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      Recent Advances in 19Fluorine Magnetic Resonance Imaging with Perfluorocarbon Emulsions

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          Abstract

          The research roots of 19fluorine ( 19F) magnetic resonance imaging (MRI) date back over 35 years. Over that time span, 1H imaging flourished and was adopted worldwide with an endless array of applications and imaging approaches, making magnetic resonance an indispensable pillar of biomedical diagnostic imaging. For many years during this timeframe, 19F imaging research continued at a slow pace as the various attributes of the technique were explored. However, over the last decade and particularly the last several years, the pace and clinical relevance of 19F imaging has exploded. In part, this is due to advances in MRI instrumentation, 19F/ 1H coil designs, and ultrafast pulse sequence development for both preclinical and clinical scanners. These achievements, coupled with interest in the molecular imaging of anatomy and physiology, and combined with a cadre of innovative agents, have brought the concept of 19F into early clinical evaluation. In this review, we attempt to provide a slice of this rich history of research and development, with a particular focus on liquid perfluorocarbon compound-based agents.

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          Most cited references141

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          Principles and applications of balanced SSFP techniques.

          During the past 5 years balanced steady-state free precession (SSFP) has become increasingly important for diagnostic and functional imaging. Balanced SSFP is characterized by two unique features: it offers a very high signal-to noise ratio and a T2/T1-weighted image contrast. This article focuses on the physical principles, on the signal formation, and on the resulting properties of balanced SSFP. Mechanisms for contrast modification, recent clinical application, and potential extensions of this technique are discussed.
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            Artificial reporter gene providing MRI contrast based on proton exchange.

            Existing magnetic resonance reporter genes all rely on the presence of (super)paramagnetic substances and employ water relaxation to gain contrast. We designed a nonmetallic, biodegradable, lysine rich-protein (LRP) reporter, the prototype of a potential family of genetically engineered reporters expressing artificial proteins with frequency-selective contrast. This endogenous contrast, based on transfer of radiofrequency labeling from the reporter's amide protons to water protons, can be switched on and off.
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              CEST: from basic principles to applications, challenges and opportunities.

              Chemical Exchange Saturation Transfer (CEST) offers a new type of contrast for MRI that is molecule specific. In this approach, a slowly exchanging NMR active nucleus, typically a proton, possessing a chemical shift distinct from water is selectively saturated and the saturated spin is transferred to the bulk water via chemical exchange. Many molecules can act as CEST agents, both naturally occurring endogenous molecules and new types of exogenous agents. A large variety of molecules have been demonstrated as potential agents, including small diamagnetic molecules, complexes of paramagnetic ions, endogenous macromolecules, dendrimers and liposomes. In this review we described the basic principles of the CEST experiment, with emphasis on the similarity to earlier saturation transfer experiments described in the literature. Interest in quantitative CEST has also resulted in the development of new exchange-sensitive detection schemes. Some emerging clinical applications of CEST are described and the challenges and opportunities associated with translation of these methods to the clinical environment are discussed.

                Author and article information

                Journal
                101673395
                44680
                Engineering (Beijing)
                Engineering (Beijing)
                Engineering (Beijing, China)
                2095-8099
                2096-0026
                20 January 2016
                16 March 2016
                December 2015
                22 April 2016
                : 1
                : 4
                : 475-489
                Affiliations
                [1 ]Division of Cardiology, Washington University School of Medical, St. Louis, MO 63110, USA
                [2 ]Toshiba Medical Research Institute USA, Inc., Cleveland, OH 44143, USA
                [3 ]Department of Biomedical Engineering, Washington University, St. Louis, MO 63130, USA
                [4 ]Philips Research Hamburg, Hamburg 22335, Germany
                Author notes
                [* ]Correspondence author. greg.lanza@ 123456me.com
                Article
                NIHMS749862
                10.15302/J-ENG-2015103
                4841681
                27110430
                bf558163-6cd4-4c84-9960-590863a79284

                This is an open access article under the CC BY license ( http://creativecommons.org/licenses/by/4.0/)

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                Categories
                Article

                fluorine,magnetic resonance imaging (mri),dual-tuned coil,perfluorocarbon,angiogenesis,cell labeling

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