TY - JOUR
T1 - Simultaneous determination of neuroactive amino acids in serum by CZE coupled with amperometric detection
AU - Ge, Shuli
AU - Wang, Huan
AU - Wang, Zhifang
AU - Cheng, Shuang
AU - Wang, Qingjiang
AU - He, Pingang
AU - Fang, Yuzhi
PY - 2013/2
Y1 - 2013/2
N2 - A quantitative determination of six neuroactive amino acids (NAAs) was performed by capillary zone electrophoresis with amperometric detection (CZE-AD). This CZE-AD method utilized two electrolytes: the borate solution flowing in a capillary has the NAAs-separation effects, and the sodium hydroxide (NaOH) solution filled in the detection reservoir for the amperometric analysis of NAAs. The following experimental parameters were optimized: the working electrode potential, the pH value, the component, and the concentration of running buffer, the separation voltage, and the injection time on CZE-AD. Then, under the optimum conditions, the six NAAs could be completely separated in 30 min and had well-shaped AD responses at 0.75 V (versus SCE) on a copper electrode. The linear calibration range of NAAs was from 5 × 10 -4 to 5 × 10-6 mol L-1 with the limits of detection (LODs) ranging from 10-6 to 10-7 mol L -1 (signal-to-noise ratio = 3), and the relative standard deviations (RSDs) of the migration time and peak area were 0.45-0.55 and 3.8-6.3 %, respectively. Moreover, this method has succeeded in human serum analysis, and the determined contents of the six NAAs in human serum were in an average recovery range of 85.3-117.9 %, which confirmed the validity and practicability of this method.
AB - A quantitative determination of six neuroactive amino acids (NAAs) was performed by capillary zone electrophoresis with amperometric detection (CZE-AD). This CZE-AD method utilized two electrolytes: the borate solution flowing in a capillary has the NAAs-separation effects, and the sodium hydroxide (NaOH) solution filled in the detection reservoir for the amperometric analysis of NAAs. The following experimental parameters were optimized: the working electrode potential, the pH value, the component, and the concentration of running buffer, the separation voltage, and the injection time on CZE-AD. Then, under the optimum conditions, the six NAAs could be completely separated in 30 min and had well-shaped AD responses at 0.75 V (versus SCE) on a copper electrode. The linear calibration range of NAAs was from 5 × 10 -4 to 5 × 10-6 mol L-1 with the limits of detection (LODs) ranging from 10-6 to 10-7 mol L -1 (signal-to-noise ratio = 3), and the relative standard deviations (RSDs) of the migration time and peak area were 0.45-0.55 and 3.8-6.3 %, respectively. Moreover, this method has succeeded in human serum analysis, and the determined contents of the six NAAs in human serum were in an average recovery range of 85.3-117.9 %, which confirmed the validity and practicability of this method.
KW - Amperometric detection
KW - Capillary zone electrophoresis
KW - Neuroactive amino acids
KW - Serum
UR - https://www.scopus.com/pages/publications/84878367320
U2 - 10.1007/s10337-012-2378-2
DO - 10.1007/s10337-012-2378-2
M3 - 文章
AN - SCOPUS:84878367320
SN - 0009-5893
VL - 76
SP - 149
EP - 155
JO - Chromatographia
JF - Chromatographia
IS - 3-4
ER -