Abstract
An inclusion complex of β-cyclodextrin with andrographolide (Andro) was prepared by using a convenient new method of microwave irradiation. The structure of the inclusion complex was determined by UV and IR analyses as well as 1H NMR, 13C NMR and two dimensional NOE spectroscopic measurements. The results indicated that the possible stoichiometry of complex formation is 1:1 (guest:host ratio) and the two isomeric 1:1 inclusion complexes are present simultaneously in solution. Thermal studies proved the thermal stability of the inclusion complex.
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Zhao, D., Liao, K., Ma, X. et al. Study of the Supramolecular Inclusion of β-Cyclodextrin with Andrographolide. Journal of Inclusion Phenomena 43, 259–264 (2002). https://doi.org/10.1023/A:1021223407297
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DOI: https://doi.org/10.1023/A:1021223407297