Nanostructural control of the release of macromolecules from silica sol-gels.
Nanostructural control of the release of macromolecules from silica sol-gels.
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DOI：
10.1016/j.actbio.2013.04.039
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发表时间：
2013-08
影响因子：
9.7
通讯作者：
Ducheyne, Paul
中科院分区：
文献类型：
--
作者：
Radin, Shula;Bhattacharyya, Sanjib;Ducheyne, Paul
The therapeutic use of biological molecules such as growth factors and monoclonal antibodies is challenging in view of their limited half-life in vivo. This has elicited the interest in delivery materials that can protect these molecules until released over extended periods of time. Although previous studies have shown controlled release of biologically functional BMP-2 and TGF-β from silica sol–gels, more versatile release conditions are desirable. This study focuses on the relationship between room temperature processed silica sol–gel synthesis conditions and the nanopore size and size distribution of the sol–gels. Furthermore, the effect on release of large molecules with a size up to 70 kDa is determined. Dextran, a hydrophilic polysaccharide, was selected as a large model molecule at molecular sizes of 10, 40 and 70 kDa, as it enabled us to determine a size effect uniquely without possible confounding chemical effects arising from the various molecules used. Previously, acid catalysis was performed at a pH value of 1.8 below the isoelectric point of silica. Herein the silica synthesis was pursued using acid catalysis at either pH 1.8 or 3.05 first, followed by catalysis at higher values by adding base. This results in a mesoporous structure with an abundance of pores around 3.5 nm. The data show that all molecular sizes can be released in a controlled manner. The data also reveal a unique in vivo approach to enable release of large biological molecules: the use more labile sol–gel structures by acid catalyzing above the pH value of the isoelectric point of silica; upon immersion in a physiological fluid the pores expand to reach an average size of 3.5 nm, thereby facilitating molecular out-diffusion.
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影响因子：
10.8
作者：
Hiemstra, Christine;Zhong, Zhiyuan;Feijen, Jan
通讯作者：
Feijen, Jan
影响因子：
2.5
作者：
Viitala, R;Jokinen, M;Jalonen, H
通讯作者：
Jalonen, H
影响因子：
3
作者：
BRAUN, S;RAPPOPORT, S;OTTOLENGHI, M
通讯作者：
OTTOLENGHI, M
影响因子：
5.5
作者：
Ok S;Steinhart M;Serbescu A;Franz C;Vaca Chávez F;Saalwächter K
通讯作者：
Saalwächter K
影响因子：
2.7
作者：
Tonelli AE
通讯作者：
Tonelli AE