标题:Studies on the preparation, characterization and pharmacokinetics of Amoitone B nanocrystals
作者:Hao, Leilei; Wang, Xiaoyong; Zhang, Dianrui; Xu, Qingyan; Song, Siyang; Wang, Feihu; Li, Caiyun; Guo, Hejian; Liu, Yue; Zheng, Danda 更多
作者机构:[Hao, Leilei; Zhang, Dianrui; Wang, Feihu; Li, Caiyun; Guo, Hejian; Liu, Yue; Zheng, Dandan] Shandong Univ, Dept Pharmaceut, Coll Pharm, Jinan 250012, 更多
通讯作者:Zhang, DR
通讯作者地址:[Zhang, DR]Shandong Univ, Dept Pharmaceut, Coll Pharm, 44 Wenhua Xilu, Jinan 250012, Peoples R China.
来源:INTERNATIONAL JOURNAL OF PHARMACEUTICS
出版年:2012
卷:433
期:1-2
页码:157-164
DOI:10.1016/j.ijpharm.2012.05.002
关键词:Amoitone B; Nanocrystals; Microfluidization method; In vitro; dissolution; Pharmacokinetics
摘要:Amoitone B, as a new derivative of cytosporone B, has been proved to be a natural agonist for Nur77. It exhibits remarkable anticancer activity in vivo and has the potential to be a therapeutic agent for cancer treatment. However, the poor solubility and dissolution rate result in low therapeutic index for injection and low bioavailability for oral administration, therefore limiting its application. In order to magnify the clinical use of Amoitone B, nanocrystal was selected as an application technology to solve the above problems. In this study, the optimized Amoitone B nanocrystals with small and uniform particle size were successfully prepared by microfluidization method and investigated by morphology, size distribution, and zeta potential. The differential scanning calorimetry (DSC) and X-ray diffraction (XRD) confirmed there was no crystalline state changed in the size reduction process. For Amoitone B nanocrystals, an accelerated dissolution velocity and increased saturation solubility were achieved in vitro and a markedly different pharmacokinetic property in vivo was exhibited with retarded clearance and magnified AUC compared with Amoitone B solution. These results implied that developing Amoitone B as nanocrystals is a promising choice for intravenous delivery and further application for cancer therapy. (C) 2012 Elsevier B. V. All rights reserved.
收录类别:SCOPUS;SCIE
WOS核心被引频次:32
Scopus被引频次:36
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84862842183&doi=10.1016%2fj.ijpharm.2012.05.002&partnerID=40&md5=d075b05cfb74d4c0da27952db80bb49e
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