磁共振成像
化学
纳米颗粒
氧化铁纳米粒子
氧化铁
纳米技术
信号(编程语言)
磁性纳米粒子
核磁共振
材料科学
计算机科学
放射科
医学
物理
有机化学
程序设计语言
作者
Jinhong Hou,Hongqian Liu,Ma Qian,Suying Xu,Leyu Wang
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2022-11-03
卷期号:94 (45): 15578-15585
被引量:16
标识
DOI:10.1021/acs.analchem.2c01341
摘要
Accurate diagnosis of diseases located in deep tissues is always challenging. The “always-on” probe often leads to false-positive signals due to nonspecific interaction of nanoprobes. Thus, stimuli-responsive nanoprobes are highly desirable, which, however, require complicated surface modification so as to achieve trigger-induced signal changes. Here pH-triggered switchable magnetic resonance imaging (MRI) nanoprobes were constructed by coordination-driven self-assembly of monodispersed iron oxide nanoparticles (MIONPs) with simple amino acid derivatives, which displayed typical T2-weighted MRI features, yet, were turned into T1-weighted MRI under slightly acidic conditions at the tumor site. The dynamic assembly and disassembly properties of MIONPs afford T2/T1 switchable contrast imaging, enabling selective “turn-on” signals at the tumor site with high specificity.
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