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Intracellular redox-responsive nanocarrier for plasmid delivery: in vitro characterization and in vivo studies in mice
Although some modifications of polyethyleneimine (PEI) properties have been explored to balance the transfection efficiency and cytotoxicity, its successful plasmid delivery in vitro and in vivo to realize its true therapeutic potentials remains a major challenge, mainly due to intracellular traffic...
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/PMC5066853/ https://www.ncbi.nlm.nih.gov/pubmed/27785025 http://dx.doi.org/10.2147/IJN.S94995 |
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author | Zhang, Lifen Zhang, Yushun Chen, Zhenzhen He, Yuling |
author_facet | Zhang, Lifen Zhang, Yushun Chen, Zhenzhen He, Yuling |
author_sort | Zhang, Lifen |
collection | PubMed |
description | Although some modifications of polyethyleneimine (PEI) properties have been explored to balance the transfection efficiency and cytotoxicity, its successful plasmid delivery in vitro and in vivo to realize its true therapeutic potentials remains a major challenge, mainly due to intracellular trafficking barriers. Herein, we present a delivery nanocarrier Pluronic-PEI-SS by conjugating reducible disulfide-linked PEI (PEI-SS) to biocompatible Pluronic for enhanced DNA delivery and transfection efficiency in vitro and in vivo. Pluronic-PEI-SS strongly condensed plasmid DNA to low positively charged nanocomplexes, exhibited good stability against deoxyribonuclease I digestion, and tended to be easily degraded in the presence of reducing agent 1,4-dithiothreitol. The in vitro transfection of the complex Pluronic-PEI-SS/DNA into HeLa and 293T cells resulted in lower cytotoxicity as well as significantly higher cellular uptake, nucleus transfection, and gene expression than Pluronic-PEI (25 kDa), PEI-SS, and PEI 25 kDa given alone. Furthermore, the in vivo transfection study demonstrated that Pluronic-PEI-SS/DNA complexes induced a higher enrichment than the commercial PEI/DNA complex in the tumor, indicating their potential application as biocompatible vector in gene delivery. |
format | Online Article Text |
id | pubmed-5066853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50668532016-10-26 Intracellular redox-responsive nanocarrier for plasmid delivery: in vitro characterization and in vivo studies in mice Zhang, Lifen Zhang, Yushun Chen, Zhenzhen He, Yuling Int J Nanomedicine Original Research Although some modifications of polyethyleneimine (PEI) properties have been explored to balance the transfection efficiency and cytotoxicity, its successful plasmid delivery in vitro and in vivo to realize its true therapeutic potentials remains a major challenge, mainly due to intracellular trafficking barriers. Herein, we present a delivery nanocarrier Pluronic-PEI-SS by conjugating reducible disulfide-linked PEI (PEI-SS) to biocompatible Pluronic for enhanced DNA delivery and transfection efficiency in vitro and in vivo. Pluronic-PEI-SS strongly condensed plasmid DNA to low positively charged nanocomplexes, exhibited good stability against deoxyribonuclease I digestion, and tended to be easily degraded in the presence of reducing agent 1,4-dithiothreitol. The in vitro transfection of the complex Pluronic-PEI-SS/DNA into HeLa and 293T cells resulted in lower cytotoxicity as well as significantly higher cellular uptake, nucleus transfection, and gene expression than Pluronic-PEI (25 kDa), PEI-SS, and PEI 25 kDa given alone. Furthermore, the in vivo transfection study demonstrated that Pluronic-PEI-SS/DNA complexes induced a higher enrichment than the commercial PEI/DNA complex in the tumor, indicating their potential application as biocompatible vector in gene delivery. Dove Medical Press 2016-10-11 /pmc/articles/PMC5066853/ /pubmed/27785025 http://dx.doi.org/10.2147/IJN.S94995 Text en © 2016 Zhang et al. This work is published and licensed by Dove Medical Press Limited The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. 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 Zhang, Lifen Zhang, Yushun Chen, Zhenzhen He, Yuling Intracellular redox-responsive nanocarrier for plasmid delivery: in vitro characterization and in vivo studies in mice |
title | Intracellular redox-responsive nanocarrier for plasmid delivery: in vitro characterization and in vivo studies in mice |
title_full | Intracellular redox-responsive nanocarrier for plasmid delivery: in vitro characterization and in vivo studies in mice |
title_fullStr | Intracellular redox-responsive nanocarrier for plasmid delivery: in vitro characterization and in vivo studies in mice |
title_full_unstemmed | Intracellular redox-responsive nanocarrier for plasmid delivery: in vitro characterization and in vivo studies in mice |
title_short | Intracellular redox-responsive nanocarrier for plasmid delivery: in vitro characterization and in vivo studies in mice |
title_sort | intracellular redox-responsive nanocarrier for plasmid delivery: in vitro characterization and in vivo studies in mice |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066853/ https://www.ncbi.nlm.nih.gov/pubmed/27785025 http://dx.doi.org/10.2147/IJN.S94995 |
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