The potential of toxin-based drug delivery systems for enhanced nucleic acid therapeutic delivery

Shorter, Susan A. and Gollings, Alexander S. and Gorringe-Pattrick, Monique A. M. and Coakley, J. Emma and Dyer, Paul D. R. and Richardson, Simon C. W. (2017) The potential of toxin-based drug delivery systems for enhanced nucleic acid therapeutic delivery. Expert Opinion on Drug Delivery, 14 (5). pp. 685-696. ISSN 1744-7593

Full text not available from this repository.
Official URL: https://doi.org/10.1080/17425247.2016.1227781

Abstract

Introduction: The potential of gene replacement therapy has been underscored by the market authorization of alipogene tiparvovec (Glybera) and GSK2696273 (Strimvelis) in the EU and recombinant adenovirus-p53 (Gendicine) in China. Common to these systems is the use of attenuated viruses for ‘drug’ delivery. Whilst viral delivery systems are being developed for siRNA, their application to antisense delivery remains problematic. Non-viral delivery remains experimental, with some notable successes. However, stability and the ‘PEG dilemma’, balancing toxicity and limited (often liver-tropic) pharmacokinetics/oharmacodynamics, with the membrane destabilizing activity, necessary for nucleocytosolic access and transfection remain a problem. Areas covered: Here we review the use of attenuated protein toxins as a delivery vehicle for nucleic acids, their relationship to the PEG dilemma, and their biological properties with specific reference to their intracellular trafficking. Expert opinion: The possibility of using attenuated toxins as antisense and siRNA delivery systems has been demonstrated in vitro. Systems based upon attenuated anthrax toxin have been shown to have high activity (equivalent to nucleofection) and low toxicity whilst not requiring cationic ‘helpers’ or condensing agents, divorcing these systems from the problems associated with the PEG dilemma. It remains to be seen whether these systems can operate safely, efficiently and reproducibly, in vivo or in the clinic.

Item Type: Journal Article
Additional Information: An author accepted manuscript copy can be found in the University of Greenwich's repository: http://gala.gre.ac.uk/15700/
Keywords: antisense, drug delivery, endocytosis
Faculty: Faculty of Science & Technology
Depositing User: Ian Walker
Date Deposited: 19 Mar 2018 16:43
Last Modified: 24 Apr 2019 11:27
URI: http://arro.anglia.ac.uk/id/eprint/702847

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