Preparation, characterisation and cell transfection of cationic liposomes in gene therapy

Abstract

Cationic lipid-mediated gene transfer is one of the most commonly used non-viralvectors. It has been shown to be a safe and effective carrier. However, its use ingene delivery was hampered by its low transfection efficiency and stability.DOTAP, DOPE, cholesterol (CHO) and carboxymethyl-β-cyclodextrin (CD) wereused to prepare cationic liposomes. Cationic liposomes were prepared using both,thin film hydration and a microfluidic method. Formulation stability wasevaluated using liposome size, zeta potential and polydispersity index (PDI).Promega QuantiFluor® ONE dsDNA System was used to investigate theencapsulation efficiency. COS7 and SH-SY5Y cell lines were used to determinetransfection efficiency. Results show that carboxymethyl-β-cyclodextrin increasedencapsulation efficiency by 15.5% and 8% using NanoAssemblr® and rotaryevaporator, respectively compared to liposomes without CD. The addition ofcarboxymethyl-β-cyclodextrin to cationic liposomes resulted in an increase intransfection efficiency in both cell lines.B

Keywords

pDNA, Cyclodextrin, Cationic lipid

How to Cite

Elsana H. , Carr-Wilkinson J. , Elkordy A. A. & Faheem A. M. (2019) “Preparation, characterisation and cell transfection of cationic liposomes in gene therapy”, British Journal of Pharmacy. 4(1). doi: https://doi.org/10.5920/bjpharm.618

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Authors

Hassan Elsana (University of Sunderland)
Jane Carr-Wilkinson (University of Sunderland)

Amal Ali Elkordy (University of Sunderland)

Ahmed M Faheem (University of Sunderland)

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Creative Commons Attribution 4.0

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This article has been peer reviewed.

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