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Title: Simultaneous and enantioselective liquid chromatographic determination of eslicarbazepine acetate, S-licarbazepine, R-licarbazepine and oxcarbazepine in mouse tissue samples using ultraviolet detection
Authors: Alves, Gilberto 
Figueiredo, Isabel 
Castel-Branco, Margarida 
Loureiro, Ana 
Falcão, Amílcar 
Caramona, Margarida 
Keywords: Eslicarbazepine acetate; Oxcarbazepine; Mouse tissue samples; Enantioselective liquid chromatography; Bioanalytical method validation
Issue Date: 2007
Citation: Analytica Chimica Acta. 596:1 (2007) 132-140
Abstract: Herein is reported, for the first time, a simple and reliable chiral reversed-phase liquid chromatographic method coupled to ultraviolet (UV) detection for simultaneous determination of eslicarbazepine acetate (ESL) and its metabolites, S-licarbazepine (S-LC), R-licarbazepine (R-LC) and oxcarbazepine (OXC), in mouse plasma and brain, liver and kidney tissue homogenates. All analytes and the internal standard were extracted from plasma and tissue homogenates by a solid-phase extraction procedure using Waters Oasis® hydrophilic-lipophilic balance cartridges. The chromatographic separation was performed by isocratic elution with water/methanol (88:12, v/v), pumped at a flow rate of 0.7 mL min-1, on a LichroCART 250-4 ChiraDex ([beta]-cyclodextrin, 5 [mu]m) column at 30 °C. The UV detector was set at 225 nm. Calibration curves were linear (r2 >= 0.996) in the ranges 0.4-8 [mu]g mL-1, 0.1-1.5 [mu]g mL-1 and 0.1-2 [mu]g mL-1 for ESL and OXC and in the ranges 0.4-80 [mu]g mL-1, 0.1-15 [mu]g mL-1 and 0.1-20 [mu]g mL-1 for R-LC and S-LC in plasma, brain and liver/kidney homogenates, respectively. The overall precision not exceeded 11.6% (%CV) and the accuracy ranged from -3.79 to 3.84% (%bias), considering all analytes in all matrices. Hence, this method will be a useful tool to characterize the pharmacokinetic disposition of ESL in mice.
DOI: 10.1016/j.aca.2007.05.056
Rights: openAccess
Appears in Collections:FFUC- Artigos em Revistas Internacionais

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