Rapid assay of rufinamide in dried blood spots by a new liquid chromatography-tandem mass spectrometric method

被引:41
|
作者
la Marca, Giancarlo [1 ,2 ,6 ]
Malvagia, Sabrina [1 ,6 ]
Filippi, Luca [3 ]
Innocenti, Marzia [4 ]
Rosati, Anna [6 ]
Falchi, Melania [6 ]
Pellacani, Simona [6 ]
Moneti, Gloriano [5 ]
Guerrini, Renzo [1 ,6 ]
机构
[1] A Meyer Childrens Hosp, Clin Pediat Neurol, Mass Spectrometry Lab, Florence, Italy
[2] Univ Florence, Dept Pharmacol, I-50121 Florence, Italy
[3] A Meyer Univ Childrens Hosp, Neonatal Intens Care Unit, Florence, Italy
[4] Univ Florence, Dept Pharmaceut, I-50121 Florence, Italy
[5] Univ Florence, Mass Spectrometry Ctr, CISM, I-50121 Florence, Italy
[6] Univ Florence, Dept Neurosci, I-50121 Florence, Italy
关键词
Rufinamide; Liquid chromatography-tandem mass spectrometry; Epilepsy; Anticonvulsant; PHARMACOKINETICS;
D O I
10.1016/j.jpba.2010.07.015
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Rufinamide (RUF) is a new antiepiletic drug with efficacy in several types of seizures. The aim of this study was to evaluate the use of dried blood spot (DBS) specimens to determinate RUF levels during treatment. Therapeutic drug monitoring of RUF could be useful in routine clinical practice. Advantages of DBS include short collection time, low invasiveness, ease and low cost of sample collection, transport and storage. The analysis was performed in selected reaction monitoring (SRM) mode. The calibration curve in matrix was linear in the concentration range of 0.008-0.8 mg/L (0.48-47.60 mg/L in DBS) of rufinamide with correlation coefficient value of 0.996. In the concentration range of 0.48-47.6 mg/L, the coefficients of variation in DBS were in the range 1.58-4.67% and the accuracy ranged from 89.73% to 107.32%. The sensitivity and specificity of tandem mass spectrometry allow now high throughput rufinamide analysis. This new assay has favourable characteristics being highly precise and accurate. The published HPLC-UV methods also proved to be precise and accurate, but required not less than 0.2-0.5 mL of plasma and are therefore unsuitable for sample collection in neonates in whom obtaining larger blood samples is not convenient or possible. (c) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:192 / 197
页数:6
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