Department of Biotechnology, Faculty of Biological Sciences and Technology, University of Isfahan, Isfahan 81746-73441, Iran.
Faculty of Physics, University of Isfahan, Isfahan 81746-73441, Iran.
Molecules. 2020 Sep 4;25(18):4053. doi: 10.3390/molecules25184053.
In recent years, the intrinsic magnetic properties of magnetic nanoparticles (MNPs) have made them one of the most promising candidates for magnetic resonance imaging (MRI). This study aims to evaluate the effect of different coating agents (with and without targeting agents) on the magnetic property of MNPs. In detail, iron oxide nanoparticles (IONPs) were prepared by the polyol method. The nanoparticles were then divided into two groups, one of which was coated with silica (SiO) and hyperbranched polyglycerol (HPG) (SPION@SiO@HPG); the other was covered by HPG alone (SPION@HPG). In the following section, folic acid (FA), as a targeting agent, was attached on the surface of nanoparticles. Physicochemical properties of nanostructures were characterized using Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), and a vibrating sample magnetometer (VSM). TEM results showed that SPION@HPG was monodispersed with the average size of about 20 nm, while SPION@SiO@HPG had a size of about 25 nm. Moreover, HPG coated nanoparticles had much lower magnetic saturation than the silica coated ones. The MR signal intensity of the nanostructures showed a relation between increasing the nanoparticle concentrations inside the MCF-7 cells and decreasing the signal related to the relaxation time. The comparison of coating showed that SPION@SiO@HPG (with/without a targeting agent) had significantly higher value in comparison to FeO@HPG. Based on the results of this study, the FeO@SiO@HPG-FA nanoparticles have shown the best magnetic properties, and can be considered promising contrast agents for magnetic resonance imaging applications.
近年来,磁性纳米粒子(MNPs)的固有磁性能使其成为磁共振成像(MRI)最有前途的候选者之一。本研究旨在评估不同涂层剂(有和没有靶向剂)对 MNPs 磁性能的影响。具体而言,通过多元醇法制备氧化铁纳米粒子(IONPs)。然后将纳米粒子分为两组,一组用硅(SiO)和超支化聚甘油(HPG)进行涂层(SPION@SiO@HPG);另一组仅用 HPG 覆盖(SPION@HPG)。在接下来的部分中,叶酸(FA)作为靶向剂被附着在纳米粒子的表面上。使用傅里叶变换红外光谱(FT-IR)、透射电子显微镜(TEM)和振动样品磁强计(VSM)对纳米结构的物理化学性质进行了表征。TEM 结果表明,SPION@HPG 呈单分散性,平均尺寸约为 20nm,而 SPION@SiO@HPG 的尺寸约为 25nm。此外,HPG 涂层纳米粒子的磁饱和强度远低于 SiO 涂层纳米粒子。纳米结构的磁共振信号强度与 MCF-7 细胞内纳米粒子浓度的增加和与 T2 弛豫时间相关的信号的降低有关。涂层的比较表明,SPION@SiO@HPG(有/没有靶向剂)的 值明显高于 FeO@HPG。基于这项研究的结果,FeO@SiO@HPG-FA 纳米粒子表现出了最佳的磁性能,可以被认为是磁共振成像应用中很有前途的对比剂。
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