Fast fabric phase sorptive extraction of selected β-blockers from human serum and urine followed by UHPLC-ESI-MS/MS analysis

被引:23
|
作者
Mazaraki, Konstantina [1 ]
Kabir, Abuzar [2 ]
Furton, Kenneth G. [2 ]
Fytianos, Konstantinos [3 ]
Samanidou, Victoria F. [4 ]
Zacharis, Constantinos K. [1 ]
机构
[1] Aristotle Univ Thessaloniki, Sch Pharm, Dept Pharmaceut Technol, Lab Pharmaceut Anal, GR-54124 Thessaloniki, Greece
[2] Florida Int Univ, Dept Chem & Biochem, Miami, FL 33199 USA
[3] Aristotle Univ Thessaloniki, Chem Dept, Environm Pollut Control Lab, GR-54124 Thessaloniki, Greece
[4] Aristotle Univ Thessaloniki, Dept Chem, Lab Analyt Chem, GR-54124 Thessaloniki, Greece
关键词
Carbowax; 20M; Cellulose; Microextraction; beta-Blockers; Biological fluid; Liquid chromatography-tandem mass spectrometry; PERFORMANCE LIQUID-CHROMATOGRAPHY; HUMAN PLASMA; PROPRANOLOL; SAMPLES; QUANTIFICATION; ATENOLOL;
D O I
10.1016/j.jpba.2021.114053
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A fast fabric phase sorptive extraction method is presented herein for the rapid isolation of selected beta-blocker drugs from human serum and urine. Among many high efficiency sol-gel sorbent coated FPSE membranes, sol-gel CW20 M coated FPSE membrane was identified as the best FPSE membrane for the target beta-blocker drugs possessing logP values ranging from 0.1 (highly polar) to 3.1 (moderately polar). Due to the engineered affinity towards the analytes via complementary intermolecular interactions and high mass transfer rate of the analytes from the bulk sample solution to the FPSE membrane, the extraction is accomplished in relatively short time (15 min) while its high permeability permits the direct extraction of biological samples without any other pretreatment. The advantages of the fabricated extraction membrane were exploited for the determination of six beta-blockers (namely atenolol, nadolol, metoprolol, oxprenolol, labetalol and propranolol) in biological matrices in combination with UHPLC-ESI-MS/MS. Important parameters including extraction time, sample volume, sorbent size, elution solvent, etc. affecting the performance of the extraction were systematically investigated. The linearity of the method was evaluated in the range of 50-5000 ng mL(-1) by constructing weighted (1/X) matrix-matched calibration curves. The intra-day and inter-day trueness were ranged between - 17.2 to 13.3% and - 10.8 to 12.6%, respectively. The intra-day and inter-day precision were less than 11.5 and 14.5 %, respectively. The proposed analytical scheme was successfully applied to the determination of the target drugs in human serum and urine. (C) 2021 Elsevier B.V. All rights reserved.
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页数:8
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