Das Ruchita, Agrawal Y K
Institute of Research and Development, Gujarat Forensic Sciences University, Sector 18/A, Gandhinagar-382007, Gujarat, India.
J Chromatogr Sci. 2013 Feb;51(2):146-54. doi: 10.1093/chromsci/bms119. Epub 2012 Aug 21.
A simple and rapid reverse-phase high-performance liquid chromatography method is developed for the simultaneous determination of selective serotonin reuptake inhibitors (sertraline, citalopram, paroxetine and fluoxetine) in urine, plasma and oral fluid. Separation was performed on a Crestpack-18 column (4.6 × 250 mm × 5 µ) within 17.5 min. The mobile phase was composed of water (50 mL) [with glacial acetic acid (0.15 mL) + triethyl amine (0.30 mL)]-acetonitrile (40 mL)-methanol (10 mL), delivered isocratically (0.6 mL/min) at 270 nm. Liquid-liquid extraction was performed for isolation of analytes from biofluids. The developed methodology was validated in terms of sensitivity, linearity, accuracy, precision, stability and selectivity. The calibration curves were linear in the range of 5-1,000 ng/mL for all the compounds in three matrices, with coefficients of determination between 0.9991 to 0.9998. The average extraction recoveries for all the four analytes were above 90%. The limits of detection and limits of quantification were in the ranges of 0.02-1.20 and 0.12-2.51 ng/mL, respectively. The intra-day and inter-day variation coefficients were less than 8.0 and 11%, respectively. Moreover, the results were compared statistically for each analyte in three matrices and found to be equivalent, which signifies the absence of matrix effect. Thus, the method can be applied for the determination of selective serotonin reuptake inhibitors in urine, plasma and oral fluid for routine therapeutic and toxicological screening.
建立了一种简单快速的反相高效液相色谱法,用于同时测定尿液、血浆和口腔液中的选择性5-羟色胺再摄取抑制剂(舍曲林、西酞普兰、帕罗西汀和氟西汀)。在Crestpack-18柱(4.6×250 mm×5µ)上于17.5分钟内完成分离。流动相由水(50 mL)[含冰醋酸(0.15 mL)+三乙胺(0.30 mL)]-乙腈(40 mL)-甲醇(10 mL)组成,在270 nm波长下等度洗脱(0.6 mL/分钟)。采用液-液萃取法从生物流体中分离分析物。所建立的方法在灵敏度、线性、准确度、精密度、稳定性和选择性方面进行了验证。三种基质中所有化合物的校准曲线在5-1000 ng/mL范围内呈线性,决定系数在0.9991至0.9998之间。所有四种分析物的平均萃取回收率均高于90%。检测限和定量限分别在0.02-1.20和0.12-2.51 ng/mL范围内。日内和日间变异系数分别小于8.0%和11%。此外,对三种基质中每种分析物的结果进行了统计学比较,发现结果相当,这表明不存在基质效应。因此,该方法可用于尿液、血浆和口腔液中选择性5-羟色胺再摄取抑制剂的测定,用于常规治疗和毒理学筛查。