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dc.contributor.authorMunoz, MM
dc.contributor.authorPena, MA
dc.contributor.authorAlmanza, OA
dc.contributor.authorJouyban, A
dc.contributor.authorMartinez, F
dc.contributor.authorAcree, WE
dc.date.accessioned2018-08-26T07:26:40Z
dc.date.available2018-08-26T07:26:40Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/46800
dc.description.abstractEquilibrium solubility of sodium naproxen (Na.NAP), procaine hydrochloride (PC.HCl), and lysine clonixinate (Lys.Clon), was determined in methanol + water mixtures at 298.15 K. Mole fraction solubility of Na.NAP increases from neat water (x(3) = 1.71 x 10(-2)) to reach a maximum in the mixture with w(1) = 0.90 (x(3) = 5.05 x 10(-2)); the solubility of PC.HCI increases from neat water (x(3) = 9.68 x 10(-2)) to reach a maximum in the mixture with w(1) = 0.20 (x(3) = 0.1032); whereas, the solubility of Lys.Clon increases from neat water (x(3) = 3.54 x 10(-2)) to reach a maximum in the mixture with w(1) = 0.60 (x(3) = 6.33 x 10(-2)). The generated solubility data are mathematically represented by using the Jouyban-Acree model with very good error level (average of 1.2% for molar solubilities). In addition, the apparent specific volumes at saturation of these drugs were also calculated in all the mixtures under study using the measured densities of the saturated solutions. In this way, the average apparent volumes at saturation in these mixtures could be considered as follows: 0.699 cm(3) g(-1) for Na.NAP, 0.821 cm(3) g(-1) for PC-HCl, and 0.730 cm(3) g(-1) for Lys.Clon. (C) 2016 Elsevier B.V. All rights reserved.
dc.language.isoEnglish
dc.relation.ispartofJOURNAL OF MOLECULAR LIQUIDS
dc.subjectSodium naproxen
dc.subjectProcaine hydrochloride
dc.subjectLysine clonixinate
dc.subjectMethanol plus water mixtures
dc.subjectSolubility
dc.subjectCosolvency
dc.subjectApparent specific volume
dc.titleSolubility and apparent specific volume at saturation of some pharmaceutical salts in methanol plus water mixtures at 298.15 K
dc.typeArticle
dc.citation.volume220
dc.citation.spage842
dc.citation.epage847
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1016/j.molliq.2016.04.116


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