[A. A. Noyes and W. R. Whitney, The rate of solution of solid substances in their own solutions, J. Am. Chem. Soc. 19 (1987) 930--934.]Search in Google Scholar
[A. Nokhodchi, N. Bolourtchian and R. Dinarvand, Dissolution and mechanical behaviors of recrystallized carbamazepine from alcohol solution in the presence of additives, J. Cryst. Growth 274 (2005) 573--584; DOI:10.1016/j.jcrysgro.2004.10.158.10.1016/j.jcrysgro.2004.10.158]Search in Google Scholar
[Y. Kobayashi, Sh. Ito, Sh. Itai and K. Yamamoto, Physicochemical properties and bioavailability of carbamazepine polymorphs and dehydrate, Int. J. Pharm. 193 (2000) 137--146; DOI: 10.1016/S0378-5173(99)00315-4.10.1016/S0378-5173(99)00315-4]Search in Google Scholar
[A. L. Grzesiak, M. Lang, K. Kim and A. J. Matzger, Comparison of the four anhydrous polymorphs of carbamazepine and the crystal structure of form I, J. Pharm. Sci. 92 (2003) 2260--2271; DOI: 10.1002/jps.10455.10.1002/jps.10455]Search in Google Scholar
[P. Costa, An alternative method to the evaluation of similarity factor in dissolution testing, Int. J. Pharm. 220 (2001) 77--83; DOI: 10.1016/S0378-5173(01)00651-2.10.1016/S0378-5173(01)00651-2]Search in Google Scholar
[M. M. J. Lowes, M. R. Caira, A. P. Lotter and J. G. Van der Watt, Physicochemical properties and X-ray structural studies of the trigonal polymorph of carbamazepine, J. Pharm. Sci. 76 (1987) 744--752; DOI: 10.1002/jps.2600760914.10.1002/jps.260076091411002813]Search in Google Scholar
[H. Kala, U. Haack, P. Pollandt and G. Brezesinski, Zur Polymorphie des Carbamazepine, Acta Pharm. Technol. 32 (1986) 72--77.]Search in Google Scholar
[F. U. Krahn and J. B. Mielck, Relation between several polymorphic forms and the dehydrate of carbamazepine, Pharm. Acta Helv. 62 (1987) 247--254.]Search in Google Scholar
[R. J. Davey, Solvent Effects in Crystallization Processes, in Current Topics in Materials Science (Ed. R. J. Davey), North-Holland Publishing Co., New York 1982, p. 8.]Search in Google Scholar
[V. L. Himes, A. D. Mighell and W. H. De Camp, Structure of carbamazepine 5H-dibenz[b, f]azepine-5-carboxamide, Acta Crystallogr. B 37 (1981) 2242--2245.10.1107/S0567740881008522]Search in Google Scholar
[G. S. Banker and N. R. Anderson, Tablets, in The Theory and Practice of Industrial Pharmacy (Eds. L. Lachman, H. Lieberman and J. Kanig), 3rd ed., Lea & Febiger, Philadelphia 1986, pp. 316--317.]Search in Google Scholar
[A. K. Tiwary, Crystal Habit Changes and Dosage Form Performance, in Encyclopedia of Pharmaceutical Technology (Eds. J. Swarbick and J. C. Boylan), 2nd ed., Informa Health Care, New York 2004, pp. 73--74.]Search in Google Scholar
[G. Alderborn, Particle Dimensions, in Pharmaceutical Powder Compaction Technology (Eds. G. Alderborn and C. Nystrom), Marcel Dekker, New York 1996, pp. 245--282.10.1201/9780367803971]Search in Google Scholar
[G. Alderborn and C. Nystrom, Studies on direct compression of tablets. IV. The effect of particle size on the mechanical strength of tablets, Acta Pharm. Suec. 19 (1982) 381--390.]Search in Google Scholar