Noninvasive glucose sensing by transcutaneous Raman spectroscopy
Name
Shih-2015-Noninvasive Glucose.pdf
Size
1.15 MB
Format
Adobe PDF
Checksum (MD5)
16f65f625d1b210d0759894f3ee2a967
Author(s) • •
Shih, Wei-Chuan
Bechtel, Kate L.
Rebec, Mihailo V.
Date Issued
February 2015
Journal
Journal of Biomedical Optics
Publisher
Society of Photo-Optical Instrumentation Engineers (SPIE)
Citation
Shih, Wei-Chuan, Kate L. Bechtel, and Mihailo V. Rebec. “Noninvasive Glucose Sensing by Transcutaneous Raman Spectroscopy.” Journal of Biomedical Optics 20, no. 5 (February 17, 2015): 051036. © 2015 SPIE.
Version
Final published version
Abstract
We present the development of a transcutaneous Raman spectroscopy system and analysis algorithm for noninvasive glucose sensing. The instrument and algorithm were tested in a preclinical study in which a dog model was used. To achieve a robust glucose test system, the blood levels were clamped for periods of up to 45 min. Glucose clamping and rise/fall patterns have been achieved by injecting glucose and insulin into the ear veins of the dog. Venous blood samples were drawn every 5 min and a plasma glucose concentration was obtained and used to maintain the clamps, to build the calibration model, and to evaluate the performance of the system. We evaluated the utility of the simultaneously acquired Raman spectra to be used to determine the plasma glucose values during the 8-h experiment. We obtained prediction errors in the range of ∼1.5−2 mM. These were in-line with a best-case theoretical estimate considering the limitations of the signal-to-noise ratio estimates. As expected, the transition regions of the clamp study produced larger predictive errors than the stable regions. This is related to the divergence of the interstitial fluid (ISF) and plasma glucose values during those periods. Two key contributors to error beside the ISF/plasma difference were photobleaching and detector drift. The study demonstrated the potential of Raman spectroscopy in noninvasive applications and provides areas where the technology can be improved in future studies.
MIT Department
Massachusetts Institute of Technology. Spectroscopy Laboratory
Terms of Use
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
DOI of Published Version
https://doi.org/10.1117/1.jbo.20.5.051036