Abstract
.Significance: We recently developed a model for the reflectance measured with (multi-diameter) single-fiber reflectance (SFR) spectroscopy as a function of the reduced scattering coefficient , the absorption coefficient , and the phase function parameter . We validated this model with simulations.Aim: We validate our model experimentally. To prevent overfitting, we investigate the wavelength-dependence of and propose a parametrization with only three parameters. We also investigate whether this parametrization enables measurements with a single fiber, as opposed to multiple fibers used in multi-diameter SFR (MDSFR).Approach: We validate our model on 16 phantoms with two concentrations of Intralipid-20% ( and at 500 nm) and eight concentrations of Evans Blue ( to at 605 nm). We parametrize as .Results: Average errors were 7% for , 11% for , and 16% with the parametrization of ; and 7%, 17%, and 16%, respectively, without. The parametrization of improved the fit speed 25 times (94 s to ). Average errors for only one fiber were 50%, 33%, and 186%, respectively.Conclusions: Our recently developed model provides accurate results for MDSFR measurements but not for a single fiber. The parametrization prevents overfitting and speeds up the fit.
Highlights
Reflectance spectroscopy techniques are used to determine optical properties of tissue and relate these to various types of disease
In single-fiber reflectance (SFR) spectroscopy light is emitted and collected through the same fiber, connected to a broadband light source and a spectrograph to detect the reflectance versus wavelength
Compared to diffuse reflectance techniques, the sampling depth of SFR spectroscopy is smaller, in the order of a few hundred micrometers.[1]. This small sampling depth makes SFR spectroscopy suitable to detect small-scale, superficial changes, such as changes related to early-stage or epithelial cancers
Summary
Reflectance spectroscopy techniques are used to determine optical properties of tissue and relate these to various types of disease. In single-fiber reflectance (SFR) spectroscopy light is emitted and collected through the same fiber, connected to a broadband light source and a spectrograph to detect the reflectance versus wavelength. Compared to diffuse reflectance techniques, the sampling depth of SFR spectroscopy is smaller, in the order of a few hundred micrometers.[1] This small sampling depth makes SFR spectroscopy suitable to detect small-scale, superficial changes, such as changes related to early-stage or epithelial cancers. We recently developed a model for the reflectance measured by SFR spectroscopy as a function of the fiber diameter d, the reduced scattering coefficient μs[0], the absorption coefficient μa, and the phase function parameter psb. Post et al.: Experimental validation of a recently developed model for single-fiber reflectance spectroscopy. RSFR;dif equals the collection efficiency of the fiber (ηc) times the fraction of photons that are diffuse and reach the fiber face (Rdif):[26]
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