The ornidazole drug substance presents melt at approximately 90 °C (ΔT = 85–98 °C), which is critical for its use on pharmaceutical manufacturing process. This work aimed the thermal characterization of ornidazole raw-material synthesized by three different manufacturers from India, China, and Italy, using the thermoanalytical techniques of DTA, DSC, and TG, besides the verification of its stability and compatibility as a solid pharmaceutical product by the analysis of its binary mixtures (BM) with excipients and a tablet formulation. The characterization includes the thermal decomposition kinetic investigation by Ozawa model using Arrhenius equation and drug purity determination by Van't Hoff equation. The DSC purity determination and precision were compared with results from UV–Vis spectrophotometric and liquid chromatography, showing an adequate correlation before being recommended as a general method for purity assay. The drug raw-materials presented similar quality and zero-order kinetic behavior, besides showing differences on thermal stability. The drug presented compatibility with the tested excipients since the BM studied presented melting at the same temperature range as the drug and a decomposition temperature similar to the drug for two of the BM, and at a higher temperature for the others three of the BM evaluated, which presented excipients with higher molecular structure, capable of spatial coating on the small drug molecule promoting a physical interaction pharmaceutical acceptable. The tablet was processed by wet granulation and compressed under normal conditions of pressure and temperature, maintaining the physical properties of solid drug approving the manufacturing process used. In this study, the thermal analysis was used with success as an alternative method to characterize, quantify, and perform a preformulation study.
1. Özkan, AS, Senturk, Z, Biryol, I 1997 Determination of ornidazole in pharmaceutical dosage forms based on reduction at an activated glassy carbon electrode. Int J Pharm 157 2 137–144 .
2. Wang, MH, Tan, ZC, Sun, XH, Xu, F, Liu, YF, Sun, LX, Zhang, T 2004 Heat capacity and thermodynamic properties of crystalline ornidazole (C7H10ClN3O3). Thermochim Acta 414:25–30 .
3. Singh, P, Mittal, R, Sharma, GC, Singh, S, Singh, A 2003 Ornidazole. Profiles Drug Subst Excip Relat Methodol 30:123–184 .
4. Rossignol, JF, Maisonneuve, H, Cho, YW 1984 Nitroimidazoles in the treatment of trichomoniasis, giardiasis, and amebiasis. Int J Clin Pharmacol Ther Toxicol 6 22 63–72.
5. Araújo, AAS, Storpirtis, S, Mercuri, LP, Carvalho, MFS, Filho, MS, Matos, JR 2003 Analysis of the antiretroviral zidovudine (AZT) and evaluation of the compatibility with excipients used in solid dosage forms. Int J Pharm 260 2 303–314 .
6. Giron, DJ Microcalorimetry and combined techniques for the study of pharmaceuticals. J Therm Anal Calorim 1999 56 3 1285–1304 .
7. Macêdo, RO, Souza, AG, Macêdo, AMC 1997 Comparative studies on some analytical methods. J Therm Anal Calorim 49:937–941 .
8. Silvia, RMF, Medeiros, FPM, Nascimento, TG, Macêdo, RO, Rolim-Neto, PJ 2009 Thermal characterization of indinavir sulfate using TG, DSC and DSC-photovisual. J Therm Anal Calorim 95 3 965–968 .
9. Schimidt, AC 2005 Solid-state characterization of chloroprocaine hydrochloride. Part VI. Crystal polymorphism of local anaesthetic drugs. J Therm Anal Calorim 81:291–297 .
10. Kanaze, FI, Kokkalou, E, Niopas, I, Georgarakis, M, Stergiou, A, Bikiares, D 2006 Thermal analysis study of flavonoid solid dispersions having enhanced solubility. J Therm Anal Calorim 83 2 283–292 .
11. Souza, FS, Gomes, APB, Macedo, RO 2001 Characterisation of starch pharmaceuticals for DSC coupled to the photovisual system. J Therm Anal Calorim 64:739–743 .
12. Gomes, APB, Pinto, LP, Simões, MOS, Macedo, RO 2007 Development thermogravimetric method to quantitative determination of Mebendazole. J Therm Anal Calorim 87:919–925 .
13. Glass, BD, Novák, CS, Brown, ME 2004 The thermal and photostability of solid pharmaceuticals: a review. J Therm Anal Calorim 77:1013–1036 .
14. Marciniec, B, Kozak, M, Dettlaff, K 2004 Thermal analysis in evaluation of the radiochemical stability of some fungicidal drugs. J Therm Anal Calorim 77:305–317 .
15. Cervantes, NAB, Medeiros, ACD, Santos, AFO, Macedo, RO 2003 Thermal stability of Metronidazole drug and tablets. J Therm Anal Calorim 72:535–538 .
16. Basu, P, Alexander, KS, Riga, A 2006 A statistical model for the optimization of DSC performance in the evaluation of drugs for preformulation studies. J Therm Anal Calorim 83:19–22 .
17. Oliveira, GGG, Ferraz, H, Matos, JSR 2005 Thermoanalytical study of glibenclamide and excipients. J Therm Anal Calorim 79:267–270 .
18. Nascimento, TG, Basílio-Júnior, ID, Macêdo, RO, Moura, EA, Dornelas, CB, Bernardo, VB, Rocha, VN, Nóvak, C 2009 Characterization of the indinavir raw materials stability in some pharmaceutical processes. J Therm Anal Calorim 98:13–19 .
19. Ozawa, T Kinetics of non-isothermal crystallization. Polymer 1971 12:150–158 .
20. Sovizi MR . Thermal behavior of drugs: investigation on decomposition kinetic of naproxen and celecoxib. J Therm Anal Calorim. 2010. doi: .
21. Ford, JL, Timmins, P 1989 Pharmaceutical thermal analysis: techniques and applications Ellis Horwood Limited England.
22. Soares, MFR, Soares-Sobrinho, JL, Grangeiro-Júnior, S, Silva, KER, Rolim-Neto, PJ 2008 Métodos de determinação do ornidazol em comprimidos revestidos: desenvolvimento, validação e comparação estatística. Lat Am J Pharm 27 5 688–694.