Timm U, Saner A
J Chromatogr. 1986 May 28;378(1):25-34. doi: 10.1016/s0378-4347(00)80696-9.
An automated high-performance liquid chromatographic assay for the determination of an aldosterone antagonist (I) is described using column switching for direct injection of urine samples. After dilution with buffered internal standard solution, the sample was injected onto a clean-up column (17 X 4.6 mm I.D.), dry-packed with C18 reversed-phase material (particle size 30 micron). Polar urine components were removed by flushing the clean-up column with water. Retained substances, including I and the internal standard, were desorbed by backflush elution onto a 5-micron ODS-silica analytical column (125 X 4 mm I.D.), separated with water-methanol-tetrahydrofuran, and detected at 295 nm. After backflushing the analytical column and re-equilibrating the clean-up column, the system was ready for the next injection. The limit of quantification was ca. 100 ng/ml, using a 100-microliter specimen of diluted urine. The mean inter-assay precision of the method up to 25.6 micrograms/ml was 2%. Practicability and accuracy of the new method were demonstrated by the application to excretion studies performed with human volunteers.
描述了一种用于测定醛固酮拮抗剂(I)的自动化高效液相色谱分析方法,该方法采用柱切换技术直接进样尿液样本。用缓冲内标溶液稀释后,将样品注入装填有C18反相材料(粒径30微米)的净化柱(内径17×4.6毫米)。用水冲洗净化柱以去除极性尿液成分。包括I和内标在内的保留物质通过反冲洗脱解吸到5微米的ODS硅胶分析柱(内径125×4毫米)上,用水 - 甲醇 - 四氢呋喃进行分离,并在295纳米处检测。在反冲分析柱并使净化柱重新平衡后,系统即可准备下一次进样。使用100微升稀释尿液样本时,定量限约为100纳克/毫升。该方法在高达25.6微克/毫升时的平均批间精密度为2%。通过应用于人体志愿者的排泄研究证明了该新方法的实用性和准确性。