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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
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.
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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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