Suckow R F, Cooper T B
J Pharm Sci. 1984 Dec;73(12):1745-8. doi: 10.1002/jps.2600731221.
A procedure for the determination of trimipramine, the demethyl, 2-hydroxy, and 2-hydroxy demethyl metabolites in plasma by liquid chromatography with electrochemical detection is described. A 1-mL plasma sample is made alkaline with a carbonate buffer (pH 9.8) and extracted with 20% ethyl acetate in n-heptane. After back-extraction into an acid phosphate buffer, an aliquot is injected onto a reverse-phase trimethylsilyl-packed column and eluted with a phosphate buffer-acetonitrile mobile phase (65:35) containing n-butylamine. The peaks were detected at +1.1 V versus the silver-silver chloride reference electrode. The method provides absolute recoveries of 60-91% and a day-to-day precision of less than 9% for all compounds. The minimum quantifiable level for all compounds was 3 ng/mL. Steady-state plasma concentration data for 29 depressed patients receiving either 75 mg or 150 mg/d is reported.
本文描述了一种采用液相色谱-电化学检测法测定血浆中三甲丙咪嗪、去甲基、2-羟基和2-羟基去甲基代谢物的方法。取1 mL血浆样品,用碳酸盐缓冲液(pH 9.8)碱化,并用20%乙酸乙酯的正庚烷溶液萃取。反萃取至酸性磷酸盐缓冲液后,取一份注入反相三甲基硅烷基填充柱,用含正丁胺的磷酸盐缓冲液-乙腈流动相(65:35)洗脱。相对于银-氯化银参比电极,在+1.1 V处检测峰。该方法对所有化合物的绝对回收率为60-91%,日常精密度小于9%。所有化合物的最低可定量水平为3 ng/mL。报告了29例接受75 mg或150 mg/d治疗的抑郁症患者的稳态血浆浓度数据。