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Anal Chim Acta. 2006 Nov 24;580(2):200-5. doi: 10.1016/j.aca.2006.07.073. Epub 2006 Aug 04.

Sensitive analysis of two barbiturates in human urine by capillary electrophoresis with sample stacking induced by moving reaction boundary.

Analytica chimica acta

Qiu-Ling Wang, Liu-Yin Fan, Wei Zhang, Cheng-Xi Cao

Affiliations

  1. Laboratory of Analytical Biochemistry & Bioseparation, School of Life Science & Biotechnology, Shanghai Jiao Tong University, Shanghai 200240, China.

PMID: 17723774 DOI: 10.1016/j.aca.2006.07.073

Abstract

An on-line stacking method based on moving reaction boundary (MRB) was developed for the sensitive determination of barbital and phenobarbital in human urine via capillary electrophoresis (CE). The optimized conditions for the method are: 60 mmol L(-1) pH 11.0 Gly-NaOH as the background electrolyte, 10 mmol L(-1) pH 5.5 Gly-HCl as sample buffer, secobarbital as the internal standard (IS), 12.5 kV, 1.4 psi 10s sample injection, 75 microm ID 60.2 cm total length (50 cm effective length) capillary and 214 nm detect wavelength. Under the optimized conditions, the method can well stack and separate barbital and phenobarbital in urine samples and result in 20.5-fold and 22.6-fold improvement in concentration sensitivity for barbital and phenobarbital, respectively. Furthermore, the method holds: (1) good linear calibration functions for the two target compounds (correlation coefficients r>0.999), (2) low limits of detection (0.27 microg mL(-1) for barbital and 0.26 microg mL(-1) for phenobarbital), (3) low limits of quantification (0.92 microg mL(-1) for barbital and 0.87 microg mL(-1) for phenobarbital), (4) good precision (R.S.D. of intra-day and inter-day less than 5.38% for barbital and 1.67% for phenobarbital, respectively) and (5) high recoveries at three concentration levels (90.27-106.36% for barbital and 93.05-113.60% for phenobarbital in urine). The method is simple, sensitive and efficient, and can fit to the need of clinical and forensic toxicology.

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