JP4974533B2 - ジスルフィド架橋したタンパク質ナノ粒子 - Google Patents
ジスルフィド架橋したタンパク質ナノ粒子 Download PDFInfo
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- JP4974533B2 JP4974533B2 JP2006020019A JP2006020019A JP4974533B2 JP 4974533 B2 JP4974533 B2 JP 4974533B2 JP 2006020019 A JP2006020019 A JP 2006020019A JP 2006020019 A JP2006020019 A JP 2006020019A JP 4974533 B2 JP4974533 B2 JP 4974533B2
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- transferrin
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- 239000007787 solid Substances 0.000 description 1
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- 150000003431 steroids Chemical class 0.000 description 1
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- MUTNCGKQJGXKEM-UHFFFAOYSA-N tamibarotene Chemical compound C=1C=C2C(C)(C)CCC(C)(C)C2=CC=1NC(=O)C1=CC=C(C(O)=O)C=C1 MUTNCGKQJGXKEM-UHFFFAOYSA-N 0.000 description 1
- 229960003454 tamoxifen citrate Drugs 0.000 description 1
- FQZYTYWMLGAPFJ-OQKDUQJOSA-N tamoxifen citrate Chemical compound [H+].[H+].[H+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.C=1C=CC=CC=1C(/CC)=C(C=1C=CC(OCCN(C)C)=CC=1)/C1=CC=CC=C1 FQZYTYWMLGAPFJ-OQKDUQJOSA-N 0.000 description 1
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- RZWIIPASKMUIAC-VQTJNVASSA-N thromboxane Chemical compound CCCCCCCC[C@H]1OCCC[C@@H]1CCCCCCC RZWIIPASKMUIAC-VQTJNVASSA-N 0.000 description 1
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Description
好ましくは、本発明のタンパク質ナノ粒子は、タンパク質の重量に対して、0.1〜100重量%の活性成分を含有する。
好ましくは、化粧品用成分は保湿剤、美白剤、又はアンチエイジング剤であり、機能性食品用成分はビタミン又は抗酸化剤であり、医薬品成分は制癌剤、抗アレルギー剤、抗血栓剤、又は抗炎症剤である。
好ましくは、タンパク質はアルブミン、オバルブミン、トランスフェリン、又はグロブリンである。
好ましくは、タンパク質の重量に対して、0.1〜100重量%のカチオン性又はアニオン性多糖が添加されている。
好ましくは、タンパク質を酸化剤で処理する工程を、有機溶媒中に分散したタンパク質ナノ粒子を酸化剤で処理することによって行う。
本発明のさらに別の側面によれば、タンパク質を還元剤で処理してタンパク質分子内のジスルフィド結合を切断した後、該タンパク質のナノ粒子を形成し、さらに該タンパク質を酸化剤で処理することにより得られる、水不溶性タンパク質ナノ粒子の製造方法が提供される。
本発明のタンパク質ナノ粒子は、タンパク質を還元剤で処理してタンパク質分子内のジスルフィド結合を切断した後、該タンパク質のナノ粒子を形成し、さらに該タンパク質を酸化剤で処理することにより得られることを特徴とする。
以下の実施例により本発明を更に具体的に説明するが、本発明の範囲はこれらの実施例に限定されるものではない。
アルブミン20mgを5mLの7Mグアニジン塩酸塩および10mM EDTAを含む0.5Mトリス−塩酸緩衝液(pH8.5)に溶解し、ジチオトレイトール20mgを加えて混合、室温で2時間還元する。ゲルろ過精製し、得られたアルブミン溶液に、ポリリジン2mg、下記構造を有する活性物質モデルを0.4mgを混合する。前記溶液1mLを、外設40℃、800rpmの攪拌条件で、マイクロシリンジを用いて、エタノール10mL中に注入した。得られた分散液を空気中で40℃、3時間攪拌することで、架橋されたアルブミンナノ粒子が得られた。上記粒子の平均粒経は、光散乱光度計(大塚電子(株)製DLS−7000)を用い測定したところ、200nmであった。
ゲルろ過性精製後、タンパク質呈色試薬Protein Assay Dye Reagent Concentrate(Bio Rad製)を用いて、アルブミン濃度を検量し、SHの理論量を計算した。SH基呈色試薬DTNB(同仁化学研究所製)を用いて、グルタチオンを標品として検量線を引き、エタノール分散直後のアルブミンナノ粒子中のSH基を定量したところ、上記アルブミン量から算出した理論量とほぼ一致し、ジスルフィド結合が定量的に還元されたことがわかった。空気中、3時間攪拌した後、再びアルブミンナノ粒子中のSH基を定量し、攪拌前後のSH基の量を比較したところ、空気酸化によって72%のジスルフィド架橋が生成したことが確認された。
