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E Sevick-Muraca

Publications and source records attributed to E Sevick-Muraca.

2 recordsLinked to original sources

Fluorescence-enhanced absorption imaging using frequency-domain photon migration: tolerance to measurement error.

Enhanced contrast of frequency-domain photon migration (FDPM) measurements for successful biomedical optical imaging may be theoretically achieved with exogenous fluorescence contrast agents. However in practice, the reduced fluorescence signals detected at the air-tissue interface possess significant noise when compared to the signals collected at the incident wavelength. In this study, we experimentally assess signal to noise ratios (SNRs) for FDPM measurements in homogeneous tissue-like scattering media which absorb and fluorescence. At 100 MHz, the SNR for our single-pixel FDPM signals at the incident wavelength is approximately constant at 55 dB while the corresponding fluorescence signal SNR is variable with signal power and is approximately 35 dB. Using these SNR values to guide our studies on the tolerance of absorption and fluorescence-enhanced absorption imaging, we show that the noise tolerance of a Born iterative method for reconstruction of absorption from FDPM measurements at the incident wavelength cannot handle the reduced SNR that is tolerated by a Born iterative type approach for reconstruction of absorption from measurements at the emission wavelength.

Absorption↗

Quantitative optical spectroscopy for tissue diagnosis.

The interaction of light within tissue has been used to recognize disease since the mid-1800s. The recent developments of small light sources, detectors, and fiber optic probes provide opportunities to quantitatively measure these interactions, which yield information for diagnosis at the biochemical, structural, or (patho)physiological level within intact tissues. However, because of the strong scattering properties of tissues, the reemitted optical signal is often influenced by changes in biochemistry (as detected by these spectroscopic approaches) and by physiological and pathophysiological changes in tissue scattering. One challenge of biomedical optics is to uncouple the signals influenced by biochemistry, which themselves provide specificity for identifying diseased states, from those influenced by tissue scattering, which are typically unspecific to a pathology. In this review, we describe optical interactions pursued for biomedical applications (fluorescence, fluorescence lifetime, phosphorescence, and Raman from cells, cultures, and tissues) and then provide a descriptive framework for light interaction based upon tissue absorption and scattering properties. Finally, we review important endogenous and exogenous biological chromophores and describe current work to employ these signals for detection and diagnosis of disease.

Animals↗