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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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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. |
format | Online Article Text |
id | pubmed-5117883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
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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