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A Proton Magnetic Resonance Study of Fexofenadine/β-Cyclodextrin Inclusion Complexes in Aqueous Solution

  • Published : 2005.12.20

Abstract

Keywords

References

  1. Simpson, K.; Jarvis, B. Drugs 2000, 59, 301 https://doi.org/10.2165/00003495-200059020-00020
  2. Bender, M. L.; Komiyama, M. Cyclodextrin Chemistry; Springer Verlag: New York, 1978; pp 1
  3. Saenger, W. Angew. Chem. Int. Ed. Engl. 1980, 19, 344 https://doi.org/10.1002/anie.198003441
  4. Szejtli, J. Cyclodextrin Technology; Kluwer: Dordrecht, 1988; pp 450
  5. Vogtle, F. Supramolecular Chemistry: An Introduction; John Wiley & Sons Ltd: New York, 1991
  6. Wenz, G. Angew. Chem. Int. Ed. Engl. 1994, 33, 803 https://doi.org/10.1002/anie.199408031
  7. Esclusa-Diaz, M. T.; Gayo-Otero, M.; Perez-Marcos, M. B.; Villa- Jato, J. L. Int. J. Pharm. 1996, 142, 183 https://doi.org/10.1016/0378-5173(96)04666-2
  8. Obaidat, A. A.; Matalgah, S. M.; Najib, N. M. Acta Pharm. 2002, 52, 9
  9. Torres-Labandeira, J. J.; Blanco-Mendez, J.; Villa-Jato, J. L. STP Pharm. Sci. 1994, 4, 235
  10. Szejtli, J. Med. Res. Rev. 1994, 14, 353 https://doi.org/10.1002/med.2610140304
  11. Schneider, H.-J.; Hacket, F.; Rudiger, V.; Ikeda, H. Chem. Rev. 1998, 98, 1755 and references cited therein https://doi.org/10.1021/cr970019t
  12. Rekharsky, M. V.; Goldberg, R. N.; Schwarz, F. P.; Tewari, Y. B.; Ross, P. D.; Yamashoji, Y.; Inoue, Y. J. Am. Chem. Soc. 1995, 117, 8830 https://doi.org/10.1021/ja00139a017
  13. Nakajima, T.; Sunagawa, M.; Hirohashi, T.; Fujioka, F. Chem. Pharm. Bull. Jpn. 1984, 32, 400
  14. Qi, Z. H.; Mak, V.; Diaz, L.; Grant, D. M.; Chang, C. J. Org. Chem. 1991, 56, 1537 https://doi.org/10.1021/jo00004a037
  15. Neuhaus, D.; Williamson, M. In The Nuclear Overhauser Effect in Structural and Conformational Analysis; VCH Publishers: New York, 1989; p 1
  16. Szejtli, J. Chem. Rev. 1998, 98, 1743 https://doi.org/10.1021/cr970022c
  17. Ali, S. M.; Maheshwari, A.; Asmat, F. Pharmazie 2004, 59, 653
  18. Ali, S. M.; Asmat, F.; Maheshwari, A. IL Farmaco 2004, 59, 835 https://doi.org/10.1016/j.farmac.2004.05.009
  19. Fronza, G.; Mele, A.; Redenti, E.; Ventura, P. J. Pharm. Sci. 1992, 81, 1162 https://doi.org/10.1002/jps.2600811206
  20. Yoshida, N. J. Chem. Soc. Perk. Trans. 2 1995, 2249

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