Issue 15, 2016

Hybrid lanthanide nanoparticles as a new class of binary contrast agents for in vivo T1/T2 dual-weighted MRI and synergistic tumor diagnosis

Abstract

Lanthanide nanoparticles (NPs), which are known as upconversion fluorescence probes for multimodal bioimaging, including magnetic resonance imaging (MRI), have attracted much attentions. In MRI, conventional contrast agents are generally employed separately in a single type of MRI. T1- and T2-weighted MRI alone have unique limitations; therefore, it is urgently necessary to combine the two modalities so as to be able to provide more comprehensive and synergistic diagnostic information than the single modality of MRI. Unfortunately, there is a lack of advanced materials as enhancing agents which are fully suitable for bimodal MRI. Here, we report a new class of hybrid lanthanide nanoparticles as synergistic contrast agents in T1/T2 dual-weighted MRI and imaging-directed tumor diagnosis. The r2/r1 value of BaGdF5 NPs can be readily adjusted from 2.8 to 334.8 by doping with 0%, 50%, or 100% Ln3+ (Ln3+ = Yb3+, Er3+, or Dy3+), respectively. Among these, BaGdF5:50% Er3+ NPs were successfully used as binary contrast agents for T1/T2 dual-weighted MRI and synergistic tumor diagnosis in vivo. These findings reveal that the longitudinal and transverse relaxivities of these Gd3+-based NPs can be controlled by tuning the Ln3+ dopants and their concentrations, providing a simple and general method for designing simultaneous T1/T2 enhancing agents.

Graphical abstract: Hybrid lanthanide nanoparticles as a new class of binary contrast agents for in vivo T1/T2 dual-weighted MRI and synergistic tumor diagnosis

Associated articles

Supplementary files

Article information

Article type
Paper
Submitted
13 Nov 2015
Accepted
22 Mar 2016
First published
22 Mar 2016

J. Mater. Chem. B, 2016,4, 2715-2722

Hybrid lanthanide nanoparticles as a new class of binary contrast agents for in vivo T1/T2 dual-weighted MRI and synergistic tumor diagnosis

Z. Yi, X. Li, W. Lu, H. Liu, S. Zeng and J. Hao, J. Mater. Chem. B, 2016, 4, 2715 DOI: 10.1039/C5TB02375K

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