Determination of ranitidine in human plasma by SPE and ESI-LC-MS/MS for use in bioequivalence studies

dc.creatorBellorio, Karini Bruno
dc.creatorAlves, Maria Isabel Ribeiro
dc.creatorAntoniosi Filho, Nelson Roberto
dc.date.accessioned2018-04-06T14:48:45Z
dc.date.available2018-04-06T14:48:45Z
dc.date.issued2013
dc.description.resumoA method for determining ranitidine in human plasma by ESI-LC-MS/MS was validated, using propranolol as internal standard. e extraction method used was solid phase extraction (SPE). Chromatographic separation was performed in a Chromolith C18 (50 mm × 4.6 mm i.d.) analytical column, which provided good separation of ranitidine and propranolol peaks with an analysis time of 2.5 minutes. Extraction yields of 94.4% for ranitidine and 89.4% for the internal standard were obtained. e lower limit of quanti􀄕cation (LLO􀀲) was 3.00 ng/mL, and limit of detection (LOD) was 0.05 ng/mL, with linearity ranging from 3.00 to 500 ng/mL. e results, thus, showed that this method is suitable for application in bioequivalence studies of ranitidine in human plasma.pt_BR
dc.identifier.citationBELLORIO, Karini B.; ALVES, Maria Isabel R.; Antoniosi Filho, Nelson R. Determination of ranitidine in human plasma by SPE and ESI-LC-MS/MS for use in bioequivalence studies. ISRN Chromatography, London, v. 2013, p. 1-7, 2013.pt_BR
dc.identifier.doi10.1155/2013/484592
dc.identifier.urihttp://repositorio.bc.ufg.br/handle/ri/14391
dc.language.isoengpt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.departmentInstituto de Química - IQ (RG)pt_BR
dc.rightsAcesso Abertopt_BR
dc.titleDetermination of ranitidine in human plasma by SPE and ESI-LC-MS/MS for use in bioequivalence studiespt_BR
dc.typeArtigopt_BR

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