JP2010043032A - 高濃度アスタキサンチン抽出物 - Google Patents
高濃度アスタキサンチン抽出物 Download PDFInfo
- Publication number
- JP2010043032A JP2010043032A JP2008208786A JP2008208786A JP2010043032A JP 2010043032 A JP2010043032 A JP 2010043032A JP 2008208786 A JP2008208786 A JP 2008208786A JP 2008208786 A JP2008208786 A JP 2008208786A JP 2010043032 A JP2010043032 A JP 2010043032A
- Authority
- JP
- Japan
- Prior art keywords
- astaxanthin
- weight
- extract
- acid
- fatty acid
- 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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Abstract
10重量%以上の高含有量のアスタキサンチンを含みながら、流動性が良く、安定性が高く、臭気が少なく、取り扱いの容易な高濃度アスタキサンチン含有抽出物が求められている。高濃度アスタキサンチン含有抽出物は、粉末や乳化液など高濃度のアスタキサンチンを含む製品に用いることができる。
【解決手段】
アスタキサンチンを含有する天然物の破砕物を抽出槽内に充填し、超臨界溶媒で油脂など夾雑物を除去した後、さらに超臨界溶媒などでアスタキサンチンを抽出し、溶媒を除去してアスタキサンチン含有抽出物にMCTなどを添加することによって、高濃度ので流動性の高いアスタキサンチン抽出物を得る。
【選択図】なし
Description
(1) 全量100重量%に対してアスタキサンチン12〜40重量%、中鎖脂肪酸トリグリセリド10〜60重量%、抽出試料に由来する脂質20〜60重量%からなり、室温で流動性のある液状を呈することを特徴とする天然アスタキサンチン含有抽出物。
(2) 全量100重量%に対してアスタキサンチン20〜40重量%、中鎖脂肪酸トリグリセリド20〜40重量%、抽出試料に由来する脂質30〜60重量%からなり、25℃における粘度が2500cp以下で、流動性のある液状を呈することを特徴とする天然アスタキサンチン含有抽出物。
(3) 酸素下安定性試験で4時間後の残存率が90%以上である(1)〜(2)のいずれか1項に記載の抽出物。
(4) 製造直後及び/又は開封後の臭気がGC/MS測定試験において、臭気成分のピーク面積が10×108以下、及び/又は臭気官能試験において評価点2以下である(1)〜(3)のいずれか1項に記載の抽出物。
(5) (1)〜(4)のいずれか1項に記載の抽出物を含有する粉末状、錠剤状、乳化液状、ジェル状、オイル状の組成物。
(6) (1)〜(5)のいずれか1項に記載の抽出物又は組成物を含有する飲食物、機能性食品、医薬品、化粧品、飼料。
本発明のアスタキサンチン高含有抽出物は、全量100重量%に対してアスタキサンチン12〜40重量%、中鎖脂肪酸グリセライド10〜60重量%、抽出試料に由来する脂質20〜60重量%からなることを特徴とするアスタキサンチン高含有抽出物である。すなわち抽出原料に含まれる脂質のうち、アスタキサンチンおよびアスタキサンチンエステル以外の夾雑画分の一部あるいは全部を取り除いた後、アスタキサンチンおよびアスタキサンチンエステルを豊富に含む画分を抽出し、工程中で適宜中鎖脂肪酸グリセライドを加えることにより濃度調整を行い得られるアスタキサンチン濃縮オイルである。
脂肪酸の誘導体としては、上記脂肪酸のリン脂質型、アルコール型、エーテル型、ショ糖エステル型、ポリグリセリンエステル型があげられる。
