[1] S.L. Childs, P.A. Wood, N. Rodríguez-Hornedo, L.S. Reddy, K.I. Hardcastle, Analysis of 50 Crystal structures containing carbamazepine using the Materials Module of Mercury CSD, Cryst. Growth Des. 9(4) (2009) 1869-1888. [2] A.L. Grzesiak, M.D. Lang, K. Kim, A.J. Matzger, Comparison of the four anhydrous polymorphs of carbamazepine and the crystal structure of form I, J. Pharm. Sci. 92(11) (2003) 2260-2271. [3] M.D. Lang, J.W. Kampf, A.J. Matzger, Form IV of carbamazepine, J. Pharm. Sci. 91(4) (2002) 1186-1190. [4] Y. Kobayashi, S. Ito, S. Itai, K. Yamamoto, Physicochemical properties and bioavailability of carbamazepine polymorphs and dihydrate, Int. J. Pharm. 193(2) (2000) 137-146. [5] H.Y. Qu, M. Louhi-Kultanen, J. Kallas, Solubility and stability of anhydrate/ hydrate in solvent mixtures, Int. J. Pharm. 321(1-2) (2006) 101-107. [6] H.Y. Qu, M. Louhi-Kultanen, J. Kallas, Additive effects on the solvent-mediated anhydrate/hydrate phase transformation in a mixed solvent, Cryst. Growth Des. 7(4) (2007) 724-729. [7] D. Murphy, F. Rodríguez-Cintrón, B. Langevin, R.C. Kelly, N. RodríguezHornedo, Solution-mediated phase transformation of anhydrous to dihydrate carbamazepine and the effect of lattice disorder, Int. J. Pharm. 246(2002) 121-134. [8] W.J. Lu, L.P. Dang, S. Black, H.Y. Wei, Solubility of carbamazepine (Form III) in different solvents from (275 to 343) K, J. Chem. Eng. Data. 53(2008) 2204-2206. [9] J.A. Dean, Lange’s Handbook of Chemistry, 13th ed., McGraw-Hill, New York, USA, 1985. [10] A. Apelblat, E. Manzurola, Solubilities of L-aspartic, DL-aspartic, DL-glutamic, p-hydroxybenzoic, o-anisic, p-anisic, and itaconic acids in water from T = 278 K to T = 345 K, J. Chem. Thermodyn. 29(1997) 1527-1533. [11] H. Buchowski, A. Ksiazczak, S. Pietrzyk, Solvent activity along a saturation line and solubility of hydrogen-bonding solids, J. Phys. Chem. 84(1980) 975-979. [12] Y. Wang, W.F. Ge, M.M. Wang, X.Q. Wang, Studies on dissolution equilibrium of chlorfenapyr in five mono-solvents and two mixed solvents ranging from 288.15 to 328.15K, Fluid Phase Equilib. 514(2020) 112560. [13] D. Li, R.Y. He, K.P. Yang, J. Sha, Y.M. Wan, Y. Li, X.D. Yao, T. Li, B.Z. Ren, Thermodynamic studies of thiamethoxam in nine pure solvents and one mixed solvent, solubility and correlation ranged from 278.15 to 323.15 K, J. Chem. Thermodyn. 146(2020) 106116. [14] L.F. Ning, X.F. Gong, P. Li, X.F. Chen, H.P. Wang, J. Xu, Measurement and correlation of the solubility of estradiol and estradiol-urea co-crystal in fourteen pure solvents at temperatures from 273.15 K to 318.15 K, J. Mol. Liq. 304(2020) 112599. [15] X.Y. Hao, X.R. Wu, G.P. Shen, L.F. Wen, H.C. Li, Q. Huang, Thermodynamic models for determination of the solubility of (-)-shikimic acid in different pure solvents and in (H2O+ethanol) binary solvent mixtures, J. Chem. Thermodyn. 88(2015) 8-14. [16] Y. Cheng, Z.H. Wang, S.Z. Ding, J.C. Li, Determination and correlation of the solubility of tricin in water and ethanol mixtures, J. Chem. Thermodyn. 89(2015) 89-92. [17] T. Li, Z.X. Jiang, F.X. Chen, B.Z. Ren, Solubilities of d -xylose in water +(acetic acid or propionic acid) mixtures at atmospheric pressure and different temperatures, Fluid Phase Equilib. 65(2013) 7-10. [18] Y.M. Wan, H.X. He, P.S. Zhang, Z.B. Huang, R. Zhao, J. Sha, T. Li, B.Z. Ren, Solidliquid equilibrium solubility and thermodynamic properties of cis-5-norbornene-endo-2,3-dicarboxylic anhydride in fourteen pure solvents and three binary solvents at various temperatures, J. Mol. Liq. 297(2020) 111396. [19] W.E. Acree, Mathematical representation of thermodynamic properties. Part 2. Derivation of the combined nearly ideal binary solvent (NIBS)/Redlich-Kister mathematical representation from a two-body and three-body interactional mixing model, Thermochim. Acta 198(1992) 71-79. [20] W.E. Acree, Comments concerning ‘model for solubility estimation in mixed solvent systems’, Int. J. Pharm. 127(1996) 27-30. [21] M. Barzegar-Jalali, E.M.H. Agha, K. Adibkia, F. Martinez, A. Jouyban, The solubility of ketoconazole in binary carbitol + water mixtures at T = (293.2-313.2) K, J. Mol. Liq. 297(2020) 111756. [22] J.Q. Zhu, Y.S. Yu, C.H. He, Calculation of solid’s solubilities in mixed liquid solvents by the kh equation using mixing rules, Fluid Phase Equilib. 155(1) (1999) 85-94. |