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介孔二氧化硅改性的含钛金属有机框架的制备及其在药物传递中的应用。

Small Titanium-Based MOFs Prepared with the Introduction of Tetraethyl Orthosilicate and Their Potential for Use in Drug Delivery.

机构信息

Graduate School at Shenzhen , Tsinghua University , Shenzhen 518055 , People's Republic of China.

State Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering , Tsinghua University , Beijing 100084 , People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2018 Apr 25;10(16):13325-13332. doi: 10.1021/acsami.8b01175. Epub 2018 Apr 11.

Abstract

Metal-organic frameworks (MOFs) have attracted much attention in the areas of biomedicine and medicine owing to their versatile porous structure. However, the oversize and high cellular toxicity of some metal-based MOF particles have hindered their development. Therefore, a series of small Ti-based MOFs are prepared with the introduction of tetraethyl orthosilicate (TEOS) into the reaction system. Compared with the Ti-based MOFs prepared by traditional methods, the size of the Ti-based MOFs prepared with this method is decreased by 42.78%. Meanwhile, the good biocompatibility of the prepared Ti-based MOF particles toward the L929 cell lines is proven using CCK-8 assays. Furthermore, the controlled release property of the Ti-based MOFs is evaluated by using ibuprofen (IBU) as a model drug. The amount of drug loaded in the samples is shown to be approximately 10%, and approximately 95% of the IBU is released from the MOFs after exposure to PBS for 24 h. We conclude that the size-decreased Ti-based MOFs prepared with the introduction of TEOS into the reaction systems are potential drug carriers in terms of their good biocompatibility and effective performance in the controlled release of a drug.

摘要

金属有机骨架(MOFs)由于其多样的多孔结构,在生物医药和医学领域引起了广泛关注。然而,一些基于金属的 MOF 颗粒过大和细胞毒性过高,阻碍了它们的发展。因此,通过在反应体系中引入正硅酸乙酯(TEOS),制备了一系列小尺寸的 Ti 基 MOFs。与传统方法制备的 Ti 基 MOFs 相比,该方法制备的 Ti 基 MOFs 的尺寸减小了 42.78%。同时,通过 CCK-8 测定法证明了所制备的 Ti 基 MOF 颗粒对 L929 细胞系具有良好的生物相容性。此外,通过将布洛芬(IBU)作为模型药物来评估 Ti 基 MOFs 的控制释放性能。结果表明,样品的载药量约为 10%,在 PBS 中暴露 24 小时后,约 95%的 IBU 从 MOFs 中释放出来。我们得出结论,通过在反应体系中引入 TEOS 制备的尺寸减小的 Ti 基 MOFs 在药物的控制释放方面具有良好的生物相容性和有效性能,是潜在的药物载体。

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