No dia 25 de Setembro de 2023, faremos a migração do Repositório Institucional para a versão 7.6 do sistema DSpace. Por este motivo, o Repositório Institucional ficará indisponível neste dia. Contamos com a compreensão de todos.

Show simple item record

dc.contributor.authorKogawa, Ana Carolina [UNESP]
dc.contributor.authorAntonio, Selma Gutierrez [UNESP]
dc.contributor.authorNunes Salgado, Herida Regina [UNESP]
dc.date.accessioned2018-11-26T16:48:29Z
dc.date.available2018-11-26T16:48:29Z
dc.date.issued2016-07-01
dc.identifierhttp://dx.doi.org/10.5740/jaoacint.16-0053
dc.identifier.citationJournal Of Aoac International. Gaithersburg: Aoac Int, v. 99, n. 4, p. 964-971, 2016.
dc.identifier.issn1060-3271
dc.identifier.urihttp://hdl.handle.net/11449/161753
dc.description.abstractRifaximin is a gut-selective oral antimicrobial that has no systemic adverse effects compared with placebo. It is used for the treatment of hepatic encephalopathy, traveler's diarrhea, irritable bowel syndrome, Clostridium difficile infection, ulcerative colitis, and acute diarrhea. The crystalline form present in rifaximin, a, has minimal systemic absorption compared to the amorphous form. The objective of this study was to obtain polymorphic forms of rifaximin using recrystallization processes. The forms were characterized and studied by thermal analysis, X-ray powder diffraction, scanning electron microscopy, and solubility testing. Six polymorphic forms of rifaximin, designated I VI, were obtained by the crystallization process by evaporation of the solvent. Some polymorphic forms obtained in this work may not have the same excellent tolerability as the reference medicine; therefore, studies such as these are extremely important and point to the need for greater requirements by the regulatory agencies overseeing polymorph analysis of the raw materials used in the manufacture of medicines marketed globally. These analyses are not required in the majority of official compendia. Partnerships among industries, research centers, and universities would be a viable way to consolidate research in this area and contribute to improving the quality of solid drugs.en
dc.format.extent964-971
dc.language.isoeng
dc.publisherAoac Int
dc.relation.ispartofJournal Of Aoac International
dc.sourceWeb of Science
dc.titleCharacterization of Polymorphic Forms of Rifaximinen
dc.typeArtigo
dcterms.rightsHolderAoac Int
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.description.affiliationUniv Estadual Paulista, Sch Pharmaceut Sci Araraquara, Dept Pharmaceut, Rodovia Araraquara Jau,Km 1, BR-14801902 Sao Paulo, Brazil
dc.description.affiliationUniv Estadual Paulista, Dept Phys Chem, Inst Chem, Ave Prof Francisco Degni,55 Jardim Quitandinha, BR-14800900 Sao Paulo, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Sch Pharmaceut Sci Araraquara, Dept Pharmaceut, Rodovia Araraquara Jau,Km 1, BR-14801902 Sao Paulo, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Dept Phys Chem, Inst Chem, Ave Prof Francisco Degni,55 Jardim Quitandinha, BR-14800900 Sao Paulo, Brazil
dc.identifier.doi10.5740/jaoacint.16-0053
dc.identifier.wosWOS:000380384900018
dc.rights.accessRightsAcesso restrito
dc.relation.ispartofsjr0,324
Localize o texto completo

Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record