Hybrid lanthanide nanoparticles as a new class of binary contrast agents for in vivo T1/T2 dual-weighted MRI and synergistic tumor diagnosis. Issue 15 (5th April 2016)

• Record Type: Journal Article
• Authors: Yi, Zhigao; Li, Xiaolong; Lu, Wei; Liu, Hongrong; Zeng, Songjun; Hao, Jianhua
• Is Part Of: Journal of materials chemistry. Volume 4:Issue 15(2016)
• Page Start: 2715
• Page End: 2722
• Publication Date: 2016-04-05
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Biomedical materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c5tb02375k
• Languages: English
• ISSNs: 2050-750X

Abstract

Abstract : A new class of hybrid lanthanide nanoparticles has been demonstrated as synergistic contrast agents in T 1 / T 2 dual-weighted MRI and imaging-directed 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. T 1 - and T 2 -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 T 1 / T 2 dual-weighted MRI and imaging-directed tumor diagnosis. The r 2 / r 1 value of BaGdF5 NPs can be readily adjusted from 2.8 to 334.8 by doping with 0%, 50%, or 100% Ln 3+ (Ln 3+ = Yb 3+, Er 3+, or Dy 3+ ), respectively. Among these, BaGdF5 :50% Er 3+ NPs were successfully used as binary contrast agents for T 1 / T 2 dual-weighted MRI and synergistic tumor diagnosis in vivo . These findings reveal that the longitudinal and transverse relaxivities of these Gd 3+ -based NPs can be controlled by tuning the Ln 3+ dopants and their concentrations, providing a simple and general method for designing simultaneous T 1 / T 2 enhancing agents.