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dc.contributor.authorRathi, P
dc.contributor.authorJouyban, A
dc.contributor.authorKhoubnasabjafari, M
dc.contributor.authorKale, M
dc.date.accessioned2018-08-26T07:42:43Z
dc.date.available2018-08-26T07:42:43Z
dc.date.issued2015
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/47865
dc.description.abstractModel's for predicting the solubility of drugs in monosolvents and their mixtures have a practical importance in design and development of new products in pharmaceutical industries. Thus, present investigation pertains to the utility of a correlative model for solubility prediction of etoricoxib (ETR). The molar solubilities of ETR in a number of monosolvents and various mass fractions of their binary aqueous solvent mixtures were determined using the shake-flask method at 298.2 K. Densities of ETR saturated solutions in the monosolvents and their binary solvent mixtures were measured and then correlated using a well-established method proposed by Jouyban and Acree. Overall mean percentage deviations (OMPDs) between experimental and predicted values were 3.4 % for the molar solubilities and 0.1 % for the densities of the saturated solutions.
dc.language.isoEnglish
dc.relation.ispartofJOURNAL OF CHEMICAL AND ENGINEERING DATA
dc.titleSolubility of Etoricoxib in Aqueous Solutions of 1,4-Butanediol, 1,4-Dioxane, N,N-Dimethylacetamide, N,N-Dimethylformamide, Dimethyl Sulfoxide, and Ethanol at 298.2 K
dc.typeArticle
dc.citation.volume60
dc.citation.issue7
dc.citation.spage2128
dc.citation.epage2134
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1021/acs.jced.5b00201


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