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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/74643
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dc.contributor.authorPerpétuo, G. L.-
dc.contributor.authorGálico, D. A.-
dc.contributor.authorFugita, R. A.-
dc.contributor.authorCastro, R. A E-
dc.contributor.authorEusébio, M. E S-
dc.contributor.authorTreu-Filho, O.-
dc.contributor.authorSilva, A. C M-
dc.contributor.authorBannach, Gilbert-
dc.date.accessioned2014-05-27T11:28:33Z-
dc.date.accessioned2016-10-25T18:44:52Z-
dc.date.available2014-05-27T11:28:33Z-
dc.date.available2016-10-25T18:44:52Z-
dc.date.issued2013-03-01-
dc.identifierhttp://dx.doi.org/10.1007/s10973-012-2247-0-
dc.identifier.citationJournal of Thermal Analysis and Calorimetry, v. 111, n. 3, p. 2019-2028, 2013.-
dc.identifier.issn1388-6150-
dc.identifier.urihttp://hdl.handle.net/11449/74643-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/74643-
dc.description.abstractThermogravimetry (TG), differential scanning calorimetry (DSC), polarized light thermal microscopy (PLTM), as well as X-ray powder diffraction (XRD) and Fourier transformed infrared spectroscopy (FTIR) were used to study the thermal behavior and the chemical structure of cimetidine, famotidine, ranitidine-HCl, and nizatidine. The TG-DSC curves show that the famotidine and ranitidine-HCl suffer decomposition during melting and they are thermally less stable in comparison with cimetidine and nizatidine, the latter being the most stable of all the drugs studied in this study. The DSC curves of famotidine and ranitidine-HCl show exothermic peaks immediately after the melting, confirming the occurrence of thermal decomposition. The DSC curves also show that the cimetidine and nizatidine have some thermal stability after melting. The thermal events shown in the PLTM images are consistent with the results shown in the TG-DSC and DSC curves. The XRD patterns show that the cimetidine and famotidine are less crystalline compared with ranitidine-HCl and nizatidine. The theoretical FTIR bands are in agreement with those obtained experimentally, and in some cases, no difference is observed between the theoretical and experimental values, even being identical in one of the cases. © 2012 Akadémiai Kiadó, Budapest, Hungary.en
dc.format.extent2019-2028-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAntihistamines-
dc.subjectCimetidine-
dc.subjectFamotidine-
dc.subjectNizatidine-
dc.subjectRanitidine-
dc.subjectThermal behavior-
dc.subjectThermal behaviors-
dc.subjectDifferential scanning calorimetry-
dc.subjectInfrared spectroscopy-
dc.subjectThermogravimetric analysis-
dc.subjectX ray powder diffraction-
dc.subjectMelting-
dc.titleThermal behavior of some antihistaminesen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de Coimbra-
dc.description.affiliationDepartamento de Química Falculdade de Ciências UNESP, Bauru, SP, CEP 17033-260-
dc.description.affiliationCEF Faculdade de Farmácia Universidade de Coimbra, CEP 3000-548, Coimbra-
dc.description.affiliationCQC Departamento de Química Universidade de Coimbra, CEP 3004-535, Coimbra-
dc.description.affiliationInstituto de Química - UNESP, Araraquara, SP, CEP 14800-900-
dc.description.affiliationUnespDepartamento de Química Falculdade de Ciências UNESP, Bauru, SP, CEP 17033-260-
dc.description.affiliationUnespInstituto de Química - UNESP, Araraquara, SP, CEP 14800-900-
dc.identifier.doi10.1007/s10973-012-2247-0-
dc.identifier.wosWOS:000315298800048-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Thermal Analysis and Calorimetry-
dc.identifier.scopus2-s2.0-84881475988-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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