Low-cost microfluidic mixers: are they up to the task?

Jade Forrester, Callum G. Davidson, May Blair, Lynn Donlon, Daragh M. McLoughlin, Chukwuebuka R. Obiora, Heather Stockdale, Ben Thomas, Martina Nutman, Sarah Brockbank, Zahra Rattray, Yvonne Perrie

Research output: Contribution to journalArticlepeer-review

Abstract

Background/Objectives: Microfluidic mixing has become the gold standard procedure for manufacturing nucleic acid lipid-based delivery systems, offering precise control over critical process parameters. The choice and design of microfluidic mixers are often seen as a key driving force affecting the critical quality attributes of the resulting lipid nanoparticles (LNPs). Methods: This study aimed to evaluate LNPs manufactured using two low-cost microfluidic mixers alongside manual mixing (pipette mixing (PM)), followed by characterization studies using orthogonal analytics as well as expression studies to establish whether low-cost microfluidic manufacturing methods are suitable for bench-scale and high-throughput research. Results: The results show that all manufacturing methods can produce LNPs with sizes ranging between 95 and 215 nm with high encapsulation (70–100%), and enhanced analytics showed variations between the LNPs produced using the different mixers. Despite these differences, pipette mixing production of LNPs demonstrated its application as a high-throughput screening tool for LNPs, effectively distinguishing between different formulations and predicting consistent expression patterns both in vitro and in vivo. Conclusions: Overall, these results validate the use of low-cost microfluidic mixers without compromising the efficiency and integrity of the resulting LNPs. This study supports the increased accessibility of small-scale LNP manufacturing and high-throughput screening.
Original languageEnglish
Article number566
Number of pages21
JournalPharmaceutics
Volume17
Issue number5
DOIs
Publication statusPublished - 25 Apr 2025

Funding

The work was carried out as part of the Intracellular Drug Delivery Centre, using funding from Innovate UK (Project Number: 10058505) (S.B., M.N., and Y.P.), the James Weir Foundation, the University of Strathclyde Nanomedicines Centre for Doctoral Training (J.F.), and the UK Engineering and Physical Sciences Research Council (C.G.D.). The authors acknowledge funding from the Engineering and Physical Sciences Research Council (EP/V028960/1), for Z.R. and Y.P. This project was also conducted in collaboration with CPI, funded by the Engineering and Physical Sciences Research Council’s Innovation Launchpad Network+ Researcher in Residence scheme (Y.P.) [grant numbers EP/W037009/1, EP/X528493/1]. Access to instrumentation at the Scottish Centre for Macromolecular Imaging (SCMI) for cryo-EM experiments was funded by the MRC (MC_PC_17135, MC_UU_00034/7) and SFC (H17007).

Keywords

  • lipid nanoparticle
  • mRNA
  • microfluidic mixing
  • manufacture
  • characterization

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