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Rational Design of Magnetic Nanoparticles as T1–T2 Dual-Mode MRI Contrast Agents

超顺磁性 磁共振成像 对比度(视觉) 顺磁性 核磁共振 双模 合理设计 材料科学 纳米颗粒 放松(心理学) 镧系元素 体内 磁化 生物医学工程 化学 纳米技术 离子 计算机科学 磁场 放射科 医学 物理 凝聚态物理 人工智能 航空航天工程 工程类 生物 生物技术 量子力学 内科学 有机化学
作者
Carlos F. G. C. Geraldes
出处
期刊:Molecules [MDPI AG]
卷期号:29 (6): 1352-1352 被引量:14
标识
DOI:10.3390/molecules29061352
摘要

Magnetic nanoparticles (MNPs), either paramagnetic or superparamagnetic depending on their composition and size, have been thoroughly studied as magnetic resonance imaging (MRI) contrast agents using in vitro and in vivo biomedical preclinical studies, while some are clinically used. Their magnetic properties responsible in some cases for high magnetization values, together with large surface area-to-volume ratios and the possibility of surface functionalization, have been used in MRI-based diagnostic and theranostics applications. MNPs are usually used as positive (T1) or negative (T2) MRI contrast agents, causing brightening or darkening of selected regions in MRI images, respectively. This review focusses on recent developments and optimization of MNPs containing Gd, Mn, Fe and other lanthanide ions which may function as dual-mode T1–T2 MRI contrast agents (DMCAs). They induce positive or negative contrast in the same MRI scanner upon changing its operational mode between T1-weighted and T2-weighted pulse sequences. The type of contrast they induce depends critically on their r2/r1 relaxivity ratio, which for DMCAs should be in the 2–10 range of values. After briefly discussing the basic principles of paramagnetic relaxation in MNPs, in this review, the basic strategies for the rational design of DMCAs are presented and typical examples are discussed, including in vivo preclinical applications: (1) the use of NPs with a single type of contrast material, Gd- or Mn-based NPs or superparamagnetic NPs with appropriate size and magnetization to provide T2 and T1 contrast; and (2) inclusion of both types of T1 and T2 contrast materials in the same nanoplatform by changing their relative positions.

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