| Literature DB >> 30856326 |
Zijuan Hai1,2, Yanhan Ni1, Dilizhatai Saimi1, Hongyi Yang3, Haiyang Tong3, Kai Zhong3, Gaolin Liang1.
Abstract
Magnetic resonance imaging (MRI) is advantageous in the diagnosis of deep internal cancers, but contrast agents (CAs) are always needed to improve MRI sensitivity. Gadolinium (Gd)-based agents are routinely used as T1-dominated CAs in clinic but using intracellularly formed Gd nanoparticles to enhance the T2-weighted MRI of tumor in vivo at high magnetic field has not been reported. Herein, we rationally designed a "smart" Gd-based probe Glu-Cys(StBu)-Lys(DOTA-Gd)-CBT (1), which was subjected to γ-glutamyltranspeptidase (GGT) cleavage and an intracellular CBT-Cys condensation reaction to form Gd nanoparticles (i.e., 1-NPs) to enhance the T2-weighted MR contrast of tumor in vivo at 9.4 T. Living cell experiments indicated that the 1-treated HeLa cells had an r2 value of 27.8 mM-1 s-1 and an r2/r1 ratio of 10.6. MR imaging of HeLa tumor-bearing mice indicated that the T2 MR contrast of the tumor enhanced 28.6% at 2.5 h post intravenous injection of 1. We anticipate that our probe 1 could be employed for T2-weighted MRI diagnosis of GGT-related cancers in the future when high magnetic field is available in clinic.Entities:
Keywords: T2-weighted magnetic resonance imaging; gadolinium nanoparticle; γ-Glutamyltranspeptidase
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Year: 2019 PMID: 30856326 DOI: 10.1021/acs.nanolett.8b05154
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189