An Overhauser‐enhanced‐MRI platform for dynamic free radical imaging in vivo
Overhauser‐enhanced MRI (OMRI) is an electron‐proton double‐resonance imaging technique of interest for its ability to non‐invasively measure the concentration and distribution of free radicals. In vivo OMRI experiments are typically undertaken at ultra‐low magnetic field (ULF), as both RF power abs...
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Veröffentlicht in: | NMR in biomedicine 2018-05, Vol.31 (5), p.e3896-n/a |
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creator | Waddington, David E. J. Sarracanie, Mathieu Salameh, Najat Herisson, Fanny Ayata, Cenk Rosen, Matthew S. |
description | Overhauser‐enhanced MRI (OMRI) is an electron‐proton double‐resonance imaging technique of interest for its ability to non‐invasively measure the concentration and distribution of free radicals. In vivo OMRI experiments are typically undertaken at ultra‐low magnetic field (ULF), as both RF power absorption and penetration issues—a consequence of the high resonance frequencies of electron spins—are mitigated. However, working at ULF causes a drastic reduction in MRI sensitivity. Here, we report on the design, construction and performance of an OMRI platform optimized for high NMR sensitivity and low RF power absorbance, exploring challenges unique to probe design in the ULF regime. We use this platform to demonstrate dynamic imaging of TEMPOL in a rat model. The work presented here demonstrates improved speed and sensitivity of in vivo OMRI, extending the scope of OMRI to the study of dynamic processes such as metabolism.
Overhauser‐enhanced MRI is a powerful tool for imaging of free radicals in vivo however its application to dynamic processes has been limited by low signal‐to‐noise ratios. Here, we detail the development of a high‐sensitivity OMRI platform that combines steady‐state acquisition with a custom double‐resonance probe. We use this platform to demonstrate dynamic imaging of TEMPOL in a rat model with 15 s time resolution. |
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Overhauser‐enhanced MRI is a powerful tool for imaging of free radicals in vivo however its application to dynamic processes has been limited by low signal‐to‐noise ratios. Here, we detail the development of a high‐sensitivity OMRI platform that combines steady‐state acquisition with a custom double‐resonance probe. We use this platform to demonstrate dynamic imaging of TEMPOL in a rat model with 15 s time resolution.</description><identifier>ISSN: 0952-3480</identifier><identifier>EISSN: 1099-1492</identifier><identifier>DOI: 10.1002/nbm.3896</identifier><identifier>PMID: 29493032</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Animals ; Biological products ; Electron spin ; Electron Spin Resonance Spectroscopy ; free radical imaging ; Free radicals ; Free Radicals - metabolism ; In vivo methods and tests ; Magnetic fields ; Magnetic Resonance Imaging ; Magnetic Resonance Spectroscopy ; Male ; Metabolism ; NMR ; Nuclear magnetic resonance ; Overhauser‐enhanced MRI (OMRI) ; Radio Waves ; Rats, Sprague-Dawley ; Resonance ; RF coil design ; Sensitivity ; Tempol ; ultra‐low magnetic field</subject><ispartof>NMR in biomedicine, 2018-05, Vol.31 (5), p.e3896-n/a</ispartof><rights>Copyright © 2018 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4156-e9ababdfa524f3e5a424de5386212ddf98a6dde395859a666d60e4c890ba263a3</citedby><cites>FETCH-LOGICAL-c4156-e9ababdfa524f3e5a424de5386212ddf98a6dde395859a666d60e4c890ba263a3</cites><orcidid>0000-0002-7017-1556</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fnbm.3896$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fnbm.3896$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29493032$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Waddington, David E. J.</creatorcontrib><creatorcontrib>Sarracanie, Mathieu</creatorcontrib><creatorcontrib>Salameh, Najat</creatorcontrib><creatorcontrib>Herisson, Fanny</creatorcontrib><creatorcontrib>Ayata, Cenk</creatorcontrib><creatorcontrib>Rosen, Matthew S.</creatorcontrib><title>An Overhauser‐enhanced‐MRI platform for dynamic free radical imaging in vivo</title><title>NMR in biomedicine</title><addtitle>NMR Biomed</addtitle><description>Overhauser‐enhanced MRI (OMRI) is an electron‐proton double‐resonance imaging technique of interest for its ability to non‐invasively measure the concentration and distribution of free radicals. In vivo OMRI experiments are typically undertaken at ultra‐low magnetic field (ULF), as both RF power absorption and penetration issues—a consequence of the high resonance frequencies of electron spins—are mitigated. However, working at ULF causes a drastic reduction in MRI sensitivity. Here, we report on the design, construction and performance of an OMRI platform optimized for high NMR sensitivity and low RF power absorbance, exploring challenges unique to probe design in the ULF regime. We use this platform to demonstrate dynamic imaging of TEMPOL in a rat model. The work presented here demonstrates improved speed and sensitivity of in vivo OMRI, extending the scope of OMRI to the study of dynamic processes such as metabolism.
