单宁酸-铁(iii)配合物†包被的介孔二氧化硅纳米颗粒中姜黄素的pH和谷胱甘肽响应释放

IF 3.9 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
RSC Advances Pub Date : 2015-10-19 DOI:10.1039/C5RA16004A
Sanghoon Kim, Stéphanie Philippot, Stéphane Fontanay, Raphaël E. Duval, Emmanuel Lamouroux, Nadia Canilho and Andreea Pasc
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引用次数: 60

摘要

通过在介孔二氧化硅纳米颗粒(MSN)表面沉积单宁酸(TA) -铁(III)配合物,开发了一种pH和谷胱甘肽响应的新型药物递送系统。通过在MSN的水分散体(如MCM-41)中连续添加氯化铁(FeCl3)和单宁酸,可以在30秒内轻松完成涂层。疏水模型药物姜黄素在生理条件下(pH 7.4)表现出持续的药物释放,而当pH降至6.0或4.5时,姜黄素会快速释放。此外,调节谷胱甘肽水平可以控制姜黄素的释放,从而通过竞争配体加速TA-Fe (III)复合物的分解。因此,这些结果将允许开发新的和简单的pH和谷胱甘肽响应的药物传递系统,具有潜在的应用,如生物医学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

pH- and glutathione-responsive release of curcumin from mesoporous silica nanoparticles coated using tannic acid–Fe(iii) complex†

pH- and glutathione-responsive release of curcumin from mesoporous silica nanoparticles coated using tannic acid–Fe(iii) complex†

A novel pH- and glutathione-responsive drug delivery system has been developed by deposition of tannic acid (TA)–Fe(III) complex on the surface of mesoporous silica nanoparticles (MSN). The coating was easily accomplished within 30 seconds by successive addition of iron chloride (FeCl3) and tannic acid in aqueous dispersion of MSN (e.g. MCM-41). A hydrophobic model drug, curcumin, showed sustainable drug release under physiological condition (pH 7.4), while a rapid curcumin release was triggered by lowering the pH to 6.0 or 4.5. Moreover, curcumin release could be controlled by adjusting the glutathione level, which accelerate the decomposition of TA–Fe(III) complex by competitive liganding. Therefore, these results would allow developing novel and simple pH- and glutathione-responsive drug delivery systems with potential applications such as in biomedicine.

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来源期刊
RSC Advances
RSC Advances chemical sciences-
CiteScore
7.50
自引率
2.60%
发文量
3116
审稿时长
1.6 months
期刊介绍: An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.
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