共 49 条
Preparation and characterization of zedoary turmeric oil-loaded insulin-modified sterically stabilized liposomes
被引:3
|作者:
Yang, Zhiwen
[1
]
Fu, Dahua
[2
]
Zhu, Liang
[3
]
Yang, Muhua
[1
]
Cheng, Qilai
[1
]
机构:
[1] Gannan Med Coll, Dept Pharmaceut Sci, Ganzhou 341000, Jiangxi, Peoples R China
[2] Zhangzhou Hlth Coll, Dept Med, Zhangzhou, Peoples R China
[3] Guangdong Pharmaceut Univ, Dept Pharmaceut, Guangzhou, Guangdong, Peoples R China
关键词:
Liposomes;
insulin receptor;
targeted drug delivery;
cancer;
IN-VITRO;
ANTICANCER ANTIBODY;
CIRCULATION TIME;
FOLATE RECEPTOR;
PEG-LIPOSOMES;
DOXORUBICIN;
CANCER;
CELLS;
SIZE;
BIODISTRIBUTION;
D O I:
10.3109/08982100903015017
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The poor selectivity of anticancer drugs often leads to their multiplicate dose-limiting toxicities in humans, which severely restricts their clinical application. In this study, a novel liposomal formulation of zedoary turmeric oil (ZTO) targeting the insulin receptor (IR) was prepared by covalently conjugating insulin to the terminal of the polyethylene glycol (PEG) chain of sterically stabilized liposomes. In vitro assays indicated that a higher uptake of insulin-modified sterically stabilized liposomes (ISSLs) was observed in SMMC-7721 hepatocarcinoma cells overexpressing insulin receptors. IC(50) values of ISSLs, NTLs (nontargeted liposomes), and ZTO injection (free ZTO) against SMMC-7721, determined by MTT assays, were 157.2, 256.7, and 43.3 mu g center dot ml(-1), respectively. Plasma-clearance profiles of ZTO in the liposomal formulations were then compared with that of ZTO injection. The liposomal formulations showed much longer terminal half-lives (11.24 and 14.73 hours for ISSLs and NTLs, respectively) than that of ZTO injection (1.45 hours). All results above indicated the ISSLs were potentially useful for the treatment of IR (+) tumors and are worthy of further investigation.
引用
收藏
页码:9 / 15
页数:7
相关论文