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Preparation of protein-loaded microspheres with size≤10 μm by electrostatic droplet generation technology
作者姓名:XUE  Weiming  LIU  Xiudong  YU  Weiting  MA  Xiaojun
作者单位:[1]College of Chemical Engineering of Northwest University, Xi'an 710069, China [2]Department of Biotechnology, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China
基金项目:This work was supported by the National Natural Science Foundation of China (Grant Nos. 50373046 and 20176056).
摘    要:AT PRESENT, ALMOST ALL PROTEIN DRUGS HAVE TO BE CLINI- CALLY ADMINISTERED VIA INJECTION ROUTES SUCH AS INTRAVE- NOUS INJECTION. ONE OF THE IMPORTANT PROBLEMS CON- FRONTED IS THAT THESE DRUGS SHOULD BE INJECTED REPEATEDLY DUE TO SHORT HALF-LIFE IN BLOOD. I…

关 键 词:胰岛素  血色素  藻酸盐  蛋白质微球  微囊化  静电液滴发电技术
收稿时间:2005-04-15
修稿时间:2005-04-152005-06-23

Preparation of protein-loaded microspheres with size ?10 μm by electrostatic droplet generation technology
XUE Weiming LIU Xiudong YU Weiting MA Xiaojun.Preparation of protein-loaded microspheres with size ?10 μm by electrostatic droplet generation technology[J].Chinese Science Bulletin,2006,51(3):279-286.
Authors:Weiming Xue  Xiudong Liu  Weiting Yu  Xiaojun Ma
Institution:(1) College of Chemical Engineering of Northwest University, Xi’an, 710069, China;(2) Department of Biotechnology, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China
Abstract:The development of non-injection route for protein drugs, especially oral administration, has been the main focus of controlled release of drugs. To overcome obstacles unsolved such as enzyme degradation and penetration barrier of intestinal epithelium, technologies using microspheres as carrier of protein drugs have been proven potential to realize oral administration. It has been demonstrated that microspheres can not only protect proteins, but also facilitate the penetration and absorption through Peyer’s patches when the size is smaller than 10 μm. Therefore, the objective of this paper is to prepare protein-loaded microspheres with size ⩽ 10 μm. Electrostatic droplet generation technology was used with insulin and hemoglobin as drug models and sodium alginate as microsphere material. By decreasing the surface tension of feed solution by adding surfactant, and improving electric field distribution by changing the shape of container and electrode for gelation solution, protein-loaded microspheres with mean size less than 10 μm were successfully produced through needle with diameter of 400 μm. The microspheres showed good sphericity and narrow size distribution. The mean standard variance of size distribution was 1.61. The encapsulation efficiency of proteins was over 70%. Moreover, the significance analysis of factors influencing the size of protein loaded microspheres was carried out through orthogonal experiments, which showed that output voltage (U), needle diameter (D) and the distance between needle tips to the surface of gelation solution (δ) influenced significantly the size of microspheres. Finally, the statistic analysis showed that when confidence level was α=0.05, and α=0.1, confidence interval of microsphere size can be (6.2545, 10.1735) and (6.6022, 9.8258) correspondingly, suggesting that there is good repeatability and reliability for improving electrostatic droplet generation technology to prepare protein-loaded microspheres with size ⩽10 μm.
Keywords:electrostatic droplet generation technology  insulin  he- moglobin  alginate  microsphere  size  encapsulation efficiency  
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