Issue 16, 2020

High-speed particle detection and tracking in microfluidic devices using event-based sensing

Abstract

Visualising fluids and particles within channels is a key element of microfluidic work. Current imaging methods for particle image velocimetry often require expensive high-speed cameras with powerful illuminating sources, thus potentially limiting accessibility. This study explores for the first time the potential of an event-based camera for particle and fluid behaviour characterisation in a microfluidic system. Event-based cameras have the unique capacity to detect light intensity changes asynchronously and to record spatial and temporal information with low latency, low power and high dynamic range. Event-based cameras could consequently be relevant for detecting light intensity changes due to moving particles, chemical reactions or intake of fluorescent dyes by cells to mention a few. As a proof-of-principle, event-based sensing was tested in this work to detect 1 μm and 10 μm diameter particles flowing in a microfluidic channel for average fluid velocities of up to 1.54 m s−1. Importantly, experiments were performed by directly connecting the camera to a standard fluorescence microscope, only relying on the microscope arc lamp for illumination. We present a data processing strategy that allows particle detection and tracking in both bright-field and fluorescence imaging. Detection was achieved up to a fluid velocity of 1.54 m s−1 and tracking up to 0.4 m s−1 suggesting that event-based cameras could be a new paradigm shift in microscopic imaging.

Graphical abstract: High-speed particle detection and tracking in microfluidic devices using event-based sensing

Supplementary files

Article information

Article type
Paper
Submitted
29 May 2020
Accepted
16 Jul 2020
First published
17 Jul 2020
This article is Open Access
Creative Commons BY license

Lab Chip, 2020,20, 3024-3035

High-speed particle detection and tracking in microfluidic devices using event-based sensing

J. Howell, T. C. Hammarton, Y. Altmann and M. Jimenez, Lab Chip, 2020, 20, 3024 DOI: 10.1039/D0LC00556H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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