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dc.contributor.authorRojas Camargo, John Jairo-
dc.contributor.authorKumar, Vijay-
dc.date.accessioned2023-06-09T14:06:32Z-
dc.date.available2023-06-09T14:06:32Z-
dc.date.issued2012-
dc.identifier.citationRojas J, Kumar V. Coprocessing of cellulose II with amorphous silicon dioxide: effect of silicification on the powder and tableting properties. Drug Dev Ind Pharm. 2012 Feb;38(2):209-26. doi: 10.3109/03639045.2011.597400.spa
dc.identifier.issn0363-9045-
dc.identifier.urihttps://hdl.handle.net/10495/35421-
dc.description.abstractABSTRACT: Aim: In recent years, coprocessing has been the most successful approach to improve and correct the functionality of excipients. The aim of this study is to coprocessed cellulose II with SiO(2) and to evaluate the resulting powder and tableting properties. Methods: Novel cellulose II:SiO(2) (98:2, 95:5, 90:10 and 80:20 w/w ratios) composites were produced by spray drying, wet granulation and spheronization techniques and the resulting powder and tableting properties were assessed. Results: Cellulose II:SiO(2) composites produced by spray- drying exhibited spherical/oblongate shape, narrow distribution and mean diameter from 51 to 75 µm. The composites produced by wet granulation had larger distribution, granular shape and a mean diameter from 105 to 129 µm. The spheronized composites showed the highest size (from 148 to 450 µm) and round shape. Bulk and tap densities and flow were reduced as the silicification level increased in the spray dried and wet granulated materials. Likewise, silicification increased the true density, porosity and surface roughness of these materials. Water sorption decreased only at silicification level of 20% being comparable to the ones shown by Prosolv(®) samples. Contact angles of all cellulose II materials were lower than those of cellulose I except for Celphere203 indicating better wettability. A 5% and 10% silicification levels rendered the strongest compacts for the spray dried and wet granulated materials, respectively. Silicification did not affect the fast disintegration properties of MCCII. Conclusions: Coprocessing proved to be useful tool to modify the powder and tableting properties of cellulose II.spa
dc.format.extent19spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherTaylor and Francisspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.5/co/*
dc.titleCoprocessing of cellulose II with amorphous silicon dioxide: effect of silicification on the powder and tableting propertiesspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupDiseño y Formulación de Medicamentos Cosméticos y Afinesspa
dc.identifier.doi10.3109/03639045.2011.597400-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1520-5762-
oaire.citationtitleDrug Development and Industrial Pharmacyspa
oaire.citationstartpage209spa
oaire.citationendpage226spa
oaire.citationvolume38spa
oaire.citationissue2spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc-nd/4.0/spa
oaire.fundernameUniversidad de Antioquia. Vicerrectoría de investigación. Comité para el Desarrollo de la Investigación - CODIspa
dc.publisher.placeLondres, Inglaterraspa
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 - Química-
dc.subject.decsCellulose - Chemistry-
dc.subject.decsComposición de Medicamentos - métodos-
dc.subject.decsDrug Compounding - methods-
dc.subject.decsExcipientes - Química-
dc.subject.decsExcipients - Chemistry-
dc.subject.decsTamaño de la Partícula-
dc.subject.decsParticle Size-
dc.subject.decsPolvos - Química-
dc.subject.decsPowders - Chemistry-
dc.subject.decsDióxido de Silicio - Química-
dc.subject.decsSilicon Dioxide - Chemistry-
dc.subject.decsComprimidos - Química-
dc.subject.decsTablets - Chemistry-
dc.description.researchgroupidCOL0003623spa
dc.relation.ispartofjournalabbrevDrug Dev. Ind. Pharm.spa
oaire.funderidentifier.rorRoR:03bp5hc83-
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