Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology and University of Tübingen, Stuttgart, Germany.
Anal Bioanal Chem. 2012 Apr;403(1):301-8. doi: 10.1007/s00216-012-5813-1. Epub 2012 Feb 25.
Letrozole is an efficient endocrine treatment of postmenopausal breast cancer, however, not all patients benefit from this treatment, and moreover, severe side-effects like arthralgia frequently lead to discontinuation. To better understand inter-individual variability in drug response and side-effects, plasma analysis of steady-state concentrations of letrozole and its major metabolites is crucial. We developed a rapid, sensitive, and specific method for the simultaneous quantification of letrozole and its metabolites 4,4'-(hydroxymethylene)dibenzonitrile (carbinol) and bis(4-cyanophenyl)methyl hexopyranosiduronic acid (carbinol-gluc) by UHPLC-ESI-MS/MS using in-house synthesized, stable isotope-labeled internal standards. Following solid-phase extraction in BondElut C18 96-well plates, the analytes were separated on a ZORBAX Eclipse XDB-C18 column (1.8 μm, 4.6 × 50 mm) with a gradient of acetonitrile in 0.1% acetic acid in water and detected on a triple quadrupole mass spectrometer with electrospray ionization in the multiple reaction monitoring mode. Lower limits of quantification were 20, 0.2, and 2 nM for letrozole, carbinol, and carbinol-gluc, respectively. The assay has been validated according to FDA guidance and applied to the analysis of 20 plasma samples of postmenopausal breast cancer patients treated with 2.5 mg of letrozole per day. Mean plasma levels (±SD) were 366 ± 173, 0.38 ± 0.09, and 34 ± 12 nM for letrozole, carbinol, and carbinol-gluc, respectively. Our rapid and sensitive mass spectrometry based method enables future pharmacokinetic investigations of letrozole outcome.
来曲唑是一种有效的绝经后乳腺癌内分泌治疗药物,但并非所有患者均从中获益,且严重的关节痛等副作用常导致治疗中断。为了更好地了解药物反应和副作用的个体间差异,测定来曲唑及其主要代谢物的稳态浓度的血浆分析至关重要。我们建立了一种采用超高效液相色谱-电喷雾串联质谱(UHPLC-ESI-MS/MS)同时定量分析来曲唑及其代谢物 4,4'-(羟亚甲基)二苯甲腈(甲醇)和双(4-氰基苯基)甲基己吡喃糖醛酸(甲醇-葡)的快速、灵敏和特异的方法,该方法采用了自行合成的稳定同位素标记的内标。样品经 BondElut C18 96 孔板固相萃取后,在 ZORBAX Eclipse XDB-C18 柱(1.8μm,4.6×50mm)上进行梯度洗脱,以乙腈和 0.1%乙酸水溶液作为流动相,采用电喷雾串联质谱三重四极杆在多反应监测模式下进行检测。来曲唑、甲醇和甲醇-葡的定量下限分别为 20、0.2 和 2 nM。该方法已根据 FDA 指南进行验证,并应用于 20 例每天接受 2.5mg 来曲唑治疗的绝经后乳腺癌患者的血浆样本分析。来曲唑、甲醇和甲醇-葡的平均血浆水平(±SD)分别为 366±173、0.38±0.09 和 34±12 nM。我们的快速灵敏的基于质谱的方法将能够进行来曲唑结局的未来药代动力学研究。