Determination of topiramate in dried blood spots using single-quadrupole gas chromatography-mass spectrometry after flash methylation with trimethylanilinium hydroxide

被引:24
作者
Hahn, Roberta Zilles [1 ]
Antunes, Marina Venzon [1 ]
Arnhold, Priscila Costa [1 ]
Andriguetti, Natalia Bordin [1 ]
Verza, Simone Gasparin [1 ]
Linden, Rafael [1 ]
机构
[1] Univ Feevale, Inst Ciencias Saude, Grad Program Toxicol & Analytical Toxicol, Toxicol Analysis Lab, Novo Hamburgo, Brazil
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2017年 / 1046卷
关键词
Topiramate; Dried blood spots; Gas chromatography-mass spectrometry; Therapeutic drug monitoring; LIQUID-CHROMATOGRAPHY; PLASMA; LEVETIRACETAM; HEMATOCRIT; EPILEPSY;
D O I
10.1016/j.jchromb.2017.01.047
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Dried blood spots (DBS) sampling obtained from fingerpricks is a promising and patient friendly alternative for obtaining samples for drug quantification, that could be of interest for topiramate (TOP) therapeutic drug monitoring. The aim of this study was to develop and validate a simple and fast GC-MS assay for TOP measurement in dried blood spots (DBS). The method uses a liquid extraction of one 8 mm DBS, followed by a flash methylation with TMAH, and separation in a DB-5 ms capillary column. Total analytical run time was 15 min. Precision assays presented CV% lower than 9.1% and accuracy was in the range of 94.5-115%. TOP was stable at 25 and 45 degrees C up to 21 days. TOP presents saturable binding to red blood cells, resulting in a fraction in plasma (f(p)) of 0.09-0.03 at 0.8 mu g ml(-1) and 0.71-0.45 at 20 mu g ml(-1) (both at 25-50 Hct% range). The method was applied to DBS samples obtained after phlebotomy and fingerpicks from an adult individual after oral intake of 100 mg TOP (0.25-96 h post dose). Plasma and DBS concentrations were moderately correlated (r=0.61), with estimated f(p) values in the range of 0.06-0.18. Translation of TOP DES to plasma concentrations is challenging due to its concentration-dependent binding to erythrocytes. Thus, the use of whole blood concentrations for patients monitoring should be considered, which favors to the use of DBS in the clinical context. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:131 / 137
页数:7
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