<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Whiting N</submitter><funding>NCI NIH HHS</funding><pagination>12842</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4523869</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5</volume><pubmed_abstract>Visualizing the movement of angiocatheters during endovascular interventions is typically accomplished using x-ray fluoroscopy. There are many potential advantages to developing magnetic resonance imaging-based approaches that will allow three-dimensional imaging of the tissue/vasculature interface while monitoring other physiologically-relevant criteria, without exposing the patient or clinician team to ionizing radiation. Here we introduce a proof-of-concept development of a magnetic resonance imaging-guided catheter tracking method that utilizes hyperpolarized silicon particles. The increased signal of the silicon particles is generated via low-temperature, solid-state dynamic nuclear polarization, and the particles retain their enhanced signal for ≥ 40 minutes--allowing imaging experiments over extended time durations. The particles are affixed to the tip of standard medical-grade catheters and are used to track passage under set distal and temporal points in phantoms and live mouse models. With continued development, this method has the potential to supplement x-ray fluoroscopy and other MRI-guided catheter tracking methods as a zero-background, positive contrast agent that does not require ionizing radiation.</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Real-Time MRI-Guided Catheter Tracking Using Hyperpolarized Silicon Particles.</pubmed_title><pmcid>PMC4523869</pmcid><funding_grant_id>CA016672</funding_grant_id><funding_grant_id>P30 CA016672</funding_grant_id><funding_grant_id>U54 CA151668</funding_grant_id><funding_grant_id>R21 CA185536</funding_grant_id><funding_grant_id>R25T CA057730</funding_grant_id><funding_grant_id>R25 CA057730</funding_grant_id><funding_grant_id>U54CA151668-03</funding_grant_id><pubmed_authors>Millward NZ</pubmed_authors><pubmed_authors>Whiting N</pubmed_authors><pubmed_authors>Shah JV</pubmed_authors><pubmed_authors>Marcus CM</pubmed_authors><pubmed_authors>Hu J</pubmed_authors><pubmed_authors>Menter DG</pubmed_authors><pubmed_authors>Bhattacharya PK</pubmed_authors><pubmed_authors>Cassidy MC</pubmed_authors><pubmed_authors>Cressman E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Real-Time MRI-Guided Catheter Tracking Using Hyperpolarized Silicon Particles.</name><description>Visualizing the movement of angiocatheters during endovascular interventions is typically accomplished using x-ray fluoroscopy. There are many potential advantages to developing magnetic resonance imaging-based approaches that will allow three-dimensional imaging of the tissue/vasculature interface while monitoring other physiologically-relevant criteria, without exposing the patient or clinician team to ionizing radiation. Here we introduce a proof-of-concept development of a magnetic resonance imaging-guided catheter tracking method that utilizes hyperpolarized silicon particles. The increased signal of the silicon particles is generated via low-temperature, solid-state dynamic nuclear polarization, and the particles retain their enhanced signal for ≥ 40 minutes--allowing imaging experiments over extended time durations. The particles are affixed to the tip of standard medical-grade catheters and are used to track passage under set distal and temporal points in phantoms and live mouse models. With continued development, this method has the potential to supplement x-ray fluoroscopy and other MRI-guided catheter tracking methods as a zero-background, positive contrast agent that does not require ionizing radiation.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Aug</publication><modification>2025-04-26T18:10:15.841Z</modification><creation>2019-03-27T01:56:13Z</creation></dates><accession>S-EPMC4523869</accession><cross_references><pubmed>26239953</pubmed><doi>10.1038/srep12842</doi></cross_references></HashMap>