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Development and validation of a rapid reverse-phase HPLC method for the determination of methotrexate from nanostructured liquid crystalline systems

dc.contributor.authorVon Zuben, E. S. [UNESP]
dc.contributor.authorOliveira, A. G. [UNESP]
dc.contributor.authorChorilli, M. [UNESP]
dc.contributor.authorScarpa, M. V. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:18:36Z
dc.date.available2018-12-11T17:18:36Z
dc.date.issued2018-01-01
dc.description.abstractA reversed-phase liquid chromatography (RP-LC) method was successfully developed and validated for the determination of methotrexate in nanostructured liquid crystalline systems composed by polyether functional siloxane and silicone polyether copolymer. The LC method was performed on RP C18-ODS column, Agilent Zorbax® (4.6 x 250 mm, 5 μm), maintained at room temperature, with a mobile phase constituted by a mixture of 50 mM ammonium acetate buffer (pH 6.0) and methanol (77:23,v/v) with a flow rate of 1.0 mL/min, using ultraviolet detection at 313 nm. The parameters used in the validation process were linearity, specificity, intra and inter-day precision, accuracy, robustness. The quantitation and detection limits yielded good results. The calibration plot assumed linear behavior from 5.0-150.0 μg. mL-1 (r2= 0.9999). The methotrexate was subjected to oxidation, acid, base and neutral degradation, photolysis and heat as stress conditions. There were no interfering peaks at or near the retention time of methotrexate. The nanostructured liquid crystalline systems did not interfere with the analysis and the recovery was quantitative. The intra and inter-day assay relative standard deviation were less than 0.20 %. The method developed proved to be simple, sensitive, accurate, precise, reproducible and therefore adequate for routine analysis of methotrexate in nanostructured liquid crystalline systems.en
dc.description.affiliationDepartment of Drugs and Medicines College of Pharmaceutical Sciences State University of São Paulo (UNESP)
dc.description.affiliationUnespDepartment of Drugs and Medicines College of Pharmaceutical Sciences State University of São Paulo (UNESP)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipForest Conservation Fund
dc.description.sponsorshipFundação de Ensino e Pesquisa de Uberaba
dc.format.extent128-132
dc.identifierhttp://dx.doi.org/10.1691/ph.2018.7140
dc.identifier.citationPharmazie, v. 73, n. 3, p. 128-132, 2018.
dc.identifier.doi10.1691/ph.2018.7140
dc.identifier.issn0031-7144
dc.identifier.scopus2-s2.0-85044136420
dc.identifier.urihttp://hdl.handle.net/11449/176024
dc.language.isoeng
dc.relation.ispartofPharmazie
dc.relation.ispartofsjr0,375
dc.rights.accessRightsAcesso restritopt
dc.sourceScopus
dc.titleDevelopment and validation of a rapid reverse-phase HPLC method for the determination of methotrexate from nanostructured liquid crystalline systemsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
unesp.author.lattes9114495952533044[2]
unesp.author.orcid0000-0002-0107-9940[2]
unesp.departmentFármacos e Medicamentos - FCFpt

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