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Authordc.contributor.authorTapia Villanueva, Cristián 
Authordc.contributor.authorCorbalán, V. es_CL
Authordc.contributor.authorCosta, Edda es_CL
Authordc.contributor.authorGai, María Nella es_CL
Authordc.contributor.authorYazdani-Pedram Zobeiri, Mehrdad es_CL
Admission datedc.date.accessioned2008-11-13T10:18:08Z
Available datedc.date.available2008-11-13T10:18:08Z
Publication datedc.date.issued2005-09
Cita de ítemdc.identifier.citationAMER CHEMICAL SOCen
Identifierdc.identifier.issn1525-7797
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/120560
Abstractdc.description.abstractThe aim of this work was to establish the diltiazem hydrochloride release mechanism from the chitosan-alginate matrix tablet (MCB/AS) and chitosan-carrageenan matrix tablet (MCS/CSI). The weight loss for MCS/CSI is mainly due to the weight loss of the matrix while for MCB/AS it is mainly due to the diltiazem hydrochloride released from the tablet. Using the Peppa's model the release order for MCS/CSI was n = 1.07 +/- 0.13 and for MCB/AS was n = 0.76 +/- 0.02. Thus, MCS/CSI has a transport mechanism, and for MCB/AS the drug release mechanism is a combined process of diffusion and relaxation. MCB/AS has an elastic modulus (G' = 10(5) Pa) one order of magnitude higher than MCS/CSI (G' = 10(4) Pa). MCB/AS is able to uptake solvent without disrupting the microstructure due to its high elastic modulus. Instead MCS/ CSI showed a quick erosion process, which conducted to the tablet disintegration due to a fast solvent uptake process.en
Lenguagedc.language.isoenen
Publisherdc.publisherBIOMACROMOLECULES 6(5):2389-2395en
Keywordsdc.subjectDiltiazemhydrochlorideen
Títulodc.titleStudy of the release mechanism of diltiazem hydrochloride from matrices based on chitosan-alginate and chitosan-carrageenan mixturesen
Document typedc.typeArtículo de revista


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