摘要

An acid-labile and PEGylated polyphosphoester-doxorubicin prodrug (PBYP-g-PEG-g-DOX) was prepared via a combination of ring-opening polymerization (ROP) and Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) "click" chemistry. The resulting multifunctional prodrug was then used to interact with alpha-cyclodextrin (alpha-CD) to fabricate a novel supramolecular hydrogel based on inclusion complexation.