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长循环 Gd(2)O(3):Yb(3+), Er(3+) 上转换纳米探针作为多模态成像的高性能造影剂。

Long-circulating Gd(2)O(3):Yb(3+), Er(3+) up-conversion nanoprobes as high-performance contrast agents for multi-modality imaging.

机构信息

State Key Laboratory of Rare Earth Resources Utilization and Laboratory of Chemical Biology, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin 130022, China.

出版信息

Biomaterials. 2013 Feb;34(6):1712-21. doi: 10.1016/j.biomaterials.2012.11.009. Epub 2012 Nov 29.

DOI:10.1016/j.biomaterials.2012.11.009
PMID:23199744
Abstract

Due to their unique electric, magnetic, and optical properties, engineered nanostructures have been applied to provide diagnostic, therapeutic, as well as prognostic information about the status of disease. In this study, we report a multifunctional nanoprobe based on PEGylated Gd(2)O(3):Yb(3+), Er(3+) nanorods (denoted as PEG-UCNPs) for in vivo up-conversion luminescence (UCL), T(1)-enhanced magnetic resonance (MR), and X-ray computed tomography (CT) multi-modality imaging. A facile and large-scale hydrothermal system combining the merits of an in situ thermal decomposition method and a surface-modified approach is introduced to construct high-quality PEG-UCNPs. By grafting PEG molecules on the surface of PEG-UCNPs, the nanostructures possess excellent stability against in vivo environment and hold long blood circulation time. Cell-cytotoxicity assay, hemolyticity, as well as post-injection histology, hematology, and inflammation analysis further demonstrate their non-cytotoxic character and indicate further in vivo application. In detail, the capability of PEG-UCNPs as high-performance contrast agents for UCL/MR/CT imaging is evaluated successfully through small-animal experiments. Additionally, pharmacokinetics, biodistribution, and clearance route are studied after intravenous injection in a mouse model, reflecting their overall safety.

摘要

由于其独特的电、磁和光学特性,工程纳米结构已被应用于提供有关疾病状态的诊断、治疗和预后信息。在本研究中,我们报告了一种基于 PEGylated Gd(2)O(3):Yb(3+)、Er(3+)纳米棒(表示为 PEG-UCNPs)的多功能纳米探针,用于体内上转换发光(UCL)、T(1)增强磁共振(MR)和 X 射线计算机断层扫描(CT)多模态成像。我们介绍了一种简便且大规模的水热系统,该系统结合了原位热分解法和表面修饰方法的优点,用于构建高质量的 PEG-UCNPs。通过在 PEG-UCNPs 的表面接枝 PEG 分子,这些纳米结构具有出色的抗体内环境稳定性,并且具有较长的血液循环时间。细胞毒性测定、溶血以及注射后组织学、血液学和炎症分析进一步证明了它们的非细胞毒性特征,并表明了进一步的体内应用。具体来说,通过小动物实验成功评估了 PEG-UCNPs 作为 UCL/MR/CT 成像的高性能造影剂的能力。此外,在小鼠模型中进行了静脉注射后的药代动力学、生物分布和清除途径研究,反映了其整体安全性。

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