Amine containing cationic methacrylate copolymers as efficient gene delivery vehicles to retinal epithelial cells |
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| Authors: | Jon Zarate Gustavo Puras David Mecerreyes Haritz Sardon J L Pedraz |
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| Affiliation: | 1. NanoBioCel Group, University of the Basque Country UPV/EHU, Vitoria‐Gasteiz, Spain;2. Biomedical Research Networking Centre in Bioengineering, Biomaterials and Nanomedicine (CIBER‐BBN), Vitoria‐Gasteiz, Spain;3. POLYMAT University of the Basque Country UPV/EHU, Joxe Mari Korta Center, Donostia‐San Sebastian, Spain;4. Basque Foundation for Science, Ikerbasque, Bilbao, Spain |
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| Abstract: | Non‐viral gene delivery vectors have emerged as potential alternatives in the field of gene therapy by replacing the biological viral vectors. DNA–cationic polymer complexes are one of the most promising systems to target many inborn or acquired diseases without the utilization of conventional drugs. Despite the excellent binding efficiency of cationic polymers, the gene transfection seems limited to date. In this work, a series of ammonium‐based block‐copolymers with different alkyl side chains (ethyl, butyl, and hexyl) and functionality (alcohol, amine, and alkyl) have been prepared to evaluate their capacity to deliver genetic material. First, different ionic liquid monomers with different pendent functional groups were prepared and characterized. Then, polyplexes elaborated with different polymers at several polymer DNA ratios (w/w) were characterized in terms of size, zeta potential, and DNA binding, release, and protection capacity. Finally, the transfection efficiency and cell viability was evaluated in ARPE19 cells. We found that only the systems containing the amine pendent group were able to transfect ARPE19 cell and, that this amine containing polymer was less cytotoxic even at high polymer/DNA ratios (30:1). In conclusion, our studies suggested that the proper selection of the pendent group substantially impacts overall transfection efficiency of cationic polymers. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 280–287 |
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| Keywords: | block copolymers copolymers drug delivery systems gene therapy epithelial cells polyelectrolytes |
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