Tumor-targeting
nano-drug-delivery
systems hold great potential
to improve the therapeutic efficacy and alleviate the side effects
of cancer treatments. Herein, folic acid (FA)-decorated amphiphilic
copolymer of FA-P(MPC-co-MaPCL) (MPC: 2-methacryloxoethyl
phosphorylcholine, MaPCL: poly(ε-caprolactone) macromonomer)
is synthesized and its micelles are fabricated for doxorubicin (DOX)
delivery. And non-FA-decorated P(MPC-co-MaPCL) micelles
are used as the control. Dynamic light scattering and scanning electron
microscopy measurements reveal that FA-P(MPC-co-MaPCL)
and P(MPC-co-MaPCL) micelles are spherical with average
diameters of 140 and 90 nm, respectively. The evaluation in vitro
demonstrates that the blank micelles are nontoxic, while DOX-loaded
FA-P(MPC-co-MaPCL) micelles show significant cytotoxicity
to HeLa cells and slight cytotoxicity to L929 cells. Moreover, the
cellular uptake of DOX-loaded FA-P(MPC-co-MaPCL)
micelles in HeLa cells are 4.3-fold and 1.7-fold higher than that
of DOX-loaded P(MPC-co-MaPCL) micelles and free DOX
after 6 h of incubation, respectively. These results indicate the
great potential of this system in anticancer target drug-delivery
applications.