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                  <mods:namePart>Velasco, Carlos</mods:namePart>
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                  <mods:namePart>Mota-Cobian, Adriana</mods:namePart>
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                  <mods:namePart>Ministerio de Educación (España)</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Ministerio de Ciencia, Innovación y Universidades (España)</mods:namePart>
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               <mods:name>
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               <mods:identifier type="citation">EJNMMI Phys. 2020; 7(1):7</mods:identifier>
               <mods:identifier type="doi">10.1186/s40658-020-0277-4</mods:identifier>
               <mods:identifier type="issn">2197-7364</mods:identifier>
               <mods:identifier type="journal">EJNMMI physics</mods:identifier>
               <mods:identifier type="pubmedID">32030519</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/9241</mods:identifier>
               <mods:abstract>BACKGROUND: Conventional PET imaging has usually been limited to a single tracer per scan. We propose a new technique for multi-tracer PET imaging that uses dynamic imaging and multi-tracer compartment modeling including an explicitly derived arterial input function (AIF) for each tracer using blood sampling spectroscopy. For that purpose, at least one of the co-injected tracers must be based on a non-pure positron emitter. METHODS: The proposed technique was validated in vivo by performing cardiac PET/CT studies on three healthy pigs injected with 18FDG (viability) and 68Ga-DOTA (myocardial blood flow and extracellular volume fraction) during the same acquisition. Blood samples were collected during the PET scan, and separated AIF for each tracer was obtained by spectroscopic analysis. A multi-tracer compartment model was applied to the myocardium in order to obtain the distribution of each tracer at the end of the PET scan. Relative activities of both tracers and tracer uptake were obtained and compared with the values obtained by ex vivo analysis of excised myocardial tissue segments. RESULTS: A high correlation was obtained between multi-tracer PET results, and those obtained from ex vivo analysis (18FDG relative activity: r = 0.95, p &lt; 0.0001; SUV: r = 0.98, p &lt; 0.0001). CONCLUSIONS: The proposed technique allows performing PET scans with two tracers during the same acquisition obtaining separate information for each tracer.</mods:abstract>
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               <mods:subject>
                  <mods:topic>Arterial input function</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Gamma spectroscopy</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Multi-tracer PET</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Positron emission tomography</mods:topic>
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               <mods:titleInfo>
                  <mods:title>Explicit measurement of multi-tracer arterial input function for PET imaging using blood sampling spectroscopy</mods:title>
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