Suppr超能文献

溶菌酶从双层聚(丙交酯-共-乙交酯)(PLGA)微球中的控释。

Controlled Release of Lysozyme from Double-Walled Poly(Lactide-Co-Glycolide) (PLGA) Microspheres.

作者信息

Ansary Rezaul H, Rahman Mokhlesur M, Mohamad Nasir, Arrif Tengku M, Latif Ahmad Zubaidi A, Katas Haliza, Nik Wan Sani B Wan, Awang Mohamed B

机构信息

Faculty of Pharmacy, International Islamic University Malaysia, Kuantan 25200, Malaysia.

Department of Chemistry, University of Rajshahi, Rajshahi 6205, Bangladesh.

出版信息

Polymers (Basel). 2017 Oct 3;9(10):485. doi: 10.3390/polym9100485.

Abstract

Double-walled microspheres based on poly(lactide--glycolide) (PLGA) are potential delivery systems for reducing a very high initial burst release of encapsulated protein and peptide drugs. In this study, double-walled microspheres made of glucose core, hydroxyl-terminated poly(lactide--glycolide) (Glu-PLGA), and carboxyl-terminated PLGA were fabricated using a modified water-in-oil-in-oil-in-water (w1/o/o/w2) emulsion solvent evaporation technique for the controlled release of a model protein, lysozyme. Microspheres size, morphology, encapsulation efficiency, lysozyme in vitro release profiles, bioactivity, and structural integrity, were evaluated. Scanning electron microscopy (SEM) images revealed that double-walled microspheres comprising of Glu-PLGA and PLGA with a mass ratio of 1:1 have a spherical shape and smooth surfaces. A statistically significant increase in the encapsulation efficiency (82.52% ± 3.28%) was achieved when 1% (/) polyvinyl alcohol (PVA) and 2.5% (/) trehalose were incorporated in the internal and external aqueous phase, respectively, during emulsification. Double-walled microspheres prepared together with excipients (PVA and trehalose) showed a better control release of lysozyme. The released lysozyme was fully bioactive, and its structural integrity was slightly affected during microspheres fabrication and in vitro release studies. Therefore, double-walled microspheres made of Glu-PLGA and PLGA together with excipients (PVA and trehalose) provide a controlled and sustained release for lysozyme.

摘要

基于聚(丙交酯-乙交酯)(PLGA)的双壁微球是一种潜在的给药系统,可减少包封的蛋白质和肽类药物非常高的初始突释。在本研究中,采用改进的水包油包油包水(w1/o/o/w2)乳液溶剂蒸发技术制备了由葡萄糖核、羟基封端的聚(丙交酯-乙交酯)(Glu-PLGA)和羧基封端的PLGA组成的双壁微球,用于模型蛋白溶菌酶的控释。对微球的大小、形态、包封效率、溶菌酶的体外释放曲线、生物活性和结构完整性进行了评估。扫描电子显微镜(SEM)图像显示,质量比为1:1的Glu-PLGA和PLGA组成的双壁微球呈球形且表面光滑。在乳化过程中,分别在内部和外部水相中加入1%(/)聚乙烯醇(PVA)和2.5%(/)海藻糖时,包封效率有统计学意义的显著提高(82.52%±3.28%)。与辅料(PVA和海藻糖)一起制备的双壁微球对溶菌酶显示出更好的控释效果。释放的溶菌酶具有完全的生物活性,其结构完整性在微球制备和体外释放研究过程中受到轻微影响。因此,由Glu-PLGA和PLGA以及辅料(PVA和海藻糖)制成的双壁微球为溶菌酶提供了控释和缓释作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25cc/6418743/347f05b8abd2/polymers-09-00485-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验