(1)ヘマトコッカス藻を粉砕し、有機溶媒や超臨界二酸化炭素を溶媒として、アスタキサンチンを含むオイルを抽出し、抽出溶媒を除去し、粗抽出オイルを得る。
(2)次いで、この粗抽出オイルを、カラム分離、リパーゼによる脂肪酸の分離、超臨界抽出による油脂の除去や高濃度画分の分取など公知の高濃度化方法によって、油脂を除去し濃縮アスタキサンチンオイルを得る。
(3)次いで、濃縮アスタキサンチンオイルに中鎖脂肪酸トリグリセライドを添加し、公知の方法によって強く混合する。
中鎖脂肪酸トリグリセライドが分離せず、アスタキサンチンと含有して得られるので有れば、どの工程で中鎖脂肪酸トリグリセライドを加えても良い。市販のアスタキサンチン含有抽出物を用いるので有れば、(2)〜(3)の工程を行えばよい。
ヘマトコッカス藻は、ボルボックス目クラミドモナス科に属する緑藻類であり、通常は緑藻であるためクロロフィル含量が高く緑色であり、2本の鞭毛によって水中を遊泳しているが、栄養源欠乏や温度変化等の飢餓条件では休眠胞子を形成し、アスタキサンチン含量が高くなり赤い球形となる。本発明においては、いずれの状態でのヘマトコッカスを用いることができるが、アスタキサンチンを多く含有した休眠胞子となったヘマトコッカスを用いるのが好ましい。また、ヘマトコッカス属に属する緑藻類では、例えば、ヘマトコッカス・プルビアリス(Haematococcus pluviaris)が好ましい。
また抽出温度は、通常、−10〜120℃、好ましくは−10〜60℃、より好ましくは−10〜30℃の範囲である。タンク内は処理中の劣化を防ぐため窒素などの不活性ガスの雰囲気下としたほうがよい。
抽出原料となるヘマトコッカスの破砕藻体中のアスタキサンチン含量は、適量の試料からアスタキサンチンをアセトンで抽出したのち、これをアセトンで希釈して適当な濃度とし、吸光度法(波長474nm、溶媒アセトン)で測定した。また抽出物中のアスタキサンチン含量は、適量の抽出物をアセトンで希釈して適当な濃度とし、吸光度法(波長474nm、溶媒アセトン)で測定した。
ビーズミルで粉砕し噴霧乾燥したヘマトコッカス藻破砕藻の100gを超臨界抽出装置[(株)AKICO製]の抽出槽に充填し、流速3mL/分、温度40℃、圧力50MPaの条件で、S/Nで100に相当する二酸化炭素で抽出を行って抽出物を得、70%ミックストコフェロール2gを添加、均一になるように混合して、濃縮アスタキサンチン抽出物32g(収率80%、アスタキサンチン含有濃度12.5重量%、脂質87.5%)を得た。形状はやや流動性のある液状であった。
ビーズミルで粉砕し噴霧乾燥したヘマトコッカス藻破砕藻の100gを超臨界抽出装置[(株)AKICO製]の抽出槽に充填し、流速3mL/分、温度40℃、圧力30MPaの条件で、S/Nで75に相当する二酸化炭素で抽出を行いその部分を取り除いた。続いて、流速3mL/分、温度40℃、圧力50MPaで、S/Nで120に相当する二酸化炭素で抽出を行って抽出物を得た。この操作を2回繰り返して抽出物を混合し、70%ミックストコフェロール4gを添加混合して、濃縮アスタキサンチン抽出物26g(収率88%アスタキサンチン含有濃度30重量%、脂質70%)を得た。形状は固形状であった。
参考例1で得た濃縮アスタキサンチン抽出物と希釈調整用パーム油由来の中鎖脂肪酸グリセライド(MCT)を16:22の割合で混合し、12.5%(w/w)のアスタキサンチン含有の濃縮アスタキサンチン抽出物を得た。形状は通常の溶液と同様の溶液であった。
参考例1で得た濃縮アスタキサンチン抽出物と希釈調整用パーム油由来の中鎖脂肪酸グリセライドを16:5の割合で混合し、25%(w/w)のアスタキサンチン含有の濃縮アスタキサンチン抽出物を得た。形状は流動性のある液状であった。
参考例1で得た濃縮アスタキサンチン抽出物全量と希釈剤としてオリーブ油5gを16:5の割合で混合し、25%(w/w)のアスタキサンチン含有の濃縮アスタキサンチン抽出物を得た。形状は半固形状であった。
