Quantitative Prediction of the Suppression of Drug-Induced Hemolysis by Cyclodextrins from Surface Tension Data

Langmuir

Volumn 15, Issue 2, 1999, Pages 594-599

  Funasaki, Noriaki ^a   Ohigashi, Mariko ^a   Hada, Sakae ^a   Neya, Saburo ^a  

^a KYOTO PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD; CHLORINE COMPOUNDS; COMPOSITION EFFECTS; DIMERS; DRUG PRODUCTS; SURFACE TENSION;

CHLORPROMAZINE HYDROCHLORIDE; CYCLODEXTRIN; HEMOLYSIS;

AROMATIC POLYMERS;

EID: 0032785498     PISSN: 07437463     EISSN: None     Source Type: Journal    
DOI: 10.1021/la980643g     Document Type: Article

References (25)

1. Szejtli, J. Cyclodextrin Technology; Kluwer Academic Publishers: Dordrecht, The Netherlands, 1988; Chapters 1 and 3.
2. Bender, M. L.; Komiyama, M. Cyclodextrin Chemistry; Springer-Verlag: Berlin, 1978; Chapters 2 and 3.
3. Saenger, W. Angew, Chem., Int. Ed. Engl. 1980, 19, 344.
4. Connors, K. A. Chem. Rev. 1997, 97, 1325.
5. Frǒmming, K.-H.; Szejtli, J Cyclodextrins in Pharmacy; Kluwer Academic Publishers: Dordrecht, The Netherlands, 1994; Chapters 3, 6, and 10.
6. Ohtani, Y.; Irie, T.; Uekama, K.; Fukunaga, K.; Pitha, J. Eur. J. Biochem. 1989, 186, 17.
7. Ishikawa, S.; Neya, S.; Funasaki, N. J. Phys. Chem. 1998, 102, 2502.
8. Funaiaki, N.; Uemura, Y.; Hada, S.; Neya, S. J. Phys. Chem. 1996, 100, 16298.
9. Funasaki, N.; Hada, S.; Paiement, J. J. Phys. Chem. 1991, 95, 4131.
10. Attwood, D.; Florence, A. T. Surfactant Systems; Chapman and Hall: London, 1983; Chapter 4.
11. Furmsaki, N. Adv. Colloid Interface Sci. 1993, 43, 87. Funasaki, N.; Hada, S.; Neya, S. Trends Phys. Chem. 1997, 6, 253.
12. Furmsaki, N. Adv. Colloid Interface Sci. 1993, 43, 87. Funasaki, N.; Hada, S.; Neya, S. Trends Phys. Chem. 1997, 6, 253.
13. Seeman, P. Pharmacol. Rev. 1972, 24, 583.
14. Uekama, K.; Irie, T.; Sunada, M.; Otagiri, M.; Iwasaki, K.; Okano, Y.; Miyata, T.; Kase, Y. J. Pharm. Pharmacol. 1981, 33, 707.
15. Otagiri, M.; Uekama, K.; Ikeda, K. Chem. Pharm. Bull. 1975, 23, 188.
16. Uekama, K.; Irie, T. Chem. Lett. 1978, 1109.
17. Takamura, K.; Inoue, S.; Kusu, F. Chem. Lett. 1983, 233.
18. Funasaki, N.; Uemura, Y.; Hada, S.; Neya, S. Langmuir 1996, 12, 2214.
19. Funasaki, N.; Yodo, H.; Hada, S.; Neya, S. Bull. Chem. Soc. Jpn. 1992, 65, 1323, and references therein.
20. Dharmawardana, U. R.; Christian, S. D.; Tucker, E. E.; Taylor, R. W.; Scamehom, J. F. Langmuir 1993, 9, 2258.
21. Fujii, T.; Sato, T.; Tamura, A.; Wakatsuki, M.; Kanaho, Y. Biochem. Pharmacol. 1979, 28, 613.
22. We have used the binding constants defined by the molarity of each species, but those values defined by the mole fraction are better thermodynamically (see ref 22). This difference in concentration units influences the absolute values for the standard free energy and entropy of complexation, but we are not concerned with these thermodynamic values in the present work. The standard enthalpy of complexation is independent of these concentration units.
23. Gurney, R. W. Ionic Processes in Solution; McGraw-Hill: New York, 1953; Chapters 5 and 6.
24. Cramer, F.; Saenger, W.; Spatz, H. C. J. Am. Chem. Soc. 1967, 89, 14.
25. Attwood, D.; Waigh, R.; Blundell, R.; Bloor, D.; Thévand, A.; Boitard, E. Dubès, J.-B.; Tachoire, H. Magn. Reson. Chem. 1994, 32, 468.