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Peer-reviewed journal article

Large field of view fluorescence imaging of microfluidic devices with a tandem-lens macroscope

Daniel Alexander MokhtariiD, Ali LashkaripouriD, Polly Morrell FordyceiD

Abstract

Microfluidic devices enable high-throughput sample processing with remarkable parallelization and miniaturization. While fluorescence microscopy provides a convenient method for reading out signal from microfluidic assays, commercially-available microscopes impose a fundamental tradeoff between temporal resolution, spatial resolution, and numerical aperture (NA). Spatially tiled imaging enables high-resolution and high-NA imaging over a large area but reduces temporal resolution. Conversely, low magnification, low NA imaging captures large areas in one shot, but typically sacrifices spatial resolution and fluorescence sensitivity. To address this, we introduce an automated transfluorescence tandem-macro-lens optomechanical system (macroscope) capable of sensitive, multi-channel fluorescence imaging over a very large field of view (34 mm diameter, 740 mm2), with resolution determined by the sensor pixel size. We demonstrate bright-field resolution of low-micron features and detection of low-to mid-nanomolar concentrations of common fluorophores within microfluidic device channels. To demonstrate the utility of this macroscope, we image enzyme turnover within valved microfluidic devices (the HT-MEK system, for High-Throughput Microfluidic Enzyme Kinetics) and achieve >50-fold increased temporal resolution over common commercial instruments while maintaining high sensitivity. This macroscope imaging solution costs substantially less than commercially available alternatives, providing a powerful new imaging approach for microfluidic applications requiring sensitive and rapid wide-field fluorescence imaging.

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02 /Specification & Classification

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