CAS Key Lab for Biomedical Effects of Nanomaterials and Nanosafety, National Center for Nanoscience and Technology of China , Beijing 100190, P. R. China.
Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University , Hangzhou 310058, P. R. China.
ACS Nano. 2015 Dec 22;9(12):12425-35. doi: 10.1021/acsnano.5b05783. Epub 2015 Nov 23.
Magnetic resonance imaging (MRI) contrast agents with high relaxivity are highly desirable because they can significantly increase the accuracy of diagnosis. However, they can be potentially toxic to the patients. In this study, using a mouse model, we investigate the toxic effects and subsequent tissue damage induced by three T1 MRI contrast agents: gadopentetate dimeglumine injection (GDI), a clinically used gadolinium (Gd)-based contrast agent (GBCAs), and oxide nanoparticle (NP)-based contrast agents, extremely small-sized iron oxide NPs (ESIONs) and manganese oxide (MnO) NPs. Biodistribution, hematological and histopathological changes, inflammation, and the endoplasmic reticulum (ER) stress responses are evaluated for 24 h after intravenous injection. These thorough assessments of the toxic and stress responses of these agents provide a panoramic description of safety concerns and underlying mechanisms of the toxicity of contrast agents in the body. We demonstrate that ESIONs exhibit fewer adverse effects than the MnO NPs and the clinically used GDI GBCAs, providing useful information on future applications of ESIONs as potentially safe MRI contrast agents.
磁共振成像(MRI)对比剂具有高弛豫率是非常理想的,因为它们可以显著提高诊断的准确性。然而,它们可能对患者有潜在的毒性。在这项研究中,我们使用小鼠模型研究了三种 T1 MRI 对比剂:钆喷酸葡胺注射液(GDI)、临床使用的基于钆(Gd)的对比剂(GBCAs)和基于氧化物纳米颗粒(NP)的对比剂,即超小尺寸氧化铁 NPs(ESIONs)和氧化锰(MnO) NPs,引起的毒性作用和随后的组织损伤。在静脉注射后 24 小时内评估其分布、血液学和组织病理学变化、炎症和内质网(ER)应激反应。这些对这些药物的毒性和应激反应的全面评估提供了对体内对比剂安全性问题和毒性机制的全面描述。我们证明,ESIONs 比 MnO NPs 和临床使用的 GDI GBCAs 表现出更少的不良反应,为 ESIONs 作为潜在安全的 MRI 对比剂的未来应用提供了有用的信息。