Poggiarelli Linda, Bernetti Caterina, Pugliese Luca, Greco Federico, Beomonte Zobel Bruno, Mallio Carlo A
School of Medicine, Università Campus Bio-Medico di Roma, via Alvaro Del Portillo, 21, 00128 Rome, Italy.
Research Unit of Diagnostic Imaging, Department of Medicine and Surgery, Università Campus Bio-Medico di Roma, 00128 Rome, Italy.
Clin Pract. 2025 Jul 25;15(8):137. doi: 10.3390/clinpract15080137.
BACKGROUND/OBJECTIVES: Magnetic resonance imaging (MRI) is a powerful, non-invasive diagnostic tool capable of capturing detailed anatomical and physiological information. MRI contrast agents enhance image contrast but, especially linear gadolinium-based compounds, have been associated with safety concerns. This has prompted interest in alternative contrast agents. Manganese-based contrast agents offer a promising substitute, owing to manganese's favorable magnetic properties, natural biological role, and strong T1 relaxivity. This review aims to critically assess the structure, mechanisms, applications, and challenges of manganese-based contrast agents in MRI.
This review synthesizes findings from preclinical and clinical studies involving various types of manganese-based contrast agents, including small-molecule chelates, nanoparticles, theranostic platforms, responsive agents, and controlled-release systems. Special attention is given to pharmacokinetics, biodistribution, and safety evaluations.
Mn-based agents demonstrate promising imaging capabilities, with some achieving relaxivity values comparable to gadolinium compounds. Targeted uptake mechanisms, such as hepatocyte-specific transport via organic anion-transporting polypeptides, allow for enhanced tissue contrast. However, concerns remain regarding the in vivo release of free Mn ions, which could lead to toxicity. Preliminary toxicity assessments report low cytotoxicity, but further comprehensive long-term safety studies should be carried out.
Manganese-based contrast agents present a potential alternative to gadolinium-based MRI agents pending further validation. Despite promising imaging performance and biocompatibility, further investigation into stability and safety is essential. Additional research is needed to facilitate the clinical translation of these agents.
背景/目的:磁共振成像(MRI)是一种强大的非侵入性诊断工具,能够获取详细的解剖和生理信息。MRI造影剂可增强图像对比度,但尤其是基于线性钆的化合物,已引发安全担忧。这促使人们对替代造影剂产生兴趣。基于锰的造影剂由于锰具有良好的磁性、天然生物学作用和较强的T1弛豫率,提供了一种有前景的替代物。本综述旨在严格评估基于锰的造影剂在MRI中的结构、机制、应用和挑战。
本综述综合了涉及各种类型基于锰的造影剂的临床前和临床研究结果,包括小分子螯合物、纳米颗粒、诊疗平台、响应剂和控释系统。特别关注药代动力学、生物分布和安全性评估。
基于锰的造影剂显示出有前景的成像能力,一些造影剂的弛豫率值可与钆化合物相媲美。靶向摄取机制,如通过有机阴离子转运多肽的肝细胞特异性转运,可增强组织对比度。然而,对于游离锰离子在体内的释放仍存在担忧,这可能导致毒性。初步毒性评估报告细胞毒性较低,但应进行进一步全面的长期安全性研究。
在进一步验证之前,基于锰的造影剂是钆基MRI造影剂的潜在替代品。尽管具有有前景的成像性能和生物相容性,但对稳定性和安全性的进一步研究至关重要。需要更多研究以促进这些造影剂的临床转化。