Solubility and preferential solvation of meloxicam in ethanol+water mixtures

Daniel R. Delgado, Andrés R. Holguín, Ovidio A. Almanza, Fleming Martínez*, Yizhak Marcus

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

120 Scopus citations

Abstract

The solubilities of the analgesic drug meloxicam (MEL) in ethanol. +. water cosolvent mixtures were determined at several temperatures from 293.15 to 313.15. K. The Gibbs energy, enthalpy, and entropy of solution and of mixing were obtained from these solubility data. The solubility was maximal in 0.85 mass fraction of ethanol at several temperatures and very low in pure water at all the temperatures studied. A non-linear plot of ΔHsoln0 vs. ΔGsoln0 with negative slope from pure water up to 0.85 mass fraction of ethanol and positive beyond this composition up to neat ethanol was obtained. Accordingly, the driving mechanism for MEL solubility in almost all mixtures is the entropy, probably due to water-structure loss around the drug non-polar moieties caused by the ethanol. The preferential solvation of MEL by the components of the solvent was estimated by means of the quasi-lattice quasi-chemical and by the inverse Kirkwood-Buff integral method, showing the preferential solvation of MEL by ethanol except at very low water contents, where water preferentially solvates the drug.

Original languageEnglish
Pages (from-to)88-95
Number of pages8
JournalFluid Phase Equilibria
Volume305
Issue number1
DOIs
StatePublished - 15 Jun 2011

Keywords

  • Activity coefficients
  • Ethanol
  • Meloxicam
  • Preferential solvation
  • Solubility
  • Solution thermodynamics

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