Solubility–pH profiles of some acidic, basic and amphoteric drugs
Tài liệu tham khảo
Avdeef, 2007, Dissolution and solubility, 5, 399
Avdeef, 2007, Solubility of sparingly-soluble ionizable drugs, Adv. Drug Deliv. Rev., 59, 568, 10.1016/j.addr.2007.05.008
Avdeef, 1998, pH-metric solubility. 1. Solubility–pH profiles from Bjerrum plots. Gibbs buffer and and pKa in the solid state, Pharm. Pharmacol. Commun., 4, 165
Avdeef, 2000, pH-metric solubility. 2: Correlation between the acid-base titration and the saturation shake-flask solubility-pH methods, Pharm. Res., 17, 85, 10.1023/A:1007526826979
Baka, 2008, Study of equilibrium solubility measurement by saturation shake-flask method using hydrochlorothiazide as model compound, J. Pharm. Biomed. Anal., 46, 335, 10.1016/j.jpba.2007.10.030
Bergström, 2004, Accuracy of calculated pH-dependent aqueous drug solubility, Eur. J. Pharm. Sci., 22, 387, 10.1016/j.ejps.2004.04.006
Bevan, 2000, A high-throughput screening method for the determination of aqueous drug solubility using laser nephelometry in microtiter plates, Anal. Chem., 72, 1781, 10.1021/ac9912247
Box, 2006, Equilibrium versus kinetic measurements of aqueous solubility, and the ability of compounds to supersaturate in solution – a validation study, J. Pharm. Sci., 95, 1298, 10.1002/jps.20613
EPA, 1998. EPA Product Properties Test Guidelines, OPPTS 830.7840, Water Solubility: Column Elution Method; Shake Flask Method. OPPTS 830.7840.
Garrido, 2006, Acidity constants in methanol/water mixtures of polycarboxylic acids used in drug salt preparations: Potentiometric determination of aqueous pKa values of quetiapine formulated as hemifumarate, Eur. J. Pharm. Sci., 22, 118, 10.1016/j.ejps.2006.01.005
Grant, 1990, XXI
Hansch, C., Leo, A., Medlin, M.H., 2011. Bio-Loom, BioByte Corp. <http://www.biobyte.com>.
Karickhoff, S., Carreira, L., Hilal, S., 2011. SPARC On-line Calculator. <http://ibmlc2.chem.uga.edu/sparc>.
Kortüm, 1961
Lennernäs, 2005, The use of biopharmaceutic classification of drugs in drug discovery and development: current status and future extension, J. Pharm. Pharmacol., 57, 273, 10.1211/0022357055263
Mosharraf, 1995, Solubility characterization of practically insoluble drugs using the Coulter counter principle, Int. J. Pharm., 122, 57, 10.1016/0378-5173(95)00035-H
Omari, 2006, Effect of buffer species on the inclusion complexation of acidic drug celecoxib with cyclodextrin in solution, J. Inclusion Phenom. Macrocyclic Chem., 55, 247, 10.1007/s10847-005-9041-6
Pan, 2001, Comparison of chromatographic and spectroscopic methods used to rank compounds for aqueous solubility, J. Pharm. Sci., 90, 521, 10.1002/1520-6017(200104)90:4<521::AID-JPS1009>3.0.CO;2-B
Pudipeddi, 2002, Solubility and dissolution of weak acids, bases, and salts, 19
Roy, 1989, Solubility behavior of narcotic analgesics in aqueous-media – solubilities and dissociation-constants of morphine, fentanyl, and sufentanil, Pharm. Res., 6, 147, 10.1023/A:1015932610010
Shoghi, 2009, Kinetic and thermodynamic solubility values of some bioactive compounds, Chem. Biodivers., 6, 1789, 10.1002/cbdv.200900121
Stuart, 2005, Chasing equilibrium: measuring the intrinsic solubility of weak acids and bases, Anal. Chem., 77, 983, 10.1021/ac048767n
Van de Waterbeemd, 2008, Physicochemical properties in drug profiling, 37, 25
Van de Waterbeemd, 2003, Physico-chemical approaches to drug absorption, 18, 1
Völgyi, 2010, Study of pH-dependent solubility of organic bases. Revisit of Henderson–Hasselbalch relationship, Anal. Chim. Acta, 673, 40, 10.1016/j.aca.2010.05.022