Simulated Measurements of the Magnetic Behavior of New Dual-Mode Nanosized Contrast Agents

被引:2
作者
Franchini, Roberto [1 ]
Casciaro, Ernesto [1 ]
Conversano, Francesco [1 ]
Lay-Ekuakille, Aime [2 ]
Casciaro, Sergio [1 ]
机构
[1] CNR, Inst Clin Physiol, I-73100 Lecce, Italy
[2] Univ Salento, Dept Innovat Engn, I-73100 Lecce, Italy
关键词
Blood flow measurements; magnetic resonance imaging; multimodal contrast agents; nanoparticles; numerical simulations; superparamagnetic nanocrystals; ultrasound; venography; IRON-OXIDE NANOPARTICLES; SILICA NANOPARTICLES; FEPT NANOPARTICLES; MRI; RESOLUTION; NANOMEDICINE; MICROBUBBLES; HYPERTHERMIA; VENOGRAPHY;
D O I
10.1109/TNANO.2017.2681460
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Aim of this work was to perform simulated measurements of the magnetic behavior of a novel class of bimodal nanosized contrast agents (CAs), made of a silica core covered by smaller superparamagnetic nanoparticles (NPs) and designed to be detected through both ultrasound and magnetic resonance imaging (MRI), in order to compare their performance in terms of MRI signal enhancement with that of the superparamagnetic NPs alone. The considered bimodal nanocomposites consisted of 330-nm silica nanospheres covered by either superparamagnetic iron oxide NPs or dumbbell-like FePt-IO nanocrystals. We simulated the MRI signal generated by each of the considered CAs during a brain venography in standard clinical conditions. Quantitative assessments of signal enhancement were carried out as a function of the main model parameters. The performed numerical simulations showed that the magnetic response of the novel nanocomposites was similar or better compared to that of the superparamagnetic NPs alone for echo times longer than 20 ms, leading to an easier detection of smaller vessels. Obtained results suggest that the bimodal NPs have an exciting potential for the development of innovative clinical protocols for multimodal imaging, combining quantitative measurements of cerebral blood flow and targeted molecular imaging of specific diseases.
引用
收藏
页码:842 / 850
页数:9
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