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dc.contributor.authorBarzegar-Jalali, M
dc.contributor.authorHanaee, J
dc.contributor.authorOmidi, Y
dc.contributor.authorGhanbarzadeh, S
dc.contributor.authorZiaee, S
dc.contributor.authorBairami-Atashgah, R
dc.contributor.authorAdibkia, K
dc.date.accessioned2018-08-26T09:32:21Z
dc.date.available2018-08-26T09:32:21Z
dc.date.issued2013
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57321
dc.description.abstractThe aim of this study was to develop sustained release dosage forms of acetazolamide (ACZ) preparing its calcium alginate beads and matrix tablets. ACZ was incorporated into calcium alginate beads using microencapsulation method. Two methods were applied to prolong ACZ release rate. In the first method, the drug was incorporated into calcium alginate beads either alone or with various polymers in internal phase. The second method involved the preparation of matrix tablet from the beads benefiting direct compression method with or without various polymers in external phase. The release rate of these prepared formulations and an innovator's sustained-release capsule (Diamox) were assessed. In-vitro dissolution studies revealed that the matrix tablets prepared by the second method containing NaCMC could sustain ACZ release properly and the drug released until 9 h. It was also found that several parameters such as concentration of sodium alginate, calcium chloride and ACZ; type and concentration of polymers; syringe needle size as well as distance between needle tip and surface of the calcium chloride could affect the properties of beads, matrix tablets and subsequently release profile. Preparation of polymer free beads, incorporation of polymers in internal phase of the beads and direct compression of the beads did not give sustained release property. Whereas, incorporation of NaCMC in the external phase of the beads in matrix tablets or in combination with alginate powder in directly compressed conventional tablets could produce dosage form with sustained release property similar to reference formulation. © Georg Thieme Verlag KG Stuttgart · New York.
dc.language.isoEnglish
dc.relation.ispartofDrug Research
dc.subjectacetazolamide
dc.subjectalginic acid
dc.subjectcalcium alginate
dc.subjectcalcium chloride
dc.subjectacetazolamide
dc.subjectalginic acid
dc.subjectglucuronic acid
dc.subjecthexuronic acid
dc.subjectarticle
dc.subjectdrug formulation
dc.subjectdrug screening
dc.subjectdrug solubility
dc.subjectdrug synthesis
dc.subjectin vitro study
dc.subjectmatrix tablet
dc.subjectsustained release preparation
dc.subjectsyringe needle
dc.subjectchemistry
dc.subjectdelayed release formulation
dc.subjectsolubility
dc.subjecttablet
dc.subjectAcetazolamide
dc.subjectAlginates
dc.subjectDelayed-Action Preparations
dc.subjectGlucuronic Acid
dc.subjectHexuronic Acids
dc.subjectSolubility
dc.subjectTablets
dc.titlePreparation and evaluation of sustained release calcium alginate beads and matrix tablets of acetazolamide
dc.typeArticle
dc.citation.volume63
dc.citation.issue2
dc.citation.spage60
dc.citation.epage64
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1055/s-0032-1331755


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