Issue 101, 2015

High throughput imaging cytometer with acoustic focussing

Abstract

We demonstrate an imaging flow cytometer that uses acoustic levitation to assemble cells and other particles into a sheet structure. This technique enables a high resolution, low noise CMOS camera to capture images of thousands of cells with each frame. While ultrasonic focussing has previously been demonstrated for 1D cytometry systems, extending the technology to a planar, much higher throughput format and integrating imaging is non-trivial, and represents a significant jump forward in capability, leading to diagnostic possibilities not achievable with current systems. A galvo mirror is used to track the images of the moving cells permitting exposure times of 10 ms at frame rates of 50 fps with motion blur of only a few pixels. At 80 fps, we demonstrate a throughput of 208 000 beads per second. We investigate the factors affecting motion blur and throughput, and demonstrate the system with fluorescent beads, leukaemia cells and a chondrocyte cell line. Cells require more time to reach the acoustic focus than beads, resulting in lower throughputs; however a longer device would remove this constraint.

Graphical abstract: High throughput imaging cytometer with acoustic focussing

Supplementary files

Article information

Article type
Paper
Submitted
15 Jul 2015
Accepted
23 Sep 2015
First published
24 Sep 2015
This article is Open Access
Creative Commons BY license

RSC Adv., 2015,5, 83206-83216

High throughput imaging cytometer with acoustic focussing

R. Zmijan, U. S. Jonnalagadda, D. Carugo, Y. Kochi, E. Lemm, G. Packham, M. Hill and P. Glynne-Jones, RSC Adv., 2015, 5, 83206 DOI: 10.1039/C5RA19497K

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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