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dc.contributor.authorJimenez, DM
dc.contributor.authorCardenas, ZJ
dc.contributor.authorDelgado, DR
dc.contributor.authorJouyban, A
dc.contributor.authorMartinez, F
dc.date.accessioned2018-08-26T07:46:09Z
dc.date.available2018-08-26T07:46:09Z
dc.date.issued2014
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/48452
dc.description.abstractThe equilibrium solubility of meloxicam in 1,4-dioxane and water binary mixtures at temperatures from 293.15 to 313.15 K was determined, and the respective thermodynamic quantities of solution were calculated. Additionally, the preferential solvation parameters of the drug were derived from their thermodynamic solution properties by means of the inverse KirkwoodBuff integrals method. From solvent effect studies, it is found that this drug is sensitive to specific solvation effects. The preferential solvation parameter by 1,4-dioxane, dx(1,3), is negative in water-rich mixtures but positive in compositions in which 0.18 < x(1) < 1.00. It could be possible that in water-rich mixtures the hydrophobic hydration around aromatic rings and/or methyl groups plays a relevant role in the drug solvation. The greater solvation by 1,4-dioxane in mixtures of similar cosolvent compositions and 1,4-dioxane-rich mixtures could be explained in terms of the greater basic behavior of the cosolvent interacting with the hydrogen-donor groups of the drug.
dc.language.isoEnglish
dc.relation.ispartofINDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
dc.titleSolubility and Solution Thermodynamics of Meloxicam in 1,4-Dioxane and Water Mixtures
dc.typeArticle
dc.citation.volume53
dc.citation.issue42
dc.citation.spage16550
dc.citation.epage16558
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1021/ie503101h


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