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Biology subjects

Bethiana, T.

Publications and source records attributed to Bethiana, T..

2 recordsLinked to original sources

Identifying differential effects from eleven mixing techniques on mRNA lipid nanoparticle physicochemistry and biological performance

Lipid nanoparticle (LNP) formulation requires a mixing step. Many studies, especially from academic groups, utilize either microfluidic mixers or hand mixing to prepare LNPs, but commercial-scale processes use turbulent-flow mixers. This discrepancy in mixing techniques has been underexplored, as LNPs made by different techniques may exhibit different performance, such that bench-scale results cannot be replicated using materials manufactured at scale. We here isolate and interrogate the effect of primary mixing. Lipid nanoparticles are produced from ten mixers (one used in two ways), holding all other formulation parameters constant, to directly compare across techniques. LNPs produced from the different mixers exhibit widely different physical properties and biological performance. Notably, manual pipetting common in academic practice yields particles that do not resemble those produces by turbulent-flow mixers. Findings are connected mechanistically to physicochemical characteristics that arise from the different flow regimes. Further establishing the relationship between mixing and LNP properties is critical. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=132 SRC="FIGDIR/small/687311v1_ufig1.gif" ALT="Figure 1"> View larger version (33K): org.highwire.dtl.DTLVardef@79cac0org.highwire.dtl.DTLVardef@1ee037eorg.highwire.dtl.DTLVardef@12763eforg.highwire.dtl.DTLVardef@111e394_HPS_FORMAT_FIGEXP M_FIG C_FIG

bioengineering↗

Effects of mixing technique and ethanol removal on lipidnanoparticle physicochemical properties

Optimizing the production of lipid nanoparticle (LNP) therapeutics is necessary for drug delivery efficiency, stability, and scalability. A small but growing body of literature has begun to recognize that LNP properties (e.g., size, shape, and internal structure) depend on the flow conditions during mixing for antisolvent precipitation, in which LNPs are formulated. Here, we use different mixers, varying flow patterns (e.g., laminar or turbulent mixing) and flow rate ratios (FRR), i.e., 3:1 and 1:1, to prepare a standard LNP formulation. We then characterize the resulting formulations using small angle x-ray scattering (SAXS) to provide insights into particle shape/morphology, internal organization (L and HII phases) of yeast RNA (yRNA), and structural differences/similarities that arise from the different mixing methods. The effect of ethanol removal on the LNPs structure, formulated from each mixing technique, is also discussed. We observed the 3:1 FRR mixers outperform the 1:1 configurations in certain desired LNP physiochemical properties. The differences observed in the LNPs produced across the two configurations are discussed. Furthermore, we use computational fluid dynamics to explain the turbulent mixing schemes among the 3:1 and 1:1 mixers.

biophysics↗