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Characterization and dissolution of resveratrol/hydroxypropyl-β-cyclodextrin inclusion complex
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DOI   10.11656/j.issn.1672-1519.2013.08.19
Key Words   resveratrol;hydroxypropyl-β-cyclodextrin;inclusion complex;solubility
Author NameAffiliationE-mail
QI Xue-jie袁 Chinese Medicine School of TCM, Tianjin University of TCM, Tianjin 300193, China
Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin 300193, China
 
 
QIU Chao Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin 300193, China
Research Center of TCM, Tianjin University of TCM, Tianjin 300193, China 
 
JIANG Heng-li Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin 300193, China
Research Center of TCM, Tianjin University of TCM, Tianjin 300193, China 
 
CUI Yuan-lu Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin 300193, China
Research Center of TCM, Tianjin University of TCM, Tianjin 300193, China 
cuiyl@tjutcm.edu.cn 
Abstract
    [Objective] Resveratrol hydroxypropyl-β-cyclodextrin (HP-β-CD) inclusion complex is prepared and characterized, stoichiometry of host and guest is determined and the dissolubility is also investigated.[Methods] The inclusion complex was prepared by freezedrying method, and characterized by Fourier-transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC) and X-ray diffractometry (XRD).Drug content and release in vitro were determined by HPLC.[Results] It was defined that Resveratrol/HP-β-CD inclusion complex formed.Resveratrol/HP-β-CD was classified as AL-type with the ratio of 1:1 between host and guest, and the complexation constant was 1621M-1 by the phase solubility diagram method.Compared to the drug alone, solubility and dissolving rate of inclusion complex increased.[Conclusion] The solubility, stability and dissolving rate of drug increases in inclusion complex of Resveratrol/HP-β- CD.

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