Kabra P M, Wall J H, Blanckaert N
Clin Chem. 1985 Oct;31(10):1717-20.
In this simple, precise, accurate, and specific isocratic liquid chromatographic procedure for determining cyclosporine, the cyclosporine is extracted from 1 mL of whole blood or from plasma, with 500 micrograms of cyclosporin D added per liter as internal standard, by elution from a Bond-ElutTM C18 extraction column with 300 microL of a mixture of ethanol and tetrahydrofuran. A 100-microL aliquot of the eluate, injected onto a cyano-phase analytical column, is eluted with a mixture of acetonitrile and pH 7.0 phosphate buffer at a flow rate of 1.0 mL/min and at 50 degrees C. Detection is at 210 nm. The chromatography is complete in less than 14.0 min. The method can measure less than 10.0 micrograms/L. Analytical recovery of cyclosporine added to whole blood ranged from 99 to 109% for concentrations up to 2000 micrograms/L. Between-run CVs ranged from 6.4 to 6.6%. None of numerous drugs and steroids tested interfered. Results by radioimmunoassay exceeded by 20 to 350% those measured by the present method.
在这个用于测定环孢素的简单、精确、准确且特异的等度液相色谱法中,环孢素从1 mL全血或血浆中提取,每升添加500微克环孢菌素D作为内标,通过用300微升乙醇和四氢呋喃的混合物从Bond-ElutTM C18萃取柱上洗脱。取100微升洗脱液注入氰基分析柱,用乙腈和pH 7.0磷酸盐缓冲液的混合物以1.0 mL/分钟的流速在50℃下洗脱。检测波长为210 nm。色谱分析在不到14.0分钟内完成。该方法可检测低至10.0微克/升的环孢素。添加到全血中的环孢素在浓度高达2000微克/升时的分析回收率为99%至109%。批间变异系数在6.4%至6.6%之间。所测试的众多药物和类固醇均无干扰。放射免疫分析法的结果比本方法测得的结果高出20%至350%。