抽出物20mgをキャップ付き試験管(10ml)に入れ、酸素で置換し、封をした後、80℃で加温した状態で、4時間後のアスタキサンチン含量を含有率測定試験と同様に吸光度法で測定した。
B型粘度計を用いて、試料を25℃、40℃、50℃に保ち、操作開始から1分後の粘度を測定した。
あらかじめ室温と同じ温度にしておいた密閉容器中の抽出物を社内の試験員10名による官能試験により、5段階で臭気を評価し、その平均値をとった。
(評 価 点) (内 容)
5: きわめて不快な臭気、あるいは強い酸敗臭がある。
4: 特有の不快な臭気、あるいは酸敗臭がある。
3: あきらかに特有の臭気があるが、不快な程度ではない。
2: 僅かに特異臭を感じる。
1: ほとんどにおいを感じない。
抽出物1mLをナスフラスコに入れ、捕集カラムTenaxTA(GLサイエンス)を取り付け、抽出物を43℃に加温した。パージガスとして高純度窒素ガスを流速50mL/minで10分間流し、試料に含まれる揮発性成分を捕集カラムに吸着させた。捕集カラムをガスクロマトグラフィー質量分析装置の試料注入口にセットし、150℃にて試料からの揮発成分を気化、キャリアーガス(高純度へキサン)によりカラムDB−WAX(φ0.25mm×60m)、カラム温度40℃(10min hold)40℃→230℃ (rate 5℃/min)にて分離し検出器となる質量分析計にてピークを得た。得られたクロマトグラムから規定の成分(2-methyl-Butanal,3-methyl-Butanal,Pentanal,Hexanal, Acetic acid,Propanoic acid)のピーク面積を算出した。
また加速安定性試験では、分別抽出後MCTで希釈した実施例1の安定性は、分別抽出を行わなかった比較例1の安定性に比べて有意に高く、また分別抽出後MCTでアスタキサンチンの濃度を25%に希釈調整した実施例2の安定性は、分別抽出後オリーブ油でアスタキサンチンの濃度を25%に希釈調整した比較例2よりも有意には高かった。
グリセリン脂肪酸エステル0.8g、カルボキシメチルセルロース0.8g、ミックストコフェロール0.4g、アラビアガム28g、デキストリン30g、実施例1の高濃度アスタキサンチン抽出物40g、精製水200gからなる均一な乳化懸濁液を、入口温度200℃、出口温度100℃、ディスク回転速度24000rpm、噴霧速度1.8L/hrの条件により噴霧乾燥し、流動性粉末70gを得た。粉末中のアスタキサンチン含量は10%であった。
下記の処方からなる分散液を、高圧ホモジナイザーで処理し、乳化安定性の優れた高度乳化分散液を得た。乳化液中のアスタキサンチン含量は2.5%であり、アスタキサンチンの安定性も優れていた。
水 31.2重量部
グリセリン 50重量部
グリセリン脂肪酸エステル 3重量部
ショ糖脂肪酸エステル 5重量部
ミックストコフェロール 0.5重量部
アスコルビン酸ナトリウム 0.3重量部
アスタキサンチン(*) 10重量部
*アスタキサンチンオイルは実施例1のアスタキサンチン抽出物に中鎖脂肪酸トリグリセリドを添加して粘度を下げて取り扱い安くしたアスタキサンチン5%濃度のオイルである。
下記の処方に従って、常法により、均一に乳化、混合し、クリームを得た。水を加えて全量を100とした。
水 67.84重量部
エタノール 3.00重量部
スクワラン 0.50重量部
ポリソルベート80 0.30重量部
ポリグリセリン 3.00重量部
ブチレングリコール 25.00重量部
フェニキシエタノール 0.30重量部
アスタキサンチンオイル(*) 0.06重量部
*アスタキサンチンオイルは実施例1のアスタキサンチン抽出物に中鎖脂肪酸トリグリセリドを添加して粘度を下げて取り扱い安くしたアスタキサンチン5%濃度のオイルである。
下記成分を配合し、常法に従って、水10kgを加えてドリンク剤を調製した。
