参考文献:1. Ivandini, T.A., Sarada, B.V., Terashima, C., Rao, T.N., Tryk, D.A., Ishiguro, H., Kubota, Y.A., and Fujishima, A., / J. Electroanal. Chem., 2002, vol. 521, nos. 1-, p. 117. CrossRef 2. Foglia, J.P., Sorisio, D., and Perel, J.M., / J. Chromatogr., B, 1991, vol. 572, nos. 1-, p. 247. CrossRef 3. Hu, L., Liu, Y., and Cheng, S., / J. Chromatogr. Sci., 2011, vol. 49, no. 2, p. 124. CrossRef 4. Yoo, S.D., Holladay, J.W., Fincher, T.K., and Dewey, M.J., / J. Chromatogr. B, 1995, vol. 668, no. 2, p. 338. CrossRef 5. Wozniakiewicz, M., Wietecha-Posluszny, R., Garbacik, A., and Koscielniak, P., / J. Chromatogr. A, 2008, vol. 1190, nos. 1-, p. 52. CrossRef 6. Cruz-Vera, M., Lucena, R., Cardenas, S., and Valcarcel, M., / J. Chromatogr. B, 2007, vol. 857, no. 2, p. 275. CrossRef 7. Bouquet, S., Guyon, S., Chapelle, G., Perault, M.C., and Barthes, D., / J. Liq. Chromatogr., 1992, vol. 15, no. 11, p. 1993. CrossRef 8. Koyama, E., Kikuchi, Y., Echizen, H., Chiba, K., and Ishizaki, T., / Therap. Drug Monitor., 1993, vol. 15, no. 3, p. 224. CrossRef 9. Messiha, F.S., / Alcohol, 1986, vol. 3, no. 2, p. 135. CrossRef 10. Virgili, P. and Henry, J.A., / J. Chromatogr. B, 1989, vol. 496, p. 228. CrossRef 11. Suckow, R.F. and Cooper, T.B., / J. Pharm. Sci., 1981, vol. 70, no. 3, p. 257. CrossRef 12. Reece, P.A., Zacest, R., and Barrow, C.G., / J. Chromatogr., 1979, vol. 163, no. 3, p. 310. CrossRef 13. Hussein, S.A., El-Kommos, M.E., Hassan, H.Y., and Mohamed, A.I., / Talanta, 1989, vol. 36, no. 9, p. 941. CrossRef 14. Wang, J., Golden, T., Ozsoz, M., and Lu, Z., / Bioelectrochem. Bioenerg., 1990, vol. 23, no. 3, p. 217. CrossRef 15. Rekharsky, M.V. and Inoue, Y., / Chem. Rev., 1998, vol. 98, no. 5, p. 1875. CrossRef 16. Bader, M., / J. Chem. Educ., 1980, vol. 57, no. 10, p. 703. CrossRef 17. Dodziuk, H., / Cyclodextrins and Their Complexes, Weinheim: Wiley, 2006. CrossRef 18. Singh, M., Sharma, R., and Banerjee, U.C., / Biotech. Adv., 2002, vol. 20, no. 5, p. 341. CrossRef 19. Ingle, J.D. and Crouch, S.R., / Spectrochemical Analysis, Englewood Cliffs: Prentice Hall, 1988. 20. Nicely, V.A. and Dye, J.L., / J. Chem. Educ., 1971, vol. 48, no. 7, p. 443. CrossRef
作者单位:Fahimeh Jalali (1) Negin Ezzati (1)
1. Department of Chemistry, Razi Universit, 67346, Kermanshah, Iran
ISSN:1608-3199
文摘
The native fluorescence intensity of desipramine was enhanced in the presence of β-cyclodextrin in aqueous solution. The inclusion complex formation between these compounds was studied by spectrofluorimetry. A stable complex with a 2: 1 stoichiometry of β-cyclodextrin to desipramine was formed (logβ2 = 9.29 ± 0.01). In the presence of an optimum concentration of β-cyclodextrin, the fluorescence intensity was linearly proportional to desipramine concentration in the range of 0.1-00 μg/mL (7.2 × 10??.0 × 10? M) with a limit of detection of 7 × 10? M. The method was successfully applied to the detection of desipramine in its tablets.