Abstract
Optical microscopy is the staple technique in the examination of microscale material structure in basic science and applied research. Of particular importance to biology and medical research is the visualization and analysis of the weakly scattering biological cells and tissues. However, the resolution of optical microscopy is limited to ≥200 nm due to the fundamental diffraction limit of light. We review one distinct form of the spectroscopic microscopy (SM) method, which is founded in the analysis of the second-order spectral statistic of a wavelength-dependent bright-field far-zone reflected-light microscope image. This technique offers clear advantages for biomedical research by alleviating two notorious challenges of the optical evaluation of biomaterials: The diffraction limit of light and the lack of sensitivity to biological, optically transparent structures. Addressing the first issue, it has been shown that the spectroscopic content of a bright-field microscope image quantifies structural composition of samples at arbitrarily small length scales, limited by the signal-to-noise ratio of the detector, without necessarily resolving them. Addressing the second issue, SM utilizes a reference arm, sample arm interference scheme, which allows us to elevate the weak scattering signal from biomaterials above the instrument noise floor.
Original language | English (US) |
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Article number | 030901 |
Journal | Journal of Biomedical Optics |
Volume | 22 |
Issue number | 3 |
DOIs | |
State | Published - Mar 1 2017 |
Funding
This study was supported by the National Institutes of Health under Grant Nos: R01CA200064, R01CA155284, R01CA165309, R01EB016983, and U54CA193419, and by the National Science Foundation under Grant No. CBET- 1240416, and by the Lungevity Foundation.
Keywords
- cell analysis
- microscopy
- scattering
- spectroscopy
ASJC Scopus subject areas
- Electronic, Optical and Magnetic Materials
- Biomaterials
- Atomic and Molecular Physics, and Optics
- Biomedical Engineering