Prediction of drug solubility in ethanol-ethyl acetate mixtures at various temperatures using the Jouyban-Acree model

Journal of Drug Delivery Science and Technology

Volumn 17, Issue 2, 2007, Pages 159-160

  Jouyban, A ^a   Acree Jr , W E ^b  

^a TABRIZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b UNIVERSITY OF NORTH TEXAS   (United States)

Author keywords

Ethanol ethyl acetate; Jouyban Acree model; Maximum solubility; Optimized solvent composition; Solubility prediction

Indexed keywords

ACETIC ACID ETHYL ESTER; ALCOHOL; SOLVENT;

ARTICLE; DRUG SOLUBILITY; MATHEMATICAL COMPUTING; MATHEMATICAL MODEL; PREDICTION; SCORING SYSTEM; SOLUBILIZATION; TEMPERATURE MEASUREMENT;

EID: 34247150611     PISSN: 17732247     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1773-2247(07)50025-0     Document Type: Article

References (17)

1. Jouyban A., Chew N.Y.K., Chan H.K., Sabour M., Acree Jr. W.E. - A unified cosolvency model for calculating solute solubility in mixed solvents. - Chem. Pharm. Bull., 53, 634-637, 2005.
2. Jouyban-Gharamaleki A., Valaee L., Barzegar-Jalali M., Clark B.J., Acree Jr. W.E.- Comparison of various cosolvency models for calculating solute solubility in water-cosolvent mixtures. - Int. J. Pharm., 177, 93-101, 1999.
3. Jouyban-Gharamaleki A., Barzegar-Jalali M., Acree Jr. W.E.-Solubility correlation of structurally related drugs in binary solvent mixtures. - Int. J. Pharm., 166, 205-209, 1998.
4. Jouyban-Gharamaleki A., Acree Jr.W.E.-Comparison of models for describing multiple peaks in solubility profiles. - Int. J. Pharm., 167, 177-182, 1998.
5. Jouyban A., Clark B.J.- Describing solubility of polymorphs in mixed solvents by CNIBS/R-K equation. - Pharmazie, 57, 861-862, 2002.
6. Jouyban A., Khoubnasabjafari M., Acree Jr.W.E.-Mathematical representation of solubility of amino acids in binary aqueous-organic solvent mixtures at various temperatures using the Jouyban-Acree model. - Pharmazie, 61, 789-792, 2006.
7. Khoubnasabjafari M., Jouyban A., Acree Jr. W.E.- Mathematical representation of solubility of electrolytes in binary solvent mixtures using Jouyban-Acree model. - Chem. Pharm. Bull., 53, 1591-1593, 2005.
8. Jouyban A., Chew N.Y.K., Chan H.K., Khoubnasabjafari M., Acree Jr. W.E.- Solubility prediction of salicylic acid in water-ethanol-propylene glycol mixtures using the Jouyban-Acree model. - Pharmazie, 61, 318-321, 2006.
9. Jouyban A.- In silico prediction of drug solubility in water-dioxane mixtures using Jouyban-Acree model. - Pharmazie, in press, 2006.
10. Acree Jr. W.E.- Model for solubility estimation in mixed solvent systems - Comments. - Int. J. Pharm., 127, 27-30, 1996.
11. Pena M.A., Reillo A., Escalera B., Bustamante P.- Solubility parameter of drugs for predicting the solubility profile type of a wide polarity range in solvent mixtures. - Int. J. Pharm., 321, 155-161, 2006.
12. Bustamante P., Navarro J., Romero S., Escalera B.- Thermodynamic origin of the solubility profile of drugs showing one or two maxima against the polarity of aqueous and nonaqueous mixtures: Niflumic acid and caffeine. - J. Pharm. Sci., 91, 874-883, 2002.
13. Romero S., Escalera B., Bustamante P.- Solubility behavior of polymorphs I and II of mefenamic acid in solvent mixtures. - Int. J. Pharm., 178, 193-202, 1999.
14. Jouyban A., Romero S., Chan H.K., Clark B.J., Bustamante P.- A cosolvency model to predict solubility of drugs at several temperatures from a limited number of solubility measurements. - Chem. Pharm. Bull., 50, 594-599, 2002.
15. Romero S., Reillo A., EscaleraA B., Bustamante P.- The behaviour of paracetamol in mixtures of aprotic and amphiprotic-aprotic solvents. Relationship of solubility curves to specific and nonspecific interactions. - Chem. Pharm. Bull., 44, 1061-1066, 1996.
16. Bustamante P., Ochoa R., Reillo A., Escalera J.B.-Chameleonic effect of sulfanilamide and sulfamethazine in solvent mixtures - solubility curves with 2 maxima. - Chem. Pharm. Bull., 42, 1129-1133, 1994.
17. Escalera J.B., Bustamante P., Martin A.-Predicting the solubility of drugs in solvent mixtures - multiple solubility maxima and the chameleonic effect. - J. Pharm. Pharmacol., 46, 172-176, 1994.