Kunsman G W, Manno J E, Przekop M A, Manno B R, Llorens K A, Kunsman C M
Department of Pharmacology, Louisiana State University Medical Center, Shreveport 71130-3932.
J Chromatogr. 1991 Aug 23;568(2):427-36. doi: 10.1016/0378-4347(91)80180-k.
A rapid and sensitive method for extracting temazepam from human serum and urine is presented. Free temazepam is extracted from plasma and urine samples using n-butyl chloride with nitrazepam as the internal standard. Temazepam glucuronide is analyzed as free temazepam after incubating extracts with beta-glucuronidase. Separation is achieved using a C8 reversed-phase column with a methanol-water-phosphate buffer mobile phase. An ultraviolet detector operated at 230 nm is used and a linear response is observed from 20 ng/ml to 10 micrograms/ml. The limit of detection is 15.5 ng/ml and the limit of quantitation is 46.5 ng/ml. Coefficients of variation are less than 10% for concentrations greater than 50 ng/ml. Application of the methodology is demonstrated in a pharmacokinetic study using eight healthy male subjects.
本文介绍了一种从人血清和尿液中提取替马西泮的快速灵敏方法。以硝西泮为内标,用正丁基氯从血浆和尿液样本中提取游离替马西泮。提取物与β-葡萄糖醛酸酶孵育后,将替马西泮葡萄糖醛酸苷作为游离替马西泮进行分析。使用C8反相柱和甲醇-水-磷酸盐缓冲液流动相进行分离。采用在230 nm波长下操作的紫外检测器,在20 ng/ml至10 μg/ml范围内观察到线性响应。检测限为15.5 ng/ml,定量限为46.5 ng/ml。浓度大于50 ng/ml时变异系数小于10%。该方法在一项使用八名健康男性受试者的药代动力学研究中得到了应用。