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用于miRNA递送的聚乙烯亚胺包覆量子点及其在HepG2细胞中的增强抑制作用。

Polyethyleneimine-coated quantum dots for miRNA delivery and its enhanced suppression in HepG2 cells.

作者信息

Liang Gaofeng, Li Yang, Feng Wenpo, Wang Xinshuai, Jing Aihua, Li Jinghua, Ma Kaiwang

机构信息

Department of Biomedical Engineering, School of Medical Technology & Engineering.

Department of Oncology, The First Affiliated Hospital, Henan University of Science & Technology, Luoyang, People's Republic of China.

出版信息

Int J Nanomedicine. 2016 Nov 15;11:6079-6088. doi: 10.2147/IJN.S120828. eCollection 2016.

DOI:10.2147/IJN.S120828
PMID:27895481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5117883/
Abstract

Quantum dots (QDs) have been intensively investigated for bioimaging, drug delivery, and labeling probes because of their unique optical properties. In this study, CdSe/ZnS QDs-based nonviral vectors with the dual functions of delivering miR-26a plasmid and bioimaging were formulated by capping the surface of CdSe/ZnS QDs with polyethyleneimine (PEI). The PEI-coated QDs were capable of condensing miR-26a expression vector into nanocomplexes that can emit strong red luminescence when loaded with CdSe/ZnS QDs. Further results showed that PEI-modified nanoparticles (NPs) could transfect miR-26a plasmid into HepG2 cells in vitro. Meanwhile, imaging of living cells could be achieved based on the CdSe/ZnS QDs. Further study suggested that miR-26a transfection up-regulated miR-26a expression, induced cycle arrest, and triggered proliferation inhibition in HepG2 cells. The results indicated that PEI-coated QD NPs possess the capability of bioimaging and gene delivery and could be a promising vehicle with the engineering of QD NPs for gene therapy in the future.

摘要

由于量子点(QDs)具有独特的光学性质,因此已被广泛研究用于生物成像、药物递送和标记探针。在本研究中,通过用聚乙烯亚胺(PEI)覆盖CdSe/ZnS量子点的表面,制备了具有递送miR-26a质粒和生物成像双重功能的基于CdSe/ZnS量子点的非病毒载体。PEI包被的量子点能够将miR-26a表达载体浓缩成纳米复合物,当装载CdSe/ZnS量子点时,该纳米复合物能发出强烈的红色荧光。进一步的结果表明,PEI修饰的纳米颗粒(NPs)能够在体外将miR-26a质粒转染到HepG2细胞中。同时,基于CdSe/ZnS量子点可以实现活细胞成像。进一步的研究表明,miR-26a转染上调了miR-26a的表达,诱导了细胞周期停滞,并触发了HepG2细胞的增殖抑制。结果表明,PEI包被的量子点纳米颗粒具有生物成像和基因递送能力,未来有望成为用于基因治疗的量子点纳米颗粒工程载体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/8382a53a1979/ijn-11-6079Fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/a08fa3aeff40/ijn-11-6079Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/46b6c5c40472/ijn-11-6079Fig2.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/dda83cb1d73f/ijn-11-6079Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/bd9bcd382d8c/ijn-11-6079Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/c5ecdb47673b/ijn-11-6079Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/8b606e578aae/ijn-11-6079Fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/8382a53a1979/ijn-11-6079Fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/a08fa3aeff40/ijn-11-6079Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/46b6c5c40472/ijn-11-6079Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/48ad052092d5/ijn-11-6079Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/dda83cb1d73f/ijn-11-6079Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/bd9bcd382d8c/ijn-11-6079Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/c5ecdb47673b/ijn-11-6079Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/8b606e578aae/ijn-11-6079Fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a5/5117883/8382a53a1979/ijn-11-6079Fig8.jpg

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