Overhauser‐enhanced MRI is a powerful tool for imaging of free radicals in vivo however its application to dynamic processes has been limited by low signal‐to‐noise ratios. Here, we detail the development of a high‐sensitivity OMRI platform that combines steady‐state acquisition with a custom double‐resonance probe. We use this platform to demonstrate dynamic imaging of TEMPOL in a rat model with 15 s time resolution.</description><subject>Animals</subject><subject>Biological products</subject><subject>Electron spin</subject><subject>Electron Spin Resonance Spectroscopy</subject><subject>free radical imaging</subject><subject>Free radicals</subject><subject>Free Radicals - metabolism</subject><subject>In vivo methods and tests</subject><subject>Magnetic fields</subject><subject>Magnetic Resonance Imaging</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Male</subject><subject>Metabolism</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Overhauser‐enhanced MRI (OMRI)</subject><subject>Radio Waves</subject><subject>Rats, Sprague-Dawley</subject><subject>Resonance</subject><subject>RF coil design</subject><subject>Sensitivity</subject><subject>Tempol</subject><subject>ultra‐low magnetic field</subject><issn>0952-3480</issn><issn>1099-1492</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMtOwzAQRS0EglKQ-AJkiQ2bFMd2TLwsFY9KFBCCdTSJJ5AqcYrdFHXHJ_CNfAkuTwmJzcwsjo7mXkL2YjaIGeNHNm8GItVqjfRipnUUS83XSY_phEdCpmyLbHs_ZYylUvBNssW11IIJ3iM3Q0uvF-geofPo3l5e0T6CLdCEc3I7prMa5mXrGhoGNUsLTVXQ0iFSB6YqoKZVAw-VfaCVpYtq0e6QjRJqj7tfu0_uz07vRhfR5fX5eDS8jAoZJypCDTnkpoSEy1JgApJLg4lIFY-5MaVOQRmDQidpokEpZRRDWaSa5cCVANEnh5_emWufOvTzrKl8gXUNFtvOZ5yF9CpZxeyTgz_otO2cDd8Fih9LzrRiv8LCtd47LLOZC9ncMotZtmo5Cy1nq5YDuv8l7PIGzQ_4XWsAok_guapx-a8ouzqZfAjfAWYphts</recordid><startdate>201805</startdate><enddate>201805</enddate><creator>Waddington, David E. J.</creator><creator>Sarracanie, Mathieu</creator><creator>Salameh, Najat</creator><creator>Herisson, Fanny</creator><creator>Ayata, Cenk</creator><creator>Rosen, Matthew S.</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7017-1556</orcidid></search><sort><creationdate>201805</creationdate><title>An Overhauser‐enhanced‐MRI platform for dynamic free radical imaging in vivo</title><author>Waddington, David E. J. ; Sarracanie, Mathieu ; Salameh, Najat ; Herisson, Fanny ; Ayata, Cenk ; Rosen, Matthew S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4156-e9ababdfa524f3e5a424de5386212ddf98a6dde395859a666d60e4c890ba263a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Biological products</topic><topic>Electron spin</topic><topic>Electron Spin Resonance Spectroscopy</topic><topic>free radical imaging</topic><topic>Free radicals</topic><topic>Free Radicals - metabolism</topic><topic>In vivo methods and tests</topic><topic>Magnetic fields</topic><topic>Magnetic Resonance Imaging</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Male</topic><topic>Metabolism</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Overhauser‐enhanced MRI (OMRI)</topic><topic>Radio Waves</topic><topic>Rats, Sprague-Dawley</topic><topic>Resonance</topic><topic>RF coil design</topic><topic>Sensitivity</topic><topic>Tempol</topic><topic>ultra‐low magnetic field</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Waddington, David E. J.