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

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...

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Autores principales: Liang, Gaofeng, Li, Yang, Feng, Wenpo, Wang, Xinshuai, Jing, Aihua, Li, Jinghua, Ma, Kaiwang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117883/
https://www.ncbi.nlm.nih.gov/pubmed/27895481
http://dx.doi.org/10.2147/IJN.S120828
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author Liang, Gaofeng
Li, Yang
Feng, Wenpo
Wang, Xinshuai
Jing, Aihua
Li, Jinghua
Ma, Kaiwang
author_facet Liang, Gaofeng
Li, Yang
Feng, Wenpo
Wang, Xinshuai
Jing, Aihua
Li, Jinghua
Ma, Kaiwang
author_sort Liang, Gaofeng
collection PubMed
description 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.
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spelling pubmed-51178832016-11-28 Polyethyleneimine-coated quantum dots for miRNA delivery and its enhanced suppression in HepG2 cells Liang, Gaofeng Li, Yang Feng, Wenpo Wang, Xinshuai Jing, Aihua Li, Jinghua Ma, Kaiwang Int J Nanomedicine Original Research 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. Dove Medical Press 2016-11-15 /pmc/articles/PMC5117883/ /pubmed/27895481 http://dx.doi.org/10.2147/IJN.S120828 Text en © 2016 Liang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Liang, Gaofeng
Li, Yang
Feng, Wenpo
Wang, Xinshuai
Jing, Aihua
Li, Jinghua
Ma, Kaiwang
Polyethyleneimine-coated quantum dots for miRNA delivery and its enhanced suppression in HepG2 cells
title Polyethyleneimine-coated quantum dots for miRNA delivery and its enhanced suppression in HepG2 cells
title_full Polyethyleneimine-coated quantum dots for miRNA delivery and its enhanced suppression in HepG2 cells
title_fullStr Polyethyleneimine-coated quantum dots for miRNA delivery and its enhanced suppression in HepG2 cells
title_full_unstemmed Polyethyleneimine-coated quantum dots for miRNA delivery and its enhanced suppression in HepG2 cells
title_short Polyethyleneimine-coated quantum dots for miRNA delivery and its enhanced suppression in HepG2 cells
title_sort polyethyleneimine-coated quantum dots for mirna delivery and its enhanced suppression in hepg2 cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117883/
https://www.ncbi.nlm.nih.gov/pubmed/27895481
http://dx.doi.org/10.2147/IJN.S120828
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