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Efficient Self‐Assembled DNA Nanoparticles through Rolling Circle Amplification for siRNA Delivery in v itro
Author(s) -
Yao Qian,
Chen Yuqi,
Wu Fan,
Wu Fan,
Liu Chaoxing,
Hong Tingting,
Li Wei,
Chen Yi,
Zhou Xiang
Publication year - 2019
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.201900064
Subject(s) - rolling circle replication , lipofectamine , small interfering rna , chemistry , nuclease , hela , gene knockdown , rna interference , gene silencing , dna , nanoparticle , biophysics , rna , green fluorescent protein , microbiology and biotechnology , nanotechnology , gene , cell , biochemistry , biology , materials science , polymerase , vector (molecular biology) , recombinant dna
Summary of main observation and conclusion Effective and low toxicity delivery of siRNA is of great importance for clinical gene therapy. Herein, self‐assembled DNA nanoparticles (NPs) based on rolling circle amplification (RCA) with a small interfering RNA (siRNA) payload were successfully developed as a facile and efficient siRNA delivery strategy. This intracellular gene silencing strategy exhibits various advantages including low toxicity, high efficiency, and good stability. The synthesized DNA NPs serve as siRNA carriers, protecting the siRNA against nuclease degradation. We demonstrate that the obtained self‐assembled siRNA/NP/PEI system can successfully deliver enhanced green fluorescent protein (EGFP)‐siRNA into HeLa cells, realizing the same EGFP knockdown efficiency with less toxicity as that of commercial Lipofectamine 2000.