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Microfluidic production of nanogels as alternative triple transfection reagents for the manufacture of adeno-associated virus vectors

Whiteley, Zoe; Massaro, Giulia; Gkogkos, Georgios; Gavriilidis, Asterios; Waddington, Simon N; Rahim, Ahad A; Craig, Duncan QM; (2023) Microfluidic production of nanogels as alternative triple transfection reagents for the manufacture of adeno-associated virus vectors. Nanoscale 10.1039/d2nr06401d. (In press). Green open access

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Abstract

Adeno-associated viral vectors (AAVs) have proved a mainstay in gene therapy, owing to their remarkable transduction efficiency and safety profile. Their production, however, remains challenging in terms of yield, the cost-effectiveness of manufacturing procedures and large-scale production. In this work, we present nanogels produced by microfluidics as a novel alternative to standard transfection reagents such as polyethylenimine-MAX (PEI-MAX) for the production of AAV vectors with comparable yields. Nanogels were formed at pDNA weight ratios of 1 : 1 : 2 and 1 : 1 : 3, of pAAV cis-plasmid, pDG9 capsid trans-plasmid and pHGTI helper plasmid respectively, where vector yields at a small scale showed no significant difference to those of PEI-MAX. Weight ratios of 1 : 1 : 2 showed overall higher titers than 1 : 1 : 3, where nanogels with nitrogen/phosphate ratios of 5 and 10 produced yields of ≈8.8 × 10^{8} vg mL^{-1} and ≈8.1 × 10^{8} vg mL^{-1} respectively compared to ≈1.1 × 10^{9} vg mL^{-1} for PEI-MAX. In larger scale production, optimised nanogels produced AAV at a titer of ≈7.4 × 10^{11} vg mL^{-1}, showing no statistical difference from that of PEI-MAX at ≈1.2 × 10^{12} vg mL^{-1}, indicating that equivalent titers can be achieved with easy-to-implement microfluidic technology at comparably lower costs than traditional reagents.

Type: Article
Title: Microfluidic production of nanogels as alternative triple transfection reagents for the manufacture of adeno-associated virus vectors
Location: England
Open access status: An open access version is available from UCL Discovery
DOI: 10.1039/d2nr06401d
Publisher version: https://doi.org/10.1039/D2NR06401D
Language: English
Additional information: © The Royal Society of Chemistry 2023. This article is Open Access (http://creativecommons.org/licenses/by/3.0/).
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > UCL BEAMS
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Engineering Science
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > UCL School of Pharmacy
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL EGA Institute for Womens Health
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Engineering Science > Dept of Chemical Engineering
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > UCL School of Pharmacy > Pharmaceutics
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > UCL School of Pharmacy > Pharmacology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL EGA Institute for Womens Health > Maternal and Fetal Medicine
URI: https://discovery.ucl.ac.uk/id/eprint/10166033
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