| Literature DB >> 29364558 |
Fei Ding1, Quanbing Mou1, Yuan Ma1, Gaifang Pan1, Yuanyuan Guo1, Gangsheng Tong1, Chung Hang Jonathan Choi2, Xinyuan Zhu1, Chuan Zhang1.
Abstract
Functional siRNAs are employed as cross-linkers to direct the self-assembly of DNA-grafted polycaprolactone (DNA-g-PCL) brushes to form spherical and nanosized hydrogels via nucleic acid hybridization in which small interfering RNAs (siRNAs) are fully embedded and protected for systemic delivery. Owing to the existence of multivalent mutual crosslinking events inside, the crosslinked nanogels with tunable size exhibit not only good thermostability, but also remarkable physiological stability that can resist the enzymatic degradation. As a novel siRNA delivery system with spherical nucleic acid (SNA) architecture, the crosslinked nanogels can assist the delivery of siRNAs into different cells without any transfection agents and achieve the gene silencing effectively both in vitro and in vivo, through which a significant inhibition of tumor growth is realized in the anticancer treatment.Entities:
Keywords: RNase resistance; antitumor therapy; crosslinked nanogels; gene silencing; siRNA delivery
Mesh:
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Year: 2018 PMID: 29364558 DOI: 10.1002/anie.201711242
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336