Ardakani Yalda H, Rouini Mohammad-Reza
Biopharmaceutics and Pharmacokinetic Division, Department of Pharmaceutics, Faculty of Pharmacy, Medical Sciences/University of Tehran, 14155-6451 Tehran, Iran.
J Pharm Biomed Anal. 2007 Sep 3;44(5):1168-73. doi: 10.1016/j.jpba.2007.04.012. Epub 2007 Apr 18.
Tramadol, an analgesic agent, and its main metabolites O-desmethyltramadol (M1), N-desmethyltramadol (M2) and O,N-didesmethyltramadol (M5) were determined simultaneously in human plasma, saliva and urine by a rapid and specific HPLC method. The sample preparation was a simple, one-step, extraction with ethyl acetate. Chromatographic separation was achieved with a Chromolith Performance RP-18e 100 mm x 4.6 mm column, using a mixture of methanol:water (19:81, v/v) adjusted to pH 2.5 by phosphoric acid, in an isocratic mode at flow rate of 2 ml/min. Fluorescence detection (lambda(ex) 200 nm/lambda(em) 301 nm) was used. The calibration curves were linear (r(2)>0.996) in the concentration ranges in plasma, saliva and urine. The lower limit of quantification was 2.5 ng/ml for all compounds. The within- and between-day precisions in the measurement of QC samples at four tested concentrations were acceptable in all analyzed body fluids The developed procedure was applied to assess the pharmacokinetics of tramadol and its main metabolites following administration of 100mg single oral dose of tramadol to healthy volunteers.
采用快速、特异的高效液相色谱法同时测定人血浆、唾液和尿液中的镇痛药曲马多及其主要代谢物O-去甲基曲马多(M1)、N-去甲基曲马多(M2)和O,N-二去甲基曲马多(M5)。样品制备简单,一步用乙酸乙酯萃取。使用Chromolith Performance RP-18e 100 mm×4.6 mm色谱柱,以甲醇∶水(19∶81,v/v)混合液(用磷酸调至pH 2.5)等度洗脱,流速为2 ml/min,进行色谱分离。采用荧光检测(激发波长200 nm/发射波长301 nm)。血浆、唾液和尿液中各化合物的校准曲线在相应浓度范围内呈线性(r²>0.996)。所有化合物的定量下限均为2.5 ng/ml。在四个测试浓度下,质控样品在所有分析体液中的日内和日间精密度均可接受。所建立的方法用于评估健康志愿者单次口服100 mg曲马多后曲马多及其主要代谢物的药代动力学。