Determination of Antiepileptic Drugs Using Dried Saliva Spots

被引:36
作者
Carvalho, Joana [1 ]
Rosado, Tiago [1 ,2 ]
Barroso, Mario [3 ]
Gallardo, Eugenia [1 ,2 ]
机构
[1] Univ Beira Interior, Ctr Invest Ciencias Saude CICS UBI, Ave Infante D Henrique, P-6201556 Covilha, Portugal
[2] Univ Beira Interior, UBIMed, Lab Farmacotoxicol, EM506, P-6201556 Covilha, Portugal
[3] Inst Nacl Med Legal & Ciencias Forenses Delegacao, Rua Manuel Bento de Sousa 3, P-1169201 Lisbon, Portugal
关键词
BIOANALYTICAL METHOD VALIDATION; LIQUID-CHROMATOGRAPHIC ANALYSIS; CARBAMAZEPINE 10,11-EPOXIDE; BLOOD SPOTS; LC-MS/MS; PLASMA; EXTRACTION; PHENYTOIN; SAMPLES; SERUM;
D O I
10.1093/jat/bky064
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The present work describes the development and validation of an analytical method for the determination of the antiepileptic drugs (AEDs) phenytoin, phenobarbital, carbamazepine and its active metabolite carbamazepine-10,11-epoxide, in oral fluid using liquid chromatography coupled to a diode array detector. Correlation between plasma and oral fluid for these compounds has been proven before, making this matrix a great non-invasive alternative for drug-monitoring purposes. The adaptation of cards, commonly applied in dried blood spots (DBS) sampling, to oral fluid resulted in dried saliva spots (DSS). The extraction procedure consisted of applying 50 L of oral fluid to Whatman(TM) 903 protein saver cards and drying for 1 h. The extraction was performed with 1 mL of acidified methanol (pH = 5.5) for 5 min with agitation. Afterward, the sample was centrifuged for 15 min at 3,500 rpm and the supernatant was evaporated and reconstituted with 80 L of mobile phase. For the AEDs separation, a Zorbax SB-C18 column (1.8 m, 4.6 x 250 mm i.d.) maintained at 35 degrees C was used, and the mobile phase consisted of 35% acetonitrile and 65% of water:methanol:triethylamine (75.5%:24.2%:0.3%) isocratically with a flow of 0.5 mL/min, and the wavelength was monitored at 210 nm. The method was validated according to internationally accepted criteria, and linearity between 0.1-10 g/mL was obtained for all AEDs. This is the first method using DSS for the determination of AEDs, showing great potential for routine use in a laboratory for its simplicity, in addition to the advantages inherent to the use of oral fluid as a sample.
引用
收藏
页码:61 / 71
页数:11
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