Hepatocellular carcinoma (HCC) poses a great threat to human health.
The elegant combination of gene therapy and chemotherapy by nanocarriers
has been repeatedly highlighted to realize enhanced therapeutic efficacy
relative to monotreatment. However, the leading strategy to achieve
the efficient codelivery of the gene and drug remains the electrostatic
condensation with the nucleic acid and the hydrophobic encapsulation
of drug molecules by the nanocarriers, which suffers substantially
from premature drug leakage during circulation and severe off-target-associated
side effects. To address these issues, we reported in this study the
codelivery of liver-specific miRNA-122 and anti-cancer drug 5-fluorouracil
(5-Fu) using a macromolecular prodrug approach, that is, electrostatic
condensation with miRNA-122 using galactosylated-chitosan-5-fluorouracil (GC-FU). The delivery
efficacy was evaluated comprehensively in vitro and in vivo. Specifically,
the biocompatibility of GC-FU/miR-122 nanoparticles (NPs) was assessed
by hemolysis activity analysis, BSA adsorption test, and cell viability
assay in both normal liver cells (L02 cells) and endothelial cells.
The resulting codelivery systems showed enhanced blood and salt stability,
efficient proliferation inhibition of HCC cells, and further induction
apoptosis of HCC cells, as well as downregulated expression of ADAM17
and Bcl-2. The strategy developed herein is thus a highly promising
platform for an effective codelivery of miRNA-122 and 5-Fu with facile
fabrication and great potential for the clinical translation toward
HCC synergistic therapy.