| Literature DB >> 30829039 |
Xuewen He1,2, Feng Yin1,3, Dongyuan Wang3, Ling-Hong Xiong1,2,4, Ryan T K Kwok1,2, Peng Fei Gao1,2, Zheng Zhao1,2, Jacky W Y Lam1,2, Ken-Tye Yong5, Zigang Li3, Ben Zhong Tang1,2,6.
Abstract
RNA interference (RNAi) is demonstrated as one of the most powerful technologies for sequence-specific suppression of genes in disease therapeutics. Exploration of novel vehicles for small interfering RNA (siRNA) delivery with high efficiency, low cytotoxicity, and self-monitoring functionality is persistently pursued. Herein, by taking advantage of aggregation-induced emission luminogen (AIEgen), we developed a novel class of Ag@AIE core@shell nanocarriers with regulable and uniform morphology. It presented excellent efficiencies in siRNA delivery, target gene knockdown, and cancer cell inhibition in vitro. What's more, an anticancer efficacy up to 75% was achieved in small animal experiments without obvious toxicity. Attributing to the unique AIE properties, real-time intracellular tracking of siRNA delivery and long-term tumor tissue imaging were successfully realized. Compared to the commercial transfection reagents, significant improvements were obtained in biocompatibility, delivery efficiency, and reproducibility, representing a promising future of this nanocarrier in RNAi-related cancer therapeutics.Entities:
Keywords: Aggregation-induced emission (AIE); apoptosis; nanocarrier; real-time; siRNA
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Year: 2019 PMID: 30829039 DOI: 10.1021/acs.nanolett.8b04677
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189