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单臂和多臂钆磁共振对比剂在脑胶质瘤靶向成像中的应用。

Single- and Multi-Arm Gadolinium MRI Contrast Agents for Targeted Imaging of Glioblastoma.

机构信息

Nanomedicine Research Center, Department of Neurosurgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.

Biomedical Imaging Research Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.

出版信息

Int J Nanomedicine. 2020 May 1;15:3057-3070. doi: 10.2147/IJN.S238265. eCollection 2020.

Abstract

BACKGROUND

Position of gadolinium atom(s) plays a key role in contrast enhancement of gadolinium-based contrast agents. To gain a better understanding of effects of distance of gadolinium in relation to the nanoconjugate platform, we designed and synthesized single- and multi-arm ("star") gadolinium conjugates equipped with antibody and peptides for targeting. The contrast agents were studied for their tumor imaging performance in a glioma mouse model.

MATERIALS AND METHODS

Antibody- and peptide-targeted nano contrast agents (NCAs) were synthesized using polymalic acid platforms of different sizes. Gadolinium-DOTA and intermediates were attached as amides and targeting agents such as antibodies and peptides as thioethers. For in vivo experiments, we used human U87MG xenografts as glioma models. Magnetic resonance imaging (MRI) was performed on a Bruker BioSpec 94/20USR 9.4 T small-animal scanner. Delivery of contrast agents across the blood-brain barrier was studied by fluorescent microscopy.

RESULTS

All contrast agents accumulated into tumor and showed composition-dependent imaging performance. Peptide-targeted mini-NCAs had hydrodynamic diameters in the range 5.2-9.4 nm and antibody-targeted NCAs had diameters in the range 15.8-20.5 nm. Zeta potentials were in the range of -5.4--8.2 mV and -4.6--8.8 mV, respectively. NCAs showed superior relaxivities compared to MultiHance at 9.4 T. The signal enhancement indicated maximum accumulation in tumor 30-60 minutes after intravenous injection of the mouse tail vein. Only targeted NCAs were retained in tumor for up to 3 hours and displayed contrast enhancement.

CONCLUSION

The novel targeted NCAs with star-PEG features displayed improved relaxivity and greater contrast compared with commercial MultiHance contrast agent. The enhancement by mini-NCAs showed clearance of tumor contrast after 3 hours providing a suitable time window for tumor diagnosis in clinics. The technology provides a great tool with the promise of differential MRI diagnosis of brain tumors.

摘要

背景

镓原子的位置在基于镓的对比剂的对比增强中起着关键作用。为了更好地了解镓与纳米缀合物平台之间的距离的影响,我们设计并合成了带有抗体和肽的单臂和多臂(“星型”)镓缀合物用于靶向。这些对比剂在神经胶质瘤小鼠模型中进行了肿瘤成像性能研究。

材料和方法

使用不同大小的聚马来酸平台合成了抗体和肽靶向的纳米对比剂(NCAs)。将镓-DOTA 和中间体作为酰胺连接,并将抗体和肽等靶向剂作为硫醚连接。对于体内实验,我们使用人 U87MG 异种移植作为神经胶质瘤模型。磁共振成像(MRI)在 Bruker BioSpec 94/20USR 9.4 T 小动物扫描仪上进行。通过荧光显微镜研究了对比剂穿过血脑屏障的传递情况。

结果

所有对比剂都聚集在肿瘤中,并表现出与组成相关的成像性能。肽靶向的迷你 NCAs 的水动力直径在 5.2-9.4nm 范围内,抗体靶向的 NCAs 的直径在 15.8-20.5nm 范围内。Zeta 电位分别在-5.4--8.2mV 和-4.6--8.8mV 范围内。NCAs 在 9.4T 下的弛豫率优于 MultiHance。信号增强表明,在静脉注射小鼠尾静脉后 30-60 分钟,肿瘤内的最大积累。只有靶向 NCAs 在肿瘤中保留长达 3 小时,并显示出对比增强。

结论

具有星型-PEG 特征的新型靶向 NCAs 与商业 MultiHance 造影剂相比,显示出更高的弛豫率和更大的对比度。迷你 NCAs 的增强在 3 小时后清除了肿瘤对比,为临床肿瘤诊断提供了合适的时间窗口。该技术提供了一种很好的工具,有望实现脑肿瘤的磁共振成像诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30df/7200230/1d7f4a3f891e/IJN-15-3057-g0001.jpg

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