Kasel Dirk, Jetter Alexander, Harlfinger Steffi, Gebhardt Wilhelm, Fuhr Uwe
Department of Pharmacology, Clinical Pharmacology, University of Cologne, Gleueler Str. 24, 50931 Cologne, Germany.
Rapid Commun Mass Spectrom. 2004;18(13):1472-8. doi: 10.1002/rcm.1508.
A reliable and easy to use liquid chromatography/tandem mass spectrometry (LC/MS/MS) method was developed for the simultaneous quantification of urinary concentrations of cyclophosphamide (CP) and its main metabolites excreted in urine, i.e. N-dechloroethylcyclophosphamide (DCL-CP), 4-ketocyclophosphamide (4KetoCP), and carboxyphosphamide (CarboxyCP). Sample preparation consisted of dilution of urine with an aqueous solution of the internal standard D(4)-CP and methanol, and centrifugation. LC/MS/MS detection was performed using a triple-quadrupole mass spectrometer working in selected reaction monitoring mode. All analytes were quantified in a single run within 11.5 min. The limits of detection were 5 ng/mL for CP and 4KetoCP, 1 ng/mL for DCL-CP, and 30 ng/mL for CarboxyCP. Quantification ranges were adjusted to the expected concentrations in 24-h urine collections of patients treated with a polychemotherapy regimen (3-175 microg/mL for CP, 0.5-27 microg/mL for 4KetoCP and 0.17-9 microg/mL for CarboxyCP and DCL-CP, respectively). The method was validated according to international guidelines of the ICH and the FDA.
开发了一种可靠且易于使用的液相色谱/串联质谱(LC/MS/MS)方法,用于同时定量尿液中环磷酰胺(CP)及其主要尿排泄代谢物,即N-去氯乙基环磷酰胺(DCL-CP)、4-酮环磷酰胺(4KetoCP)和羧基磷酰胺(CarboxyCP)。样品制备包括用内标D(4)-CP的水溶液和甲醇稀释尿液,然后离心。LC/MS/MS检测使用在选择反应监测模式下工作的三重四极杆质谱仪进行。所有分析物在11.5分钟内单次进样定量。CP和4KetoCP的检测限为5 ng/mL,DCL-CP为1 ng/mL,CarboxyCP为30 ng/mL。定量范围根据接受多药化疗方案治疗的患者24小时尿液收集的预期浓度进行调整(CP为3-175 μg/mL,4KetoCP为0.5-27 μg/mL,CarboxyCP和DCL-CP分别为0.17-9 μg/mL)。该方法根据ICH和FDA的国际指南进行了验证。