TY - JOUR
T1 - Determination of human blood glucose levels using microchip electrophoresis
AU - Maeda, Eiki
AU - Kataoka, Masatoshi
AU - Hino, Mami
AU - Kajimoto, Kazuaki
AU - Kaji, Noritada
AU - Tokeshi, Manabu
AU - Kido, Jun Ichi
AU - Shinohara, Yasuo
AU - Baba, Yoshinobu
PY - 2007/8
Y1 - 2007/8
N2 - A high-performance monitoring system for human blood glucose levels was developed using microchip electrophoresis with a plastic chip. The combination of reductive amination as glucose labeling with fluorescent 2-aminoacridone (AMAC) and glucose-borate complex formation realized the highly selective detection of glucose even in a complex matrix such as a blood sample. The migration time of a single peak, observed on an electropherogram of AMAC-labeled plasma, closely resembled that of glucose standard solution. The treatment of plasma with hexokinase or glucokinase for glucose phosphorylation resulted in a peak shift from approximately 145 to 70 s, corresponding to glucose and glucose-6-phosphate, respectively. A double-logarithm plot revealed a linear relationship between glucose concentration and fluorescence intensity in the range of 1-300 μM of glucose (r2 = 0.9963; p <0.01), and the detection limit was 0.92 μM. Furthermore, blood glucose concentrations estimated from the standard curves of three subjects were compared with results obtained by conventional colorimetric analysis using glucose dehydrogenase. Good correlation was observed between methods according to simple linear regression analysis (p <0.05). The reproducibility of the assay was about 6.3-9.1% (RSD) and the within-days and between-days reproducibility were 1.6-8.4 and 5.2-7.2%, respectively. This system enables us to determine blood glucose with high sensitivity and accuracy, and will be applicable to clinical diagnosis.
AB - A high-performance monitoring system for human blood glucose levels was developed using microchip electrophoresis with a plastic chip. The combination of reductive amination as glucose labeling with fluorescent 2-aminoacridone (AMAC) and glucose-borate complex formation realized the highly selective detection of glucose even in a complex matrix such as a blood sample. The migration time of a single peak, observed on an electropherogram of AMAC-labeled plasma, closely resembled that of glucose standard solution. The treatment of plasma with hexokinase or glucokinase for glucose phosphorylation resulted in a peak shift from approximately 145 to 70 s, corresponding to glucose and glucose-6-phosphate, respectively. A double-logarithm plot revealed a linear relationship between glucose concentration and fluorescence intensity in the range of 1-300 μM of glucose (r2 = 0.9963; p <0.01), and the detection limit was 0.92 μM. Furthermore, blood glucose concentrations estimated from the standard curves of three subjects were compared with results obtained by conventional colorimetric analysis using glucose dehydrogenase. Good correlation was observed between methods according to simple linear regression analysis (p <0.05). The reproducibility of the assay was about 6.3-9.1% (RSD) and the within-days and between-days reproducibility were 1.6-8.4 and 5.2-7.2%, respectively. This system enables us to determine blood glucose with high sensitivity and accuracy, and will be applicable to clinical diagnosis.
UR - http://www.scopus.com/inward/record.url?scp=34548245626&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=34548245626&partnerID=8YFLogxK
U2 - 10.1002/elps.200600795
DO - 10.1002/elps.200600795
M3 - Article
C2 - 17640093
AN - SCOPUS:34548245626
SN - 0173-0835
VL - 28
SP - 2927
EP - 2933
JO - ELECTROPHORESIS
JF - ELECTROPHORESIS
IS - 16
ER -