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用于测定人乙二胺四乙酸(EDTA)血浆、锂肝素血浆、人尿液以及山羊和猪EDTA血浆中碘海醇的超高效液相色谱-串联质谱法。

UHPLC-MS/MS method for iohexol determination in human EDTA and lithium-heparin plasma, human urine and in goat- and pig EDTA plasma.

作者信息

Stevens Jasper, Wessels Mireille A, Roggeveld Jan, Koster Remco A, Dekkers Claire Cj, van Gelder Maaike K, Gansevoort Ron T, Heerspink Hiddo Jl, Touw Daan J

机构信息

Department of Clinical Pharmacy & Pharmacology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Bioanalytical Laboratory, PRA Health Sciences, Assen, The Netherlands.

出版信息

Bioanalysis. 2020 Jul;12(14):981-990. doi: 10.4155/bio-2020-0122. Epub 2020 Jul 22.

Abstract

Iohexol plasma clearance is used as an indicator of kidney function in clinical and preclinical settings. To investigate the pharmacokinetic profile of iohexol, a rapid, simple method for measurement of iohexol in different matrices and species was needed. Iohexol was separated on an Accucore C18 column (Thermo Fisher Scientific, CA, USA). Detection was performed on a Thermo Scientific Quantiva tandem quadrupole mass spectrometer. The method was validated according to the requirements for bioanalytical methods issued by the US FDA and European Medicines Agency. We developed and validated a fast and efficient analytical method, suitable for analyzing iohexol in human EDTA plasma, human lithium-heparin plasma, human urine and goat- and pig EDTA plasma, using only one calibration line prepared in human EDTA plasma.

摘要

碘海醇血浆清除率在临床和临床前环境中被用作肾功能的指标。为了研究碘海醇的药代动力学特征,需要一种快速、简单的方法来测量不同基质和物种中的碘海醇。碘海醇在Accucore C18柱(美国加利福尼亚州赛默飞世尔科技公司)上分离。检测在赛默飞世尔科技公司的Quantiva串联四极杆质谱仪上进行。该方法根据美国食品药品监督管理局和欧洲药品管理局发布的生物分析方法要求进行了验证。我们开发并验证了一种快速高效的分析方法,该方法仅使用在人乙二胺四乙酸(EDTA)血浆中制备的一条校准曲线,适用于分析人EDTA血浆、人锂肝素血浆、人尿液以及山羊和猪的EDTA血浆中的碘海醇。

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