dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorAlves, Claudete
dc.creatorGomes, Paulo Clairmont Feitosa de Lima
dc.creatordos Santos-Neto, Álvaro José
dc.creatorRodrigues, José Carlos
dc.creatorLanças, Fernando Mauro
dc.date2015-05-15T13:30:21Z
dc.date2016-10-25T20:48:38Z
dc.date2015-05-15T13:30:21Z
dc.date2016-10-25T20:48:38Z
dc.date2012
dc.date.accessioned2017-04-06T08:16:52Z
dc.date.available2017-04-06T08:16:52Z
dc.identifierAnalytical Methods, v. 4, p. 1519-1524, 2012.
dc.identifier1759-9660
dc.identifierhttp://hdl.handle.net/11449/123522
dc.identifierhttp://acervodigital.unesp.br/handle/11449/123522
dc.identifierhttp://dx.doi.org/10.1039/C2AY25047K
dc.identifier0049857977635051
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/934133
dc.descriptionA simple and sensitive method using solid phase microextraction (SPME) and liquid chromatography (LC) with heated online desorption (SPME-LC) was developed and validated to analyze anticonvulsants (AEDs) in human plasma samples. A heated lab-made interface chamber was used in the desorption procedure, which allowed the transference of the whole extracted sample. The SPME conditions were optimized by applying an experimental design. Important factors are discussed such as fiber coating types, pH, extraction time and desorption conditions. The drugs were analyzed by LC, using a C18 column (150 mm 4.6 mm 5 mm); and 50 mmol L1 , pH ¼ 5.50 ammonium acetate buffer : acetonitrile : methanol (55 : 22 : 23 v/v) as the mobile phase with a flow rate of 0.8 mL min1 . The suggested method presented precision (intra-assay and inter-assay), linearity and limit of quantification (LOQ) all adequate for the therapeutic drug monitoring (TDM) of AEDs in plasma.
dc.languageeng
dc.relationAnalytical Methods
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleDetermination of anticonvulsants in human plasma using SPME in a heated interface coupled online to liquid chromatography (SPME-LC)
dc.typeOtro


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