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dc.contributor.authorAli, Hany S.M.*
dc.contributor.authorYork, Peter*
dc.contributor.authorBlagden, Nicholas*
dc.contributor.authorSoltanpour, S.*
dc.contributor.authorAcree, W.E. Jr.*
dc.contributor.authorJouyban, A.*
dc.date.accessioned2011-03-25T12:13:32Z
dc.date.available2011-03-25T12:13:32Z
dc.date.issued2010-01
dc.identifier.citationAli, H.S.M., York, P., Blagden, P., Soltanpour, S., Acree, Jr., W.E. and Jouyban, A. (2010). Solubility of Budesonide, Hydrocortisone, and Prednisolone in Ethanol plus Water Mixtures at 298.2 K. Journal of Chemical and Engineering Data. Vol. 55, No. 1, pp. 578-582.en_US
dc.identifier.urihttp://hdl.handle.net/10454/4853
dc.descriptionnoen_US
dc.description.abstractExperimental solubilities of budesonide, hydrocortisone, and prednisolone in ethanol + water mixtures at 298.2 K are reported. The solubility of drugs was increased with the addition of ethanol and reached the maximum values of the volume fractions of 90 %, 80 %, and 80 % of ethanol. The Jouyban-Acree model was used to fit the experimental data, and the solubilities were reproduced using previously trained versions of the Jouyban-Acree model and the solubility data in monosolvents in which the overall mean relative deviations (OMRDs) of the models were 5.1 %, 6.4 %, 37.7 %, and 35.9 %, respectively, for the fitted model, the trained version for ethanol + water mixtures, and generally trained versions for various organic solvents + water mixtures. Solubilities were also predicted by a previously established log-linear model of Yalkowsky with the OMRD of 53.8 %.en_US
dc.language.isoenen_US
dc.relation.isreferencedbyhttp://dx.doi.org/10.1021/je900376ren_US
dc.subjectSolubilityen_US
dc.subjectCrystal engineeringen_US
dc.subjectBudesonideen_US
dc.subjectHydrocortisoneen_US
dc.subjectPrednisoloneen_US
dc.subjectEthanol and water mixturesen_US
dc.titleSolubility of Budesonide, Hydrocortisone, and Prednisolone in Ethanol plus Water Mixtures at 298.2 Ken_US
dc.status.refereedYesen_US
dc.typeArticleen_US


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