Equilibrium solubility and apparent specific volume at saturation of sodium sulfadiazine in some aqueous cosolvent mixtures at 298.2 K

References

• Rubino JT. Cosolvents and cosolvency. In: Swarbrick JC, Boylan J, editors. Encyclopedia of pharmaceutical technology. Vol. 3. New York (NY): Marcel Dekker; 1988. p. 375–398.
   Google Scholar
• Martin A, Bustamante P, Chun AHC. Physical chemical principles in the pharmaceutical sciences. 4th ed. Philadelphia: Lea & Febiger; 1993.
   Google Scholar
• Yalkowsky SH. Solubility and solubilization in aqueous media. New York: American Chemical Society and Oxford University Press; 1999.
   Google Scholar
• Martinez F, Jouyban A, Acree WE Jr. Pharmaceuticals solubility is still nowadays widely studied everywhere (Editorial). Pharm Sci (Tabriz). 2017;23:1–2.
   Google Scholar
• Budavari S, O’Neil MJ, Smith A, et al. The Merck index, an encyclopedia of chemicals, drugs, and biologicals. 13th ed. Whitehouse Station (NJ): Merck & Co., Inc.; 2001.
   Google Scholar
• Martínez F, Gómez A. Thermodynamics of partitioning of some sulfonamides in 1-octanol/buffer and liposome systems. J Phys Org Chem. 2002;15:874–880.
   Web of Science ®Google Scholar
• Gelone S, O’Donell JA. Anti-infectives. In: Gennaro AR, editor. Remington: the science and practice of pharmacy. 21 ed. Philadelphia (PA): Lippincott Williams & Wilkins; 2005. p. 1630–1633.
   Google Scholar
• Delgado DR, Martínez F. Thermodynamic study of the solubility of sodium sulfadiazine in some ethanol + water cosolvent mixtures. Vitae Rev Fac Quím Farm. 2010;17:191–198.
   Google Scholar
• Delgado DR, Martínez F, Fakhree MAA, et al. Study of the solubility of some sodium sulfonamides in ethanol + water cosolvent mixtures and correlation with the Jouyban-Acree model. Biomed Int. 2011;2:5–11.
   Google Scholar
• Delgado DR, Vargas EF, Martínez F. Thermodynamics of mixing of some sodium sulfonamides in ethanol + water cosolvent mixtures. Vitae Rev Fac Quím Farm. 2011;18:192–200.
   Google Scholar
• Muñoz MM, Rodríguez CJ, Delgado DR, et al. Solubility and saturation apparent specific volume of some sodium sulfonamides in propylene glycol + water mixtures at 298.15 K. J Mol Liq. 2015;211:192–196.
   Web of Science ®Google Scholar
• Martínez F, Gómez A, Ávila CM. Partial molal volumes of transfer of some sulfonamides from water to the (x = 0.5) ethanol-water mixture. Acta Farm Bonaerense. 2002;21:107–118.
   Google Scholar
• Delgado DR, Vargas EF, Martínez F. Apparent molar volumes of some sodium sulfonamides in water at several concentrations and temperatures. J Solution Chem. 2011;40:1955–1963.
   Web of Science ®Google Scholar
• Rodríguez GA, Martínez F, Vargas EF. Volumetric and acoustic properties of some sodium sulfonamides in dilute aqueous solutions at several temperatures. J Chem Thermodyn. 2018;118:159–164.
   Web of Science ®Google Scholar
• Galindres DM, Rodríguez GA, Martínez F, et al. Molar electrical conductivity of sodium sulfonamides in aqueous solution at several temperatures. J Mol Liq. 2019;287:110984.
   Web of Science ®Google Scholar
• Jouyban A. Handbook of solubility data for pharmaceuticals. Boca Raton (FL): CRC Press; 2010. p. 69–505.
   Google Scholar
• Pérez DC, Guevara CC, Cárdenas CA, et al. Solubility and displacement volumes of acetaminophen in binary mixtures formed by propylene glycol, ethanol, and water at 25.0 °C. Rev Colomb Cienc Quím Farm. 2003;32:116–136.
   Google Scholar
• Cárdenas ZJ, Jiménez DM, Martínez F. Solubility and saturation apparent volume of propranolol.HCl in some binary aqueous cosolvent mixtures at 298.15 K. J Chem Eng Data. 2015;60:1520–1525.
   Web of Science ®Google Scholar
• Jiménez DM, Cárdenas ZJ, Martínez F. Solubility and apparent specific volume of some pharmaceutical salts in propylene glycol + water mixtures at 298.15 K. Chem Eng Commun. 2016;203:1013–1019.
   Web of Science ®Google Scholar
• Muñoz MM, Almanza OA, Peña MÁ, et al. Solubility and apparent specific volume at saturation of some pharmaceutical salts in methanol + water mixtures at 298.15 K. J Mol Liq. 2016;220:842–847.
   Web of Science ®Google Scholar
• Tinjacá DA, Muñoz MM, Rahimpour E, et al. Solubility and apparent specific volume of sucrose in some aqueous polyethylene glycol mixtures at 298.2 K. Pharm Sci (Tabriz). 2018;24:163–167.
   Web of Science ®Google Scholar
• Tinjacá DA, Muñoz MM, Jouyban A, et al. Equilibrium solubility, preferential solvation and apparent specific volume of sucrose in some {cosolvent (1) + water (2)} mixtures at 298.2 K. Phys Chem Liq. 2019;57(259–273).
   Google Scholar
• Romdhani A, Martínez F, Almanza OA, et al. Solubility of sulfacetamide in (ethanol + water) mixtures: measurement, correlation, thermodynamics, preferential solvation and volumetric contribution at saturation. J Mol Liq. 2019;290:111219.
