Jie Chen, Xiaoming Wang, Yinan Bai, Zhiqian Li, Haonan Li, Bing Wang, Qiyong Gong, Kui Luo
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引用次数: 0
摘要
开发用于肝癌靶向磁共振成像(MRI)的新型钆基造影剂仍然是一个巨大的挑战。在此,我们报道了一种新型的基于gd的MRI造影剂,它具有改进的弛豫性,可用于特异性诊断肝癌。采用RAFT聚合法制备gsh反应性大分子造影剂POLDGd,其乳酸片段可以精确靶向肝癌细胞上的ASGP-R表面蛋白,而不含乳酸片段的PODGd作为对照。POLDGd分子量为45 kDa,粒径为103 nm。3.0 T MR扫描仪测得其纵向弛缓度(11.39 mM-1 s-1)是临床使用造影剂DTPA-Gd的3倍。与podgd治疗组相比,肿瘤部位的信号增强明显延长,荷瘤小鼠静脉注射POLDGd后,最大增强峰约为190%。荧光成像也证实了肝脏肿瘤中POLDGd的高积累水平。POLDGd显示出最小的副作用,这可能归因于其通过肾脏的代谢。因此,POLDGd可作为一种高效的生物安全纳米造影剂用于肝癌的靶向MRI。
An ASGP-R-targeting magnetic resonance imaging contrast agent for liver cancer diagnosis.
Development of novel Gd-based contrast agents for targeted magnetic resonance imaging (MRI) of liver cancer remains a great challenge. Herein we reported a novel Gd-based MRI contrast agent with improved relaxivity for specifically diagnosing liver cancer. This GSH-responsive macromolecular contrast agent (mCA), POLDGd, was prepared by RAFT polymerization, and its lactic acid moiety could precisely target the ASGP-R surface protein on liver cancer cells, whereas PODGd without the lactic acid moiety was prepared as a control. POLDGd had a high molecular weight of 45 kDa and a particle size of 103 nm. Its longitudinal relaxivity (11.39 mM-1 s-1) measured via a 3.0 T MR scanner was three times that of the clinically used contrast agent DTPA-Gd. In comparison with the PODGd-treated group, the signal enhancement at the tumor site was significantly prolonged, with a maximum enhancement peak of about 190% after intravenous injection of POLDGd into tumor-bearing mice. A high accumulation level of POLDGd in the liver tumors observed via MRI was also confirmed by fluorescence imaging. POLDGd showed minimal side effects, which may be ascribed to its metabolism through the kidneys. Therefore, POLDGd may be used as a highly effective biosafe nanoscale contrast agent for targeted MRI of liver cancer.