Geometry-Dependent Efficiency of Dean-Flow Affected Lateral Particle Focusing and Separation in Periodically Inhomogeneous Microfluidic Channels

In this study, inertial focusing phenomenon was investigated, which can be used as a passive method for sample preparation and target manipulation in case of particulate suspensions. Asymmetric channel geometry was designed to apply additional inertial forces besides lift forces to promote laterally ordered particles to achieve sheathless focusing or size-dependent sorting. The evolving hydrodynamic forces were tailored with altered channel parameters (width and height), and different flow rates, to get a better understanding of smaller beads’ lateral migration. Fluorescent beads (with the diameter of 4.8 µm and 15.8 µm) were used to distinguish the focusing position in continuous flow, and experimental results were compared to in silico models for particle movement prediction, made in COMSOL Multiphysics. The focusing behaviour of the applied microfluidic system was mainly characterised for particle size in the range close to blood cells and bacteria

Dean-Flow Affected Lateral Focusing and Separation of Particles and Cells in Periodically Inhomogeneous Microfluidic Channels

The purpose of the recent work is to give a better explanation of how Dean vortices affect lateral focusing, and to understand how cell morphology can alter the focusing position compared to spherical particles. The position and extent of the focused region were investigated using polystyrene fluorescent beads with different bead diameters (Ø = 0.5, 1.1, 1.97, 2.9, 4.8, 5.4, 6.08, 10.2, 15.8, 16.5 µm) at different flow rates (0.5, 1, 2 µL/s). Size-dependent focusing generated a precise map of the equilibrium positions of the spherical beads at the end of the periodically altering channels, which gave a good benchmark for focusing multi-dimensional particles and cells. The biological samples used for experiments were rod-shaped Escherichia coli (E. coli), discoid biconcave-shaped red blood cells (RBC), round or ovoid-shaped yeast, Saccharomyces cerevisiae, and soft-irregular-shaped HeLa cancer-cell-line cells to understand how the shape of the cells affects the focusing position at the end of the channel

Design, realisation and validation of microfluidic stochastic mixers integrable in bioanalytical systems using CFD modeling

In this work we present the design aspects of special microfluidic structures applicable to dilute and transport analyte solutions (such as whole blood) to the sensing area of biosensors. Our goal is to design and realise a reliable microfluidic system which is applicable for effective sample transport and can accomplish simple sample preparation functions such as mixing to ensure homogeneous concentration distribution of the species along the fluidic channel. The behaviour of different chaotic mixers were analysed by numerical modeling and experimentally to determine their efficiency. At first we used the concentration distribution method, however because of numerical diffusion this required higher mesh resolutions. Using the particle tracing method is more efficient according to the experimental results and requires lower computational effort. The microstructures were realised by micro-fabrication in polydimethylsiloxane (PDMS) and integrated into a real microfluidic transport system. The functional performance was verified by biological analyte