Oxidation-Responsive Nanoassemblies for Light-Enhanced Gene Therapy.

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State Key Laboratory of Chemical Resource Engineering and Beijing Laboratory of Biomedical Materials, Beijing University of Chemical Technology, Beijing, 100029, China.

Published: November 2019

AI Article Synopsis

  • Microenvironment-responsive supramolecular assemblies, specifically oxidation-responsive CPAs, are developed for effective nucleic acid delivery.
  • The presence of reactive oxygen species (ROS) enhances the disassembly of CPA/pDNA complexes, improving the release and transfection of pDNA in targeted cells, particularly A549.
  • Light exposure increases ROS levels, further augmenting transfection efficiency and leading to significant antitumor effects from the delivery of the p53 suppressor gene in various cell lines.

Article Abstract

Microenvironment-responsive supramolecular assemblies have attracted great interest in the biomedical field due to their potential applications in controlled drug release. In this study, oxidation-responsive supramolecular polycationic assemblies named CPAs are prepared for nucleic acid delivery via the host-guest interaction of β-cyclodextrin based polycations and a ferrocene-functionalized zinc tetraaminophthalocyanine core. The reactive oxygen species (ROS) can accelerate the disassembly of CPA/pDNA complexes, which would facilitate the release of pDNA in the complexes and further benefit the subsequent transfection. Such improvement in transfection efficiency is proved in A549 cells with high H O concentration. Interestingly, the transfection efficiencies mediated by CPAs are also different in the presence or absence of light in various cell lines such as HEK 293 and 4T1. The single oxygen ( O ), produced by photosensitizers in the core of CPAs under light, increases the ROS amount and accelerates the disassembly of CPAs/pDNA complexes. In vitro and in vivo studies further illustrate that suppressor tumor gene p53 delivered by CPAs exhibits great antitumor effects under illumination. This work provides a promising strategy for the design and fabrication of oxidation-responsive nanoassemblies with light-enhanced gene transfection performance.

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http://dx.doi.org/10.1002/smll.201904017DOI Listing

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