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.