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FeO@SiO 纳米粒子的改良绿色合成及其 pH 响应性药物释放。

Modified green synthesis of FeO@SiO nanoparticles for pH responsive drug release.

机构信息

Fujian Key Laboratory of Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Fujian Normal University, Fuzhou 350007, Fujian Province, China.

Centre for Marine Bioproducts Development, Flinders University, Bedford Park, SA 5042, Australia.

出版信息

Mater Sci Eng C Mater Biol Appl. 2020 Jul;112:110900. doi: 10.1016/j.msec.2020.110900. Epub 2020 Mar 26.


DOI:10.1016/j.msec.2020.110900
PMID:32409056
Abstract

A magnetic field activated drug delivery and pH-sensitive controlled drug release system based on carboxyl-modified green synthesized FeO@SiO (FeO@SiO-Glu) nanoparticles was established. Doxorubicin hydrochloride (DOX), as a drug model, was adsorbed onto the FeO@SiO-Glu nanoparticles' surface, where the observed drug loading capacity of 34.6 mg/g was attributed to electrostatic interaction between -COO on the surface of FeO@SiO-Glu and -NH of DOX. The structure, morphology and physiochemical properties of FeO@SiO-Glu were characterized via TEM, FTIR, XRD, N adsorption/desorption isotherms, and Zeta potential measurements. The green synthesized FeO@SiO-Glu nanoparticles exhibited multilayer architecture with a BET surface area of 79.9 m/g and a magnetization saturation of 25.9 emu/g. Drug release experiments indicated that DOX was pH trigger released with 60.8% released within 72 h at pH 3.5. This system has important potential implications for the design of more effective and stable magnetic FeO@SiO-Glu materials as drug carriers for targeted and controlled drug release.

摘要

建立了一种基于羧基修饰的绿色合成 FeO@SiO(FeO@SiO-Glu)纳米粒子的磁场激活药物输送和 pH 敏感控制药物释放系统。盐酸阿霉素(DOX)作为药物模型,被吸附到 FeO@SiO-Glu 纳米粒子的表面上,观察到的药物负载能力为 34.6mg/g,这归因于 FeO@SiO-Glu 表面上的-COO 与 DOX 的-NH 之间的静电相互作用。通过 TEM、FTIR、XRD、N 吸附/解吸等温线和 Zeta 电位测量对 FeO@SiO-Glu 的结构、形态和物理化学性质进行了表征。绿色合成的 FeO@SiO-Glu 纳米粒子具有多层结构,BET 表面积为 79.9m/g,磁化饱和为 25.9emu/g。药物释放实验表明,DOX 是 pH 触发释放的,在 pH 3.5 下 72 小时内释放了 60.8%。该系统对于设计更有效和稳定的磁性 FeO@SiO-Glu 药物载体用于靶向和控制药物释放具有重要的潜在意义。

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