DSpace DSpace

Biblioteca Digital do IPG >
Escola Superior de Saúde (ESS) >
Artigos em Revista Internacional (ESS) >

Utilize este identificador para referenciar este registo: http://hdl.handle.net/10314/3099

Título: An easy-to-use liquid chromatography assay for the analysis of lamotrigine in rat plasma and brain samples using microextraction by packed sorbent:Application to a pharmacokinetic study
Autores: Ventura, Sandra
Rodrigues, Márcio
Pousinho, Sarah
Falcão, Amílcar
Alves, Gilberto
Palavras Chave: Bioanalytical method validation
High-performance liquid chromatography
Lamotrigine
Microextraction by packed sorbent
Rat plasma and brain
Data: 27-Sep-2016
Editora: Elsevier B.V
Resumo: A simple and rapid high-performance liquid chromatography method with diode-array detection (HPLC-DAD) using microextraction by packed sorbent (MEPS) during the sample preparation step was developed and validated to quantify lamotrigine (LTG) in rat plasma and brain samples. MEPS variables such as pH, number of draw-eject cycles, and washing and desorption conditions were optimized. The chromatographic resolution of LTG and chloramphenicol, used as internal standard (IS), was accomplished in less than 5min on a C18 column, at 35°C, using an isocratic elution with acetonitrile (13%), methanol (13%) and water-triethylamine (99.7:0.3, v/v; pH 6.0) pumped at a flow rate of 1mL/min. Detection was performed at 215nm. Calibration curves were linear over the range of 0.1-20μg/mL (r2≥0.9947) for LTG in both rat plasma and brain homogenate samples. The intra and interday imprecision did not exceed 8.6% and the intra and interday inaccuracy ranged from -8.1 to 13.5%. LTG was extracted from rat plasma and brain homogenate samples with an average absolute recovery ranging from 68.0 to 86.7%, and its stability was demonstrated in the assayed conditions. No interferences were observed at the retention times of the analyte (LTG) and IS. To the best of our knowledge, this is the first bioanalytical assay that uses MEPS procedure for the determination of LTG not only in rat plasma but also in tissue (brain) samples. This novel method was successfully applied to a preliminary pharmacokinetic study in rats and it seems to be a cost-effective tool to support non-clinical pharmacokinetic-based studies involving LTG treatment.
URI: http://hdl.handle.net/10314/3099
ISSN: 1570-0232
Aparece nas Colecções:Artigos em Revista Internacional (ESS)

Ficheiros deste Registo:

Ficheiro Descrição TamanhoFormato
1_Ventura 2016.pdf477KbAdobe PDFVer/Abrir
Sugerir este item a um colega