Abstract
We report a method to capture a multifocus image stack based on recording multiple reflections generated by imaging through a custom etalon. The focus stack is collected in a single camera exposure and consequently the information needed for 3D reconstruction is recorded in the camera integration time, which is only 100 µs. We have used the VIDA microscope to temporally resolve the multi-lobed 3D morphology of neutrophil nuclei as they rotate and deform through a microfluidic constriction. In addition, we have constructed a 3D imaging flow cytometer and quantified the nuclear morphology of nearly a thousand white blood cells flowing at a velocity of 3 mm per second. The VIDA microscope is compact and simple to construct, intrinsically achromatic, and the field-of-view and stack number can be easily reconfigured without redesigning diffraction gratings and prisms.
Original language | English |
---|---|
Pages (from-to) | 1044-1049 |
Number of pages | 6 |
Journal | Journal of Biophotonics |
Volume | 9 |
Issue number | 10 |
Early online date | 23 Dec 2015 |
DOIs | |
Publication status | Published - 1 Oct 2016 |
Keywords
- cytometry
- microfluidics
- microscopy
- high-speed 3D microscopy
- multifocus image stack
- VIDA microscope
- 3D imaging flow cytometer