Kim Tae Hyoung, Lee Haeshin, Park Tae Gwan
Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Taejon, South Korea.
Biomaterials. 2002 Jun;23(11):2311-7. doi: 10.1016/s0142-9612(01)00365-9.
Recombinant human epidermal growth factor (rhEGF) was conjugated with polyethylene glycol (PEG) to improve its physical stability during microencapsulation in biodegradable poly(lactic-co-glycolic acid) microspheres. rhEGF was conjugated with N-hydroxysuccimide (NHS)-derivatized methoxy-PEG (mPEG) of MW 2000 and 5000 under various reaction conditions to optimize the extent of pegylation. Pegylated rhEGF showed much enhanced physical stability against homogenization. Pegylated rhEGF was encapsulated in PLGA microspheres by a double emulsion solvent evaporation method to achieve a sustained release. Pegylated rhEGF exhibited a tri-phasic release profile with a reduced initial burst, compared with unpegylated rhEGF. This study demonstrated that protein pegylation enhanced physical stability of protein and could be a good approach to achieve a sustained protein release profile from biodegradable microspheres.
重组人表皮生长因子(rhEGF)与聚乙二醇(PEG)偶联,以提高其在可生物降解的聚乳酸-乙醇酸共聚物微球中微囊化过程中的物理稳定性。在各种反应条件下,将rhEGF与分子量为2000和5000的N-羟基琥珀酰亚胺(NHS)衍生化甲氧基聚乙二醇(mPEG)偶联,以优化聚乙二醇化程度。聚乙二醇化的rhEGF在匀浆处理中显示出大大增强的物理稳定性。通过双乳液溶剂蒸发法将聚乙二醇化的rhEGF包封在聚乳酸-乙醇酸共聚物微球中以实现缓释。与未聚乙二醇化的rhEGF相比,聚乙二醇化的rhEGF呈现出三相释放曲线,初始突释减少。这项研究表明,蛋白质聚乙二醇化增强了蛋白质的物理稳定性,并且可能是从可生物降解微球实现蛋白质缓释曲线的一种好方法。