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Study on preparation of glabridin hydroxypropyl -β -cyclodextrin inclusion compound and its effect of transdermal absoption
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DOI   10.11656/j.issn.1672-1519.2015.10.11
Key Words   glabridin;HP-β-CD;transdermal absoption
Author NameAffiliationE-mail
YE Liu-qing School of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China  
WANG Yan School of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China paozhijiaoxue@126.com 
HAN Wan-ying School of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China  
ZHOU Xiao-xia School of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China  
MA Zong-wu School of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China  
GUI Guang-zhi School of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China  
Abstract
    [Objective] To optimize the preparation technology of glabridin hydroxypropyl-β-cyclodextrin (HP-β-CD) inclusion compound and investigate its effect of transdermal absoption. [Methods] With inclusion efficiency as the indice, the optimum preparation condition was studied by orthogonal test. Franz vertical diffusion cell was adopted to investigate transdermal performance of glabridin HP-β-CD. [Results] The optimal inclusion conditions were as follows: the ratio of glabridin to HP-β-CD was 1∶15 (m/m), inclusion temperature was 40 ℃, inclusion time was 1.5 h. The cumulative permeation of glabridin HP-β-CD was higher than glabridin group. [Conclusion] HP-β-CD have significant effect on transdermal of glabridin.

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