NIR-II aza-BODIPY Platform for the Development of a Fluorescent Antibody Drug Conjugate

Real-time imaging of antibody-drug conjugates (ADCs) offers valuable insights for assessing tumor targeting specificity, monitoring therapeutic efficacy, and detecting off-target accumulation that may cause adverse effects. To enable precise tracking, we developed a versatile fluorescent platform based on an NIR-II emitting aza-BODIPY dye, which can be site-specifically grafted onto an IgG1 antibody to generate well-defined fluorescent ADCs. As a proof of concept, we synthesized an HER2-targeting trastuzumab immunoconjugate bearing a NIR-II aza-BODIPY fluorophore. The cytotoxic monomethyl auristatin E (MMAE) payload was introduced in the final step, resulting in a trackable and homogeneous ADC suitable for both in vitro and in vivo investigations. The resulting Trastu-azaNIRII-MMAE selectively accumulated in HER2-positive subcutaneous tumors, significantly reducing the tumor growth. Using NIR-II optical imaging, a single injection of the NIR-II-ADC allowed for the detection of the conjugate over a period of more than one month, highlighting its potential for long-term tracking and therapeutic applications.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-03-28
DOI
https://doi.org/10.1021/acs.jmedchem.4c02777
Citations
1
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
1.36

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NIR-II aza-BODIPY Platform for the Development of a Fluorescent Antibody Drug Conjugate

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Journal of Medicinal Chemistry
Monoclonal and Polyclonal Antibodies Research
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article

NIR-II aza-BODIPY Platform for the Development of a Fluorescent Antibody Drug Conjugate

Catherine Paul, Lucie Sancey, François Ghiringhelli, K. David Wegner, Elisa Chazeau, Angélique Pipier, Christine Goze
article en
1 citations

Abstract

Real-time imaging of antibody-drug conjugates (ADCs) offers valuable insights for assessing tumor targeting specificity, monitoring therapeutic efficacy, and detecting off-target accumulation that may cause adverse effects. To enable precise tracking, we developed a versatile fluorescent platform based on an NIR-II emitting aza-BODIPY dye, which can be site-specifically grafted onto an IgG1 antibody to generate well-defined fluorescent ADCs. As a proof of concept, we synthesized an HER2-targeting trastuzumab immunoconjugate bearing a NIR-II aza-BODIPY fluorophore. The cytotoxic monomethyl auristatin E (MMAE) payload was introduced in the final step, resulting in a trackable and homogeneous ADC suitable for both in vitro and in vivo investigations. The resulting Trastu-azaNIRII-MMAE selectively accumulated in HER2-positive subcutaneous tumors, significantly reducing the tumor growth. Using NIR-II optical imaging, a single injection of the NIR-II-ADC allowed for the detection of the conjugate over a period of more than one month, highlighting its potential for long-term tracking and therapeutic applications.

Journal of Medicinal ChemistryVol. 68(7)
Centre National de la Recherche Scientifique (FR), Federal Institute For Materials Research and Testing (DE), Inserm (FR), Université de Bourgogne (FR), Université Paris Sciences et Lettres (FR), Université Grenoble Alpes (FR)
Agence Nationale de la Recherche, Ligue Contre le Cancer, Ministère de l'Education Nationale, de l'Enseignement Superieur et de la Recherche, Centre National de la Recherche Scientifique, Conseil régional de Bourgogne-Franche-Comté
Good health and well-being
Openalex Percentile: Top 22%
Monoclonal and Polyclonal Antibodies Research
1.36
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