共 33 条
Encapsulation of Basic Fibroblast Growth Factor by Polyelectrolyte Multilayer Microcapsules and Its Controlled Release for Enhancing Cell Proliferation
被引:58
作者:
She, Zhen
[1
,2
,3
]
Wang, Chuxia
[1
]
Li, Jun
[1
,2
,3
]
Sukhorukov, Gleb B.
[3
,4
]
Antipina, Maria N.
[3
]
机构:
[1] Natl Univ Singapore, Fac Engn, Dept Bioengn, Singapore 117574, Singapore
[2] Natl Univ Singapore, Ctr Life Sci, NUS Grad Sch Integrat Sci & Engn NGS, Singapore 117456, Singapore
[3] ASTAR, Inst Mat Res & Engn, Singapore 117602, Singapore
[4] Univ London, Sch Mat Sci & Engn, London E1 4NS, England
关键词:
IN-VITRO;
PROTEIN ENCAPSULATION;
CAPSULES;
HEPARIN;
MACROMOLECULES;
ANGIOGENESIS;
DEGRADATION;
SYSTEM;
VIVO;
PH;
D O I:
10.1021/bm3005879
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:
Basic fibroblast growth factor (FGF2) is an important protein for cellular activity and highly vulnerable to environmental conditions. FGF2 protected by heparin and bovine serum albumin was loaded into the microcapsules by a coprecipitation-based layer-by-layer encapsulation method. Low cytotoxic and biodegradable polyelectrolytes dextran sulfate and poly-L-arginine were used for capsule shell assembly. The shell thickness-dependent encapsulation efficiency was measured by enzyme-linked immunosorbent assay. A maximum encapsulation efficiency of 42% could be achieved by microcapsules with a shell thickness of 14 layers. The effects of microcapsule concentration and shell thickness on cytotoxicity, FGF2 release kinetics, and L929 cell proliferation were evaluated in vitro. The advantage of using microcapsules as the carrier for FGF2 controlled release for enhancing L929 cell proliferation was analyzed.
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页码:2174 / 2180
页数:7
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