The Renal Clearable Magnetic Resonance Imaging Contrast Agents: State of the Art and Recent Advances

被引:14
|
作者
Li, Xiaodong [1 ]
Sun, Yanhong [2 ]
Ma, Lina [2 ]
Liu, Guifeng [1 ]
Wang, Zhenxin [2 ]
机构
[1] Jilin Univ, Dept Radiol, China Japan Union Hosp, Xiantai St, Changchun 130033, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Peoples R China
来源
MOLECULES | 2020年 / 25卷 / 21期
基金
中国国家自然科学基金;
关键词
magnetic resonance imaging contrast agents; renal clearance; nanodots; gadolinium (III)-based composites; IRON-OXIDE NANOPARTICLES; CARBON QUANTUM DOTS; GD3+-FUNCTIONALIZED GOLD NANOCLUSTERS; MANGANESE FERRITE NANOPARTICLES; FUNCTIONALIZED NAGDF4 NANODOTS; GD2O3; NANOPARTICLES; HIGH-PERFORMANCE; POLYACRYLIC-ACID; FACILE SYNTHESIS; HIGH-RELAXIVITY;
D O I
10.3390/molecules25215072
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The advancements of magnetic resonance imaging contrast agents (MRCAs) are continuously driven by the critical needs for early detection and diagnosis of diseases, especially for cancer, because MRCAs improve diagnostic accuracy significantly. Although hydrophilic gadolinium (III) (Gd3+) complex-based MRCAs have achieved great success in clinical practice, the Gd3+-complexes have several inherent drawbacks including Gd3+ leakage and short blood circulation time, resulting in the potential long-term toxicity and narrow imaging time window, respectively. Nanotechnology offers the possibility for the development of nontoxic MRCAs with an enhanced sensitivity and advanced functionalities, such as magnetic resonance imaging (MRI)-guided synergistic therapy. Herein, we provide an overview of recent successes in the development of renal clearable MRCAs, especially nanodots (NDs, also known as ultrasmall nanoparticles (NPs)) by unique advantages such as high relaxivity, long blood circulation time, good biosafety, and multiple functionalities. It is hoped that this review can provide relatively comprehensive information on the construction of novel MRCAs with promising clinical translation.
引用
收藏
页数:26
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