Yaewon Kim, Hsin-Yu Chen, Tanner Nickles, Illia Shkliar, Duy Dang, James Slater, Charlie Wang, Jeremy W Gordon, Chou T Tan, Chris Suszczynski, Sri Maddali, Adam Gaunt, Rui Chen, Javier Villanueva-Meyer, Duan Xu, Peder E Z Larson, John Kurhanewicz, Robert A Bok, Susan Chang, Daniel B Vigneron
{"title":"Translation of hyperpolarized [<sup>13</sup>C,<sup>15</sup>N<sub>2</sub>]urea MRI for novel human brain perfusion studies.","authors":"Yaewon Kim, Hsin-Yu Chen, Tanner Nickles, Illia Shkliar, Duy Dang, James Slater, Charlie Wang, Jeremy W Gordon, Chou T Tan, Chris Suszczynski, Sri Maddali, Adam Gaunt, Rui Chen, Javier Villanueva-Meyer, Duan Xu, Peder E Z Larson, John Kurhanewicz, Robert A Bok, Susan Chang, Daniel B Vigneron","doi":"10.1038/s44303-025-00073-3","DOIUrl":null,"url":null,"abstract":"<p><p>This study developed a new approach to produce sterile, hyperpolarized [<sup>13</sup>C,<sup>15</sup>N<sub>2</sub>]urea as a novel molecular imaging probe and applied it for first-ever healthy brain volunteer studies. Hyperpolarized [<sup>13</sup>C,<sup>15</sup>N<sub>2</sub>]urea, as a small, metabolically inert molecule, offers significant advantages for perfusion imaging due to its endogenous nature and excellent safety profile. The developed methods achieved a hyperpolarized [<sup>13</sup>C,<sup>15</sup>N<sub>2</sub>]urea solution (132 ± 6 mM) with 27.4 ± 5.6% polarization and a T<sub>1</sub> = 50.4 ± 0.2 s. In healthy brain volunteer studies, high-resolution <sup>13</sup>C imaging captured blood flow with a spatial resolution of 7.76 × 7.76 × 15 (or 10) mm<sup>3</sup> over ~1 min following hyperpolarized [<sup>13</sup>C,<sup>15</sup>N<sub>2</sub>]urea injection, visualizing detailed vascular structures. Time-to-peak and centroid analyses showed consistent arterial and venous signal patterns across subjects. Findings suggest hyperpolarized [<sup>13</sup>C,<sup>15</sup>N<sub>2</sub>]urea may have applications beyond brain imaging, including the non-invasive perfusion assessment in various organs, cancer microenvironment, and renal function, paving the way for clinical translation.</p>","PeriodicalId":501709,"journal":{"name":"npj Imaging","volume":"3 1","pages":"11"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11925798/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"npj Imaging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1038/s44303-025-00073-3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/20 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
This study developed a new approach to produce sterile, hyperpolarized [13C,15N2]urea as a novel molecular imaging probe and applied it for first-ever healthy brain volunteer studies. Hyperpolarized [13C,15N2]urea, as a small, metabolically inert molecule, offers significant advantages for perfusion imaging due to its endogenous nature and excellent safety profile. The developed methods achieved a hyperpolarized [13C,15N2]urea solution (132 ± 6 mM) with 27.4 ± 5.6% polarization and a T1 = 50.4 ± 0.2 s. In healthy brain volunteer studies, high-resolution 13C imaging captured blood flow with a spatial resolution of 7.76 × 7.76 × 15 (or 10) mm3 over ~1 min following hyperpolarized [13C,15N2]urea injection, visualizing detailed vascular structures. Time-to-peak and centroid analyses showed consistent arterial and venous signal patterns across subjects. Findings suggest hyperpolarized [13C,15N2]urea may have applications beyond brain imaging, including the non-invasive perfusion assessment in various organs, cancer microenvironment, and renal function, paving the way for clinical translation.