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Pretargeted imaging beyond the blood–brain barrier

Pretargeting is a powerful nuclear imaging strategy to achieve enhanced imaging contrast for nanomedicines and reduce the radiation burden to healthy tissue. Pretargeting is based on bioorthogonal chemistry. The most attractive reaction for this purpose is currently the tetrazine ligation, which occ...

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Autores principales: Shalgunov, Vladimir, Lopes van den Broek, Sara, Vang Andersen, Ida, García Vázquez, Rocío, Raval, Nakul Ravi, Palner, Mikael, Mori, Yuki, Schäfer, Gabriela, Herrmann, Barbara, Mikula, Hannes, Beschorner, Natalie, Nedergaard, Maiken, Syvänen, Stina, Barz, Matthias, Moos Knudsen, Gitte, Battisti, Umberto Maria, Herth, Matthias Manfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034008/
https://www.ncbi.nlm.nih.gov/pubmed/36970152
http://dx.doi.org/10.1039/d2md00360k
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author Shalgunov, Vladimir
Lopes van den Broek, Sara
Vang Andersen, Ida
García Vázquez, Rocío
Raval, Nakul Ravi
Palner, Mikael
Mori, Yuki
Schäfer, Gabriela
Herrmann, Barbara
Mikula, Hannes
Beschorner, Natalie
Nedergaard, Maiken
Syvänen, Stina
Barz, Matthias
Moos Knudsen, Gitte
Battisti, Umberto Maria
Herth, Matthias Manfred
author_facet Shalgunov, Vladimir
Lopes van den Broek, Sara
Vang Andersen, Ida
García Vázquez, Rocío
Raval, Nakul Ravi
Palner, Mikael
Mori, Yuki
Schäfer, Gabriela
Herrmann, Barbara
Mikula, Hannes
Beschorner, Natalie
Nedergaard, Maiken
Syvänen, Stina
Barz, Matthias
Moos Knudsen, Gitte
Battisti, Umberto Maria
Herth, Matthias Manfred
author_sort Shalgunov, Vladimir
collection PubMed
description Pretargeting is a powerful nuclear imaging strategy to achieve enhanced imaging contrast for nanomedicines and reduce the radiation burden to healthy tissue. Pretargeting is based on bioorthogonal chemistry. The most attractive reaction for this purpose is currently the tetrazine ligation, which occurs between trans-cyclooctene (TCO) tags and tetrazines (Tzs). Pretargeted imaging beyond the blood–brain barrier (BBB) is challenging and has not been reported thus far. In this study, we developed Tz imaging agents that are capable of ligating in vivo to targets beyond the BBB. We chose to develop (18)F-labeled Tzs as they can be applied to positron emission tomography (PET) – the most powerful molecular imaging technology. Fluorine-18 is an ideal radionuclide for PET due to its almost ideal decay properties. As a non-metal radionuclide, fluorine-18 also allows for development of Tzs with physicochemical properties enabling passive brain diffusion. To develop these imaging agents, we applied a rational drug design approach. This approach was based on estimated and experimentally determined parameters such as the BBB score, pretargeted autoradiography contrast, in vivo brain influx and washout as well as on peripheral metabolism profiles. From 18 initially developed structures, five Tzs were selected to be tested for their in vivo click performance. Whereas all selected structures clicked in vivo to TCO-polymer deposited into the brain, [(18)F]18 displayed the most favorable characteristics with respect to brain pretargeting. [(18)F]18 is our lead compound for future pretargeted neuroimaging studies based on BBB-penetrant monoclonal antibodies. Pretargeting beyond the BBB will allow us to image targets in the brain that are currently not imageable, such as soluble oligomers of neurodegeneration biomarker proteins. Imaging of such currently non-imageable targets will allow early diagnosis and personalized treatment monitoring. This in turn will accelerate drug development and greatly benefit patient care.
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spelling pubmed-100340082023-03-24 Pretargeted imaging beyond the blood–brain barrier Shalgunov, Vladimir Lopes van den Broek, Sara Vang Andersen, Ida García Vázquez, Rocío Raval, Nakul Ravi Palner, Mikael Mori, Yuki Schäfer, Gabriela Herrmann, Barbara Mikula, Hannes Beschorner, Natalie Nedergaard, Maiken Syvänen, Stina Barz, Matthias Moos Knudsen, Gitte Battisti, Umberto Maria Herth, Matthias Manfred RSC Med Chem Chemistry Pretargeting is a powerful nuclear imaging strategy to achieve enhanced imaging contrast for nanomedicines and reduce the radiation burden to healthy tissue. Pretargeting is based on bioorthogonal chemistry. The most attractive reaction for this purpose is currently the tetrazine ligation, which occurs between trans-cyclooctene (TCO) tags and tetrazines (Tzs). Pretargeted imaging beyond the blood–brain barrier (BBB) is challenging and has not been reported thus far. In this study, we developed Tz imaging agents that are capable of ligating in vivo to targets beyond the BBB. We chose to develop (18)F-labeled Tzs as they can be applied to positron emission tomography (PET) – the most powerful molecular imaging technology. Fluorine-18 is an ideal radionuclide for PET due to its almost ideal decay properties. As a non-metal radionuclide, fluorine-18 also allows for development of Tzs with physicochemical properties enabling passive brain diffusion. To develop these imaging agents, we applied a rational drug design approach. This approach was based on estimated and experimentally determined parameters such as the BBB score, pretargeted autoradiography contrast, in vivo brain influx and washout as well as on peripheral metabolism profiles. From 18 initially developed structures, five Tzs were selected to be tested for their in vivo click performance. Whereas all selected structures clicked in vivo to TCO-polymer deposited into the brain, [(18)F]18 displayed the most favorable characteristics with respect to brain pretargeting. [(18)F]18 is our lead compound for future pretargeted neuroimaging studies based on BBB-penetrant monoclonal antibodies. Pretargeting beyond the BBB will allow us to image targets in the brain that are currently not imageable, such as soluble oligomers of neurodegeneration biomarker proteins. Imaging of such currently non-imageable targets will allow early diagnosis and personalized treatment monitoring. This in turn will accelerate drug development and greatly benefit patient care. RSC 2022-12-02 /pmc/articles/PMC10034008/ /pubmed/36970152 http://dx.doi.org/10.1039/d2md00360k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Shalgunov, Vladimir
Lopes van den Broek, Sara
Vang Andersen, Ida
García Vázquez, Rocío
Raval, Nakul Ravi
Palner, Mikael
Mori, Yuki
Schäfer, Gabriela
Herrmann, Barbara
Mikula, Hannes
Beschorner, Natalie
Nedergaard, Maiken
Syvänen, Stina
Barz, Matthias
Moos Knudsen, Gitte
Battisti, Umberto Maria
Herth, Matthias Manfred
Pretargeted imaging beyond the blood–brain barrier
title Pretargeted imaging beyond the blood–brain barrier
title_full Pretargeted imaging beyond the blood–brain barrier
title_fullStr Pretargeted imaging beyond the blood–brain barrier
title_full_unstemmed Pretargeted imaging beyond the blood–brain barrier
title_short Pretargeted imaging beyond the blood–brain barrier
title_sort pretargeted imaging beyond the blood–brain barrier
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034008/
https://www.ncbi.nlm.nih.gov/pubmed/36970152
http://dx.doi.org/10.1039/d2md00360k
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