| Literature DB >> 30354014 |
Xiao Xiao1, Xingxing Wang1, Haidong Gao2, Xi Chen2, Jinbo Li1,2, Yan Zhang1,2.
Abstract
Targeted delivery of microRNA (miRNA) into specific cells has been regarded as an efficient strategy to enhance miRNA-targeted therapeutics. However, concurrent delivery of therapeutic miRNAs into different target cells that is conducive to multi-target therapy is still underdeveloped. Here, we report a novel strategy for cell-selective delivery of miRNA into different target cells by using miRNA nanocomplexes (MINRCs) formed by miRNA with peptide conjugates. The peptide conjugates comprised a cationic cell-penetrating peptide nona-arginine and a targeting ligand that is cyclic RGD or folic acid. Upon mixing in buffer, the peptide conjugates and miR-34a readily formed two MINRCs, respectively. These two MINRCs facilitated the targeted delivery of miR-34a into RGD receptor-positive U87MG cells or folate receptor-positive HeLa cells via ligand-receptor interaction. We also demonstrated that co-incubation of these two MINRCs with U87MG and HeLa cells led to cell-selective delivery of miR-34a.Entities:
Keywords: cell-selective delivery; microRNA; microRNA nanocomplex; peptide conjugate; targeted delivery
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Year: 2018 PMID: 30354014 DOI: 10.1002/asia.201801396
Source DB: PubMed Journal: Chem Asian J ISSN: 1861-471X