TY - JOUR
T1 - An experimental investigation into the focusing behaviours of flagellated and elongated cells in inertial microfluidic devices
AU - Howell, Jessie
AU - Hall, Nicole
AU - Omwenga, Sulochana
AU - Hammarton, Tansy C.
AU - Jimenez, Melanie
PY - 2025/8/4
Y1 - 2025/8/4
N2 - Inertial microfluidics has demonstrated tremendous potential to impact biological – and notably medical – fields, by offering a highly versatile, portable and cost-effective approach to cell focusing and sorting. While the range of applications of inertial devices spans medical diagnostics, bioprocessing or water engineering to mention a few, translation is still impeded by the lack of clear understanding of cell interactions in such devices. This often leads to bespoke designs that take years of development and characterisation for one targeted application, and limited tools for informed optimisation. A more fundamental knowledge of inertial behaviours is key to future translational works and impact, by enabling a deeper understanding of inertial forces in biological systems. Towards this goal, this paper focuses on high-throughput morphological phenotyping of the single-celled, flagellated parasite Leishmania mexicana to better understand how variations in cell body length, width and flagellated status impact the focusing patterns of highly non-spherical cells in curved inertial devices. Some of the key findings in this study include (i) flagella do not always alter focusing if body shape is conserved, (ii) the impact of cell shape is specific to a channel design and slight changes in e.g., cell confinement can drastically change focusing patterns, (iii) elongated prolate-like cells align differently depending on their lateral position within a curved channel, and (iv) despite variabilities observed in focusing patterns for elongated versus rounder cell phenotypes, large morphological variations can be completely overcome at high Reynolds numbers so that all phenotypes tightly focus at a single and stable position (here, towards the channel outer wall). This last finding, in particular, may open new avenues for highly efficient cell enrichment processes.
AB - Inertial microfluidics has demonstrated tremendous potential to impact biological – and notably medical – fields, by offering a highly versatile, portable and cost-effective approach to cell focusing and sorting. While the range of applications of inertial devices spans medical diagnostics, bioprocessing or water engineering to mention a few, translation is still impeded by the lack of clear understanding of cell interactions in such devices. This often leads to bespoke designs that take years of development and characterisation for one targeted application, and limited tools for informed optimisation. A more fundamental knowledge of inertial behaviours is key to future translational works and impact, by enabling a deeper understanding of inertial forces in biological systems. Towards this goal, this paper focuses on high-throughput morphological phenotyping of the single-celled, flagellated parasite Leishmania mexicana to better understand how variations in cell body length, width and flagellated status impact the focusing patterns of highly non-spherical cells in curved inertial devices. Some of the key findings in this study include (i) flagella do not always alter focusing if body shape is conserved, (ii) the impact of cell shape is specific to a channel design and slight changes in e.g., cell confinement can drastically change focusing patterns, (iii) elongated prolate-like cells align differently depending on their lateral position within a curved channel, and (iv) despite variabilities observed in focusing patterns for elongated versus rounder cell phenotypes, large morphological variations can be completely overcome at high Reynolds numbers so that all phenotypes tightly focus at a single and stable position (here, towards the channel outer wall). This last finding, in particular, may open new avenues for highly efficient cell enrichment processes.
UR - https://www.scopus.com/pages/publications/105010458228
U2 - 10.1039/d4an01288g
DO - 10.1039/d4an01288g
M3 - Article
C2 - 40626926
SN - 0003-2654
VL - 150
SP - 3602
EP - 3614
JO - Analyst
JF - Analyst
IS - 16
ER -