Zell M, Timm U
J Chromatogr. 1986 Oct 31;382:175-88. doi: 10.1016/s0378-4347(00)83515-x.
A selective and highly sensitive capillary gas chromatographic method was developed for the determination of a benzodiazepine antagonist in human plasma. The analytical procedure involved extraction of the compound and its internal standard from basified plasma with n-butyl chloride-dichloromethane and chromatography of the extract on a DB-5 fused-silica column (30 m X 0.25 mm I.D.), applying automated splitless injection and nitrogen- phosphorus detection. The limit of quantification was about 50 pg/ml, using a 1-ml plasma specimen. The mean inter-assay precision was 2.6% in the concentration range 0.5-10 ng/ml. The method was shown to be specific with respect to various benzodiazepines and their main metabolites. The practicability of the method was demonstrated by the analysis of more than 300 plasma samples from a dose proportionality study performed with human volunteers. Owing to its high sensitivity, the new method can be used to obtain pharmacokinetic parameters of the benzodiazepine antagonist in man after doses near the envisaged therapeutic intravenous dose of less than 1 mg.
建立了一种选择性高、灵敏度高的毛细管气相色谱法,用于测定人血浆中的苯二氮䓬拮抗剂。分析过程包括用正丁基氯 - 二氯甲烷从碱化血浆中提取该化合物及其内标,并将提取物在DB - 5熔融石英柱(30 m×0.25 mm内径)上进行色谱分析,采用自动不分流进样和氮磷检测。使用1 ml血浆样本时,定量限约为50 pg/ml。在0.5 - 10 ng/ml浓度范围内,批间平均精密度为2.6%。该方法对各种苯二氮䓬及其主要代谢物具有特异性。通过对来自人体志愿者剂量比例研究的300多个血浆样本进行分析,证明了该方法的实用性。由于其高灵敏度,新方法可用于获得苯二氮䓬拮抗剂在人体中接近设想的治疗静脉剂量(小于1 mg)给药后的药代动力学参数。