Chitosan-DNA nanoparticles as non-viral vectors in gene therapy: strategies to improve transfection efficacy
- PMID: 14729076
- DOI: 10.1016/s0939-6411(03)00155-3
Chitosan-DNA nanoparticles as non-viral vectors in gene therapy: strategies to improve transfection efficacy
Abstract
Currently, the major drawback of gene therapy is the gene transfection rate. The two main types of vectors that are used in gene therapy are based on viral or non-viral gene delivery systems. The viral gene delivery system shows a high transfection yield but it has many disadvantages, such as oncogenic effects and immunogenicity. However, cationic polymers, like chitosan, have potential for DNA complexation and may be useful as non-viral vectors for gene therapy applications. Chitosan is a natural non-toxic polysaccharide, it is biodegradable and biocompatible, and protects DNA against DNase degradation and leads to its condensation. The objective of this paper was to summarize the state of the art in gene therapy and particularly the use of chitosan to improve the transfection efficiency in vivo and in vitro.
Similar articles
-
Polycation-based gene therapy: current knowledge and new perspectives.Curr Gene Ther. 2011 Aug;11(4):288-306. doi: 10.2174/156652311796150408. Curr Gene Ther. 2011. PMID: 21453278 Review.
-
Synthetic and natural polycations for gene therapy: state of the art and new perspectives.Curr Gene Ther. 2006 Feb;6(1):59-71. doi: 10.2174/156652306775515510. Curr Gene Ther. 2006. PMID: 16475946 Review.
-
Optimization of Chitosan-α-casein Nanoparticles for Improved Gene Delivery: Characterization, Stability, and Transfection Efficiency.AAPS PharmSciTech. 2019 Feb 28;20(3):132. doi: 10.1208/s12249-019-1342-y. AAPS PharmSciTech. 2019. PMID: 30820699
-
Enhancement of chitosan-mediated gene delivery through combination with phiC31 integrase.Acta Biomater. 2015 Apr;17:89-97. doi: 10.1016/j.actbio.2015.01.013. Epub 2015 Jan 17. Acta Biomater. 2015. PMID: 25600399
-
Chitosan and its derivatives--a promising non-viral vector for gene transfection.J Control Release. 2002 Sep 18;83(1):1-11. doi: 10.1016/s0168-3659(02)00144-x. J Control Release. 2002. PMID: 12220833 Review.
Cited by
-
DNA-based applications in nanobiotechnology.J Biomed Biotechnol. 2010;2010:715295. doi: 10.1155/2010/715295. Epub 2010 Jun 28. J Biomed Biotechnol. 2010. PMID: 20652049 Free PMC article. Review.
-
Safety and toxicology of the intravenous administration of Ang2‑siRNA plasmid chitosan magnetic nanoparticles.Mol Med Rep. 2017 Feb;15(2):736-742. doi: 10.3892/mmr.2016.6090. Epub 2016 Dec 29. Mol Med Rep. 2017. PMID: 28035391 Free PMC article.
-
Gene transfer to hemophilia A mice via oral delivery of FVIII-chitosan nanoparticles.J Control Release. 2008 Dec 18;132(3):252-9. doi: 10.1016/j.jconrel.2008.06.019. Epub 2008 Jun 27. J Control Release. 2008. PMID: 18634839 Free PMC article.
-
Generation of stable cell line by using chitosan as gene delivery system.Cytotechnology. 2016 Aug;68(4):1033-8. doi: 10.1007/s10616-015-9859-8. Epub 2015 Jul 2. Cytotechnology. 2016. PMID: 26134852 Free PMC article.
-
Self-assembled nanoparticles based on modified cationic dipeptides and DNA: novel systems for gene delivery.J Nanobiotechnology. 2013 Jun 21;11:18. doi: 10.1186/1477-3155-11-18. J Nanobiotechnology. 2013. PMID: 23800286 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical