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Tetrazine—trans-Cyclooctene Chemistry Applied to Fabricate Self-Assembled Fluorescent and Radioactive Nanoparticles for in Vivo Dual Mode Imaging
[Image: see text] Multimodal imaging agents combine two or more imaging modalities into one probe. Self-assembling fluorescent nanoparticles are a promising class of modular multimodal imaging probes as they can allow easy blending of imaging and targeting modalities. Our group recently developed a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429424/ https://www.ncbi.nlm.nih.gov/pubmed/30731039 http://dx.doi.org/10.1021/acs.bioconjchem.9b00038 |
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author | van Onzen, Arthur H. A. M. Rossin, Raffaella Schenning, Albertus P. H. J. Nicolay, Klaas Milroy, Lech-Gustav Robillard, Marc S. Brunsveld, Luc |
author_facet | van Onzen, Arthur H. A. M. Rossin, Raffaella Schenning, Albertus P. H. J. Nicolay, Klaas Milroy, Lech-Gustav Robillard, Marc S. Brunsveld, Luc |
author_sort | van Onzen, Arthur H. A. M. |
collection | PubMed |
description | [Image: see text] Multimodal imaging agents combine two or more imaging modalities into one probe. Self-assembling fluorescent nanoparticles are a promising class of modular multimodal imaging probes as they can allow easy blending of imaging and targeting modalities. Our group recently developed a class of self-assembling and intrinsically fluorescent small molecule-based nanoparticles (SMNPs) with excellent optical properties. In this article, we describe the efficient radiolabeling of these SMNPs via a two-step bioconjugation strategy involving the inverse-electron-demand Diels–Alder ligation between a tetrazine (Tz)-tagged radiolabel and a trans-cyclooctene (TCO)-tagged fluorescent small molecule building block of the SMNPs. Studies in mice revealed that the SMNPs are well tolerated and could be monitored by both radioactivity and fluorescence, thereby demonstrating the potential of SMNPs in optical and dual-mode imaging in vivo. The work also testifies to the utility of the Tz–TCO conjugation chemistry for the labeling of self-assembled nanoparticles. |
format | Online Article Text |
id | pubmed-6429424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-64294242019-03-25 Tetrazine—trans-Cyclooctene Chemistry Applied to Fabricate Self-Assembled Fluorescent and Radioactive Nanoparticles for in Vivo Dual Mode Imaging van Onzen, Arthur H. A. M. Rossin, Raffaella Schenning, Albertus P. H. J. Nicolay, Klaas Milroy, Lech-Gustav Robillard, Marc S. Brunsveld, Luc Bioconjug Chem [Image: see text] Multimodal imaging agents combine two or more imaging modalities into one probe. Self-assembling fluorescent nanoparticles are a promising class of modular multimodal imaging probes as they can allow easy blending of imaging and targeting modalities. Our group recently developed a class of self-assembling and intrinsically fluorescent small molecule-based nanoparticles (SMNPs) with excellent optical properties. In this article, we describe the efficient radiolabeling of these SMNPs via a two-step bioconjugation strategy involving the inverse-electron-demand Diels–Alder ligation between a tetrazine (Tz)-tagged radiolabel and a trans-cyclooctene (TCO)-tagged fluorescent small molecule building block of the SMNPs. Studies in mice revealed that the SMNPs are well tolerated and could be monitored by both radioactivity and fluorescence, thereby demonstrating the potential of SMNPs in optical and dual-mode imaging in vivo. The work also testifies to the utility of the Tz–TCO conjugation chemistry for the labeling of self-assembled nanoparticles. American Chemical Society 2019-02-07 2019-03-20 /pmc/articles/PMC6429424/ /pubmed/30731039 http://dx.doi.org/10.1021/acs.bioconjchem.9b00038 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | van Onzen, Arthur H. A. M. Rossin, Raffaella Schenning, Albertus P. H. J. Nicolay, Klaas Milroy, Lech-Gustav Robillard, Marc S. Brunsveld, Luc Tetrazine—trans-Cyclooctene Chemistry Applied to Fabricate Self-Assembled Fluorescent and Radioactive Nanoparticles for in Vivo Dual Mode Imaging |
title | Tetrazine—trans-Cyclooctene
Chemistry Applied to Fabricate Self-Assembled Fluorescent and Radioactive
Nanoparticles for in Vivo Dual Mode Imaging |
title_full | Tetrazine—trans-Cyclooctene
Chemistry Applied to Fabricate Self-Assembled Fluorescent and Radioactive
Nanoparticles for in Vivo Dual Mode Imaging |
title_fullStr | Tetrazine—trans-Cyclooctene
Chemistry Applied to Fabricate Self-Assembled Fluorescent and Radioactive
Nanoparticles for in Vivo Dual Mode Imaging |
title_full_unstemmed | Tetrazine—trans-Cyclooctene
Chemistry Applied to Fabricate Self-Assembled Fluorescent and Radioactive
Nanoparticles for in Vivo Dual Mode Imaging |
title_short | Tetrazine—trans-Cyclooctene
Chemistry Applied to Fabricate Self-Assembled Fluorescent and Radioactive
Nanoparticles for in Vivo Dual Mode Imaging |
title_sort | tetrazine—trans-cyclooctene
chemistry applied to fabricate self-assembled fluorescent and radioactive
nanoparticles for in vivo dual mode imaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429424/ https://www.ncbi.nlm.nih.gov/pubmed/30731039 http://dx.doi.org/10.1021/acs.bioconjchem.9b00038 |
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