Non-invasive Blood Glucose Determination using Near Infrared LED in Diffused Reflectance Method

Author(s):  
Mohammed Shahriar Arefin ◽  
Adnan Hossain Khan ◽  
Rabiul Islam
1997 ◽  
Vol 359 (1) ◽  
pp. 78-82 ◽  
Author(s):  
C. Fischbacher ◽  
K.-U. Jagemann ◽  
K. Danzer ◽  
U. A. Müller ◽  
L. Papenkordt ◽  
...  

2011 ◽  
Vol 31 (9) ◽  
pp. 0900105
Author(s):  
陈星旦 Chen Xingdan ◽  
王动民 Wang Dongmin ◽  
卢启鹏 Lu Qipeng ◽  
丁海泉 Ding Haiquan

1997 ◽  
Vol 20 (5) ◽  
pp. 285-290 ◽  
Author(s):  
U.A. Müller ◽  
B. Mertes ◽  
C. Fischbacher ◽  
K.U. Jageman ◽  
K. Danzer

The feasibility of using near infrared reflection spectroscopy for non-invasive blood glucose monitoring is discussed. Spectra were obtained using a diode-array spectrometer with a fiberoptic measuring head with a wavelength ranging from 800 nm to 1350 nm. Calibration was performed using partial least-squares regression and radial basis function networks. The results of different methods used to evaluate the quality of the recorded spectra in order to improve the reliability of the calibration models, are presented.


2012 ◽  
Vol 10 (8) ◽  
pp. 083002-83005 ◽  
Author(s):  
Wanjie Zhang Wanjie Zhang ◽  
Rong Liu Rong Liu ◽  
Wen Zhang Wen Zhang ◽  
Jiaxiang Zheng Jiaxiang Zheng ◽  
Kexin Xu Kexin Xu

2020 ◽  
Author(s):  
Lei Zhang ◽  
Yaqiong Ran ◽  
Yan Zhu ◽  
Qianna Zhen

Abstract Objective Sodium fluoride (NaF) has been applied to inhibit glycolysis in venous specimens for decades. However, it has had little effect on the rate of glycolysis in the first 1 to 2 hours, resulting in a decrease of glucose, so a more efficient method is needed. Recently, we discovered that WZB117, a specific Glut1 inhibitor, restricts glycolysis by inhibiting the passive sugar transport of human red blood cells and cancer cells. The purpose of this study was to evaluate the results of intravenous blood glucose determination after the addition of WZB117. Methods Venous specimens from 40 pairs of healthy volunteers were collected for several days and placed in tubes containing NaF plus EDTA-disodium (Na2) without WZB117 (the A group); citric acid, trisodium citrate, and EDTA-Na2 without WZB117 (B group); and NaF plus EDTA-Na2 with WZB117 (C group). The glucose concentration was measured after venipuncture and compared with test tubes treated for 1 hour, 2 hours, and 3 hours before centrifugation. Glucose level was determined by the hexokinase method. The paired t-test was used to examine differences in glucose values at baseline and at different time points. The number of misdiagnoses and the misdiagnosis rate were calculated at 2 diagnostic stages: high risk of diabetes (glucose level of 6.1 mmol/L) and diagnosis of diabetes (glucose level of 7.0 mmol/L). Results Glucose levels decreased by 1.0% at 1 hour and by 2.1% at 3 hours in the C group tubes and simultaneously decreased by 1.7% at 1 hour and by 2.5% at 3 hours in the B group tubes. In contrast, glucose levels decreased by 4.1% at 1 hour and by 6.3% at 3 hours in the A group tubes. There was a statistically significant difference in glucose levels measured in the A group tubes and B group tubes at 1 hour, 2 hours, and 3 hours. The misdiagnosis rate of clinical diagnosis in diabetes was highest in the A group tubes (7.0‰ at 1 hour, 0.1‰ at 3 hours at 7.0 mmol/L point; 14.6‰ at 1 hour, 0.4‰ at 3 hours at 6.1 mmol/L point) and lowest in the C group tubes (2.95‰ at 1 hour, 0‰ at 3 hours at 7.0 mmol/L point; 4.8‰ at 1 hour, 0.1‰ at 3 hours at 6.1 mmol/L point). Conclusion The tube addition of WZB117 is more suitable for minimizing glycolysis and has no effect on glucose levels even if specimens are left uncentrifuged for up to 3 hours.


1971 ◽  
Vol 17 (5) ◽  
pp. 440-441 ◽  
Author(s):  
Giovanni Ceriotti

Abstract A method is described for determining glucose in 25 µl of plasma. o-Toluidine is used in weak acetic acid solution. Addition of the emulsifier "Cremophor" obviates the need for deproteinization. The reaction is complete after 15 min at 100°C, and the color is stable for longer than 24 h. The blank is almost colorless. The reagent is stable, colorless, not viscous, and convenient to handle.


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