| Literature DB >> 32250633 |
Qingfei Zhang1,2, Gaizhen Kuang3, Shasha He1, Hongtong Lu1,2, Yilong Cheng4, Dongfang Zhou1, Yubin Huang1,2.
Abstract
Combination of chemotherapy and gene therapy provides an effective strategy for cancer treatment. However, the lack of suitable codelivery systems with efficient endo/lysosomal escape and controllable drug release/gene unpacking is the major bottleneck for maximizing the combinational therapeutic efficacy. In this work, we developed a photoactivatable Pt(IV) prodrug-backboned polymeric nanoparticle system (CNPPtCP/si(c-fos)) for light-controlled si(c-fos) delivery and synergistic photoactivated chemotherapy (PACT) and RNA interference (RNAi) on platinum-resistant ovarian cancer (PROC). Upon blue-light irradiation (430 nm), CNPPtCP/si(c-fos) generates oxygen-independent N3• with mild oxidation energy for efficient endo/lysosomal escape through N3•-assisted photochemical internalization with less gene deactivation. Thereafter, along with Pt(IV) prodrug activation, CNPPtCP/si(c-fos) dissociates to release active Pt(II) and unpack si(c-fos) simultaneously. Both in vitro and in vivo results demonstrated that CNPPtCP/si(c-fos) displayed excellent synergistic therapeutic efficacy on PROC with low toxicity. This PACT prodrug-backboned polymeric nanoplatform may provide a promising gene/drug codelivery tactic for treatment of various hard-to-tackle cancers.Entities:
Keywords: N3•-assisted photochemical internalization; gene delivery; photoactivatable polymeric nanoparticles; photoactivated chemotherapy; platinum-resistant ovarian cancer
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Year: 2020 PMID: 32250633 DOI: 10.1021/acs.nanolett.9b04981
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189