Zhou Zijian, Zhao Zhenghuan, Zhang Hui, Wang Zhenyu, Chen Xiaoyuan, Wang Ruifang, Chen Zhong, Gao Jinhao
ACS Nano. 2014 Aug 26;8(8):7976-85. doi: 10.1021/nn5038652.
Iron oxide has been developed as either T1 or T2 magnetic resonance imaging (MRI) contrast agents by controlling the size and composition; however, the underlying mechanism of T1 and T2 contrasts in one iron oxide entity is still not well understood. Herein, we report that freestanding superparamagnetic magnetite nanoplates with (111) exposed facets have significant but interactional T1 and T2 contrast effects. We demonstrate that the main contribution of the T1 contrast of magnetic nanoplates is the chemical exchange on the iron-rich Fe3O4(111) surfaces, whereas the T2 relaxation is dominated by the intrinsic superparamagnetism of the nanoplates with an enhanced perturbation effect. We are able to regulate the balance of T1 and T2 contrasts by controlling structure and surface features, including morphology, exposed facets, and surface coating. This study provides an insightful understanding on the T1 and T2 contrast mechanisms, which is urgently needed to allow more sophisticated design of high-performance MRI contrast agents.
通过控制尺寸和组成,氧化铁已被开发为T1或T2磁共振成像(MRI)造影剂;然而,在一个氧化铁实体中T1和T2造影的潜在机制仍未得到很好的理解。在此,我们报道具有(111)暴露面的独立超顺磁性磁铁矿纳米片具有显著但相互作用的T1和T2造影效果。我们证明磁性纳米片T1造影的主要贡献是富铁的Fe3O4(111)表面上的化学交换,而T2弛豫则由具有增强扰动效应的纳米片的固有超顺磁性主导。我们能够通过控制结构和表面特征(包括形态、暴露面和表面涂层)来调节T1和T2造影的平衡。这项研究为T1和T2造影机制提供了深刻的理解,这是高性能MRI造影剂更复杂设计迫切需要的。