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HERO ID
7175320
Reference Type
Journal Article
Title
Folate receptor targeted bufalin/beta-cyclodextrin supramolecular inclusion complex for enhanced solubility and anti-tumor efficiency of bufalin
Author(s)
Zou Aihua; Zhao Xiaotong; Handge, UA; Garamus, VM; Willumeit-Roemer, R; Peihao, Yin; ,
Year
2017
Is Peer Reviewed?
1
Journal
Materials Science and Engineering C: Materials for Biological Applications
ISSN:
0928-4931
EISSN:
1873-0191
Publisher
ELSEVIER SCIENCE BV
Location
AMSTERDAM
Page Numbers
609-618
PMID
28576029
DOI
10.1016/j.msec.2017.04.094
Web of Science Id
WOS:000404944700072
Abstract
Bufalin (BF), a traditional Chinese medicine, exhibited inhibitory activities against a broad spectrum of tumor cells. The present study elaborates that bufalin was successfully encapsulated into the cavity of beta-cyclodextrin (beta-CD), which was determined by Fourier transform infrared spectroscopy (FT-IR), proton nuclear magnetic resonance spectroscopy (H-1 NMR), differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). The best reaction mole ratio of BF/beta-CD was 1:5. The solubilities of bufalin in water and phosphate buffer solution (pH = 7.4) were increased up to 24 and 34 times after encapsulated into the cavity of S-CD respectively. The inclusion efficiency (IE) and drug loading (DL) of bufalin in the inclusion complex were (94.22 +/- 0.85)% and (14.11 +/- 0.20)%, respectively. Then beta-CD conjugated with folic acid (FA) were further prepared and employed to improve the anti-tumor efficacy of inclusion complex. The in vitro dissolution and solubility study showed better values of inclusion complex and FA targeted inclusion complex than that of pure BF. Cytotoxicity experiments by using HCT116 cell line revealed that the antitumor efficiency of bufalin were enhanced more than two folds in the presence of beta-CD and folate conjugated beta-CD (FA-PEI-beta-CD), which demonstrated the potential application of beta-CD (FA-9EI-beta-CD) as delivery vehicles of bufalin for antitumor therapy. (C) 2017 Elsevier B.V. All rights reserved.
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