Volumetric and ultraacoustic properties of sodium salts of ibuprofen/diclofenac drugs in aqueous and aqueous-β-cyclodextrin solution

Present paper reports the study of inclusion complex formation between two non-steroidal anti-inflammatory drugs namely sodium ibuprofen and diclofenac sodium in water and aqueous-β-cyclodextrin solutions through thermodynamic properties like the standard partial molar volumes and the standard parti...

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Veröffentlicht in:Journal of molecular liquids 2020-01, Vol.297, p.111812, Article 111812
Hauptverfasser: Deosarkar, S.D., Sawale, R.T., Arsule, A.D., Puyad, A.L.
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Sprache:eng
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Zusammenfassung:Present paper reports the study of inclusion complex formation between two non-steroidal anti-inflammatory drugs namely sodium ibuprofen and diclofenac sodium in water and aqueous-β-cyclodextrin solutions through thermodynamic properties like the standard partial molar volumes and the standard partial molar compressibility at 303.15, 308.15 and 313.15 K and at atmospheric pressure. For this, the densities and ultrasonic velocities of ternary sodium ibuprofen/diclofenac-β-cyclodextrin-water mixtures were measured and used for the calculation of apparent molar volume (V2,ϕ) and apparent molar compressibility (κs,2,ϕ). The concentration dependence of apparent properties has been fitted to standard relations and corresponding the standard partial molar volume (V2o) and the standard partial molar compressibility (κs,2o) and respective solute-solute interaction parameters Sv and Sk were graphically determined. The standard transfer volumes (ΔtrV2o) and standard transfer compressibility (Δtrκs,2o) were also computed and these properties have been interpreted in terms of drug hydration, inclusion complex formation, and different interactions involved. The sign of Sv and Sk revealed the weakening of solute–solute interactions in presence of cosolute β-cyclodextrin. Solubilization of hydrophobic parts, expulsion of water from hydrophobic cavity of β-cyclodextrin and inclusion complex formation of these drugs with β-cyclodextrin has been confirmed from partial molar volume and transfer properties. [Display omitted] •Thermodynamic properties of {ibuprofen/diclofenac + β-cyclodextrin + water} were studied.•Standard transfer volume and compression has been found to be positive.•Dehydration effect of temperature on studied drugs has been found.•Inclusion complex formation between studied drugs and β-cyclodextrin is confirmed.•Study will have implications in the stability and water solubility of studied drugs.
ISSN:0167-7322
1873-3166
DOI:10.1016/j.molliq.2019.111812