Utilize este identificador para referenciar este registo: http://hdl.handle.net/10451/21254
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degois.publication.firstPage95por
degois.publication.lastPage106por
degois.publication.titleDRUG DEVELOPMENT AND INDUSTRIAL PHARMACYpor
dc.contributor.authorLopes, CM
dc.contributor.authorLobo, JMS
dc.contributor.authorCosta, P
dc.contributor.authorPinto, JF
dc.date.accessioned2015-12-30T10:17:48Z-
dc.date.available2015-12-30T10:17:48Z-
dc.date.issued2006
dc.identifier.citationDRUG DEVELOPMENT AND INDUSTRIAL PHARMACY. - Vol. 32, n. 1 (2006), p. 95-106
dc.identifier.issn0363-9045
dc.identifier.urihttp://hdl.handle.net/10451/21254-
dc.description.abstractDirectly compressed mini tablets were produced containing either hydroxypropylmethylcellulose (HPMC) or ethylcellulose (EC) as release controlling agent. The dynamics of water uptake and erosion degree of polymer were investigated. By changing the polymer concentration, the ibuprofen release was modified. In identical quantities, EC produced a greater sustaining release effect than HPMC. Different grades of viscosity of HPMC did not modify ibuprofen release. For EC formulations, the contribution of diffusion was predominant in the ibuprofen release process. For HPMC preparations, the drug release approached zero-order during a period of 8 h. For comparative purposes, tablets with 10 mm diameter were produced.
dc.formatapplication/pdf
dc.language.isoeng
dc.publisherTAYLOR & FRANCIS INC
dc.rightsrestrictedAccess
dc.subjectChemistry, Medicinal
dc.subjectPharmacology & Pharmacy
dc.titleDirectly compressed mini matrix tablets containing ibuprofen
dc.titlePreparation and evaluation of sustained release
dc.typearticle
degois.publication.volumeVol. 32por
dc.identifier.doihttp://dx.doi.org/10.1080/03639040500388482
Aparece nas colecções:FF - Produção Científica 2000-2009

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