A Pt(iv)-mediated polymer architecture for facile and stimuli-responsive intracellular gene silencing with chemotherapy. (25th October 2018)

• Record Type: Journal Article
• Authors: Jung, Sungjin; Kim, Jinhwan; Pramanick, Swapan; Park, Hyeongmok; Lee, Hyori; Lee, Junseok; Kim, Won Jong
• Is Part Of: Biomaterials science. Volume 6:Number 12(2018)
• Page Start: 3345
• Page End: 3355
• Publication Date: 2018-10-25
• Subjects: Biomedical materials -- Periodicals; 610.28
• DOI: 10.1039/c8bm01019f
• Languages: English
• ISSNs: 2047-4830

Abstract

Abstract : A prodrug–polymer architecture was designed for simultaneous delivery of siRNA and a Pt(ii ) drug by exploiting the chemistry of Pt(iv ). Abstract : Conventional chemotherapy has been impeded by the inherent characteristics of cancer including fast mutagenesis and drug resistance; thus a combination therapy consisting of multiple therapeutic strategies has attracted much attention. However, the loading processes of multiple therapeutic molecules affect each other; thus the development of a nanocarrier that enables independent loading of the cargo molecules has been demanded. Herein, we report an ingeniously designed Pt(iv )-mediated polymeric architecture (Pt-PA) for combinatorial gene and chemotherapy to address the issue, prepared by crosslinking a cationic polymer (polyethylenimine, PEI) with a Pt(iv ) prodrug. Therapeutic siRNA (anti-BCL2) was simply loaded by electrostatic interaction to form a stable nanocomplex. In the cellular study, the simultaneous release of both the active Pt(ii ) drug and siRNA was monitored under the intracellular reducing environment, driven by dissociation of the polymer architecture due to an inherent characteristic of the Pt(iv ) crosslinker. Therefore, an enhanced gene silencing effect and an anticancer effect were observed. Furthermore, in the animal study, an improved therapeutic effect of the nanocomplex was observed, which can be explained by tumor targeting via the EPR effect, and enhanced drug and siRNA release at the intracellular environment simultaneously. Taken together, the overall results from in vitro and in vivo studies strongly suggest the therapeutic potential of our precisely designed Pt(iv )-mediated polymer architecture.