Feng M R, Atherton J, Knoll S, Strenkoski C A, Wright D S
Parke-Davis Pharmaceutical Research, Division of Warner-Lambert Company, Ann Arbor, MI 48105, USA.
J Chromatogr B Biomed Sci Appl. 1997 May 23;693(1):159-66. doi: 10.1016/s0378-4347(97)00015-7.
Two HPLC assays were developed and validated for simultaneous quantitation of two sulfate metabolites, PD 163637 (VI) and PD 163639 (VIII), of an investigational antipsychotic drug CI-1007 (I) in monkey plasma and urine. VI and VIII were identified as major metabolites in monkey plasma, and both were excreted in urine. Monkey plasma samples were directly injected after deproteinization, and urine samples were analyzed after a clean-up procedure using methyl-tert.-butyl ether. Liquid chromatographic separation was achieved on a Zorbax RX C8 analytical column using gradient elution. Column effluent was monitored using fluorescence detection with excitation and emission wavelengths of 254 and 330 nm, respectively. Minimum quantitation limit was 50 ng/ml in plasma and 100 ng/ml in urine. Linearity was demonstrated up to 3000 ng/ml in plasma and urine. Recoveries of the analytes from plasma and urine were greater than 85%. The assay has been applied to the determination of VI and VIII in plasma and urine samples from monkeys receiving oral administration of I.
开发并验证了两种高效液相色谱法,用于同时定量测定一种研究性抗精神病药物CI-1007(I)在猴血浆和尿液中的两种硫酸代谢物PD 163637(VI)和PD 163639(VIII)。VI和VIII被鉴定为猴血浆中的主要代谢物,且两者均经尿液排泄。猴血浆样品经去蛋白后直接进样,尿液样品经甲基叔丁基醚净化处理后进行分析。在Zorbax RX C8分析柱上采用梯度洗脱进行液相色谱分离。柱流出物采用荧光检测,激发波长和发射波长分别为254和330 nm。血浆中的最低定量限为50 ng/ml,尿液中的最低定量限为100 ng/ml。血浆和尿液中线性范围高达3000 ng/ml。分析物在血浆和尿液中的回收率大于85%。该方法已应用于口服I的猴血浆和尿液样品中VI和VIII的测定。