Silica nanoparticles with enlarged nanopore size for the loading and release of biological proteins

被引:21
作者
Eltohamy, Mohamed [1 ,5 ]
Shin, Ueon Sang [1 ,2 ,3 ]
Kim, Hae-Won [1 ,2 ,3 ,4 ]
机构
[1] Dankook Univ, ITREN, Seoul, South Korea
[2] Dankook Univ, Biomat & Tissue Engn Lab, Dept Nanobiomed Sci, Seoul, South Korea
[3] Dankook Univ, WCU Res Ctr, Seoul, South Korea
[4] Dankook Univ, Coll Dent, Dept Biomat Sci, Seoul, South Korea
[5] Natl Res Ctr, Glass Res Dept, Giza, Egypt
基金
新加坡国家研究基金会;
关键词
Ceramics; Nanoparticles; Bioceramics; DRUG-DELIVERY; DIAMETERS; SYSTEM;
D O I
10.1016/j.matlet.2011.07.112
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Silica nanoparticles (SNs) with a nanoporous structure are attractive for the delivery of biomolecules. This study developed a SNs-based protein delivery system with nanopore sizes large enough to uptake protein molecules. The use of trioctylmethylammonium bromide (TOMAB) as an auxiliary chemical facilitated a dramatic increase in pore size from 2.6 nm to 17.4 nm. The surface was highly negatively-charged with a zeta potential of approximately -35 at pH 7. positively-charged protein cytochrome C was encapsulated effectively within the large pore spaces of the SNs, with a protein loading capacity of almost 2-fold increase due to the pore size increase. The loaded protein exhibited sustained release for approximately one week with an initial burst in a day, suggesting the SNs tailored with enlarged nanopores should be useful for the delivery of large protein molecules for tissue regeneration. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:3570 / 3573
页数:4
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