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SYNTHESIS AND CONTROLLED RELEASE OF MITOMYCIN C FROM A CHITOSAN-BASED POLYMERIC PRODRUG

机译:壳聚糖基高分子药物合成丝裂霉素C及其控制释放

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摘要

A chitosan-based polymeric prodrug of mitomycin C was synthesized and the release of mitomycin C from the prodrug was measured. The results showed that the higher the degree of aldehyde formation in chitosan, the more mitomycin C was trapped by imine bond formation in the polymeric prodrug. The drug release was controlled by the number of aldehyde groups in chitosan and the mass ratios of periodate-oxidized chitosan to mitomycin C.
机译:合成了基于壳聚糖的丝裂霉素C的聚合前药,并测定了丝裂霉素C从前药中的释放。结果表明,壳聚糖中醛形成的程度越高,聚合物前药中亚胺键的形成就越容易捕获丝裂霉素C。释放的药物由壳聚糖中的醛基数量和高碘酸盐氧化的壳聚糖与丝裂霉素C的质量比控制。

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