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Pretargeted PET Imaging of trans-Cyclooctene-Modified Porous Silicon Nanoparticles

[Image: see text] Pretargeted positron emission tomography (PET) imaging based on bioorthogonal chemical reactions has proven its potential in immunoimaging. It may also have great potential in nanotheranostic applications. Here, we report the first successful pretargeted PET imaging of trans-cycloo...

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Autores principales: Keinänen, Outi, Mäkilä, Ermei M., Lindgren, Rici, Virtanen, Helena, Liljenbäck, Heidi, Oikonen, Vesa, Sarparanta, Mirkka, Molthoff, Carla, Windhorst, Albert D., Roivainen, Anne, Salonen, Jarno J., Airaksinen, Anu J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478181/
https://www.ncbi.nlm.nih.gov/pubmed/28649670
http://dx.doi.org/10.1021/acsomega.6b00269
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author Keinänen, Outi
Mäkilä, Ermei M.
Lindgren, Rici
Virtanen, Helena
Liljenbäck, Heidi
Oikonen, Vesa
Sarparanta, Mirkka
Molthoff, Carla
Windhorst, Albert D.
Roivainen, Anne
Salonen, Jarno J.
Airaksinen, Anu J.
author_facet Keinänen, Outi
Mäkilä, Ermei M.
Lindgren, Rici
Virtanen, Helena
Liljenbäck, Heidi
Oikonen, Vesa
Sarparanta, Mirkka
Molthoff, Carla
Windhorst, Albert D.
Roivainen, Anne
Salonen, Jarno J.
Airaksinen, Anu J.
author_sort Keinänen, Outi
collection PubMed
description [Image: see text] Pretargeted positron emission tomography (PET) imaging based on bioorthogonal chemical reactions has proven its potential in immunoimaging. It may also have great potential in nanotheranostic applications. Here, we report the first successful pretargeted PET imaging of trans-cyclooctene-modified mesoporous silicon nanoparticles, using (18)F-labeled tetrazine as a tracer. The inverse electron-demand Diels–Alder cycloaddition (IEDDA) reaction was fast, resulting in high radioactivity accumulation in the expected organs within 10 min after the administration of the tracer. The highest target-to-background ratio was achieved 120 min after the tracer injection. A clear correlation between the efficiency of the in vivo IEDDA labeling reaction and the injected amount of the tracer was observed. The radioactivity accumulation decreased with the increased amount of the co-injected carrier, indicating saturation in the reaction sites. This finding was supported by the in vitro results. Our study suggests that pretargeted imaging has excellent potential in nanotheranostic PET imaging when using high-specific-activity tracers.
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spelling pubmed-54781812017-06-21 Pretargeted PET Imaging of trans-Cyclooctene-Modified Porous Silicon Nanoparticles Keinänen, Outi Mäkilä, Ermei M. Lindgren, Rici Virtanen, Helena Liljenbäck, Heidi Oikonen, Vesa Sarparanta, Mirkka Molthoff, Carla Windhorst, Albert D. Roivainen, Anne Salonen, Jarno J. Airaksinen, Anu J. ACS Omega [Image: see text] Pretargeted positron emission tomography (PET) imaging based on bioorthogonal chemical reactions has proven its potential in immunoimaging. It may also have great potential in nanotheranostic applications. Here, we report the first successful pretargeted PET imaging of trans-cyclooctene-modified mesoporous silicon nanoparticles, using (18)F-labeled tetrazine as a tracer. The inverse electron-demand Diels–Alder cycloaddition (IEDDA) reaction was fast, resulting in high radioactivity accumulation in the expected organs within 10 min after the administration of the tracer. The highest target-to-background ratio was achieved 120 min after the tracer injection. A clear correlation between the efficiency of the in vivo IEDDA labeling reaction and the injected amount of the tracer was observed. The radioactivity accumulation decreased with the increased amount of the co-injected carrier, indicating saturation in the reaction sites. This finding was supported by the in vitro results. Our study suggests that pretargeted imaging has excellent potential in nanotheranostic PET imaging when using high-specific-activity tracers. American Chemical Society 2017-01-06 /pmc/articles/PMC5478181/ /pubmed/28649670 http://dx.doi.org/10.1021/acsomega.6b00269 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Keinänen, Outi
Mäkilä, Ermei M.
Lindgren, Rici
Virtanen, Helena
Liljenbäck, Heidi
Oikonen, Vesa
Sarparanta, Mirkka
Molthoff, Carla
Windhorst, Albert D.
Roivainen, Anne
Salonen, Jarno J.
Airaksinen, Anu J.
Pretargeted PET Imaging of trans-Cyclooctene-Modified Porous Silicon Nanoparticles
title Pretargeted PET Imaging of trans-Cyclooctene-Modified Porous Silicon Nanoparticles
title_full Pretargeted PET Imaging of trans-Cyclooctene-Modified Porous Silicon Nanoparticles
title_fullStr Pretargeted PET Imaging of trans-Cyclooctene-Modified Porous Silicon Nanoparticles
title_full_unstemmed Pretargeted PET Imaging of trans-Cyclooctene-Modified Porous Silicon Nanoparticles
title_short Pretargeted PET Imaging of trans-Cyclooctene-Modified Porous Silicon Nanoparticles
title_sort pretargeted pet imaging of trans-cyclooctene-modified porous silicon nanoparticles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478181/
https://www.ncbi.nlm.nih.gov/pubmed/28649670
http://dx.doi.org/10.1021/acsomega.6b00269
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