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Cysteine modified and bile salt based micelles: Preparation and application as an oral delivery system for paclitaxel
被引:17
|作者:
Xu, Wei
[1
]
Fan, Xiaohui
[2
]
Zhao, Yanli
[2
]
Li, Lingbing
[2
]
机构:
[1] Shandong Prov Qian Foshan Hosp, Dept Pharm, Jinan, Shandong, Peoples R China
[2] Shandong Univ, Sch Pharmaceut Sci, Dept Pharmaceut, Jinan 250012, Shandong, Peoples R China
关键词:
Cysteine modified;
Sodium cholate;
Micelles;
Paclitaxel;
Oral;
POLYION COMPLEX MICELLES;
MULTIDRUG-RESISTANCE;
COPOLYMER MICELLES;
GENE DELIVERY;
DRUG;
ENHANCEMENT;
ABSORPTION;
MECHANISM;
POLYMERS;
D O I:
10.1016/j.colsurfb.2015.02.031
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
The aim of the present study is to construct a cysteine modified polyion complex micelles made of Pluronic F127-chitosan (PF127-CS), Pluronic F127-cysteine (PF127-cysteine) and sodium cholate (NaC) and to evaluate the potential of the micelles as an oral drug delivery system for paclitaxel. Systematic studies on physicochemical properties including size distribution, zeta-potential and morphology were conducted to validate the formation of micelle structure. Compared with Pluronic micelles, drug-loading capacity of PF127-CS/PF127-cysteine/NaC micelles was increased from 3.35% to 12.77%. Both the critical micelle concentration and the stability test confirmed that the PF127-CS/PF127-cysteine/NaC micelles were more stable in aqueous solution than sodium cholate micelles. Pharmacokinetic study demonstrated that when oral administration the area under the plasma concentration-time curve (AUC(0-infinity)) and the absolute bioavailability of paclitaxel-loaded micelles were five times greater than that of the paclitaxel solution. In general, PF127-CS/PF127-cysteine/NaC micelles were proven to be a potential oral drug delivery system for paclitaxel. (c) 2015 Elsevier B.V. All rights reserved.
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页码:165 / 171
页数:7
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