摘要
The folic acid (FA)-conjugated pH/temperature/redox multi-stimuli responsive poly(methacrylic acid- co - N , N -bis(acryloyl)cystamine/poly( N -isopropylacrylamide- co -glycidyl methacrylate- co - N , N -bis(acryloyl)cystamine) microspheres were prepared by a two-stage distillation–precipitation polymerization with subsequent surface modification with FA . The microspheres were characterized by transmission electron microscopy, dynamical light scattering, Fourier-transform infrared spectra, UV–vis spectra and elemental analysis. The degradation of the functional microspheres could be triggered by a reductive reagent, such as glutathione, due to presence of BAC crosslinker. The drug-loaded microspheres exhibited a pH/temperature/redox multi-stimuli responsive drug release character for doxorubicin hydrochloride as a model anti-cancer drug, which was efficiently loaded into the microspheres with a high loading capacity of 208.0% and an encapsulation efficiency of 85.4%. In vitro drug delivery study indicated that the FA-conjugated microspheres could deliver Dox into MCF-7 cells more efficiently than the microspheres without functionalization of FA. Furthermore, WST-1 assay showed that the microspheres had no obvious toxicity to MCF-7 cells even at a high concentration of 2000 μg mL −1 . The resultant microsphere may be a promising vector for delivery of anti-cancer drugs as it exhibits a low cytotoxicity and degradability, precise molecular targeting property and multi-stimuli responsively controlled drug release.
危险品化学品经营许可证(带存储)