Bioanalytical method for the quantification of the monastrol derivative anticancer candidate lasom 65 in pre-clinical pharmacokinetic investigations

A simple HPLC/UV method was developed for the determination of the anticancer candidate LaSOM 65 in rat plasma. Samples were cleaned by protein precipitation with acetonitrile (recovery > 95%), after which they were subjected to chromatography under the isocratic elution of an acetonitrile:water...

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Detalles Bibliográficos
Autores: Torres, Bruna Gaelzer Silva, Uchôa, Flávia de Toni, Canto, Rômulo Faria Santos, Crestani, Allan, Eifler-Lima, Vera Lucia, Dalla Costa, Teresa Cristina Tavares
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2014
País:Brasil
Institución:Universidade Federal do Rio Grande do Sul (UFRGS)
Repositorio:Repositório Institucional da UFRGS
Idioma:portugués
OAI Identifier:oai:www.lume.ufrgs.br:10183/115510
Acceso en línea:http://hdl.handle.net/10183/115510
Access Level:acceso abierto
Palabra clave:Monastrol
Farmacocinética
Antineoplásicos
LaSOM 65
HPLC/UV
Descripción
Sumario:A simple HPLC/UV method was developed for the determination of the anticancer candidate LaSOM 65 in rat plasma. Samples were cleaned by protein precipitation with acetonitrile (recovery > 95%), after which they were subjected to chromatography under the isocratic elution of an acetonitrile:water (45:55, v/v) solution with detection at 303 nm. The method was linear (r2 > 0.98) over the concentration range (0.05–2 μg mL−1) with intra- and inter-day precision ranging from 9.6% to 13.6% and 4.3% to 5.4%, respectively. The accuracy of the method ranged from 85% to 113.6%, and it showed sufficient sensitivity to determine pharmacokinetic parameters of LaSOM 65 after intravenous administration to Wistar rats.