首页> 外文期刊>Micro & Nano Letters, IET >Stabilisation and encapsulation of protein into biodegradable microspheres with zinc ion and protein in polyethylene glycol solution formed nanoparticles by freeze-drying
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Stabilisation and encapsulation of protein into biodegradable microspheres with zinc ion and protein in polyethylene glycol solution formed nanoparticles by freeze-drying

机译:蛋白质与锌离子和蛋白质在聚乙二醇溶液中通过冷冻干燥形成的纳米颗粒中被稳定化和包封到可生物降解的微球中

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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.
机译:蛋白质的持续释放制剂具有几个未解决的问题,包括蛋白质的突然释放和/或不完全释放以及在制备过程中蛋白质的不稳定。进行该研究以找到减少蛋白质的爆发释放和不完全释放以及稳定蛋白质的出路。该方法是应用水包油固体(S / O / W)封装工艺。在制备Zn 2 + -牛血清白蛋白的过程中,通过改变锌离子(Zn 2 + ),蛋白质和聚乙二醇(PEG)的比例可获得不同的稳定作用研究了PEG溶液中的(BSA)纳米粒子,然后进行了冷冻干燥,然后使用SOW方法将上述纳米粒子封装到聚丙交酯-共-乙交酯(PLGA)微球中。尺寸排阻高效液相色谱结果表明,与原始BSA溶液相比,从PLGA微球释放的蛋白质的聚集没有明显变化。体外释放结果表明,通过改变PLGA中锌离子,蛋白质和PEG的比例可以控制猝发释放和不完全释放。

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