DOI QR코드

DOI QR Code

Drug Polymorphism and its Importance on Drug Development Process

  • Received : 2010.09.07
  • Accepted : 2010.10.07
  • Published : 2010.12.20

Abstract

Polymorphism has been recognized to be a critical issue throughout the drug product development process. Most of solid phase drugs have polymorphism, which has generated a great deal of interest and the field has been evolving rapidly. Preferably, thermodynamically most stable form of a drug substance is selected to obtain consistent bioavailability over its shelf life and various storage conditions. Moreover, it has the lowest potential for conversion from one polymorphic form to another. However, metastable or amorphous forms may be used intentionally to induce faster dissolution rate for rapid drug absorption and higher efficacy. For pharmaceutical industry, polymorphism is one of the key activities in form selection process together with salt selection. This article introduces the main features in the investigation of solid form selection especially polymorphic behavior with thermodynamic backgrounds, physicochemical properties with solubility, dissolution, and mechanical properties, and characterization techniques for proper analysis. The final form can be recommended based on the physicochemical and biopharmaceutical properties and by the processability, scalability and safety considerations. Pharmaceutical scientists especially in charge of formulation need to be well aware of the above issues to assure product quality.

Keywords

References

  1. Aguiar, A.J., Krc, J., Kinkel, A.W., Samyn, J.C., 1967. Effect of polymorphism on the absorption of chloramphenicol from chloramphenicol palmitate. J. Pharm. Sci. 56, 847-853. https://doi.org/10.1002/jps.2600560712
  2. Aguiar, A.J., Zelmer, J.E, 1969. Dissolution behavior of polymorphs of chloramphenicol palmitate and mefanamic acid. J. Pharm. Sci. 58, 983-987. https://doi.org/10.1002/jps.2600580817
  3. Beyer, T., Day, G.M., Price, S.L., 2001. The prediction, morphology and mechanical properties of the polymorphs of paracetamol. J. Am. Chem. Soc. 123, 5086-5094. https://doi.org/10.1021/ja0102787
  4. Byrn, S., Pfeiffer, R., Ganey, M., Hoiberg, C., Poochikian, G., 1995. Pharmaceutical solids: A strategic approach to regulatory considerations. Pharm. Res. 12, 945-954. https://doi.org/10.1023/A:1016241927429
  5. Byrn, S.R., Pfeiffer, R.R., Stowell, J.G., 1999. Solid-state chemistry of drugs (2nd ed.). SSCI, Inc., West Lafayette, Indiana.
  6. Bauer, J., Spanton, S., Henry, R., Quick, J., Dziki, W., Porter, W., Morris, J., 2001. Ritonavir: an extraordinary example of conformational polymorphism. Pharm. Res. 18, 859-866. https://doi.org/10.1023/A:1011052932607
  7. Center for Drug Evaluation and Research Guidance: Submitting Supporting Documentation in Drug Applications for the Manufacture of Drug Substances, February 1987.
  8. Chen, X., Morris, K.R., Griesser, U.J., Byrn S.R., Stowell, J.G., 2002. Reactivity differences of indomethacin solid forms with ammonia gas. J. Am. Chem. Soc. 124, 15012-15019. https://doi.org/10.1021/ja017662o
  9. Di Martino, P., Guyot-Hermann, A.M., Conflant, P., Drache, M., Guyot, J.C., 1996. A new pure paracetamol for direct compression: the orthorhombic form. Int. J. Pharm. 128, 1-8. https://doi.org/10.1016/0378-5173(95)04127-3
  10. Giron, D., Grant, D.J.W., 2002. Evaluation of solid-state properties of salts. In Stahl, P.H., Wermuth, C.G. (eds.) Handbook of pharmaceutical salts: properties, selection, and use. Wiley-VCH, Surich, Switzerland, pp 41-81.
  11. Giron, D., 2001. Investigation of polymorphism and pseudo-polymorphism in pharmaceuticals by combined thermoanalytical techniques. J. Therm. Anal. Calorim., 64, 37-60. https://doi.org/10.1023/A:1011572610005
  12. Grant, D.J.W., 1999. Theory and origin of polymorphism. In H. G. Brittain (ed.) Polymorphism in Pharmaceutical Solids. Marcel Dekker, Inc., New York, pp. 1-34.
  13. International Conference on Harmonization Q6A Guideline: Specifications for New Drug Substances and Products: Chemical Substances, October 1999.
  14. Joiris, E., Di Martino, P., Berneron, C., Guyot-Hermann, A.M., Guyot, J.C., 1998. Compression behavior of orthorhombic paracetamol. Pharm. Res. 15, 1122-1130. https://doi.org/10.1023/A:1011954800246
  15. Ku, M.S., 2008. Use of the Biopharmaceutical Classification System in Early Drug Development. AAPS J. 10, 208-212. https://doi.org/10.1208/s12248-008-9020-0
  16. Liebenberg, W., de Villiers, M., Wurster, D.E., Swanepoel, E., Dekker, T.G., Lotter, A.P., 1999. The effect of polymorphism on powder compaction and dissolution properties of chemically equivalent oxytetracycline hydrochloride powders. Drug Dev. Ind. Pharm. 25, 1027-1033. https://doi.org/10.1081/DDC-100102265
  17. Lohani, S., Grant, D.J.W., 2006. Thermodynamics of polymorph. In Hilfiker, R. (ed.) Polymorphism in the pharmaceutical industry. Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany, pp 21-42.
  18. Meyer, M.C., Straughn, A.B., Jarvi, E.J., Wood, G.C., Pelsor, F.R., Shah, V.P., 1992. The bioinequivalence of carbamazepine tablets with a history of clinical failures. Pharm. Res. 9, 1612-1616. https://doi.org/10.1023/A:1015872626887
  19. Nichols, G., Frampton, C.S., 1998. Physicochemical characterization of the orthorhombic polymorph of paracetamol crystallized from solution. J. Pharm. Sci. 87, 684-693. https://doi.org/10.1021/js970483d
  20. Otsuka, M., Hasegawa, H., Matsuda, Y., 1999. Effect of polymorphic forms of bulk powders on pharmaceutical properties of carbamazepine granules. Chem. Pharm. Bull. 47, 852-856. https://doi.org/10.1248/cpb.47.852
  21. Roberts, R.J., Payne, R.S., Rowe, R.C., 2000. Mechanical property predictions for polymorphs of sulphathiazole and carbamazepine. Eur. J. Pharm. Sci. 9, 277-283. https://doi.org/10.1016/S0928-0987(99)00065-2
  22. Singhhal, D., Curatolo, W., 2004. Drug polymorphism and dosage form design: a practical perspective. Adv. Drug Del. Rev. 56, 335-347. https://doi.org/10.1016/j.addr.2003.10.008
  23. Summers, M.P., Enever, R.P., Carless, J.E., 1976. The influence of crystal form on the radial stress transition characteristics of pharmaceutical materials. J. Pharm. Pharmacol. 28, 89-99. https://doi.org/10.1111/j.2042-7158.1976.tb04105.x
  24. Sun, C., Grant, D.J.W., 2001. Influence of crystal structure on the tableting properties of sulfamerazine polymorphs. Pharm. Res. 18, 274-280. https://doi.org/10.1023/A:1011038526805
  25. Young, W.W.L., Suryanarayanan, R., 1991. Kinetics of transition of anhydrous carbamazepine to carbamazepine dihydrate in aqueous suspensions. J. Pharm. Sci. 80, 496-500. https://doi.org/10.1002/jps.2600800519