Ginsenoside Drug Nanocomposites Prepared by the Aerosol Solvent Extraction System for Enhancing Drug Solubility and Stability

被引:19
作者
Tao, Cheng [1 ]
Zhang, Jianjun [1 ]
Wang, Jiexin [1 ]
Le, Yuan [1 ]
机构
[1] Beijing Univ Chem Technol, Coll Chem Engn, Beijing 100029, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
ginsenoside; drug nanocomposites; aerosol solvent extraction system (ASES); dissolution rate; anticancer activity; SUPERCRITICAL SOLUTIONS; SOLID DISPERSIONS; RAPID EXPANSION; CRYSTAL-GROWTH; DISSOLUTION; CELLS; RE; PRECIPITATION; APOPTOSIS; DELIVERY;
D O I
10.3390/pharmaceutics10030095
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ginsenosides are the pharmacologically active constituents of ginseng. So far, more than 30 ginsenosides have been identified and widely used in pharmaceutical formulations. However, the therapeutic applications of ginsenosides are hampered by their poor solubility and low bioavailability. In this study, we selected two of the most important ginsenosides-Re and Rh-2 as model drugs to prepare ginsenoside drug nanocomposites (NanoGS) using the simple aerosol solvent extraction system (ASES) technique to address the poor solubility and bioavailability of these compounds. Compared with raw ginsenosides, NanoGS exhibited significantly enhanced dissolution rate owing to their low crystallinity and high surface area. Furthermore, in vitro cellular investigations showed that NanoGS-Rh-2 exhibited outstanding anticancer activity against MCF-7 cancer cells. Therefore, this study is expected to provide a promising strategy that could optimize and broaden the applications of ginsenosides, as well as other water-insoluble drugs in pharmaceutical formulations.
引用
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页数:12
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[1]   Preparation of hydrocortisone nanosuspension through a bottom-up nanoprecipitation technique using microfluidic reactors [J].
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[2]  
[Anonymous], CHINESE MED
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[5]   THE SPRAY DRYING OF PHARMACEUTICALS [J].
BROADHEAD, J ;
ROUAN, SKE ;
RHODES, CT .
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