Comparison of fast field-cycling magnetic resonance imaging methods and future perspectives

被引:15
作者
Boedenler, Markus [1 ]
de Rochefort, Ludovic [2 ]
Ross, P. James [3 ]
Chanet, Nicolas [4 ]
Guillot, Genevieve [4 ]
Davies, Gareth R. [3 ]
Goesweiner, Christian [1 ]
Scharfetter, Hermann [1 ]
Lurie, David J. [3 ]
Broche, Lionel M. [3 ]
机构
[1] Graz Univ Technol, Inst Med Engn, Graz, Austria
[2] Aix Marseille Univ, CNRS, Ctr Magnet Resonance Biol & Med CRMBM, UMR 7339, Marseille, France
[3] Univ Aberdeen, Aberdeen Biomed Imaging Ctr, Aberdeen, Scotland
[4] Univ Paris Saclay, UMR 8081, IR4M, Orsay, France
基金
英国工程与自然科学研究理事会;
关键词
Field-cycling; FFC-MRI; delta relaxation enhanced MR; dispersion; NMRD; QUADRUPOLE RELAXATION ENHANCEMENT; CONTRAST AGENTS; INSERT COIL; RELAXOMETRY; PROTON; T1; CONSTRUCTION; SPECTROSCOPY; MECHANISMS; DEPENDENCE;
D O I
10.1080/00268976.2018.1557349
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Fast field-cycling (FFC) nuclear magnetic resonance relaxometry is a well-established method to determine the relaxation rates as a function of magnetic field strength. This so-called nuclear magnetic relaxation dispersion gives insight into the underlying molecular dynamics of a wide range of complex systems and has gained interest especially in the characterisation of biological tissues and diseases. The combination of FFC techniques with magnetic resonance imaging (MRI) offers a high potential for new types of image contrast more specific to pathological molecular dynamics. This article reviews the progress in FFC-MRI over the last decade and gives an overview of the hardware systems currently in operation. We discuss limitations and error correction strategies specific to FFC-MRI such as field stability and homogeneity, signal-to-noise ratio, eddy currents and acquisition time. We also report potential applications with impact in biology and medicine. Finally, we discuss the challenges and future applications in transferring the underlying molecular dynamics into novel types of image contrast by exploiting the dispersive properties of biological tissue or MRI contrast agents.
引用
收藏
页码:832 / 848
页数:17
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