Characterization of physical entrapment and chemical conjugation of adriamycin in polymeric micelles and their design for in vivo delivery to a solid tumor
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Yokoyama, M
Fukushima, S
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机构:Tokyo Womens Med Coll, Inst Biomed Engn, Shinjuku Ku, Tokyo 162, Japan
Fukushima, S
Uehara, R
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机构:Tokyo Womens Med Coll, Inst Biomed Engn, Shinjuku Ku, Tokyo 162, Japan
Uehara, R
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Okamoto, K
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Kataoka, K
Sakurai, Y
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机构:Tokyo Womens Med Coll, Inst Biomed Engn, Shinjuku Ku, Tokyo 162, Japan
Sakurai, Y
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Okano, T
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[1] Tokyo Womens Med Coll, Inst Biomed Engn, Shinjuku Ku, Tokyo 162, Japan
[2] Nippon Kayaku Co Ltd, Gunma 37012, Japan
[3] Sci Univ Tokyo, Fac Ind Sci & Technol, Dept Mat Sci & Technol, Chiba 278, Japan
[4] Sci Univ Tokyo, ICBS, Biosci Res Inst, Chiba 278, Japan
An anticancer drug adriamycin (ADR) was incorporated into polymeric micelles forming from poly(ethylene glycol)poly(aspartic acid) block copolymer by chemical conjugation and physical entrapment. Structural stability of the polymeric micelles was found to be dependent on both the contents of chemically conjugated and physically entrapped ADR. The polymeric micelle with high contents of the chemically conjugated ADR and the physically entrapped ADR expressed very high in vivo antitumor activity against murine C 26 tumor, while the polymeric micelle with only the chemically conjugated ADR showed negligible in vivo activity. This indicates that the physically entrapped ADR played a major role in antitumor activity in vivo. For the polymeric micelle with the high ADR contents, it was found that a dimer of adriamycin molecules formed and that this dimer was physically entrapped in the inner core of the micelle as well as intact ADR. (C) 1998 Elsevier Science B.V.