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dc.contributor.authorGulsun, Tugba
dc.contributor.authorAkdag, Yagmur
dc.contributor.authorIzat, Nihan
dc.contributor.authorOner, Levent
dc.contributor.authorSahin, Selma
dc.date.accessioned2021-06-03T08:55:44Z
dc.date.available2021-06-03T08:55:44Z
dc.date.issued2019
dc.identifier.issn2630-6344
dc.identifier.urihttp://dx.doi.org/10.35333/jrp.2019.33
dc.identifier.urihttp://hdl.handle.net/11655/24367
dc.description.abstractDeferasirox is an oral iron chelator used for the treatment of chronic iron overload in blood transfusions. Deferasirox is a BCS Class II drug with low solubility and high permeability. In the formulation development stage for BCS Class II compounds, one of the main approaches is solubility enhancement to achieve better dissolution profiles, increased bioavailability and in some cases, dose reduction. The aim of the study was to investigate the effect of particle size and surfactant on the solubility, permeability and dissolution characteristics of deferasirox. Ball milling method was used to reduce the particle size of deferasirox. Pluronic F127 or sodium lauril sulfate (SLS) were selected as surfactants at different concentrations. The maximum increase in the solubility was obtained with 10% SLS at pH 1.2 (from 0.9 mu g/mL to 333.7 mu g/mL), and with 5% Pluronic F127 at pH 6.8 (from 46.8 mu g/mL to 334.2 mu g/mL). Dissolution studies revealed that time to dissolve 85% of deferasirox was decreased as a function of ball milling time and particle size. Permeability studies showed that, in 100 mu M concentration, deferasirox permeability was significantly enhanced by all concentrations of SLS (p<0.05). With an increase in Pluronic F127 concentration, permeability of deferasirox was not altered (p>0.05). All these results clearly demonstrated that surfactant addition to the formulations was effective for solubility enhancement of deferasirox, and surfactant type in optimized concentrations was very crucial. Particle size reduction can be used as a promising approach to improve dissolution, and hence bioavailability of deferasirox.
dc.language.isoen
dc.relation.isversionof10.35333/jrp.2019.33
dc.rightsAttribution 4.0 United States
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectpermeability
dc.subjectDeferasirox
dc.subjectdissolution
dc.subjectparticle size distribution
dc.subjectsolubility
dc.subjectsurfactant
dc.titleEffect Of Particle Size And Surfactant On The Solubility, Permeability And Dissolution Characteristics Of Deferasirox
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalJournal Of Research In Pharmacy
dc.contributor.departmentFarmasötik Teknoloji
dc.identifier.volume23
dc.identifier.issue5
dc.description.indexWoS
dc.description.indexScopus


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Attribution 4.0 United States
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