Determination of Barbiturates in Biological Specimens by Flat Membrane-Based Liquid-Phase Microextraction and Liquid Chromatography-Mass Spectrometry
Autor: | Ying Dong, Chuixiu Huang, Ruiqin Zhu, Cai Xiangyang |
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Rok vydání: | 2019 |
Předmět: |
Male
Liquid Phase Microextraction Pharmaceutical Science 02 engineering and technology Mass spectrometry liver 01 natural sciences barbiturates Article Analytical Chemistry lcsh:QD241-441 lcsh:Organic chemistry Liquid chromatography–mass spectrometry Tandem Mass Spectrometry Drug Discovery medicine Animals Sample preparation simultaneous determination Physical and Theoretical Chemistry Whole blood Detection limit Chromatography medicine.diagnostic_test Chemistry 010401 analytical chemistry Organic Chemistry Extraction (chemistry) whole blood Reproducibility of Results Repeatability Hydrogen-Ion Concentration 021001 nanoscience & nanotechnology urine 0104 chemical sciences Rats Chemistry (miscellaneous) Therapeutic drug monitoring Solvents Molecular Medicine membrane-based microextraction 0210 nano-technology Chromatography Liquid |
Zdroj: | Molecules Molecules, Vol 24, Iss 8, p 1494 (2019) Volume 24 Issue 8 |
ISSN: | 1420-3049 |
Popis: | The wide abuse of barbiturates has aroused extensive public concern. Therefore, the determination of such drugs is becoming essential in therapeutic drug monitoring and forensic science. Herein, a simple, efficient, and inexpensive sample preparation technique, namely, flat membrane-based liquid-phase microextraction (FM-LPME) followed by liquid chromatography-mass spectrometry (LC-MS), was used to determine barbiturates in biological specimens. Factors that may influence the efficiency including organic extraction solvent, pH, and composition of donor and acceptor phases, extraction time, and salt addition to the sample (donor phase) were investigated and optimized. Under the optimized extraction conditions, the linear ranges of the proposed FM-LPME/LC-MS method (with correlation coefficient factors &ge 0.99) were 7.5&ndash 750 ng mL&minus 1 for whole blood, 5.0&ndash 500 ng mL&minus 1 for urine, and 25&ndash 2500 ng g&minus 1 for liver. Repeatability between 5.0 and 13.7% was obtained and the limit of detection (LOD) values ranged from 1.5 to 3.1 ng mL&minus 1, from 0.6 to 3.6 ng mL&minus 1, and from 5.2 to 10.0 ng g&minus 1 for whole blood, urine, and liver samples, respectively. This method was successfully applied for the analysis of barbiturates in blood and liver from rats treated with these drugs, and excellent sample cleanup was achieved. |
Databáze: | OpenAIRE |
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