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采用 ESI-LC-MS/MS 快速定量检测小鼠血浆中的长春新碱:在药代动力学研究中的应用。

Rapid quantification of vincristine in mouse plasma using ESI-LC-MS/MS: Application to pharmacokinetic studies.

机构信息

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.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2021 Apr 1;1168:122591. doi: 10.1016/j.jchromb.2021.122591. Epub 2021 Feb 21.

Abstract

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.

摘要

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。

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本文引用的文献

2
Murine Pharmacokinetic Studies.
Bio Protoc. 2018 Oct 20;8(20). doi: 10.21769/BioProtoc.3056.
3
Vincristine-associated Neuropathy With Antifungal Usage: A Kaiser Northern California Experience.
J Pediatr Hematol Oncol. 2018 Jul;40(5):e273-e277. doi: 10.1097/MPH.0000000000001220.
6
Vincristine-induced peripheral neuropathy in children with cancer: A systematic review.
Crit Rev Oncol Hematol. 2017 Jun;114:114-130. doi: 10.1016/j.critrevonc.2017.04.004. Epub 2017 Apr 6.
8
Vincristine-induced peripheral neuropathy in pediatric cancer patients.
Am J Cancer Res. 2016 Nov 1;6(11):2416-2430. eCollection 2016.
9
Severe Vincristine-induced Neuropathic Pain in a CYP3A5 Nonexpressor With Reduced CYP3A4/5 Activity: Case Study.
Clin Ther. 2016 Jan 1;38(1):216-20. doi: 10.1016/j.clinthera.2015.10.017. Epub 2015 Nov 10.

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