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A novel formulation of [6]-gingerol: Proliposomes with enhanced oral bioavailability and antitumor effect
被引:83
|作者:
Wang, Qilong
[1
]
Wei, Qiuyu
[1
]
Yang, Qiuxuan
[1
]
Cao, Xia
[1
]
Li, Qiang
[1
]
Shi, Feng
[1
]
Tong, Shan Shan
[1
]
Feng, Chunlai
[1
]
Yu, Qingtong
[1
]
Yu, Jiangnan
[1
]
Xu, Ximing
[1
]
机构:
[1] Jiangsu Univ, Ctr Nano Drug Gene Delivery & Tissue Engn, Sch Pharm, Dept Pharmaceut, Zhenjiang 212013, Peoples R China
基金:
中国国家自然科学基金;
中国博士后科学基金;
关键词:
6]-Gingerol;
Extraction;
Proliposome;
Antitumor;
GINGER ZINGIBER-OFFICINALE;
NF-KAPPA-B;
CELL-DEATH;
CANCER CHEMOPREVENTION;
COX-2;
EXPRESSION;
IN-VITRO;
ANTIOXIDANT;
ACTIVATION;
6-GINGEROL;
APOPTOSIS;
D O I:
10.1016/j.ijpharm.2017.11.006
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
[6]-Gingerol, one of the components of the rhizome of Ginger, has a variety of biological activities such as anticoagulant, antioxidative, antitumor, anti-inflammatory, antihypertensive, and so forth. However, as one of the homologous phenolic ketones, [6]-gingerol is insoluble in water which limits its applications. Herein, we prepared [6]-gingerol proliposomes through modified thin-film dispersion method, which was spherical or oval, and physicochemically stable with narrow size distribution. Surprisingly, in vitro release of [6]-gingerol loaded proliposome compared with the free [6]-gingerol was significantly higher and its oral bioavailability increased 5-fold in vivo. Intriguingly, its antitumor effect was enhanced in the liposome formulation. Thus, our prepared [6]-gingerol proliposome proved to be a novel formulation for [6]-gingerol, which significantly improved its antitumor effect.
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页码:308 / 315
页数:8
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