Novel iron-polysaccharide multilayered microcapsules for controlled insulin release

被引:49
|
作者
Zheng, Jian [1 ,3 ]
Yue, Xiuli [2 ]
Dai, Zhifei [1 ]
Wang, Yang [3 ]
Liu, Shaoqin [1 ]
Yan, Xiufeng [3 ]
机构
[1] Harbin Inst Technol, BioX Ctr, Nanomed & Biosensor Lab, Harbin 150080, Peoples R China
[2] Harbin Inst Technol, SKLUWRE, Harbin 150090, Peoples R China
[3] NE Forestry Univ, Coll Life Sci, Harbin 150040, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
Iron-polysaccharide complex; Insulin; Controlled release; Microencapsulation; Hypoglycemic effect; BY-LAYER ASSEMBLIES; IN-VITRO; DRUG-DELIVERY; ALTERNATING BIOACTIVITY; HUMAN BLOOD; DEXTRAN; NANOPARTICLES; CAPSULES; CHITOSAN; THERAPY;
D O I
10.1016/j.actbio.2009.01.017
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
study, insulin-loaded microcapsules were prepared via layer-by-layer deposition of oppositely charged Fe3+ and dextran sulfate (DS) onto the surface of insulin microparticles. Fe3+ was combined with DS via both electrostatic interaction and chemical complexation process, leading to the formation of a stable complex of Fe3+/DS. Subsequently, prolamine was used as the outermost layer of the insulin-loaded microcapsules to facilitate nuclear delivery. The sufficient charge reversal with successive deposition cycles and successful fabrication of hollow microcapsules provided strong evidence for the growth of (Fe3+/DS)(n) multilayer on the surface of microparticles. The experiments showed that the microcapsules successfully entrapped insulin with encapsulation efficiency of 70.56 +/- 0.97% and drug loading content of 46.15 +/- 0.97%. It was found that the release time and hypoglycemic effect increased as the number of deposited bilayers increased. The insulin-loaded microcapsules significantly improved glucose tolerance from 2 h (free insulin) to even 12 h (insulin-loaded microcapsules with 10 bilayers). Moreover, the microcapsules with protamine as the outermost layer displayed a prolonged and stable glucose-lowering profile over a period of over 6 h compared with Fe3+ as the outermost layer. These findings indicate that such microcapsules can be a promising approach for the construction of an effective controlled release delivery system of insulin as well as other proteins with short half-life time. (c) 2009 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1499 / 1507
页数:9
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