Paper
19 July 2007 In vivo measurement of the carotenoid level using portable resonance Raman spectroscopy
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Abstract
Carotenoid is an important antioxidant in human body, which can eliminate the free radicals and other harmful reactive oxygen species. The standard technique for measuring carotenoid is high-pressure liquid chromatography which involves using chemicals and is invasive. In this paper, we present a portable resonance Raman spectroscopy system for measuring carotenoid in vivo, which is noninvasive, highly sensitive and compact. A small diode-pumped all solid-state 473nm laser instead of a 488nm Argon ion laser is used to excite in vivo the carotenoid in the thumb, and the resonance Raman scattering light intensity is measured to assess the carotenoid level. Basically, it is difficult to detect the very weak resonance Raman scattering light because it is overlapping with the strong fluorescence. Our investigation shows that matching glycerol can help to reduce tissue scattering and increase light collecting efficiency. We demonstrate that the employment of optical matching technology for measuring carotenoid resonance Raman spectra in tissue can improve the signal-to-noise ratio by 3.9dB.
© (2007) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Yonghong Shao, Junle Qu D.D.S., and Yonghong He "In vivo measurement of the carotenoid level using portable resonance Raman spectroscopy", Proc. SPIE 6628, Diagnostic Optical Spectroscopy in Biomedicine IV, 662817 (19 July 2007); https://doi.org/10.1117/12.726859
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Cited by 1 scholarly publication.
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KEYWORDS
Raman spectroscopy

Raman scattering

Tissue optics

Signal to noise ratio

In vivo imaging

Light scattering

Luminescence

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