Evaluation and Validation on Sensitivity of Near-Infrared Diffuse Reflectance in Non-Invasive Human Blood Glucose Measurement

In non-invasive blood glucose measurement, the sensitivity of glucose-induced optical signals within human tissue is a crucial reference point. This study evaluates the sensitivity of glucose-induced diffuse reflectance in the 1000-1700 nm range. A key factor in understanding this sensitivity is the...

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Published inSensors (Basel, Switzerland) Vol. 24; no. 18; p. 5879
Main Authors Ge, Qing, Han, Tongshuai, Liu, Rong, Zhang, Zengfu, Sun, Di, Liu, Jin, Xu, Kexin
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 10.09.2024
MDPI
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Summary:In non-invasive blood glucose measurement, the sensitivity of glucose-induced optical signals within human tissue is a crucial reference point. This study evaluates the sensitivity of glucose-induced diffuse reflectance in the 1000-1700 nm range. A key factor in understanding this sensitivity is the rate at which the scattering coefficient changes due to glucose, as it is significantly higher than in non-living media and predominantly influences the diffuse light signal level when blood glucose levels change. The study measured and calculated the changes in the scattering coefficient at 1314 nm, a wavelength chosen for its minimal interference from glucose absorption and other bodily constituents. Based on the Mie scattering theory and the results at 1314 nm, the changes in the scattering coefficient within the 1000-1700 nm range were estimated. Subsequently, the sensitivity of the glucose signal across this range was determined through Monte Carlo (MC) simulations. The findings from 25 human trials indicate that the measured sensitivities at five other typical wavelengths within this band generally align with the sensitivities calculated using the aforementioned method. This research can guide the identification of blood glucose signals and the selection of wavelengths for non-invasive blood glucose measurements.
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These authors contributed equally to this work.
These authors also contributed equally to this work.
ISSN:1424-8220
1424-8220
DOI:10.3390/s24185879