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• W2743259782 abstract "Functionalized nanoparticles (NPs) are usually used to enhance cellular penetration for targeted drug delivery that can improve efficacy and reduce side effects. However, it is difficult to exploit intracellular targets for similar delivery applications. Herein we describe the targeted delivery of functionalized NPs by homing in on an intracellular target, histone deacetylases (HDACs). Specifically, a modified poly-lactide-co-glycolideacid (FPLGA) was yielded by conjugation with an HDAC inhibitor. Subsequently, FPLGA was used to prepare functionalized FPLGA NPs. Compared to unmodified NPs, FPLGA NPs were more efficiently uptaken or retained by MCF-7 cells and showed longer retention time intracellular. In vivo fluorescence imaging also revealed that they had a higher accumulation and a slower elimination than unmodified NPs. FPLGA NPs loaded with paclitaxel exhibited superior anticancer efficacy compared with unmodified NPs. These results offer a promising approach for intracellular drug delivery through elevating the concentration of NPs." @default.
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• W2743259782 date "2017-08-07" @default.
• W2743259782 modified "2023-09-27" @default.
• W2743259782 title "Homing in on an intracellular target for delivery of loaded nanoparticles functionalized with a histone deacetylase inhibitor" @default.
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• W2743259782 doi "https://doi.org/10.18632/oncotarget.20021" @default.
• W2743259782 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5620252" @default.
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