Timed-Release of Mitomycin C from Its Agarose Bead Conjugate
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概要
- 論文の詳細を見る
A new derivative of mitomycin C, mitomycin C-agarose bead conjugate, was synthesized by using cyanogen bromide method. Biologically active mitomycin C was released successively from the conjugate with a half-life of about 6 day in vitro, and also in vivo following subcutaneous injection of conjugate.
- 公益社団法人日本薬学会の論文
- 1977-09-25
著者
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村西 昌三
Faculty of Pharmaceutical Sciences, Kyoto University
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瀬崎 仁
Faculty Of Pharmaceutical Sciences Kyoto University
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瀬崎 仁
京都大学
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村西 昌三
Department of Biopharmaceutics, Kyoto Pharmaceutical University
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橋田 充
Faculty Of Pharmaceutical Sciences Kyoto University
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高橋 嘉輝
Pharmaceuticals Research Center Kanebo Ltd.
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村西 昌三
Department Of Biopharmaceutics Kyoto Pharmaceutical University
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小嶋 拓巳
Faculty Of Pharmaceutical Sciences Kyoto University
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高橋 嘉輝
Faculty of Pharmaceutical Sciences, Kyoto University
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