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采用 UPLC-MS/MS 法测定和处置转运蛋白缺陷型小鼠血浆和心脏中的间碘苄胍

Determination and disposition of meta-iodobenzylguanidine in plasma and heart of transporter-deficient mice by UPLC-MS/MS.

机构信息

Division of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, OH, USA.

Division of Cardiovascular Medicine, Department of Medicine, The Ohio State University, Columbus, OH, USA.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2023 May 1;1222:123699. doi: 10.1016/j.jchromb.2023.123699. Epub 2023 Apr 7.

Abstract

A simple LC-MS/MS method for the quantitative determination of the norepinephrine analogue meta-iodobenzyl-guanidine (mIBG) was developed and validated for mouse plasma and tissues, including salivary gland and heart. The assay procedure involved a one-step solvent extraction of mIBG and the internal standard N-(4-fluorobenzyl)-guandine from plasma or tissue homogenates with acetonitrile. An Accucore aQ column was used to separate analytes using a gradient elution with a total run time of 3.5 min. Validation studies with quality control samples processed on consecutive days revealed values for intra-day and inter-day precision of < 11.3%, with values for accuracy ranging 96.8-111%. Linear responses were observed over the entire calibration curves range (up to 100 ng/mL), and the lower limit of quantification was 0.1 ng/mL, using sample volumes of 5 µL. The developed method was successfully applied to evaluate the plasma pharmacokinetics and tissue distribution of mIBG in wild-type mice and animals lacking the organic cation transporters OCT1, OCT2, OCT3, and/or MATE1 to further understand mechanisms contributing to drug distribution and elimination and causes of inter-individual pharmacokinetic variability.

摘要

建立并验证了一种用于定量测定去甲肾上腺素类似物间碘苄胍(mIBG)的简单 LC-MS/MS 方法,适用于小鼠血浆和组织,包括唾液腺和心脏。该测定方法包括一步溶剂提取法,即用乙腈从血浆或组织匀浆中提取 mIBG 和内标 N-(4-氟苄基)-胍。采用 Accucore aQ 柱,以梯度洗脱方式在 3.5 分钟内分离分析物。连续几天处理质控样品的验证研究表明,日内和日间精密度<11.3%,准确度值在 96.8-111%之间。在整个校准曲线范围内(高达 100ng/mL)观察到线性响应,使用 5μL 样品量时,定量下限为 0.1ng/mL。该方法成功应用于评估野生型小鼠和缺乏有机阳离子转运体 OCT1、OCT2、OCT3 和/或 MATE1 的动物中 mIBG 的血浆药代动力学和组织分布,以进一步了解药物分布和消除的机制以及个体间药代动力学变异性的原因。

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