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dc.contributor.authorVargas Escobar, Paola-
dc.contributor.authorFlórez Acosta, Oscar Albeiro-
dc.contributor.authorGiraldo Aguirre, Ana Liliana-
dc.contributor.authorTobón Zapata, Gloria Elena-
dc.date.accessioned2022-01-08T18:06:00Z-
dc.date.available2022-01-08T18:06:00Z-
dc.date.issued2016-
dc.identifier.citationVargas Escobar P, Florez Acosta OA, Giraldo Aguirre AL, Tobón Zapata GE. Preparation and Characterization of Solid Dispersion of Tinidazole with Benzoic Acid and Tartaric Acid. AJAS [Internet]. 2016 Apr. 16 [cited 2022 Jan. 8];4(2). Available from: https://www.ajouronline.com/index.php/AJAS/article/view/3637spa
dc.identifier.issn1996-3343-
dc.identifier.urihttp://hdl.handle.net/10495/25212-
dc.description.abstractABSTRACT: Two solid dispersions (SDs) were prepared in order to increase the dissolution rate of tinidazole (TND) by applying the method of grinding and moisturizing with drops of ethanol, using tartaric acid (TTA) and benzoic acid (BZA) as carrier agents. These carrier agents showed complete miscibility with TND, according to the DSC results. The two SDs were characterized and compared with pure TND through XRPD, DSC, FT-IR, particle size, water saturation solubility, equivalent specific surface, wettability and intrinsic dissolution rate tests. All samples were evaluated in the same particle range, and it was found that the increase in the dissolution of the two SDs in comparison to the pure drug was not a result of the reduced particle size but of the partial amorphization of the TND. The carrier-drug ratio makes the TND dosage in these two dispersions a promising alternative for the tablet form.spa
dc.format.extent8spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherKnowledgia Scientificspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/2.5/co/*
dc.titlePeparation and Characterization of Solid Dispersion of Tinidazole with Benzoic Acid and Tartaric Acidspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupDiseño y Formulación de Medicamentos Cosméticos y Afinesspa
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn2321-0893-
oaire.citationtitleAsian Journal of Applied Sciencesspa
oaire.citationstartpage387spa
oaire.citationendpage394spa
oaire.citationvolume4spa
oaire.citationissue2spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc-sa/4.0/spa
dc.publisher.placePakistánspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsTinidazol-
dc.subject.decsTinidazole-
dc.subject.decsHumectabilidad-
dc.subject.decsWettability-
dc.subject.decsSolubilidad-
dc.subject.decsSolubility-
dc.subject.decsDisolución-
dc.subject.decsDissolution-
dc.identifier.urlhttps://www.ajouronline.com/index.php/AJAS/article/view/3637spa
dc.description.researchgroupidCOL0003623spa
dc.relation.ispartofjournalabbrevAsian J. Appl. Sci.spa
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