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Ruthenium-containing supramolecular nanoparticles based on bipyridine-modified cyclodextrin and adamantyl PEI with DNA condensation properties

ABSTRACT: Exploring safe and highly efficient gene carriers made from biocompatible constituents has great prospects for clinical gene therapy. Here, a supramolecular gene delivery system was readily constructed by assembling adamantyl-modified polyethylenimine (PEI-Ada) units with a versatile ruthe...

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Autores principales: Yan, Fang, Wu, Jian-Shuang, Liu, Zhi-Li, Yu, Hong-Li, Wang, Yong-Hong, Zhang, Wei-Fen, Ding, De-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300456/
https://www.ncbi.nlm.nih.gov/pubmed/30569227
http://dx.doi.org/10.1186/s11671-018-2820-y
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author Yan, Fang
Wu, Jian-Shuang
Liu, Zhi-Li
Yu, Hong-Li
Wang, Yong-Hong
Zhang, Wei-Fen
Ding, De-Jun
author_facet Yan, Fang
Wu, Jian-Shuang
Liu, Zhi-Li
Yu, Hong-Li
Wang, Yong-Hong
Zhang, Wei-Fen
Ding, De-Jun
author_sort Yan, Fang
collection PubMed
description ABSTRACT: Exploring safe and highly efficient gene carriers made from biocompatible constituents has great prospects for clinical gene therapy. Here, a supramolecular gene delivery system was readily constructed by assembling adamantyl-modified polyethylenimine (PEI-Ada) units with a versatile ruthenium bipyridine-modified cyclodextrin (Ru-CD) through host-guest interactions. The photophysical and morphological features of the PEI-Ada@Ru-CD nanoparticles were systematically characterized by techniques including UV-vis absorption spectroscopy, fluorescence spectroscopy, transmission electron microscopy, dynamic light scattering, and zeta potential experiments. The small size and suitably positive zeta potential of the nanoparticles facilitated their cellular uptake and gene transfection. As expected, DNA interaction studies, which were performed using agarose gel electrophoresis and atomic force microscopy, showed that the ability of the nanoparticles to condense DNA was higher than that of the gold standard, i.e., PEI, at low N/P ratios. The design of these ruthenium-containing supramolecular nanoparticles based on bipyridine-modified cyclodextrin and adamantyl PEI has great prospects in the development of gene delivery vehicles. GRAPHICAL ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s11671-018-2820-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-63004562019-01-04 Ruthenium-containing supramolecular nanoparticles based on bipyridine-modified cyclodextrin and adamantyl PEI with DNA condensation properties Yan, Fang Wu, Jian-Shuang Liu, Zhi-Li Yu, Hong-Li Wang, Yong-Hong Zhang, Wei-Fen Ding, De-Jun Nanoscale Res Lett Nano Express ABSTRACT: Exploring safe and highly efficient gene carriers made from biocompatible constituents has great prospects for clinical gene therapy. Here, a supramolecular gene delivery system was readily constructed by assembling adamantyl-modified polyethylenimine (PEI-Ada) units with a versatile ruthenium bipyridine-modified cyclodextrin (Ru-CD) through host-guest interactions. The photophysical and morphological features of the PEI-Ada@Ru-CD nanoparticles were systematically characterized by techniques including UV-vis absorption spectroscopy, fluorescence spectroscopy, transmission electron microscopy, dynamic light scattering, and zeta potential experiments. The small size and suitably positive zeta potential of the nanoparticles facilitated their cellular uptake and gene transfection. As expected, DNA interaction studies, which were performed using agarose gel electrophoresis and atomic force microscopy, showed that the ability of the nanoparticles to condense DNA was higher than that of the gold standard, i.e., PEI, at low N/P ratios. The design of these ruthenium-containing supramolecular nanoparticles based on bipyridine-modified cyclodextrin and adamantyl PEI has great prospects in the development of gene delivery vehicles. GRAPHICAL ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s11671-018-2820-y) contains supplementary material, which is available to authorized users. Springer US 2018-12-19 /pmc/articles/PMC6300456/ /pubmed/30569227 http://dx.doi.org/10.1186/s11671-018-2820-y Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Nano Express
Yan, Fang
Wu, Jian-Shuang
Liu, Zhi-Li
Yu, Hong-Li
Wang, Yong-Hong
Zhang, Wei-Fen
Ding, De-Jun
Ruthenium-containing supramolecular nanoparticles based on bipyridine-modified cyclodextrin and adamantyl PEI with DNA condensation properties
title Ruthenium-containing supramolecular nanoparticles based on bipyridine-modified cyclodextrin and adamantyl PEI with DNA condensation properties
title_full Ruthenium-containing supramolecular nanoparticles based on bipyridine-modified cyclodextrin and adamantyl PEI with DNA condensation properties
title_fullStr Ruthenium-containing supramolecular nanoparticles based on bipyridine-modified cyclodextrin and adamantyl PEI with DNA condensation properties
title_full_unstemmed Ruthenium-containing supramolecular nanoparticles based on bipyridine-modified cyclodextrin and adamantyl PEI with DNA condensation properties
title_short Ruthenium-containing supramolecular nanoparticles based on bipyridine-modified cyclodextrin and adamantyl PEI with DNA condensation properties
title_sort ruthenium-containing supramolecular nanoparticles based on bipyridine-modified cyclodextrin and adamantyl pei with dna condensation properties
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300456/
https://www.ncbi.nlm.nih.gov/pubmed/30569227
http://dx.doi.org/10.1186/s11671-018-2820-y
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