   Web of Science ®Google Scholar
• Echeverry LC, Muñoz MM, Tinjacá DA, et al. Equilibrium solubility and apparent specific volume of lidocaine.HCl.H2O in some {cosolvent (1) + water (2)} mixtures at 298.2 K. Phys Chem Liq. 2019;57:679–688.
   Web of Science ®Google Scholar
• Muñoz MM, Romdhani A, Tinjacá DA, et al. Equilibrium solubility and apparent specific volume at saturation of sodium diclofenac in {formamide (1)/N-methylformamide (1)/or N,N,-dimethylformamide (1) + water (2)} mixtures at 298.2 K. Phys Chem Liq. Forthcoming 2019. DOI:10.1080/00319104.2019.1608547
   Web of Science ®Google Scholar
• Marcus Y. The properties of solvents. Chichester: John Wiley & Sons; 1998.
   Google Scholar
• Marcus Y. Solvent mixtures: properties and selective solvation. New York (NY): Dekker; 2002.
   Google Scholar
• Leduc PA, Fortier JL, Desnoyers JE. Apparent molal volumes, heat capacities, and excess enthalpies of n-alkylamine hydrobromides in water as a function of temperature. J Phys Chem. 1974;78:1217–1225.
   Web of Science ®Google Scholar
• Shahidi F. Partial molar volumes of phenalkylamines and their physiologically active derivatives in water. Can J Chem. 1987;65:1924–1926.
   Web of Science ®Google Scholar
• Iqbal M, Verall RE. Apparent molar volume and adiabatic compressibility studies of aqueous solutions of some drug compounds at 25°C. Can J Chem. 1989;67:727–735.
   Web of Science ®Google Scholar
• Iqbal M, Jamal MA, Ahmed M, et al. Partial molar volumes of some drugs in water and ethanol at 35 °C. Can J Chem. 1994;72:1076–1079.
   Web of Science ®Google Scholar
• Ruso JM, Gonzalez-Perez A, Prieto G, et al. Volumetric study of two related amphiphilic beta-blockers as a function of temperature and electrolyte concentration. Colloids Surf B Biointerfaces. 2004;11:165–175.
   Web of Science ®Google Scholar
• Torres DR, Blanco L, Martínez F, et al. Apparent molal volumes of lidocaine-HCl and procaine-HCl in aqueous solution as a function of temperature. J Chem Eng Data. 2007;52:1700–1703.
   Web of Science ®Google Scholar
• Delgado DR, Jiménez-Kairuz AF, Manzo RH, et al. Apparent molar volumes of the anesthetics procaine-HCl and lidocaine-HCl in water at temperatures from 278.15 to 313.15 K. Rev Colomb Cienc Quím Farm. 2010;39:57–67.
   Google Scholar
• Aulton ME. Pharmaceutics. The Science of Dosage Forms Design. 2nd ed. London: Churchill Livingstone; 2002. p. 309–322.
   Google Scholar
• Allen LV Jr, Popovich NG, Ansel HC. Ansel’s pharmaceutical dosage forms and drug delivery systems. 8th ed. Baltimore (MD): Lippincott Williams & Wilkins; 2005. p. 336–384.
   Google Scholar
• Acree WE Jr. Mathematical representation of thermodynamic properties: part 2. Derivation of the combined nearly ideal binary solvent (NIBS)/Redlich-Kister mathematical representation from a two-body and three-body interactional mixing model. Thermochim Acta. 1992;198:71–79.
   Web of Science ®Google Scholar
• Jouyban-Gharamaleki A, York P, Hanna M, et al. Solubility prediction of salmeterol xinafoate in water-dioxane mixtures. Int J Pharm. 2001;216:33–41.
   PubMed Web of Science ®Google Scholar
• Abbasi M, Martinez F, Jouyban A. Prediction of deferiprone solubility in aqueous mixtures of ethylene glycol, propylene glycol and polyethylene glycol 400 at various temperatures. J Mol Liq. 2014;197:171–175.
   Web of Science ®Google Scholar
• Jouyban A, Acree WE Jr. Mathematical derivation of the Jouyban-Acree model to represent solute solubility data in mixed solvents at various temperatures. J Mol Liq. 2018;256:541–547.
   Web of Science ®Google Scholar
• Jouyban A, Khoubnasabjafari M, Chan HK, et al. Mathematical representation of solubility of amino acids in binary aqueous-organic solvent mixtures at various temperatures using Jouyban-Acree model. Pharmazie. 2006;61:789–792.
   PubMed Web of Science ®Google Scholar
• Jouyban A, Soltanpour S, Soltani S, et al. Prediction of drug solubility in mixed solvents using computed Abraham parameters. J Mol Liq. 2009;146:82–88.
   Web of Science ®Google Scholar
• Acree WE Jr, Grubbs LM, Abraham MH. Prediction of partition coefficients and permeability of drug molecules in biological systems with Abraham model solute descriptors derived from measured solubilities and water-to-organic solvent partition coefficients. New York: InTech Publisher; 2012. p. 100–102.
   Google Scholar
• Rahimpour E, Jouyban A, Acree WE Jr. Comment on. Measurement and correlation of the solubility of 2,6-dihydroxybenzoic acid in alcohols and binary solvents. J Chem Eng Data. 2018;63:2329–2331.
   Web of Science ®Google Scholar
• Mikhail SZ, Kimel WR. Densities and viscosities of methanol-water mixtures. J Chem Eng Data. 1961;6:533–537.
   Google Scholar
• Ruidiaz MA, Martínez F. Volumetric properties of the pharmaceutical model cosolvent system 1,4-dioxane + water at several temperatures. Vitae Rev Fac Quím Farm. 2009;16:327–337.
   Web of Science ®Google Scholar