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Comparative Study of Diethylaminoethyl-Chitosan and Methylglycol-Chitosan as Potential Non-Viral Vectors for Gene Therapy
In this paper, we compared the transfection efficiency and cytotoxicity of methylglycol-chitosan (MG-CS) and diethylaminoethyl-chitosan (DEAE-CS(I) and DEAE-CS(II) with degrees of substitution of 1.2 and 0.57, respectively) to that of Lipofectamine (used as a reference transfection vector). MG-CS co...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415247/ https://www.ncbi.nlm.nih.gov/pubmed/30966477 http://dx.doi.org/10.3390/polym10040442 |
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author | Raik, Sergei V. Andranovitš, Stanislav Petrova, Valentina A. Xu, Yingying Lam, Jenny Ka-Wing Morris, Gordon A. Brodskaia, Alexandra V. Casettari, Luca Kritchenkov, Andreii S. Skorik, Yury A. |
author_facet | Raik, Sergei V. Andranovitš, Stanislav Petrova, Valentina A. Xu, Yingying Lam, Jenny Ka-Wing Morris, Gordon A. Brodskaia, Alexandra V. Casettari, Luca Kritchenkov, Andreii S. Skorik, Yury A. |
author_sort | Raik, Sergei V. |
collection | PubMed |
description | In this paper, we compared the transfection efficiency and cytotoxicity of methylglycol-chitosan (MG-CS) and diethylaminoethyl-chitosan (DEAE-CS(I) and DEAE-CS(II) with degrees of substitution of 1.2 and 0.57, respectively) to that of Lipofectamine (used as a reference transfection vector). MG-CS contains quaternary amines to improve DNA binding, whereas the DEAE-CS exhibits pH buffering capability that would ostensibly enhance transfection efficiency by promoting endosomal escape. Gel retardation assays showed that both DEAE-CS and MG-CS bound to DNA at a polysaccharide:DNA mass ratio of 2:1. In Calu-3 cells, the DNA transfection activity was significantly better with MG-CS than with DEAE-CS, and the efficiency improved with increasing polysaccharide:DNA ratios. By contrast, the efficiency of DEAE-CS(I) and DEAE-CS(II) was independent of the polysaccharide:DNA ratio. Conversely, in the transfection-recalcitrant JAWSII cells, both Lipofectamine and MG-CS showed significantly lower DNA transfection activity than in Calu-3 cells, whereas the efficiency of DEAE-CS(I) and DEAE-CS(II) was similar in both cell lines. The toxicity of DEAE-CS increased with increasing concentrations of the polymer and its degree of substitution, whereas MG-CS demonstrated negligible cytotoxicity, even at the highest concentration studied. Overall, MG-CS proved to be a more efficient and less toxic transfection agent when compared to DEAE-CS. |
format | Online Article Text |
id | pubmed-6415247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64152472019-04-02 Comparative Study of Diethylaminoethyl-Chitosan and Methylglycol-Chitosan as Potential Non-Viral Vectors for Gene Therapy Raik, Sergei V. Andranovitš, Stanislav Petrova, Valentina A. Xu, Yingying Lam, Jenny Ka-Wing Morris, Gordon A. Brodskaia, Alexandra V. Casettari, Luca Kritchenkov, Andreii S. Skorik, Yury A. Polymers (Basel) Article In this paper, we compared the transfection efficiency and cytotoxicity of methylglycol-chitosan (MG-CS) and diethylaminoethyl-chitosan (DEAE-CS(I) and DEAE-CS(II) with degrees of substitution of 1.2 and 0.57, respectively) to that of Lipofectamine (used as a reference transfection vector). MG-CS contains quaternary amines to improve DNA binding, whereas the DEAE-CS exhibits pH buffering capability that would ostensibly enhance transfection efficiency by promoting endosomal escape. Gel retardation assays showed that both DEAE-CS and MG-CS bound to DNA at a polysaccharide:DNA mass ratio of 2:1. In Calu-3 cells, the DNA transfection activity was significantly better with MG-CS than with DEAE-CS, and the efficiency improved with increasing polysaccharide:DNA ratios. By contrast, the efficiency of DEAE-CS(I) and DEAE-CS(II) was independent of the polysaccharide:DNA ratio. Conversely, in the transfection-recalcitrant JAWSII cells, both Lipofectamine and MG-CS showed significantly lower DNA transfection activity than in Calu-3 cells, whereas the efficiency of DEAE-CS(I) and DEAE-CS(II) was similar in both cell lines. The toxicity of DEAE-CS increased with increasing concentrations of the polymer and its degree of substitution, whereas MG-CS demonstrated negligible cytotoxicity, even at the highest concentration studied. Overall, MG-CS proved to be a more efficient and less toxic transfection agent when compared to DEAE-CS. MDPI 2018-04-14 /pmc/articles/PMC6415247/ /pubmed/30966477 http://dx.doi.org/10.3390/polym10040442 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Raik, Sergei V. Andranovitš, Stanislav Petrova, Valentina A. Xu, Yingying Lam, Jenny Ka-Wing Morris, Gordon A. Brodskaia, Alexandra V. Casettari, Luca Kritchenkov, Andreii S. Skorik, Yury A. Comparative Study of Diethylaminoethyl-Chitosan and Methylglycol-Chitosan as Potential Non-Viral Vectors for Gene Therapy |
title | Comparative Study of Diethylaminoethyl-Chitosan and Methylglycol-Chitosan as Potential Non-Viral Vectors for Gene Therapy |
title_full | Comparative Study of Diethylaminoethyl-Chitosan and Methylglycol-Chitosan as Potential Non-Viral Vectors for Gene Therapy |
title_fullStr | Comparative Study of Diethylaminoethyl-Chitosan and Methylglycol-Chitosan as Potential Non-Viral Vectors for Gene Therapy |
title_full_unstemmed | Comparative Study of Diethylaminoethyl-Chitosan and Methylglycol-Chitosan as Potential Non-Viral Vectors for Gene Therapy |
title_short | Comparative Study of Diethylaminoethyl-Chitosan and Methylglycol-Chitosan as Potential Non-Viral Vectors for Gene Therapy |
title_sort | comparative study of diethylaminoethyl-chitosan and methylglycol-chitosan as potential non-viral vectors for gene therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415247/ https://www.ncbi.nlm.nih.gov/pubmed/30966477 http://dx.doi.org/10.3390/polym10040442 |
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