Division of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, OH, USA.
Division of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, OH, USA.
J Chromatogr B Analyt Technol Biomed Life Sci. 2021 Apr 1;1168:122591. doi: 10.1016/j.jchromb.2021.122591. Epub 2021 Feb 21.
A simple, rapid, and sensitive LC-MS/MS method for determining concentrations of the anticancer alkaloid vincristine in micro volumes of mouse plasma was developed and validated in positive ion mode. Separation of vincristine and the internal standard [H]-vincristine was achieved on an Accucore aQ column with a gradient mobile phase delivered at a flow rate of 0.4 mL/min and a run time of 2.2 min. Calibration curves were linear (r > 0.99, n = 8) up to 250 ng/mL, with a lower limit of quantitation of 2.5 ng/mL. The matrix effect and extraction recovery for vincristine were ranging 108-110% and 88.4-107%, respectively. The intra-day and inter-day precision of quality controls tested at 3 different concentrations were always less than 15%, and accuracy ranged from 91.7 to 107%. The method was successfully applied to evaluate the pharmacokinetic profile of vincristine in wild-type and CYP3A-deficient mice in support of a project to provide mechanistic insight into drug-drug interactions and to identify sources of inter-individual pharmacokinetic variability associated with vincristine-induced peripheral neuropathy.
建立并验证了一种在正离子模式下,用 LC-MS/MS 测定微量小鼠血浆中抗癌生物碱长春新碱浓度的简单、快速、灵敏的方法。长春新碱和内标 [H]-长春新碱在 Accucore aQ 柱上以梯度洗脱方式分离,洗脱液流速为 0.4 mL/min,运行时间为 2.2 min。在 2.5-250ng/mL 范围内,标准曲线呈线性(r>0.99,n=8),定量下限为 2.5ng/mL。长春新碱的基质效应和提取回收率分别为 108-110%和 88.4-107%。3 个不同浓度质控品的日内和日间精密度均小于 15%,准确度为 91.7-107%。该方法成功应用于评价野生型和 CYP3A 缺陷型小鼠长春新碱的药代动力学特征,为研究药物相互作用的机制以及鉴定与长春新碱诱导的周围神经病变相关的个体间药代动力学变异性的来源提供了支持。