Solubility of sulfapyridine in propylene glycol plus water mixtures and correlation with the Jouyban-Acree model

被引:69
作者
Delgado, Daniel R. [1 ]
Rodriguez, Gerson A. [1 ]
Holguin, Andres R. [1 ]
Martinez, Fleming [1 ]
Jouyban, Abolghasem [2 ,3 ]
机构
[1] Univ Nacl Colombia, Fac Ciencias, Dept Farm, Grp Invest Farmaceut Fis Quim, Bogota 14490, DC, Colombia
[2] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz 51664, Iran
[3] Tabriz Univ Med Sci, Fac Pharm, Tabriz 51664, Iran
关键词
Sulfapyridine; Propylene glycol plus water mixtures; Solubility; Solution thermodynamics; Activity coefficients; Jouyban-Acree model; FLUPHENAZINE DECANOATE SOLUBILITY; ENTHALPY-ENTROPY COMPENSATION; SOLUTION THERMODYNAMICS; COSOLVENT MIXTURES; MATHEMATICAL REPRESENTATION; PREFERENTIAL SOLVATION; 200+WATER MIXTURES; SOLVENT MIXTURES; ETHANOL; TEMPERATURES;
D O I
10.1016/j.fluid.2012.12.017
中图分类号
O414.1 [热力学];
学科分类号
070201 [理论物理];
摘要
The solubility of sulfapyridine (SP) in propylene glycol + water mixtures was determined at temperatures from 293.15 K to 313.15 K. The solubility was maximal in pure propylene glycol and minimum in pure water at all the temperatures. The thermodynamic functions; Gibbs energy, enthalpy, and entropy of solution were obtained from these solubility data by using the van't Hoff and Gibbs equations. Thermodynamic quantities of mixing were also calculated by using calorimetric values related to drug fusion process. A nonlinear enthalpy-entropy relationship was observed from a plot of enthalpy vs. Gibbs energy of solution. The plot of Delta H-soln degrees vs. Delta(soln)G degrees shows two different trends, one with negative slope from pure water up to 0.30 mass fraction of propylene glycol and the other one positive beyond this composition up to pure propylene glycol. Accordingly, the driving mechanism for SP solubility in water-rich mixtures is the entropy, probably due to water-structure loss around the drug non-polar moieties by effect of propylene glycol, whereas, above 0.30 mass fraction of propylene glycol the driving mechanism is the enthalpy, probably due to SP solvation increase by the co-solvent molecules. This behavior is similar to the one exhibited by sulfanilamide, sulfamethizole and other drugs in the same co-solvent mixtures. The Generated solubility data were calculated (correlated and/or predicted) with the Jouyban-Acree model in which the mean percentage deviation (MPD) of the correlated and predicted data were 9.3 +/- 8.6%, and 12.1 +/- 9.9%, respectively. The corresponding MPDs for the correlated and predicted solubilities using the log-linear model were 25.1 +/- 19.8%, and 55.1 +/- 32.4%. The density of saturated solutions was predicted using a previously trained model. The Delta H-soln degrees and Delta(soln)G degrees values were also correlated using a proposed model. (C) 2012 Elsevier B.V. All rights reserved.
引用
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页码:86 / 95
页数:10
相关论文
共 49 条
[2]
Almanza F, 2012, LAT AM J PHARM, V31, P427
[3]
[Anonymous], US PHARMACOPEIA
[4]
[Anonymous], 2005, REMINGTON SCI PRACTI
[5]
[Anonymous], 1981, TECHNIQUES SOLUBILIZ
[6]
ATTWOOD D., 2002, PHARM SCI DOSAGE FOR, V2nd
[7]
Barton A.F. M., 2017, CRC Handbook of Solubility Parameters and Other Cohesion Parameters, VSecond
[8]
Bevington P. R., 1969, DATA REDUCTION ERROR
[9]
Budavari S., 2001, The Merck Index, An Encyclopedia of Chemicals, Drugs, and Biologicals, V13th
[10]
Enthalpy-entropy compensation for the solubility of drugs in solvent mixtures: Paracetamol, acetanilide, and nalidixic acid in dioxane-water [J].
Bustamante, P ;
Romero, S ;
Pena, A ;
Escalera, B ;
Reillo, A .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 87 (12) :1590-1596