van Maanen R J, van Ooijen R D, Beijnen J H
University of Utrecht, Department of Pharmaceutical Analysis, The Netherlands.
J Chromatogr B Biomed Sci Appl. 1997 Sep 26;698(1-2):111-21. doi: 10.1016/s0378-4347(97)00281-8.
A sensitive assay for the determination of N,N',N"-triethylenthiophosphoramide (thioTEPA) in microvolumes of human plasma and urine has been developed. ThioTEPA was analysed using gas chromatography with selective nitrogen-phosphorus detection, after extraction with ethyl acetate from the biological matrix. Diphenylamine is the internal standard. The limit of quantitation was 0.1 ng/ml, using only 100 microl of sample; recoveries ranged between 85 and 100% and both accuracy and precision were less than 10%. Using a flame ionisation nitrogen-phosphorus detector, the assay was not linear over the concentration range of 2-1000 ng/ml for plasma and 10-1000 ng/ml for urine. Linearity was accomplished in the range of 1-1000 ng/ml for plasma and urine when a thermionic nitrogen/phosphorous detector was used. The stability of thioTEPA in plasma proved to be satisfactory over a period of 3 months, when kept at -20 degrees C, whereas it was stable in urine for at least 1 month at -80 degrees C. ThioTEPA plasma concentrations of two patients treated with thioTEPA are presented demonstrating the applicability of the assay.
已开发出一种灵敏的测定方法,用于测定微量人血浆和尿液中的N,N',N"-三亚乙基硫代磷酰胺(硫替派)。从生物基质中用乙酸乙酯萃取后,采用带选择性氮磷检测的气相色谱法分析硫替派。二苯胺为内标物。仅使用100微升样品时,定量限为0.1纳克/毫升;回收率在85%至100%之间,准确度和精密度均小于10%。使用火焰离子化氮磷检测器时,该测定方法在血浆浓度范围为2 - 1000纳克/毫升和尿液浓度范围为10 - 1000纳克/毫升内不呈线性。当使用热离子氮/磷检测器时,血浆和尿液在1 - 1000纳克/毫升范围内呈线性。硫替派在血浆中的稳定性在-20℃保存3个月期间被证明是令人满意的,而在尿液中于-80℃至少稳定1个月。给出了两名接受硫替派治疗患者的硫替派血浆浓度,证明了该测定方法的适用性。