Stabilisation and encapsulation of protein into biodegradable microspheres with zinc ion and protein in polyethylene glycol solution formed nanoparticles by freeze-drying

被引:3
|
作者
Ma, Liuqing [1 ,2 ]
Hong, Xiaoyun [2 ]
Liu, Zhenguo [1 ]
Yuan, Weien [2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Xinhua Hosp, Dept Neurol, Shanghai 200092, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Pharm, Shanghai 200240, Peoples R China
来源
MICRO & NANO LETTERS | 2012年 / 7卷 / 03期
基金
美国国家科学基金会;
关键词
HUMAN-IMMUNOGLOBULIN-G; HUMAN GROWTH-HORMONE; SUSTAINED-RELEASE; STABILITY; DELIVERY;
D O I
10.1049/mnl.2011.0640
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The sustained-release formulation of protein has several unsolved problems, including the burst release and/or incomplete release of protein and the instability of protein during the preparation process. This study was conducted to find a way out in decreasing the burst release and incomplete release of protein as well as stabilising the protein. The method was to apply the solid-in-oil-in-water (S/O/W) encapsulation process. The different stabilising effects achieved by varying the proportion of zinc ion (Zn2+), protein and polyethylene glycol (PEG) during the preparation of Zn2+-bovine serum albumin (BSA) nanoparticles in PEG solution were investigated followed by the investigation of freeze-drying and subsequently encapsulating the nanoparticles mentioned above into polylactide-co-glycolide (PLGA) microspheres using the S/O/W method. The size-exclusion high-performance liquid chromatography results showed that the aggregation of protein released from the PLGA microspheres did not change significantly compared with that of the original BSA solution. The in vitro release results showed that burst release and incomplete release might be controlled through changing the proportion of zinc ion, protein and PEG in PLGA.
引用
收藏
页码:215 / 218
页数:4
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