Publication | Closed Access
Tomographic phase microscopy with 180° rotation of live cells in suspension by holographic optical tweezers
197
Citations
21
References
2015
Year
HolographyHolographic Optical TweezersEngineeringMicroscopySingle CellsSuspended CellsBiomedical EngineeringCell MechanicsDigital HolographyLive CellsMicroscopy MethodComputational ImagingLight MicroscopyMolecular ImagingBiophysicsMedicineTomographic Phase MicroscopyLaser MicroscopyBiophotonicsComputational Optical ImagingCell BiologyMicroscope Image ProcessingBiomedical ImagingQuantitative Phase ImagingImagingCell ImagingTpm Approaches
We present a new tomographic phase microscopy (TPM) approach that allows capturing the three-dimensional refractive index structure of single cells in suspension without labeling, using 180° rotation of the cells. This is obtained by integrating an external off-axis interferometer for wide-field wave front acquisition with holographic optical tweezers (HOTs) for trapping and micro-rotation of the suspended cells. In contrast to existing TPM approaches for cell imaging, our approach does not require anchoring the sample to a rotating stage, nor is it limited in angular range as is the illumination rotation approach. Thus, it allows noninvasive TPM of suspended live cells in a wide angular range. The proposed technique is experimentally demonstrated by capturing the three-dimensional refractive index map of yeast cells, while collecting interferometric projections at an angular range of 180° with 5° steps. The interferometric projections are processed by both the filtered back-projection method and the diffraction theory method. The experimental system is integrated with a spinning disk confocal fluorescent microscope for validation of the label-free TPM results.
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