに懸濁し、3,000rpmで10分間遠心処理して、上清画分と沈殿画分とに分けた。前記沈殿画分に1N−NaOH水溶液を1ml添加し、固形物を溶解させ、次いで、1N−HCl水溶液で中和した後、精製水で全量を10mlとし、分画分子量5,000ダルトンのUF膜を用いて高分子画分と低分子画分とに分画した。各画分につき、後述するコラーゲン・アッセイ法(以下、『コラーゲン・アッセイ法』と言う。)を適用して、コラーゲン産生増強作用の有無を調べた。その結果、コラーゲン産生増強作用は、沈殿画分の低分子画分(以下、『画分A』と言う。)が最も高かった。そこで、画分A中に存在するコラーゲン産生増強成分の単離と同定を試みた。即ち、画分AをC18逆相高速液体クロマトグラフィー(以下、『HPLC』と言う。)(カラムサイズ:内径4.6×長さ250mm、充填剤:シリカゲルにオクタデシル基が結合したゲル(バイダック社製))を用いて複数の画分に分画し、コラーゲン・アッセイ法によりコラーゲン産生増強活性画分を特定し、回収した。溶出に際しては、溶出速度0.5ml/分で、0.05%(w/v)トリフルオロ酢酸水溶液を15分間、アセトニトリル20%(w/v)含有0.05%(w/v)トリフルオロ酢酸水溶液を5分間カラムに流し、更に、アセトニトリル濃度が20%(w/v)から80%(w/v)に直線的に上昇する0.05%(w/v)トリフルオロ酢酸水溶液を60分間カラムに流しつつ、波長210nmにて溶出画分の吸収ピークをモニターし、その吸収ピークが高い画分(画分B)を回収した。尚、波長210nmにてモニターした理由は、予備的実験により、画分Aに含まれるコラーゲン産生増強作用を有する成分の吸収波長であったことによる。更に、画分Bを再度、前記条件でC18逆相HPLCにて再クロマトしたところ、コラーゲン産生増強作用を示す成分(以下、『成分X』と言う。)は、43〜44分の位置に溶出した。この成分Xの吸収極大波長を調べたところ215nmであった。
ヒト線維芽細胞であるNHDF細胞(倉敷紡績株式会社販売)を細胞濃度2.5×104個/穴となるように10%(v/v)ウシ胎児血清と適量のペニシリンを添加したダルベッコ変法イーグル培地(株式会社日水販売、以下、『DMEM培地』と既述する。)(pH7.1〜7.4)を含む96穴マイクロプレート(ベクトン・ディッキンソン社販売)に播種し、5%(v/v)CO2条件下、37℃で24時間培養する。その後、培養上清を所定濃度のサンプル及び/又は50μMのL−アスコルビン酸2−グルコシド(商品名『AA2G』、純度98.0%以上、株式会社林原生物化学研究所製)とを添加したDMEM培地200μlで交換して5日間培養する。その後、前記マイクロプレートにおける各穴当たりの細胞によるコラーゲン産生量をサーコル・コラーゲン・アッセイ・キット(バイオカラー社製)にて定量する。
<10−HDAによるコラーゲン産生増強作用>
実験1中に示すコラーゲン・アッセイ法により、10−HDAによるコラーゲン産生増強作用について調べた。即ち、コラーゲン・アッセイ法において、サンプルとして、10−HDAを150μg/ml及び/又は実験1で用いたと同じAA2G50μMを含むDMEM培地を用い、10−HDAによるコラーゲン産生増強作用を調べた。対照は、サンプル不含有のAA2G50μM含有又は不含有DMEM培地を用いる2つの系を設けた。その結果を図1に示す。
<L−アスコルビン酸又はAA2G存在下でのコラーゲン産生増強作用に及ぼす10−HDAの影響>
L−アスコルビン酸又はAA2Gによるコラーゲン産生増強作用に及ぼす10−HDAの影響を調べることを目的として、下記の実験を行った。即ち、実験1中に示すコラーゲン・アッセイ法において、サンプルとして10−HDAを0、0.1、0.2又は0.5mg/ml含み、L−アスコルビン酸類として、L−アスコルビン酸又はAA2GをL−アスコルビン酸換算で50μM含有するDMEM培地、及びサンプルとして10−HDAを0、0.1、0.2又は0.5mg/ml含み、L−アスコルビン酸類不含有のDMEM培地を用いて、培養細胞におけるコラーゲン産生量を比較検討した。その結果を図4に示す。
<脂肪酸類がヒト線維芽細胞におけるTGF−β産生に与える影響>
ウシ胎児血清を10%(v/v)補足したDMEM培地を用いて、ヒト線維芽細胞であるNHDF細胞(倉敷紡績株式会社販売)を、複数の96穴マイクロプレート(ベクトン・ディッキンソン社販売)に細胞濃度2.5×104個/穴で播種し、5%(v/v)CO2インキュベータ中にて24時間培養した。その後、培養上清を除去した後、10−HDAを0、0.5、又は1.5mM、及びAA2Gを0.2μg/ml含む新鮮なDMEM培地をそれぞれ異なるマイクロプレートに添加して24時間培養した。その後、各マイクロプレートの各穴における培養上清中のTGF−β量を『TGF−β1 Eマックス イムノアッセイ・システム』(プロメガ社販売)により定量し統計処理した。その結果を表1に示す。
