Laganière S, Goernert L, Beatch G
Biopharmaceutics and Pharmacodynamics Division, Department of Health, Ottawa, Ont., Canada.
J Chromatogr B Biomed Appl. 1994 Oct 3;660(1):191-5. doi: 10.1016/0378-4347(94)00261-4.
A simple and sensitive high-performance liquid chromatographic assay for quantification of sematilide in rabbit plasma was developed. After extraction of samples via solid-phase extraction on C8 microcolumns, baseline resolution was achieved on a reversed-phase 5 microns Inertsil ODS-2 column using isocratic conditions with mobile phase consisting of water-glacial acetic acid-acetonitrile-methanol-triethylamine (93.5:4.0:1.5:0.5:0.5) and UV detection at 254 nm. The assay did not require evaporation or reconstitution steps. The injection interval was 8 minutes. The inter-day coefficient of variation for replicate analysis of spiked samples was less than 7.6% and the accuracy was more than 97% over the standard curve range (0.128 to 3.191 microM) using 0.5 ml of plasma. The assay has been successfully applied to pharmacokinetic studies in rabbits.
建立了一种简单、灵敏的高效液相色谱法用于定量测定兔血浆中的司他利定。通过在C8微柱上进行固相萃取对样品进行提取后,使用由水-冰醋酸-乙腈-甲醇-三乙胺(93.5:4.0:1.5:0.5:0.5)组成的流动相在反相5微米Inertsil ODS-2柱上采用等度洗脱条件,并在254 nm处进行紫外检测,实现了基线分离。该测定方法无需蒸发或复溶步骤。进样间隔为8分钟。使用0.5 ml血浆时,加标样品重复分析的日间变异系数小于7.6%,在标准曲线范围(0.128至3.191 microM)内准确度超过97%。该测定方法已成功应用于兔的药代动力学研究。