TY - JOUR
T1 - On the hydrodynamic mutual interactions among cells for high-throughput microfluidic holographic cyto-tomography
AU - Pirone, Daniele
AU - Villone, Massimiliano Maria
AU - Memmolo, Pasquale
AU - Wang, Zhe
AU - Tkachenko, Volodymyr
AU - Xiao, Wen
AU - Che, Leiping
AU - Xin, Lu
AU - Li, Xiaoping
AU - Pan, Feng
AU - Ferraro, Pietro
AU - Maffettone, Pier Luca
N1 - Publisher Copyright:
© 2022
PY - 2022/11
Y1 - 2022/11
N2 - In digital holography (DH) modality for lab on chip application the cells passing through the field of view (FOV) of the microscope can be detected and analyzed even if they are flowing at different depths. In fact, in-focus imaging of each cell can be easily retrieved thanks to the ability of DH to obtain numerical focus ex-post the recording process. An advantageous and preferred configuration for DH in flow-cytometry modality provides that the cells rotate along the microfluidic channel. This gives the unique chance to probing cells by light beams alongside many different directions while they cross the holographic FOV. Thus, it is possible to retrieve the 3D refractive index map of each flowing cell, i.e. a 3D phase-contrast tomogram. Although many cells can be analyzed in the same FOV, thus giving the possibility to increase the throughput of the system, until now no investigations have been made to establish how close the cells can be to avoid mutual disturbing effects on their rotation. Nevertheless, to estimate the maximum achievable throughput, it is indispensable to comprehend the effects of hydrodynamic interactions on adjacent cells in a tomographic flow cytometer. Here we show by means of an experimental and a numerical simulation of the fluid dynamics that hydrodynamic interactions have a quantitative effect on cells rotational behavior and neither on their mechanical deformation. However, in the considered scenario we demonstrate that the effect is negligible as it does not affect the possibility of recovering the tomograms. The reported results will allow to estimate which is the optimum density of cells to analyze by the holographic flow-cyto-tomograph thus opening the route for biomedical applications.
AB - In digital holography (DH) modality for lab on chip application the cells passing through the field of view (FOV) of the microscope can be detected and analyzed even if they are flowing at different depths. In fact, in-focus imaging of each cell can be easily retrieved thanks to the ability of DH to obtain numerical focus ex-post the recording process. An advantageous and preferred configuration for DH in flow-cytometry modality provides that the cells rotate along the microfluidic channel. This gives the unique chance to probing cells by light beams alongside many different directions while they cross the holographic FOV. Thus, it is possible to retrieve the 3D refractive index map of each flowing cell, i.e. a 3D phase-contrast tomogram. Although many cells can be analyzed in the same FOV, thus giving the possibility to increase the throughput of the system, until now no investigations have been made to establish how close the cells can be to avoid mutual disturbing effects on their rotation. Nevertheless, to estimate the maximum achievable throughput, it is indispensable to comprehend the effects of hydrodynamic interactions on adjacent cells in a tomographic flow cytometer. Here we show by means of an experimental and a numerical simulation of the fluid dynamics that hydrodynamic interactions have a quantitative effect on cells rotational behavior and neither on their mechanical deformation. However, in the considered scenario we demonstrate that the effect is negligible as it does not affect the possibility of recovering the tomograms. The reported results will allow to estimate which is the optimum density of cells to analyze by the holographic flow-cyto-tomograph thus opening the route for biomedical applications.
KW - 3D phase contrast tomography
KW - 3D tracking
KW - Digital holography
KW - Flow cytometry
KW - Hydrodynamic interactions
KW - Microfluidics
UR - https://www.scopus.com/pages/publications/85134694304
U2 - 10.1016/j.optlaseng.2022.107190
DO - 10.1016/j.optlaseng.2022.107190
M3 - 文章
AN - SCOPUS:85134694304
SN - 0143-8166
VL - 158
JO - Optics and Lasers in Engineering
JF - Optics and Lasers in Engineering
M1 - 107190
ER -