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Bioreducible and acid-labile poly(amido amine)s for efficient gene delivery

Intracellular processes, including endosomal escape and intracellular release, are efficiency-determining steps in achieving successful gene delivery. It has been found that the presence of acid-labile units in polymers can facilitate endosomal escape and that the presence of reducible units in poly...

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Detalles Bibliográficos
Autores principales: Yu, Zhi-Qiang, Yan, Jun-Jie, You, Ye-Zi, Zhou, Qing-Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511192/
https://www.ncbi.nlm.nih.gov/pubmed/23209367
http://dx.doi.org/10.2147/IJN.S37334
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author Yu, Zhi-Qiang
Yan, Jun-Jie
You, Ye-Zi
Zhou, Qing-Hui
author_facet Yu, Zhi-Qiang
Yan, Jun-Jie
You, Ye-Zi
Zhou, Qing-Hui
author_sort Yu, Zhi-Qiang
collection PubMed
description Intracellular processes, including endosomal escape and intracellular release, are efficiency-determining steps in achieving successful gene delivery. It has been found that the presence of acid-labile units in polymers can facilitate endosomal escape and that the presence of reducible units in polymers can lead to intracellular release. In this study, poly(amido amine)s with both bioreducible and acid-labile properties were synthesized to improve gene delivery compared with single-responsive carriers. Transfection and cytotoxicity were evaluated in three cell lines. The complexes of DNA with dual-responsive polymers showed higher gene transfection efficiency than single-responsive polymers and polyethylenimine. At the same time, these polymers were tens of times less cytotoxic than polyethylenimine. Therefore, a polymer that is both reducible and acid-labile is a promising material for efficient and biocompatible gene delivery.
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spelling pubmed-35111922012-12-03 Bioreducible and acid-labile poly(amido amine)s for efficient gene delivery Yu, Zhi-Qiang Yan, Jun-Jie You, Ye-Zi Zhou, Qing-Hui Int J Nanomedicine Original Research Intracellular processes, including endosomal escape and intracellular release, are efficiency-determining steps in achieving successful gene delivery. It has been found that the presence of acid-labile units in polymers can facilitate endosomal escape and that the presence of reducible units in polymers can lead to intracellular release. In this study, poly(amido amine)s with both bioreducible and acid-labile properties were synthesized to improve gene delivery compared with single-responsive carriers. Transfection and cytotoxicity were evaluated in three cell lines. The complexes of DNA with dual-responsive polymers showed higher gene transfection efficiency than single-responsive polymers and polyethylenimine. At the same time, these polymers were tens of times less cytotoxic than polyethylenimine. Therefore, a polymer that is both reducible and acid-labile is a promising material for efficient and biocompatible gene delivery. Dove Medical Press 2012 2012-11-23 /pmc/articles/PMC3511192/ /pubmed/23209367 http://dx.doi.org/10.2147/IJN.S37334 Text en © 2012 Yu et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Yu, Zhi-Qiang
Yan, Jun-Jie
You, Ye-Zi
Zhou, Qing-Hui
Bioreducible and acid-labile poly(amido amine)s for efficient gene delivery
title Bioreducible and acid-labile poly(amido amine)s for efficient gene delivery
title_full Bioreducible and acid-labile poly(amido amine)s for efficient gene delivery
title_fullStr Bioreducible and acid-labile poly(amido amine)s for efficient gene delivery
title_full_unstemmed Bioreducible and acid-labile poly(amido amine)s for efficient gene delivery
title_short Bioreducible and acid-labile poly(amido amine)s for efficient gene delivery
title_sort bioreducible and acid-labile poly(amido amine)s for efficient gene delivery
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511192/
https://www.ncbi.nlm.nih.gov/pubmed/23209367
http://dx.doi.org/10.2147/IJN.S37334
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