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Simultaneous quantitative analysis of letrozole, its carbinol metabolite, and carbinol glucuronide in human plasma by LC-MS/MS

机译:LC-MS / MS同时定量测定人血浆中来曲唑,其甲醇代谢物和葡萄糖醛糖苷酸含量

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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.
机译:来曲唑是绝经后乳腺癌的有效内分泌治疗方法,但是,并非所有患者都能从这种治疗中受益,而且,严重的副作用(如关节痛)经常导致停药。为了更好地了解药物反应和副作用之间的个体差异,对来曲唑及其主要代谢物的稳态浓度进行血浆分析至关重要。我们开发了一种快速,灵敏和特异的方法,用于通过UHPLC-ESI同时定量来曲唑及其代谢物4,4'-(羟基亚甲基)二苯甲腈(甲醇)和双(4-氰基苯基)甲基六吡喃葡萄糖醛酸(carbinol-gluc) -MS / MS使用内部合成的,稳定的同位素标记的内标。在BondElut C18 96孔板中进行固相萃取后,将分析物在ZORBAX Eclipse XDB-C18色谱柱(1.8μm,4.6×50 mm)上进行分离,并用乙腈在0.1%的乙酸水溶液中的溶液进行梯度洗脱并在多反应监测模式下具有电喷雾电离的三重四极杆质谱仪。来曲唑,甲醇和甲醇葡萄糖的定量下限分别为20、0.2和2 nM。该测定方法已根据FDA指南进行了验证,并已用于分析每天接受2.5 mg来曲唑治疗的绝经后乳腺癌患者的20份血浆样品。来曲唑,甲醇和甲醇葡萄糖的平均血浆水平(±SD)分别为366±173、0.38±0.09和34±12 nM。我们基于快速灵敏质谱的方法可实现来曲唑结果的未来药代动力学研究。

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