Investigation of the specificity of Raman spectroscopy in non-invasive blood glucose measurements

被引:81
作者
Dingari, Narahara Chari [1 ]
Barman, Ishan [1 ]
Singh, Gajendra P. [1 ]
Kang, Jeon Woong [1 ]
Dasari, Ramachandra R. [1 ]
Feld, Michael S. [1 ]
机构
[1] MIT, George R Harrison Spect Lab, Cambridge, MA 02139 USA
关键词
Raman spectroscopy; Non-invasive glucose monitoring; Chance correlations; Causation; Animal model; Human subject; NEAR-INFRARED SPECTROSCOPY; SUPPORT VECTOR MACHINES; CALIBRATION MODELS; ACCURACY; SPECTRA;
D O I
10.1007/s00216-011-5004-5
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Although several in vivo blood glucose measurement studies have been performed by different research groups using near-infrared (NIR) absorption and Raman spectroscopic techniques, prospective prediction has proven to be a challenging problem. An important issue in this case is the demonstration of causality of glucose concentration to the spectral information, especially as the intrinsic glucose signal is smaller compared with that of the other analytes in the blood-tissue matrix. Furthermore, time-dependent physiological processes make the relation between glucose concentration and spectral data more complex. In this article, chance correlations in Raman spectroscopy-based calibration model for glucose measurements are investigated for both in vitro (physical tissue models) and in vivo (animal model and human subject) cases. Different spurious glucose concentration profiles are assigned to the Raman spectra acquired from physical tissue models, where the glucose concentration is intentionally held constant. Analogous concentration profiles, in addition to the true concentration profile, are also assigned to the datasets acquired from an animal model during a glucose clamping study as well as a human subject during an oral glucose tolerance test. We demonstrate that the spurious concentration profile-based calibration models are unable to provide prospective predictions, in contrast to those based on actual concentration profiles, especially for the physical tissue models. We also show that chance correlations incorporated by the calibration models are significantly less in Raman as compared to NIR absorption spectroscopy, even for the in vivo studies. Finally, our results suggest that the incorporation of chance correlations for in vivo cases can be largely attributed to the uncontrolled physiological sources of variations. Such uncontrolled physiological variations could either be intrinsic to the subject or stem from changes in the measurement conditions.
引用
收藏
页码:2871 / 2880
页数:10
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