Frye R F, Branch R A
Department of Pharmacy and Therapeutics, School of Pharmacy, University of Pittsburgh, PA 15261, USA.
J Chromatogr B Biomed Appl. 1996 Feb 23;677(1):178-82. doi: 10.1016/0378-4347(95)00380-0.
A sensitive and specific reversed-phase high-performance liquid chromatographic assay was developed for the determination of debrisoquine and 4-hydroxydebrisoquine in urine. The urine samples were directly injected following an ether clean-up step which eliminated interference. Separation of the analytes was achieved using a mobile phase consisting of acetonitrile-methanol-0.02 M heptane sulfonic acid (pH 3.0) (6:37:57) and a mu Bondapak C18 analytical column. The assay utilizes fluorescence detection at 208 nm (ex) and 562 (em). The within-day and between-day coefficients of variation were < or = 10% for both components and accuracy was within 12%. The method is suitable of pharmacogenetic studies utilizing debrisoquine.
建立了一种灵敏且特异的反相高效液相色谱法,用于测定尿液中的异喹胍和4-羟基异喹胍。尿液样品在经过乙醚净化步骤以消除干扰后直接进样。使用由乙腈-甲醇-0.02M庚烷磺酸(pH 3.0)(6:37:57)组成的流动相和μ Bondapak C18分析柱实现分析物的分离。该测定法利用在208nm(激发)和562nm(发射)处的荧光检测。两种成分的日内和日间变异系数均≤10%,准确度在12%以内。该方法适用于利用异喹胍的药物遗传学研究。