<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Miller JJ</submitter><funding>British Heart Foundation</funding><funding>National Institute for Health Research (NIHR)</funding><funding>Wellcome Trust</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>2978-2991</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7986077</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>85(6)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Phosphorus saturation-transfer experiments can quantify metabolic fluxes noninvasively. Typically, the forward flux through the creatine kinase reaction is investigated by observing the decrease in phosphocreatine (PCr) after saturation of γ-ATP. The quantification of total ATP utilization is currently underexplored, as it requires simultaneous saturation of inorganic phosphate ( Pi ) and PCr. This is challenging, as currently available saturation pulses reduce the already-low γ-ATP signal present.&lt;h4>Methods&lt;/h4>Using a hybrid optimal-control and Shinnar-Le Roux method, a quasi-adiabatic RF pulse was designed for the dual saturation of PCr and Pi to enable determination of total ATP utilization. The pulses were evaluated in Bloch equation simulations, compared with a conve</pubmed_abstract><journal>Magnetic resonance in medicine</journal><pubmed_title>Rapid, B1 -insensitive, dual-band quasi-adiabatic saturation transfer with optimal control for complete quantification of myocardial ATP flux.</pubmed_title><pmcid>PMC7986077</pmcid><funding_grant_id>FS/14/17/30634</funding_grant_id><funding_grant_id>FS/19/18/34252</funding_grant_id><funding_grant_id>FS/15/68/32042</funding_grant_id><funding_grant_id>1944425</funding_grant_id><funding_grant_id>RE/13/1/30181</funding_grant_id><funding_grant_id>FS/16/7/31843</funding_grant_id><funding_grant_id>FS/17/58/33072</funding_grant_id><funding_grant_id>098436/Z/12/B</funding_grant_id><funding_grant_id>RG/11/9/28921</funding_grant_id><pubmed_authors>Tyler DJ</pubmed_authors><pubmed_authors>Tyler A</pubmed_authors><pubmed_authors>Timm KN</pubmed_authors><pubmed_authors>Lau JYC</pubmed_authors><pubmed_authors>Miller JJ</pubmed_authors><pubmed_authors>Kerr M</pubmed_authors><pubmed_authors>Watson WD</pubmed_authors><pubmed_authors>Bottomley PA</pubmed_authors><pubmed_authors>Valkovic L</pubmed_authors><pubmed_authors>Heather LC</pubmed_authors><pubmed_authors>Rodgers C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rapid, B1 -insensitive, dual-band quasi-adiabatic saturation transfer with optimal control for complete quantification of myocardial ATP flux.</name><description>&lt;h4>Purpose&lt;/h4>Phosphorus saturation-transfer experiments can quantify metabolic fluxes noninvasively. Typically, the forward flux through the creatine kinase reaction is investigated by observing the decrease in phosphocreatine (PCr) after saturation of γ-ATP. The quantification of total ATP utilization is currently underexplored, as it requires simultaneous saturation of inorganic phosphate ( Pi ) and PCr. This is challenging, as currently available saturation pulses reduce the already-low γ-ATP signal present.&lt;h4>Methods&lt;/h4>Using a hybrid optimal-control and Shinnar-Le Roux method, a quasi-adiabatic RF pulse was designed for the dual saturation of PCr and Pi to enable determination of total ATP utilization. The pulses were evaluated in Bloch equation simulations, compared with a conve</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jun</publication><modification>2025-04-18T17:41:14.766Z</modification><creation>2025-04-07T05:18:05.823Z</creation></dates><accession>S-EPMC7986077</accession><cross_references><pubmed>33538063</pubmed><doi>10.1002/mrm.28647</doi></cross_references></HashMap>