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
相关论文
共 56 条
[1]   Dried saliva spot as a sampling technique for saliva samples [J].
Abdel-Rehim, Abbi ;
Abdel-Rehim, Mohamed .
BIOMEDICAL CHROMATOGRAPHY, 2014, 28 (06) :875-877
[2]   Method of Applying Internal Standard to Dried Matrix Spot Samples for Use in Quantitative Bioanalysis [J].
Abu-Rabie, Paul ;
Denniff, Philip ;
Spooner, Neil ;
Brynjolffssen, Jan ;
Galluzzo, Paul ;
Sanders, Giles .
ANALYTICAL CHEMISTRY, 2011, 83 (22) :8779-8786
[3]  
Andre P, 2015, EPILEPTOLOGIE, V32, P78
[5]  
[Anonymous], 2018, Guidance for Industry: Bioanalytical Method Validation
[6]   Key elements of bioanalytical method validation for small molecules [J].
Bansal, Surendra ;
DeStefano, Anthony .
AAPS JOURNAL, 2007, 9 (01) :E109-E114
[7]   Determination of Morphine and 6-Acetylmorphine in Blood With Use of Dried Blood Spots [J].
Boy, Regine Garcia ;
Henseler, Joerg ;
Mattern, Rainer ;
Skopp, Gisela .
THERAPEUTIC DRUG MONITORING, 2008, 30 (06) :733-739
[8]   Determination of antiepileptic drugs in biological material [J].
Chollet, DF .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2002, 767 (02) :191-233
[9]   Simultaneous HPLC-UV analysis of rufinamide, zonisamide, lamotrigine, oxcarbazepine monohydroxy derivative and felbamate in deproteinized plasma of patients with epilepsy [J].
Contin, Manuela ;
Mohamed, Susan ;
Candela, Carmina ;
Albani, Fiorenzo ;
Riva, Roberto ;
Baruzzi, Agostino .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2010, 878 (3-4) :461-465
[10]   APPLICATION ISSUES IN BIOANALYTICAL METHOD VALIDATION, SAMPLE ANALYSIS AND DATA REPORTING [J].
DADGAR, D ;
BURNETT, PE ;
CHOC, MG ;
GALLICANO, K ;
HOOPER, JW .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1995, 13 (02) :89-97