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in the future, the combination of specific receptor modulators, molecular targeting, and immune regulation is expected to achieve personalized treatment and precise inflammation control

developed galactose-tailored poly (lactide-co-glycolide) (PLGA) nanoparticles loaded with AP (AP-GAL-NPs) for active liver targeting to treat HCC and found that AP-GAL-NPs exhibited a better protective effect against HCC in rats evidenced by the significant reduction of nodule formation, downregulation of MMP-2 and MMP-9, and induction of apoptosis in the liver (Ganguly et al., 2021)