Solubility of sulphadiazine in some {Carbitol® (1) + water (2)} mixtures: determination, correlation, and preferential solvation

被引：17

作者：

Osorio, Irmis P. ^{[1
]}

Martinez, Fleming ^{[1
]}

Pena, Maria A. ^{[2
]}

Jouyban, Abolghasem ^{[3
,4
,5
]}

Acree Jr, William E. ^{[6
]}

机构：

[1] Univ Nacl Colombia, Fac Ciencias, Dept Farm, Grp Invest Farmaceut Fisicoquim,Sede Bogota, Bogota, Colombia

[2] Univ Alcala, Fac Farm, Dept Ciencias Biomed, Alcala De Henares, Spain

[3] Tabriz Univ Med Sci, Pharmaceut Anal Res Ctr, Tabriz 51664, Iran

[4] Tabriz Univ Med Sci, Fac Pharm, Tabriz 51664, Iran

[5] Shahid Beheshti Univ Med Sci, Sch Adv Technol Med, Tehran, Iran

[6] Univ North Texas, Dept Chem, Denton, TX 76203 USA

来源：

PHYSICS AND CHEMISTRY OF LIQUIDS | 2021年 / 59卷 / 06期

关键词：

Sulphadiazine; Carbitol® solubility; Jouyban-Acree model; preferential solvation; PLUS WATER MIXTURES; ENTHALPY-ENTROPY COMPENSATION; PREFERENTIAL SOLVATION; SOLUTION THERMODYNAMICS; MATHEMATICAL REPRESENTATION; PREDICT SOLUBILITY; SOLVENT MIXTURES; DRUGS; SULFAMETHAZINE; TEMPERATURES;

D O I：

10.1080/00319104.2020.1858420

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

The mole fraction solubility of sulphadiazine (SD) in {Carbitol (R) (1) + water (2)} binary solvent mixtures at different temperatures from (278.15 to 313.15) K was determined. Solubility values were correlated with the combined nearly ideal binary solvent/Redlich-Kister, modified Wilson and Jouyban-Acree models. Preferential solvation parameters of SD by Carbitol (R) (delta x (1,3)) were derived from their thermodynamic solution properties using the inverse Kirkwood-Buff integrals method. delta x (1,3) values are negative in water-rich mixtures but positive in Carbitol (R) mole fractions higher than 0.12. In the former case is conjecturable that hydrophobic hydration around non-polar groups of SD plays a relevant role in drug solvation.

引用

页码：890 / 906

页数：17

共 68 条

[21] Experimental determination of the temperature dependence of water activities for a selection of aqueous organic solutions
Ganbavale, G.
Marcolli, C.
Krieger, U. K.
Zuend, A.
Stratmann, G.
Peter, T.
[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2014, 14 (18) : 9993 - 10012
[22] GELONE S, 2005, REMINGTON SCI PRACTI, P1630
[23] Hansen C.M., 2007, Hansen Solubility Parameters: A User's Handbook, DOI DOI 10.1201/9781420006834
[24] Higuchi T., 1965, ADV ANAL CHEM INSTRU, V4, P117, DOI DOI 10.1016/S0076-6879(82)87029-8
[25] Solubility and solution thermodynamics of sulfadiazine in polyethylene glycol 400+water mixtures
Jimenez, Daniel M.
Cardenas, Zaira J.
Martinez, Fleming
[J]. JOURNAL OF MOLECULAR LIQUIDS, 2016, 216 : 239 - 245
[26] Solubility temperature dependence and preferential solvation of sulfadiazine in 1,4-dioxane + water co-solvent mixtures
Jimenez, Daniel M.
Cardenas, Zaira J.
Delgado, Daniel R.
Pena, Maria A.
Martinez, Fleming
[J]. FLUID PHASE EQUILIBRIA, 2015, 397 : 26 - 36
[27] Jouyban A, 2006, PHARMAZIE, V61, P789
[28] Jouyban A, 2010, HANDBOOK OF SOLUBILITY DATA FOR PHARMACEUTICALS, P1
[29] A cosolvency model to predict solubility of drugs at several temperatures from a limited number of solubility measurements
Jouyban, A
Romero, S
Chan, HK
Clark, BJ
Bustamante, P
[J]. CHEMICAL & PHARMACEUTICAL BULLETIN, 2002, 50 (05) : 594 - 599
[30] Preferential solvation of apremilast in some (Transcutol® plus water) mixtures
Jouyban, Abolghasem
Acree, William E., Jr.
Martinez, Fleming
[J]. JOURNAL OF MOLECULAR LIQUIDS, 2020, 316

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