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Assessment of Gold-Coated Iron Oxide Nanoparticles as Negative T2 Contrast Agent in Small Animal MRI Studies

机译:镀金氧化铁纳米粒子的评估为小动物MRI研究中的阴性T2造影剂

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Purpose: Magnetic resonance imaging (MRI) contrast agents are pharmaceuticals that enable a better visualization of internal body structures. In this study, we present the synthesis, MRI signal enhancement capabilities, in vitro as well as in vivo cytotoxicity results of gold-coated iron oxide nanoparticles (Fesub3/subOsub4/sub@AuNPs) as potential contrast agents. Methods: Fesub3/subOsub4/sub@AuNPs were obtained by synthesizing iron oxide nanoparticles and gradually coating them with gold. The obtained Fesub3/subOsub4/sub@AuNPs were characterized by spectroscopies, transmission electron microscopy (TEM) and energy dispersive X-ray diffraction. The effect of the nanoparticles on the MRI signal was tested using a 7T Bruker PharmaScan system. Cytotoxicity tests were made in vitro on Fesub3/subOsub4/sub@AuNP-treated retinal pigment epithelium cells by WST-1 tests and in vivo by following histopathological changes in rats after injection of Fesub3/subOsub4/sub@AuNPs. Results: Stable Fesub3/subOsub4/sub@AuNPs were successfully prepared following a simple and fast protocol ( 1h worktime) and identified using TEM. The cytotoxicity tests on cells have shown biocompatibility of Fesub3/subOsub4/sub@AuNPs at small concentrations of Fe ( 1.95× 10sup? 8/sup mg/cell). Whereas, at higher Fe concentrations (eg 7.5× 10sup? 8/sup mg/cell), cell viability decreased to 80.88± 5.03%, showing a mild cytotoxic effect. MRI tests on rats showed an optimal Fesub3/subOsub4/sub@AuNPs concentration of 6mg/100g body weight to obtain high-quality images. The histopathological studies revealed significant transient inflammatory responses in the time range from 2 hours to 14 days after injection and focal cellular alterations in several organs, with the lung being the most affected organ. These results were confirmed by hyperspectral microscopic imaging of the same, but unstained tissues. In most organs, the inflammatory responses and sublethal cellular damage appeared to be transitory, except for the kidneys, where the glomerular damage indicated progression towards glomerular sclerosis. Conclusion: The obtained stable, gold covered, iron oxide nanoparticles with reduced cytotoxicity, gave a negative Tsub2/sub signal in the MRI, which makes them suitable for candidates as contrast agent in small animal MRI applications.
机译:目的:磁共振成像(MRI)造影剂是能够更好地可视化内体结构的药物。在这项研究中,我们介绍了合成,MRI信号增强能力,体外以及镀金氧化铁纳米颗粒的体内细胞毒性结果(Fe 3 O 4 @ aunps)作为潜在的造影剂。方法:通过合成氧化铁纳米颗粒并逐渐用金涂覆它们来获得Fe 3 o 3 O 4 @aunps通过光谱,透射电子显微镜(TEM)和能量分散X射线衍射。使用7T Bruker药物系统测试纳米颗粒对MRI信号的影响。通过WST-1试验和在注射后的大鼠组织病理学变化下,在Fe 3 O 4 o 4 o 4 @ a / sup> @ a / sub> @ / sub> o 3 O 4 @aunps。结果:稳定FE 3 O 4 @aunps在简单快速的协议(<1h工作时)后成功准备并使用TEM识别。细胞上的细胞毒性试验表明,在小浓度的Fe(<1.95×10 8 / sup> mg / mg /)下,细胞的生物相容性为Fe 3 O 4 @aunps。细胞)。然而,在更高的Fe浓度(例如7.5×10 α8 mg / cell),细胞活力降至80.88±5.03%,显示出轻度细胞毒性效应。对大鼠的MRI测试显示出最佳Fe 3 O 4 @aunps浓度为6mg / 100g体重,以获得高质量的图像。组织病理学研究表明,在几小时到14天的时间范围内显示出几小时至14天,几个器官的局灶性细胞改变,肺部是受影响最大的器官。通过Hyperspectral微观成像确认这些结果,但是未染色的组织。在大多数器官中,除了肾脏外,炎症反应和止吐细胞损伤似乎是暂时的,其中肾小球损伤表明肾小球硬化的进展。结论:获得的稳定,金覆盖,具有降低细胞毒性的氧化铁纳米颗粒,在MRI中产生负T <亚次> 2 信号,使其适用于小型动物MRI应用中的患者作为造影剂。

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