Separation and determination of 3-hydroxyaspartate by online concentration capillary electrophoresis/laser-induced fluorescence with microwave-assisted derivatization

被引:10
作者
Liu, Mingxia [1 ,2 ]
Chen, Lixia [2 ]
Li, Xiangjun [2 ]
Meng, Jinghua [3 ]
Bai, Yu [1 ]
Liu, Huwei [1 ]
机构
[1] Peking Univ, Coll Chem & Mol Engn, Key Lab Bioorgan Chem & Mol Engn, Beijing Natl Lab Mol Sci,Minist Educ, ChengFu Rd, Beijing 100871, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Sci, YuQuan Rd, Beijing 100049, Peoples R China
[3] Xinzhou Teachers Univ, Dept Math, Xinzhou, Shanxi, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
3-hydroxyaspartate; capillary electrophoresis; chiral separation; microwave-assisted derivatization; online sample concentration; AMINO-ACIDS; UV; CHROMATOGRAPHY; CYCLODEXTRIN; SENSITIVITY; ENZYME;
D O I
10.1002/jssc.202100398
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A chiral analytical method was proposed based on capillary electrophoresis with laser-induced fluorescence detection coupled with microwave-assisted derivatization for the simultaneous baseline separation and sensitive detection of four stereoisomers of 3-hydroxyaspartate. The derivatization reaction of 3-hydroxyaspartate with 4-chloro-7-nitrobenzo-2-oxa-1,3-diazole was greatly accelerated by microwave irradiation. Under the optimized conditions, the derivatization yield was increased by 20% and the derivatization time was shortened by 20 min when compared with those from conventional water bath heating. In addition, the sensitivity was improved by online sample concentration methods. The detection limit of l-threo-3-hydroxyaspartate obtained by large-volume sample stacking with polarity switching was 5.3 nmol/L, which was around 1000-fold lower than that of the capillary electrophoresis/laser-induced fluorescence without stacking. The excellent analytical performance in terms of linearity and precision was also achieved. Furthermore, the developed method was successfully applied to the determination of 3-hydroxyaspartate in the spiked urine, and satisfactory recoveries were obtained ranging from 90.5 to 107.0%.
引用
收藏
页码:3646 / 3653
页数:9
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