</creatorcontrib><creatorcontrib>Sarracanie, Mathieu</creatorcontrib><creatorcontrib>Salameh, Najat</creatorcontrib><creatorcontrib>Herisson, Fanny</creatorcontrib><creatorcontrib>Ayata, Cenk</creatorcontrib><creatorcontrib>Rosen, Matthew S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>NMR in biomedicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Waddington, David E. J.</au><au>Sarracanie, Mathieu</au><au>Salameh, Najat</au><au>Herisson, Fanny</au><au>Ayata, Cenk</au><au>Rosen, Matthew S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An Overhauser‐enhanced‐MRI platform for dynamic free radical imaging in vivo</atitle><jtitle>NMR in biomedicine</jtitle><addtitle>NMR Biomed</addtitle><date>2018-05</date><risdate>2018</risdate><volume>31</volume><issue>5</issue><spage>e3896</spage><epage>n/a</epage><pages>e3896-n/a</pages><issn>0952-3480</issn><eissn>1099-1492</eissn><abstract>Overhauser‐enhanced MRI (OMRI) is an electron‐proton double‐resonance imaging technique of interest for its ability to non‐invasively measure the concentration and distribution of free radicals. In vivo OMRI experiments are typically undertaken at ultra‐low magnetic field (ULF), as both RF power absorption and penetration issues—a consequence of the high resonance frequencies of electron spins—are mitigated. However, working at ULF causes a drastic reduction in MRI sensitivity. Here, we report on the design, construction and performance of an OMRI platform optimized for high NMR sensitivity and low RF power absorbance, exploring challenges unique to probe design in the ULF regime. We use this platform to demonstrate dynamic imaging of TEMPOL in a rat model. The work presented here demonstrates improved speed and sensitivity of in vivo OMRI, extending the scope of OMRI to the study of dynamic processes such as metabolism.
Overhauser‐enhanced MRI is a powerful tool for imaging of free radicals in vivo however its application to dynamic processes has been limited by low signal‐to‐noise ratios. Here, we detail the development of a high‐sensitivity OMRI platform that combines steady‐state acquisition with a custom double‐resonance probe. We use this platform to demonstrate dynamic imaging of TEMPOL in a rat model with 15 s time resolution.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29493032</pmid><doi>10.1002/nbm.3896</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-7017-1556</orcidid></addata></record> |
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subjects | Animals Biological products Electron spin Electron Spin Resonance Spectroscopy free radical imaging Free radicals Free Radicals - metabolism In vivo methods and tests Magnetic fields Magnetic Resonance Imaging Magnetic Resonance Spectroscopy Male Metabolism NMR Nuclear magnetic resonance Overhauser‐enhanced MRI (OMRI) Radio Waves Rats, Sprague-Dawley Resonance RF coil design Sensitivity Tempol ultra‐low magnetic field |
title | An Overhauser‐enhanced‐MRI platform for dynamic free radical imaging in vivo |
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