Ragot S, Marquet P, Lachâtre F, Rousseau A, Lacassie E, Gaulier J M, Dupuy J L, Lachâtre G
Department of Pharmacology and Toxicology, University Hospital, Limoges, France.
J Chromatogr B Biomed Sci Appl. 1999 Dec 24;736(1-2):175-84. doi: 10.1016/s0378-4347(99)00452-1.
A couple of sensitive and accurate liquid chromatography-electrospray mass spectrometry (LC- S-MS) methods for the determination of the total forms of irinotecan and its active metabolite SN-38 in human serum, using the same chromatographic and detection conditions, is presented. Both used camptothecin as internal standard (I.S.). The sample pretreatment for irinotecan involved a simple protein precipitation with acetonitrile, whereas a liquid-liquid extraction was necessary for SN-38. A Symmetry C18, 3.5 microm (150 x 1 mm I.D.) reversed-phase column was used for the chromatographic separation, together with a gradient elution of acetonitrile in 5 mM ammonium formate buffer (pH 3) as mobile phase. After ionisation in the pneumatically-assisted electrospray source and in-source collision induced dissociation, acquisition was performed in the selected ion monitoring mode. Recoveries were 69 and 47% on average, detection limits 2.5 and 0.25 ng/ml and quantitation limits 10 and 0.5 ng/ml for irinotecan and SN-38, respectively. Reproducibility was good and the method was linear from limits of quantitation up to 10,000 ng/ml for irinotecan, and up to 100 ng/ml for SN-38. This sensitive and highly specific method is suitable both for pharmacokinetic studies and routine therapeutic drug monitoring.
本文介绍了两种灵敏且准确的液相色谱 - 电喷雾质谱(LC - S - MS)方法,用于在相同的色谱和检测条件下测定人血清中伊立替康及其活性代谢物SN - 38的总形式。两种方法均使用喜树碱作为内标(I.S.)。伊立替康的样品预处理采用乙腈简单沉淀蛋白质的方法,而SN - 38则需要液 - 液萃取。色谱分离使用Symmetry C18,3.5微米(150×1毫米内径)反相柱,以5 mM甲酸铵缓冲液(pH 3)中的乙腈梯度洗脱作为流动相。在气动辅助电喷雾源中电离并进行源内碰撞诱导解离后,采用选择离子监测模式进行采集。伊立替康和SN - 38的平均回收率分别为69%和47%,检测限分别为2.5和0.25 ng/ml,定量限分别为10和0.5 ng/ml。重现性良好,该方法在伊立替康的定量限至10,000 ng/ml以及SN - 38的定量限至100 ng/ml范围内呈线性。这种灵敏且高度特异的方法适用于药代动力学研究和常规治疗药物监测。