アルブミン20mgを5mLの7Mグアニジン塩酸塩および10mM EDTAを含む0.5Mトリス−塩酸緩衝液(pH8.5)に溶解し、ジチオトレイトール20mgを加えて混合、室温で2時間還元する。ゲルろ過精製し、得られたアルブミン溶液に、コンドロイチン硫酸−Cを2mg、アドリアマイシンを0.4mgを混合する。前記溶液1mLを、外設40℃、800rpmの攪拌条件で、マイクロシリンジを用いて、エタノール10mL中に注入した。得られた分散液を空気中で40℃、3時間攪拌することで、架橋されたアルブミンナノ粒子が得られた。上記粒子の平均粒経は、光散乱光度計(大塚電子(株)製DLS−7000)を用い測定したところ、200nmであった。また、実施例1と同様にして、架橋度を評価した結果、70%以上の架橋が確認された。
トランスフェリン20mgを5mLの7Mグアニジン塩酸塩および10mM EDTAを含む0.5Mトリス−塩酸緩衝液(pH8.5)に溶解し、ジチオトレイトール20mgを加えて混合、室温で2時間還元する。ゲルろ過精製し、得られたトランスフェリン溶液に、アルブチンを0.4mgを混合する。前記溶液1mLを、外設40℃、800rpmの攪拌条件で、マイクロシリンジを用いて、エタノール10mL中に注入した。得られた分散液を空気中で40℃、3時間攪拌することで、架橋されたトランスフェリンナノ粒子が得られた。上記粒子の平均粒経は、光散乱光度計(大塚電子(株)製DLS−7000)を用い測定したところ、150nmであった。また、実施例1と同様にして、架橋度を評価した結果、70%以上の架橋が確認された。
グロブリン20gmを5mLの7Mグアニジン塩酸塩および10mM EDTAを含む0.5Mトリス−塩酸緩衝液(pH8.5)に溶解し、ジチオトレイトール20mgを加えて混合、室温で2時間還元する。ゲルろ過精製し、得られたアルブミン溶液に、ダイキトサン2mg、実施例1で使用したものと同じ活性物質モデルを0.4mgを混合する。前記溶液1mLとダイキトサン1mgを、外設40℃、800rpmの攪拌条件で、マイクロシリンジを用いてエタノール10mL中に注入した。得られた分散液を空気中で40℃、3時間攪拌することで、架橋したグロブリンナノ粒子が得られた。上記粒子の平均粒経は、光散乱光度計(大塚電子(株)製DLS−7000)を用い測定したところ、200nmであった。また、実施例1と同様にして、架橋度を評価した結果、70%以上の架橋が確認された。
アルブミン20mgを5mLの7Mグアニジン塩酸塩および10mM EDTAを含む0.5Mトリス−塩酸緩衝液(pH8.5)に溶解し、ジチオトレイトール20mgを加えて混合、室温で2時間還元する。ゲルろ過精製し、得られたアルブミン溶液2.5mLに塩酸を加え、pH2.5に調整し、アドリアマイシンを0.4mg添加する。この溶液を攪拌子ながらアセトン4mLを滴下した後、空気中で40℃、3時間攪拌することで、架橋されたアルブミンナノ粒子が得られた。上記粒子の平均粒経は、光散乱光度計(大塚電子(株)製DLS−7000)を用い測定したところ、100nmであった。また、実施例1と同様にして、架橋度を評価した結果、70%以上の架橋が確認された。
Claims (12)
- トランスフェリンを還元剤で処理してトランスフェリン分子内のジスルフィド結合を切断した後、該トランスフェリンのナノ粒子を形成し、さらに該トランスフェリンを酸化剤で処理することにより得られ、トランスフェリンの重量に対して、0.1〜100重量%のリン脂質が添加されている、水不溶性トランスフェリンナノ粒子。
- トランスフェリンを還元剤で処理してトランスフェリン分子内のジスルフィド結合を切断した後、該トランスフェリンのナノ粒子を形成し、さらに該トランスフェリンを酸化剤で処理することにより得られ、トランスフェリンの重量に対して、0.1〜100重量%のカチオン性又はアニオン性多糖が添加されている、水不溶性トランスフェリンナノ粒子。
- トランスフェリンを還元剤で処理してトランスフェリン分子内のジスルフィド結合を切断した後、該トランスフェリンのナノ粒子を形成し、さらに該トランスフェリンを酸化剤で処理することにより得られ、トランスフェリンの重量に対して、0.1〜100重量%のカチオン性タンパク質又はアニオン性タンパク質が添加されている、水不溶性トランスフェリンナノ粒子。
- トランスフェリンを還元剤で処理してトランスフェリン分子内のジスルフィド結合を切断した後、該トランスフェリンのナノ粒子を形成し、さらに該トランスフェリンを酸化剤で処理することにより得られ、トランスフェリンを酸化剤で処理する工程を、有機溶媒中に分散したトランスフェリンナノ粒子を酸化剤で処理することによって行う、水不溶性トランスフェリンナノ粒子。
- 有機溶媒が、エタノール、イソプロパノール、アセトン又はTHFである、請求項4に記載の水不溶性トランスフェリンナノ粒子。
- 少なくとも1種の活性成分をさらに含む、請求項1から5の何れか1項に記載のトランスフェリンナノ粒子。
- トランスフェリンの重量に対して、0.1〜100重量%の活性成分を含有する、請求項6に記載のトランスフェリンナノ粒子。
- 活性成分が、化粧品用成分、機能性食品用成分、又は医薬品成分である、請求項6又は7に記載のトランスフェリンナノ粒子。
- 化粧品用成分が保湿剤、美白剤、又はアンチエイジング剤であり、機能性食品用成分がビタミン又は抗酸化剤であり、医薬品成分が制癌剤、抗アレルギー剤、抗血栓剤、又は抗炎症剤である、請求項8に記載のトランスフェリンナノ粒子。
- 平均粒子サイズが10〜1000nmである、請求項1から9の何れかに記載のトランスフェリンナノ粒子。
- 請求項1から10の何れかに記載のトランスフェリンナノ粒子を含む、薬物送達剤。
- トランスフェリンを還元剤で処理してトランスフェリン分子内のジスルフィド結合を切断した後、該トランスフェリンのナノ粒子を形成し、さらに有機溶媒中に分散した該トランスフェリンを酸化剤で処理することにより得られる、水不溶性トランスフェリンナノ粒子の製造方法。
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