<コラーゲン産生増強剤>
以下に示す各成分を所定の配合割合で均一に混合し、常法により打錠して、一錠当たり300mgの本発明のコラーゲン産生増強剤を調製した。本品は、ヒトを含む動物のコラーゲン産生増強剤として好適に用いることができる。また、本品は、TGF−β産生増強剤としての機能をも有している。
L−アスコルビン酸2−グルコシド 20質量部
(商品名『AA2G』、株式会社林原生物化学研究所販売)
10−HDA 0.1質量部
プルラン 5質量部
精製水 5質量部
<コラーゲン産生増強剤>
以下に示す各成分を所定の配合割合で均一に混合し、プラスチック製プレート上に流延し、45℃で一夜乾燥して、一辺2cmの正方形に裁断し、厚さ0.5mmのフィルム状コラーゲン産生増強剤を得た。本品は、経口摂取するか、又は、予め水や化粧水などを塗布した皮膚部位に載置して用いる手法により日常的に用いることにより、皮膚のコラーゲン産生を効果的に増強し、小ジワを予防し、改善し、肌にはりと潤いを付与することができる。
L−アスコルビン酸2−グルコシド 1質量部
(商品名『AA2G』、株式会社林原生物化学研究所販売)
10−HDA 0.01質量部
無水結晶マルトース 1質量部
(商品名『ファイントース』(登録商標)、株式会社林原商事販売)
スクラロース 0.01質量部
プルラン 10質量部
精製水 20質量部
<コラーゲン産生増強剤>
以下に示す各成分を所定の配合割合で均一に混合し、膜濾過して、200ml容ピストン式噴霧容器に充填して、本発明のコラーゲン産生増強剤を得た。本品は、その適量をヒト又は動物の皮膚に噴霧して使用することにより、ヒトを含む動物の皮膚に於けるコラーゲン産生を増強させ、発毛・育毛、毛並みの改善に著効を発揮する。また、本品は、TGF−β産生増強剤としての機能をも有している。
L−アスコルビン酸2−グルコシド 20質量部
(商品名『AA2G』、株式会社林原生物化学研究所販売)
10−HDA 10質量部
精製水 100質量部
防腐剤 1質量部
<健康食品>
以下に示す各成分を所定の配合割合で均一に混合し、常法により常温で一晩減圧乾燥した後、粉砕機にて破砕して、本発明の粉末状コラーゲン産生増強剤として機能する健康食品を得た。本品は、ヒトを含む動物のコラーゲン産生増強剤として好適に用いることができる。また、本品は、TGF−β産生増強剤としての機能をも有している。
L−アスコルビン酸2−グルコシド 1質量部
(商品名『AA2G』、株式会社林原生物化学研究所販売)
実験1で精製して得た成分X(10−HDA) 0.05質量部
2含水結晶トレハロース 2質量部
(商品名『トレハ』(登録商標)、株式会社林原商事販売)
<健康食品>
以下に示す各成分を所定の配合割合で均一に混合した後、減圧乾燥して、水分含量5%の経口投与用粉末コラーゲン産生増強剤として機能する健康食品を得た。本品は、ヒトのみならず、家畜・家禽、ペット(昆虫も含む)、観賞魚用のコラーゲン産生増強剤として有利に用いることができる。また、本品は、TGF−β産生増強剤としての機能をも有している。
L−アスコルビン酸ナトリウム 1.5質量部
L−アスコルビン酸2−グルコシド 1.0質量部
(商品名『AA2G』、株式会社林原生物化学研究所販売)
10−HDA 0.25質量部
糖転移ルチン 1.0質量部
(商品名『αGルチン』、株式会社林原商事販売)
無水結晶マルチトール 1.5質量部
トレハロース 0.2質量部
精製水 10.0質量部
<アイスクリーム>
生クリーム(油脂含量約46質量%)15質量部、脱脂粉乳3質量部、全乳45質量部、トレハロース10質量部、プルラン1質量部の混合物を加熱溶解し、65℃で30分間保持して殺菌した後、ホモゲナイザーで乳化分散させ、次いで、4℃まで急冷し、これに、実施例1で得たコラーゲン産生増強剤0.5質量部を加え、混合した後、100gずつ適宜容器に充填し、−20℃で凍結させてアイスクリームを得た。
<フルーツゼリー>
以下に示す成分の内、スクロース、トレハロース、ゼラチン及び水を適宜容器に入れ、95℃にて加熱溶解した後、ミカン果汁を加えて混合し、80℃で30分加熱殺菌し、更に、L−アスコルビン酸2−グルコシド(商品名『AA2G』、株式会社林原生物化学研究所販売)と、加熱処理ローヤルゼリーとを加えて冷却してフルーツゼリーを調製した。
スクロース 10.0質量部
含水結晶トレハロース 2.0質量部
ゼラチン 2.5質量部
ミカン果汁(L−アスコルビン酸含量3%) 32.0質量部
精製水 45.0質量部
L−アスコルビン酸2−グルコシド 1.0質量部
(商品名『AA2G』、株式会社林原生物化学研究所販売)
10−ヒドロキシデカン酸 0.01質量部
