Solubility measurement, Hansen solubility parameters and solution thermodynamics of gemfibrozil in different pharmaceutically used solvents

References

• Chen YM, Lin PC, Tang M, et al. Solid solubility of antilipemic agents and micronization of gemfibrozil in supercritical carbon dioxide. J Supercrit Fluids. 2010;52:175–182.
   Web of Science ®Google Scholar
• Ambrus R, Amirzadi NN, Aigner Z, et al. Formulation of poorly water-soluble gemfibrozil applying power ultrasound. Ultarason Sonochem. 2012;19:286–291.
   PubMed Web of Science ®Google Scholar
• American Hospital Formulary Service. AHFS Drug Information® 95, Bethesda, MD, American Society of Health-System Pharmacists, 1995. pp. 1168–1173.
   Google Scholar
• Gennaro AR. ed. Remington: the science and practice of pharmacy, 19th Ed., Vol. II, Eastön, PA, Mack Publishing Co.; 1995. p. 968.
   Google Scholar
• Kasim NA, Whitehouse M, Ramachandran C, et al. Molecular properties of WHO essential drugs and provisional biopharmaceutical classification. Mol Pharmaceutics. 2004;1:85–96.
   PubMed Web of Science ®Google Scholar
• Kersten S, Mandard S, Tan NS, et al. Characterization of the fasting-induced adipose factor FIAF, a novel peroxisome proliferator-activated receptor target gene. J Biol Chem. 2000;275:28488–28493.
   PubMed Web of Science ®Google Scholar
• Loomba RS, Arora R. Fibrates: where are we now? Ther Adv Cardiovasc Dis. 2009;3:91–96.
   PubMedGoogle Scholar
• Fruchart JC, Duriez P. Mode of action of fibrates in the regulation of triglyceride and HDL-cholesterol metabolism. Drugs Today. 2006;42:39–64.
   PubMed Web of Science ®Google Scholar
• Saku K, Gartside PS, Hynd BA, et al. Mechanism of action of gemfibrozil on lipoprotein metabolism. J Clin Invest. 1985;75:1702–1712.
   PubMed Web of Science ®Google Scholar
• Villar AMS, Naveros BC, Campmany ACC, et al. Design and optimization of self-nanoemulsifying drug delivery systems (SNEDDS) for enhanced dissolution of gemfibrozil. Int J Pharm. 2012;431:161–175.
   PubMed Web of Science ®Google Scholar
• Hassan HB, Kata M, Erős I, et al. Preparation and investigation of inclusion complexes containing gemfibrozil and DIMEB. J Incl Phenom Macrocycl Chem. 2004;50:219–225.
   Web of Science ®Google Scholar
• Sami F, Philip B, Pathak K. Effect of auxiliary substances on complexation efficiency and intrinsic dissolution rate of gemfibrozil-βCD complexes. AAPS PharmSciTech. 2010;11:27–35.
   PubMed Web of Science ®Google Scholar
• Hussain T, Waters LJ, Parkes GMB, et al. Microwave processed solid dispersions for enhanced dissolution of gemfibrozil using non-ordered mesoporous silica. Coll Surf A. 2017;520:428–435.
   Google Scholar
• Patel RN, Tbaviskar D, Rajput AR. Development and in-vivo characterization of SMEDDS (self-microemulsifying drug delivery system) for gemfibrozil. Int J Pharm Pharm Sci. 2013;5:793–800.
   Google Scholar
• Bastami Z, Taheri A, Soltanpour S. Formulation, optimization and characterization of gemfibrozil nanocrystals prepared by wet milling technique. Asian J Pharm. 2015;9:19–22.
   Web of Science ®Google Scholar
• Kalam MA, Khan AA, Alshamsan A, et al. Solubility of a poorly soluble immunosuppressant in different pure solvents: measurement, correlation, thermodynamics and molecular interactions. J Mol Liq. 2018;249:53–60.
   Web of Science ®Google Scholar
• Shakeel F, Haq N, Alshehri S, et al. Solubility, thermodynamic properties and solute-solvent molecular interactions of luteolin in various pure solvents. J Mol Liq. 2018;255:43–50.
   Web of Science ®Google Scholar
• Shakeel F, Anwer MK. Dissolution thermodynamics and solubility of silymarin in PEG 400-water mixtures at different temperatures. Drug Develop Ind Pharm. 2015;41:1819–1823.
