Amphiphilic block copolymer of SN38 prodrugs by atom transfer radical polymerization: synthesis, kin

来源 :The Third Symposium on Innovative Polymers for Controlled De | 被引量 : 0次 | 上传用户:lvguanghuang
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  Modification of anti-cancer drugs with poly(ethylene glycol)(PEG),e.g.directly linking PEG to hydrophobic drugs and conjugating drugs to PEG-block copolymers (PEG-polyDeug),has been shown to significantly improve the physicochemical and biological properties of various drug delivery systems [1].PEG-polyDrugs are generally synthesized by conjugating anticancer drugs via cleavable bonds onto the polymer backbones.However,this method has several disadvantages including incomplete conjugation,side reactions and broad polydispersity.
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