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[Imaging Diagnosis of Ischemic Stroke Through Multiparametric Magnetic Resonance Angiography Enhanced by NaGdF4
Jin Wu1, Yuqiang Ma1,2, Saisai Yue1,2
1( 100029) Physical Examination Center, China-Japan Friendship Hospital, Beijing 100029, China.
Objective:
To develop an ultra-sensitive nanoparticle contrast agent for magnetic resonance angiography (MRA), to establish a highly sensitive imaging method for complicated vascular structures, and to provide imaging evidence for precision diagnosis, treatment, prognosis, and individualized treatment of ischemic stroke.
Methods:
A dual-modality MRA contrast agent was prepared through ligand exchange of ultra-small NaGdF4 nanocrystals synthesized via a high temperature method, with biocompatible polyethylene glycol (PEG-dp) ligands. The basic structure, morphology, size distribution, and relaxation rate of the NaGdF4 nano contrast agent were characterized using transmission electron microscopy (TEM), a particle size potential analyzer, and a 7.0 T small-animal MRI scanner. A total of 6 healthy male SPF-grade BALB/c mice were selected and randomly divided into two groups, a NaGdF4 group and a Gd-DTPA group. The mice in the two groups were injected with NaGdF4 nanoparticle contrast agent or clinical Gd-DTPA contrast agent (0.1 mmol Gd3+/kg) via the tail vein. MRA images were obtained using a 7.0 T small animal magnetic resonance imaging system before and after the injection. A total of 6 healthy male SPF-grade Sprague Dawley (SD) rats were selected to establish a right middle cerebral artery occlusion (rMCAO) model to simulate ischemic stroke. The rats were injected with NaGdF4 nano-contrast agent (0.1 mmol Gd3+/kg) via the tail vein. Before and after the injection, brain MRI images of the rats were obtained using a 7.0 T small animal magnetic resonance imaging system. The in vitro and in vivo biological safety of the nano contrast agent was verified through cytotoxicity and hemolysis experiments and HE staining.
Results:
Uniform spherical oil-phase NaGdF4 nanocrystals with an average particle size of approximately (4.43 ± 0.46) nm were successfully prepared. After ligand exchange, biocompatible water-phase nanocrystals were obtained with a hydrodynamic size of 16.1 nm and a surface potential of -1.9 mV. The relaxation performance of this nanocrystal contrast agent was significantly superior to that of the clinical contrast agent Gd-DTPA. The longitudinal molar relaxivity rate (r 1) of the NaGdF4 nano contrast agent was 8.84 mM-1s-1, while the transverse molar relaxivity rate (r 2) was 27.36 mM-1s-1, which were 1.96 times (4.52 mM-1s-1) and 3.37 times (8.13 mM-1s-1) those of Gd-DTPA, respectively. It also demonstrated excellent biocompatibility. NaGdF4-enhanced MRA achieved high-resolution vascular imaging and effectively enabled the differentiation of the ischemic area, infarct core, and ischemic penumbra in an animal model of ischemic stroke.
Conclusion:
The multi-parameter MRA based on NaGdF4 nanoparticles provides critical imaging evidence for the clinical diagnosis and prognosis of ischemic stroke.
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