Timed-release of mitomycin C from its agarose bead conjugate.

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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.

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