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dc.contributor.authorRojas Camargo, John Jairo-
dc.contributor.authorLópez López, Alvin de Jesús-
dc.contributor.authorMoreno Soto, Sebastián-
dc.date.accessioned2023-07-31T23:51:41Z-
dc.date.available2023-07-31T23:51:41Z-
dc.date.issued2011-
dc.identifier.citationRojas, John & Moren, Sebastian & Lopez, Alvin. (2011). Assessment of the Water Sorption Properties of Several Microcrystalline Celluloses. Journal of Pharmaceutical Sciences and Research. 3.spa
dc.identifier.issn0975-1459-
dc.identifier.urihttps://hdl.handle.net/10495/36094-
dc.description.abstractABSTRACT: This paper compares the water sorption behavior of commercial microcrystalline celluloses with those of cellulose II materials using several nonlinear models. Aqueous dispersions of cellulose II were spray-dried employing an inlet drying air temperature of 195 °C; atomizing air pressure of 1.0 kg-f/cm2; drying air flow-rate of 0.44 m3/min; feed flow-rate of 2.0 mL/min and nozzle diameter of 0.7 mm. Cellulose II samples were also spheronized in a Fuji Paudal spheronizer for 10 min at 1000 rpm. Products were analyzed for water sorption on a VTI® symmetrical gravimetric analyzer in triplicates. The Guggenheim-Anderson-de Boer (GAB), Hailwood-Horrobin (HH), Generalized D’Arcy and Watt (GDW) and Young and Nelson (YN) models were employed for the data analysis. Most of the sorption isotherms exhibited a type II sigmoid shape. Celphere®203, presented a type III isotherm and showed the highest monolayer capacity (m0 of 0.15 g water/g cellulose) and the lowest monolayer energy constant (C=1.0) given by the GAB model. The GDW model indicated that the monolayer capacity (m0) and the fraction of sorption sites available for multilayer sorption (w) were the highest for Celphere®203 (1.0 g/g cellulose and 1.0, respectively). The HH model indicated that Celphere®203 had the highest sorption capacity (W of 3.0 g/g sorption site). The YN model showed that this material had the largest water uptake by absorption into the core of the particles. Celphere®203 and SPCII were the most hydrophilic materials. Neither polymorphic form, nor silicification, was responsible for the difference in the hydrophilic properties of cellulose.spa
dc.format.extent8spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherPharmainfo Publicationsspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/co/*
dc.titleAssessment of the water sorption properties of several microcrystalline cellulosesspa
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
oaire.citationtitleJournal of Pharmaceutical Sciences and Researchspa
oaire.citationstartpage1302spa
oaire.citationendpage1309spa
oaire.citationvolume3spa
oaire.citationissue7spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by/4.0/spa
dc.publisher.placeIndiaspa
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.decsCelulosa-
dc.subject.decsCellulose-
dc.subject.decsIsoterma-
dc.subject.decsIsotherm-
dc.subject.decsPolímeros-
dc.subject.decsPolymers-
dc.identifier.urlhttp://www.jpsr.pharmainfo.in/spa
dc.description.researchgroupidCOL0003623spa
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