Hollow-fiber liquid phase microextraction for determination of fluoxetine in human serum by nano-liquid chromatography coupled to high resolution mass spectrometry

被引:4
作者
Cestaro, Beatriz Isabella [1 ]
Machado, Kelly Cavalcanti [2 ]
Batista, Michel [2 ]
da Silva, Bruno Jose Goncalves [1 ]
机构
[1] Univ Fed Parana, Dept Chem, BR-81531980 Curitiba, Brazil
[2] Fiocruz MS, Carlos Chagas Inst, Mass Spectrometry Facil RPT02H, BR-81350010 Curitiba, Brazil
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2024年 / 1234卷
关键词
Human serum; Fluoxetine; nano; -LC; -MS; HF-LPME; High resolution mass spectrometry; HUMAN PLASMA; SAMPLE PREPARATION; BIOLOGICAL-FLUIDS; WATER SAMPLES; LC-MS/MS; DRUGS; NORFLUOXETINE; EXTRACTION; OLANZAPINE; PRECONCENTRATION;
D O I
10.1016/j.jchromb.2024.124018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Therapeutic drug monitoring (TDM) is a personalized care tool based on the determination of a target drug concentration in human serum. An antidepressant drug of interest for such investigations is fluoxetine (FXT), due to a severe impact of genetic polymorphisms on its metabolism. A bioanalytical method employed for TDM purposes must exhibit satisfactory selectivity and detectability, which becomes more difficult due to highly complex biological matrices. In this study, a highly selective bioanalytical method for the determination of FXT in human serum is proposed, which provides excellent clean-up efficiency based on a low cost hollow fiber liquid-phase microextraction (HF-LPME) sample preparation step and nano-liquid chromatography coupled to high-resolution mass spectrometry (nano-LC-HRMS). HF-LPME was performed using a two-phase "U" configuration, with 6 cm fiber, 20 mu L of 1-octanol acting as supported liquid membrane, and ammonium hydroxide (pH 10) as the donor phase with NaCl (10 % m/v) and methanol (5 % v/v) as additives, requiring only 250 mu L of the sample. The procedure was conducted for 30 min under a 750 rpm stirring rate. Gradient elution was carried out employing an acetonitrile-water as mobile phase, the composition of 30:70 to 100:00 (v/v) for 15 min, using formic acid 0.1 % (v/v) as an additive. MS1 was acquired in an Orbitrap mass analyzer, while MS2 was acquired in a linear trap quadrupole. Satisfactory linearity (Pearson's r = 0.99709) was obtained for a concentration range of 0.02 to 2.5 mu g mL-1, which is compatible with the therapeutic and toxic range for FXT. The developed method presents adequate precision (1.61 to 7.45 %) and accuracy (95 to 114 %) and allows the dilution of high concentration samples in a 1:4 ratio (v/v), enabling its application for forensic serum samples. To our knowledge, this is the first study reporting a method based on HF-LPME and nano-LC-HRMS with any analytical purpose, especially with a TDM focus.
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页数:8
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