Chen Hongyu, Colvin Daniel C, Qi Bin, Moore Thomas, He Jian, Mefford O Thompson, Alexis Frank, Gore John C, Anker Jeffrey N
Department of Chemistry, Center for optical materials science and engineering (COMSET), and environmental toxicology program; Clemson University, Clemson, SC, 29634, USA.
Vanderbilt University Institute of Imaging Science (VUIIS), Department of Radiology and Radiological Sciences Vanderbilt University, Nashville, TN, 37232, USA.
J Mater Chem. 2012 Jul 7;22(25):12802-12809. doi: 10.1039/C2JM15444G.
When X-rays irradiate radioluminescence nanoparticles, they generate visible and near infrared light that can penetrate through centimeters of tissue. X-ray luminescence tomography (XLT) maps the location of these radioluminescent contrast agents at high resolution by scanning a narrow X-ray beam through the tissue sample and collecting the luminescence at every position. Adding magnetic functionality to these radioluminescent particles would enable them to be guided, oriented, and heated using external magnetic fields, while their location and spectrum could be imaged with XLT and complementary magnetic resonance imaging. In this work, multifunctional monodispersed magnetic radioluminescent nanoparticles were developed as potential drug delivery carriers and radioluminescence imaging agents. The particles consisted of a spindle-shaped magnetic γ-FeO core and a radioluminescent europium-doped gadolinium oxide shell. Particles with solid iron oxide cores displayed saturation magnetizations consistent with their ~13% core volume, however, the iron oxide quenched their luminescence. In order to increase the luminescence, we partially etched the iron oxide core in oxalic acid while preserving the radioluminescent shell. The core size was controlled by the etching time which in turn affected the particles' luminescence and magnetic properties. Particles with intermediate core sizes displayed both strong magnetophoresis and luminescence properties. They also served as MRI contrast agents with relaxivities of up to 58 mMs (r) and 120 mMs (r*). These particles offer promising multimodal MRI/fluorescence/X-ray luminescence contrast agents. Our core-shell synthesis technique offers a flexible method to control particle size, shape, and composition for a wide range of biological applications of magnetic/luminescent nanoparticles.
当X射线照射放射性发光纳米粒子时,它们会产生可见光和近红外光,这些光能够穿透几厘米厚的组织。X射线发光断层扫描(XLT)通过将窄X射线束扫描穿过组织样本并在每个位置收集发光信号,以高分辨率绘制这些放射性发光造影剂的位置。给这些放射性发光粒子添加磁性功能,将使它们能够利用外部磁场进行引导、定向和加热,同时它们的位置和光谱可以通过XLT和互补的磁共振成像进行成像。在这项工作中,开发了多功能单分散磁性放射性发光纳米粒子,作为潜在的药物递送载体和放射性发光成像剂。这些粒子由纺锤形磁性γ-FeO核和放射性发光的铕掺杂氧化钆壳组成。具有实心氧化铁核的粒子显示出与其约13%的核体积一致的饱和磁化强度,然而,氧化铁会淬灭它们的发光。为了增加发光,我们在草酸中部分蚀刻氧化铁核,同时保留放射性发光壳。核尺寸由蚀刻时间控制,蚀刻时间反过来又影响粒子的发光和磁性。具有中等核尺寸的粒子同时表现出强磁泳和发光特性。它们还用作MRI造影剂,弛豫率高达58 mM s⁻¹(r₁)和120 mM s⁻¹(r₂*)。这些粒子提供了有前景的多模态MRI/荧光/X射线发光造影剂。我们的核壳合成技术提供了一种灵活的方法来控制粒子的大小、形状和组成,以用于磁性/发光纳米粒子的广泛生物应用