Walter S, Bauer S, Roots I, Brockmöller J
Institut of Clinical Pharmacology, University Clinic Charité, Humboldt University of Berlin, Germany.
J Chromatogr B Biomed Sci Appl. 1998 Dec 11;720(1-2):231-7. doi: 10.1016/s0378-4347(98)00432-0.
A high-performance liquid chromatography (HPLC) method was developed for quantification of both isomers of the thioxanthene neuroleptic flupentixol and of the butyrophenone derivative haloperidol in human serum. After extraction with diethyl ether-n-heptane (50:50, v/v), an isocratic normal-phase HPLC system with a Hypersil cyanopropyl silica column (250x4.6 mm, 5 microm particle size) was used with ultraviolet detection at 254 nm and elution with a mixture of 920 ml acetonitrile, 110 ml methanol, 30 ml 0.1 M ammonium acetate, and 50 microl triethylamine. The limit of quantitation of 0.5 ng/ml and 0.3 ng/ml for flupentixol and haloperidol, respectively, was sufficient to quantify both compounds in serum after administration of clinically adjusted doses. The suitability of the described method for therapeutic drug monitoring and clinical pharmacokinetic studies was assessed by analysis of more than 100 trough level serum samples.
建立了一种高效液相色谱(HPLC)法,用于定量测定人血清中噻吨类抗精神病药物氟哌噻吨的两种异构体以及丁酰苯衍生物氟哌啶醇。用乙醚-正庚烷(50:50,v/v)萃取后,使用配备Hypersil氰丙基硅胶柱(250×4.6 mm,粒径5μm)的等度正相HPLC系统,在254 nm处进行紫外检测,并用920 ml乙腈、110 ml甲醇、30 ml 0.1 M醋酸铵和50μl三乙胺的混合物进行洗脱。氟哌噻吨和氟哌啶醇的定量限分别为0.5 ng/ml和0.3 ng/ml,足以对临床调整剂量给药后的血清中的两种化合物进行定量。通过分析100多个谷浓度血清样本,评估了所述方法用于治疗药物监测和临床药代动力学研究的适用性。