   PubMed Web of Science ®Google Scholar
• Alhalaweh A, Alzghoul A, Kaialy W. Data mining of solubility parameters for computational prediction of drug-excipient miscibility. Drug Develop Ind Pharm. 2014;40:904–909.
   PubMed Web of Science ®Google Scholar
• Kang X, Wang F, Xie Z, et al. A high performance liquid chromatography method for simultaneous determination of rosiglitazone and gemfibrozil in human plasma. J Chromatogr B. 2009;877:645–648.
   PubMedGoogle Scholar
• Higuchi T, Connors KA. Phase-solubility techniques. Adv Anal Chem Instr. 1965;4:117–122.
   Google Scholar
• Shakeel F, Haq N, Raish M, et al. Solubility and thermodynamic analysis of sinapic acid in various neat solvents at different temperatures. J Mol Liq. 2016;222:167–171.
   Web of Science ®Google Scholar
• Shakeel F, Haq N, Alanazi FK, et al. Thermodynamic modeling for solubility prediction of indomethacin in self-nanoemulsifying drug delivery system (SNEDDS) and its individual components. Drug Develop Ind Pharm. 2014;40:1240–1245.
   PubMed Web of Science ®Google Scholar
• United States Pharmacopeia and National Formulary USP 23–NF 18; The United States Pharmacopeial Convention, Inc.: Rockville, MD, 1994.
   Google Scholar
• Hansen CM. Hansen solubility parameters: a User’s handbook, 2nd ed. Boca Raton, FL, USA: CRC press, Taylor and Francis Group. 2007; p. 544.
   Google Scholar
• Kitak T, Dumicic A, Planinsek O, et al. Determination of solubility parameters of ibuprofen and ibuprofen lysinate. Molecules. 2015;20:21549–21568.
   PubMed Web of Science ®Google Scholar
• Alshehri S, Haq N, Shakeel F. Solubility, molecular interactions and mixing thermodynamic properties of piperine in various pure solvents at different temperatures. J Mol Liq. 2018;250:63–70.
   Web of Science ®Google Scholar
• Ruidiaz MA, Delgado DR, Martínez F, et al. Solubility and preferential solvation of indomethacin in 1,4-dioxane + water solvent mixtures. Fluid Phase Equilib. 2010;299:259–265.
   Web of Science ®Google Scholar
• Hildebrand JH, Prausnitz JM, Scott RL. Regular and related solutions, Van Nostrand Reinhold, New York. 1970.
   Google Scholar
• Manrique YJ, Pacheco DP, Martínez F. Thermodynamics of mixing and solvation of ibuprofen and naproxen in propylene glycol + water cosolvent mixtures. J Solution Chem. 2008;37:165–181.
   Web of Science ®Google Scholar
• Apelblat A, Manzurola E. Solubilities of o-acetylsalicylic, 4-aminosalicylic, 3,5-dinitrosalicylic and p-toluic acid and magnesium-DL-aspartate in water from T=(278–348) K. J Chem Thermodyn. 1999;31:85–91.
   Web of Science ®Google Scholar
• Manzurola E, Apelblat A. Solubilities of L-glutamic acid, 3-nitrobenzoic acid, acetylsalicylic, p-toluic acid, calcium-L-lactate, calcium gluconate, magnesium-DL-aspartate, and magnesium-L-lactate in water. J Chem Thermodyn. 2002;34:1127–1136.
   Web of Science ®Google Scholar
• Holguín AR, Rodríguez GA, Cristancho DM, et al. Solution thermodynamics of indomethacin in propylene glycol + water mixtures. Fluid Phase Equilib. 2012;314:134–139.
   Web of Science ®Google Scholar
• Krug RR, Hunter WG, Grieger RS. Enthalpy-entropy compensation. 2. Separation of the chemical from the statistic effect. J Phys Chem. 1976;80:2341–2351.
   Web of Science ®Google Scholar
• Shakeel F, Haq N, Siddiqui NA. Solubility and thermodynamic function of vanillin in ten different environmentally benign solvents. Food Chem. 2015;180:244–248.
   PubMed Web of Science ®Google Scholar
• Ahad A, Shakeel F, Raish M, et al. Solubility and thermodynamic analysis of antihypertensive agent nitrendipine in different pure solvents at temperature range of 298.15 to 318.15 K. AAPS PharmSciTech. 2017;18:2727–2743.
   PubMed Web of Science ®Google Scholar