10−HDA 0.01質量部
<健康飲料>
以下に示す成分を所定の割合で適宜容器中にて均質に混合し、得られる混合物25質量部を精製水150質量部に均一に分散・溶解させ、200gずつ褐色ガラス瓶に入れ、65℃で30分間加熱殺菌して健康飲料を得た。
無水結晶マルトース 500質量部
L−アスコルビン酸2−グルコシド 30質量部
(商品名『AA2G』、株式会社林原生物化学研究所販売)
L−アスコルビン酸ナトリウム 6質量部
10−HDA 2質量部
10−ヒドロキシデセン酸 1質量部
粉末卵黄 190質量部
脱脂粉乳 200質量部
塩化ナトリウム 4.4質量部
塩化カリウム 1.85質量部
硫酸マグネシウム 4質量部
チアミン 0.01質量部
ビタミンEアセテート 0.6質量部
ニコチン酸アミド 0.04質量部
糖転移ヘスペリジン 0.02質量部
(『αGヘスペリジンPS』、東洋精糖株式会社販売)
<皮膚外用クリーム>
所定の配合量からなる下記に示す成分1に成分2を添加し、60℃で加熱攪拌しつつ混合し、室温まで冷却した後、所定の配合量からなる成分3を加えた後、水酸化カリウムでpH6.5に調製した後、ホモゲナイザーにて乳化・分散させてコラーゲン産生増強作用を有する皮膚外用クリームを製造した。
モノステアリン酸ポリオキシエチレングリセリン 2.0質量部
自己乳化型モノステアリン酸グリセリン 5.0質量部
ベヘニン酸エイコサニル 1.0質量部
流動パラフィン 1.9質量部
トリオクタン酸トリメチロールプロパン 10.0質量部
1,3−ブチレングリコール 5.0質量部
乳酸ナトリウム液 10.0質量部
高麗人参エキス 1.5質量部
パラオキシ安息香酸メチル 0.1質量部
ヒアルロン酸ナトリウム 0.1質量部
コンドロイチン硫酸 0.1質量部
甘草エキス 0.5質量部
精製水 62.4質量部
L−アスコルビン酸2−グルコシド 2質量部
(商品名『AA2G』、株式会社林原生物化学研究所販売)
10−HDA 0.01質量部
セバシン酸 0.01質量部
Claims (3)
- 有効成分として、L−アスコルビン酸2−グルコシドと、L−アスコルビン酸2−グルコシドによるコラーゲン産生増強作用を増強するための脂肪酸類とを含んでなるコラーゲン産生増強剤であって、脂肪酸類としては、10−ヒドロキシ−2−デセン酸、10−ヒドロキシデカン酸、デカン酸、2−デセン酸、及びセバシン酸から選ばれる1種又は2種以上からなる脂肪酸類のみを含み、かつ、全組成物質量当たり、L−アスコルビン酸2−グルコシドを、L−アスコルビン酸質量換算で1質量%以上含むとともに、L−アスコルビン酸2−グルコシド1質量部(但し、L−アスコルビン酸質量換算による。)に対し、脂肪酸類を0.0001乃至1質量部含んでなるコラーゲン産生増強剤。
- 脂肪酸類が、生ローヤルゼリーを溶媒に懸濁する工程、得られる懸濁液を遠心分離及び/又は濾過して上清画分と沈殿画分とに分ける工程、得られる沈殿をアルカリ剤により溶解する工程、得られる溶液を酸剤により中和する工程、及び中和して得られる溶液を膜分離して、高分子画分と脂肪酸類を含有する低分子画分に分離し、後者の低分子画分を採取する工程を経由して得られたものである請求項1に記載のコラーゲン産生増強剤。
- コンドロイチン、コンドロイチン硫酸、デルマタン硫酸、ヘパリン、ヘパラン硫酸、ケラタン硫酸、ヒアルロン酸、及びヒアルロン酸ナトリウムから選ばれる1種又は2種以上の成分を更に含んでなる請求項1記載のコラーゲン産生増強剤。
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Also Published As
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JPWO2005034938A1 (ja) | 2006-12-21 |
EP1679071A4 (en) | 2009-04-15 |
CN1863526B (zh) | 2010-04-28 |
KR20060123727A (ko) | 2006-12-04 |
TWI340651B (ja) | 2011-04-21 |
US20070129430A1 (en) | 2007-06-07 |
EP1679071A1 (en) | 2006-07-12 |
WO2005034938A1 (ja) | 2005-04-21 |
TW200513267A (en) | 2005-04-16 |
CN1863526A (zh) | 2006-11-15 |
KR101277180B1 (ko) | 2013-06-20 |
KR20120091398A (ko) | 2012-08-17 |
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