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首页> 外文期刊>NMR in biomedicine >Manganese-enhanced MRI of rat brain based on slow cerebral delivery of manganese(II) with silica-encapsulated Mn_xFe_(1–x)O nanoparticles
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Manganese-enhanced MRI of rat brain based on slow cerebral delivery of manganese(II) with silica-encapsulated Mn_xFe_(1–x)O nanoparticles

机译:基于锰包裹的Mn_xFe_(1-x)O纳米粒子缓慢递送锰(II)的大鼠脑锰增强MRI

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In this work, we report a monodisperse bifunctional nanoparticle system, MIO@SiO_2-RITC, as an MRI contrast agent [core, manganese iron oxide (MIO); shell, amorphous silica conjugated with rhodamine B isothiocyanate (RITC)]. It was prepared by thermal decomposition and modified microemulsion methods. The nanoparticles with varying iron to manganese ratios displayed different saturated magnetizations and relaxivities. In vivo MRI of rats injected intravenously with MIO@SiO_2-RITC nanoparticles exhibited enhancement of the T_1 contrast in brain tissue, in particular a time-delayed enhancement in the hippocampus, pituitary gland, striatum and cerebellum. This is attributable to the gradual degradation of MIO@SiO_2-RITC nanoparticles in the liver, resulting in the slow release of manganese(II) [Mn(II)] into the blood pool and, subsequently, accumulation in the brain tissue. Thus, T_1-weighted contrast enhancement was clearly detected in the anatomic structure of the brain as time progressed. In addition, T_2~*-weighted images of the liver showed a gradual darkening effect. Here, we demonstrate the concept of the slow release of Mn(II) for neuroimaging. This new nanoparticle-based manganese contrast agent allows one simple intravenous injection (rather than multiple infusions) of Mn(II) precursor, and results in delineation of the detailed anatomic neuroarchitecture in MRI; hence, this provides the advantage of the long-term study of neural function.
机译:在这项工作中,我们报告了单分散双功能纳米粒子系统MIO @ SiO_2-RITC,作为MRI造影剂[核心,锰铁氧化物(MIO);壳,与罗丹明B异硫氰酸盐(RITC)共轭的无定形二氧化硅]。它是通过热分解和改进的微乳液方法制备的。铁锰比变化的纳米颗粒表现出不同的饱和磁化强度和弛豫度。静脉注射MIO @ SiO_2-RITC纳米颗粒的大鼠的体内MRI显示脑组织中T_1造影剂增强,特别是海马,垂体,纹状体和小脑的时间延迟增强。这归因于MIO @ SiO_2-RITC纳米颗粒在肝脏中逐渐降解,导致锰(II)[Mn(II)]缓慢释放到血池中,并随后在脑组织中积累。因此,随着时间的流逝,在大脑的解剖结构中可以清楚地检测到T_1加权对比度增强。另外,肝脏的T_2〜*加权图像显示逐渐变暗的作用。在这里,我们演示了Mn(II)缓慢释放的神经影像学概念。这种新的基于纳米颗粒的锰对比剂允许一次简单的静脉内注射(而不是多次输注)Mn(II)前体,从而勾勒出MRI中详细的解剖神经结构。因此,这提供了长期研究神经功能的优势。

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