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dc.contributor.authorHosseini, N
dc.contributor.authorHamidi, S
dc.contributor.authorSoleymani, J
dc.contributor.authorJouyban, A
dc.date.accessioned2018-08-26T09:35:52Z
dc.date.available2018-08-26T09:35:52Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57924
dc.description.abstractSolubility trend of naproxen in the presence of 5 and 10 mM of ?-CD was measured at 298.2 K and compared with solubility profiles in the absence of ?-CD for water + cosolvent mixtures. The saturated solutions of the given volume fractions were reached using shake-flask method, and then the solubility values were measured by UV spectrophotometric method at 256 nm. Afterwards, the experimental solubility data points of naproxen in water + ethanol (EtOH) and water + N-methyl-2-pyrrolidone with and without ?-cyclodextrin (?-CD) were correlated with Jouyban-Acree model. Calculation results revealed that the back-calculated solubilities were in good agreement with the corresponding experimental values. By applying the correlated equations, one can rapidly predict the solubility of naproxen in all solvent compositions. © 2017 Informa UK Limited, trading as Taylor & Francis Group
dc.language.isoEnglish
dc.relation.ispartofPhysics and Chemistry of Liquids
dc.subjectCyclodextrins
dc.subjectEthanol
dc.subjectIonic liquids
dc.subjectSpectrophotometry
dc.subjectCalculation results
dc.subjectExperimental solubility datum
dc.subjectExperimental values
dc.subjectN-methyl-2-pyrrolidone
dc.subjectNaproxens
dc.subjectSaturated solutions
dc.subjectSolvent composition
dc.subjectUV spectrophotometric
dc.subjectSolubility
dc.titleSolubilization of naproxen using N-methyl-2-pyrrolidone or ethanol and ?-cyclodextrin
dc.typeArticle
dc.citation.spage1
dc.citation.epage9
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1080/00319104.2017.1419474


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