液糖 4000重量部
DL−酒石酸ナトリウム 1重量部
クエン酸 50重量部
ビタミンC 50重量部
ビタミンE 150重量部
シクロデキストリン 25重量部
塩化カリウム 5重量部
硫酸マグネシウム 2重量部
アスタキサンチンオイル(*) 0.25重量部
*アスタキサンチンオイルは実施例1のアスタキサンチン抽出物に中鎖脂肪酸トリグリセリドを添加して粘度を下げて取り扱い安くしたアスタキサンチン5%濃度のオイルである。
下記成分を配合し、常法に従って、板状のチューインガムを調製した。
ガムベース 26重量部
マルチトール 32重量部
キシリトール 28重量部
還元パラチノース 10重量部
軟化剤 1重量部
香料 2重量部
アスタキサンチンオイル(*) 1重量部
*アスタキサンチンオイルは実施例1のアスタキサンチン抽出物に中鎖脂肪酸トリグリセリドを添加して粘度を下げて取り扱い安くしたアスタキサンチン5%濃度のオイルである。
Claims (6)
- 全量100重量%に対してアスタキサンチン12〜40重量%、中鎖脂肪酸トリグリセリド10〜60重量%、抽出試料に由来する脂質20〜60重量%からなり、室温で流動性のある液状を呈することを特徴とする天然アスタキサンチン含有抽出物。
- 全量100重量%に対してアスタキサンチン20〜40重量%、中鎖脂肪酸トリグリセリド20〜40重量%、抽出試料に由来する脂質30〜60重量%からなり、25℃における粘度が2500cp以下で、流動性のある液状を呈することを特徴とする天然アスタキサンチン含有抽出物。
- 酸素下安定性試験で4時間後の残存率が90%以上である請求項1〜2のいずれか1項に記載の抽出物。
- 製造直後及び/又は開封後の臭気がGC/MS測定試験において、臭気成分のピーク面積が10×108以下、及び/又は臭気官能試験において評価点2以下である請求項1〜3のいずれか1項に記載の抽出物。
- 請求項1〜4のいずれか1項に記載の抽出物を含有する粉末状、錠剤状、乳化液状、ジェル状、オイル状の組成物。
- 請求項1〜5のいずれか1項に記載の抽出物又は組成物を含有する飲食物、機能性食品、医薬品、化粧品、飼料。
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JP2020503061A (ja) * | 2016-10-06 | 2020-01-30 | ベイジン ギンコ グループ バイオロジカル テクノロジー カンパニー リミテッドBeijing Gingko Group Biological Technology Co., Ltd. | 心血管性の効率に影響を与える栄養補助食品 |
US10827775B2 (en) * | 2016-10-06 | 2020-11-10 | Beijing Gingko Group Biological Technology Co., Ltd. | Nutritional supplements affecting cardiovascular efficiency |
WO2019117224A1 (ja) * | 2017-12-15 | 2019-06-20 | 日産化学株式会社 | 疎水性クラスター及び糖類を含む抗酸化剤 |
CN108524385A (zh) * | 2018-03-27 | 2018-09-14 | 赵金椿 | 一种虾青素多效精华液及其制备方法 |
CN113214127A (zh) * | 2021-05-18 | 2021-08-06 | 昆明白鸥微藻技术有限公司 | 一种应用超临界技术高效去除虾青素异味的方法 |
KR102598627B1 (ko) * | 2022-12-23 | 2023-11-06 | 에이앤펩주식회사 | 안정성이 향상된 아스타잔틴 용액의 제조방법과 이를 포함하는 화장료 조성물 |
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