Published November 7, 2011 | Version Published
Journal Article Open

Fluorescence microscopy imaging with a Fresnel zone plate array based optofluidic microscope

  • 1. ROR icon California Institute of Technology

Abstract

We report the implementation of an on-chip microscope system, termed fluorescence optofluidic microscope (FOFM), which is capable of fluorescence microscopy imaging of samples in fluid media. The FOFM employs an array of Fresnel zone plates (FZP) to generate an array of focused light spots within a microfluidic channel. As a sample flows through the channel and across the array of focused light spots, the fluorescence emissions are collected by a filter-coated CMOS sensor, which serves as the channel's floor. The collected data can then be processed to render fluorescence microscopy images at a resolution determined by the focused light spot size (experimentally measured as 0.65 mm FWHM). In our experiments, our established resolution was 1.0 mm due to Nyquist criterion consideration. As a demonstration, we show that such a system can be used to image the cell nuclei stained by Acridine Orange and cytoplasm labeled by Qtracker.

Additional Information

© 2011 The Royal Society of Chemistry. Received 19 Jul 2011, Accepted 30 Aug 2011. First published on the web 21 Sep 2011. We would like to express our thanks to Guoan Zheng, Seung Ah Lee, Dr Jigang Wu, Dr Benjamin Judkewitz, Rick Lake, Dr Marc Sulfridge, and Dr Swarnal Borthakur for the discussions and their generous help. We acknowledge support from the Gates Foundation and a generous gift from Aptina Imaging.

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Additional details

Identifiers

PMCID
PMC3710399
Eprint ID
25507
Resolver ID
CaltechAUTHORS:20110930-090239172

Funding

Bill and Melinda Gates Foundation
Aptina Imaging

Dates

Created
2011-10-24
Created from EPrint's datestamp field
Updated
2021-11-09
Created from EPrint's last_modified field