Issue 1, 2023

A new microfluidic platform for the highly reproducible preparation of non-viral gene delivery complexes

Abstract

Transfection describes the delivery of exogenous nucleic acids (NAs) to cells utilizing non-viral means. In the last few decades, scientists have been doing their utmost to design ever more effective transfection reagents. These are eventually mixed with NAs to give rise to gene delivery complexes, which must undergo characterization, testing, and further refinement through the sequential reiteration of these steps. Unfortunately, although microfluidics offers distinct advantages over the canonical approaches to preparing particles, the systems available do not address the most frequent and practical quest for the simultaneous generation of multiple polymer-to-NA ratios (N/Ps). Herein, we developed a user-friendly microfluidic cartridge to repeatably prepare non-viral gene delivery particles and screen across a range of seven N/Ps at once or significant volumes of polyplexes at a given N/P. The microchip is equipped with a chaotic serial dilution generator for the automatic linear dilution of the polymer to the downstream area, which encompasses the NA divider to dispense equal amounts of DNA to the mixing area, enabling the formation of particles at seven N/Ps eventually collected in individual built-in tanks. This is the first example of a stand-alone microfluidic cartridge for the fast and repeatable preparation of non-viral gene delivery complexes at different N/Ps and their storage.

Graphical abstract: A new microfluidic platform for the highly reproducible preparation of non-viral gene delivery complexes

Supplementary files

Article information

Article type
Paper
Submitted
10 Aug 2022
Accepted
28 Nov 2022
First published
30 Nov 2022
This article is Open Access
Creative Commons BY-NC license

Lab Chip, 2023,23, 136-145

A new microfluidic platform for the highly reproducible preparation of non-viral gene delivery complexes

G. Protopapa, N. Bono, R. Visone, F. D'Alessandro, M. Rasponi and G. Candiani, Lab Chip, 2023, 23, 136 DOI: 10.1039/D2LC00744D

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