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Biocompatible Aza-BODIPY-Biotin Conjugates for Photodynamic Therapy of Cancer

[Image: see text] With an objective to develop efficient photosensitizers to cancerous tissues, we synthesized two novel biocompatible sensitizers based on aza-BODIPYs incorporated with heavy atoms and biotin moieties. The bioconjugates DPR2a and DPR2b exhibited a favorable absorption range (600–750...

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Autores principales: Dutta, Dhiraj, Nair, Rajshree R., Mangalath, Sreejith, Nair, S. Asha, Joseph, Joshy, Gogoi, Pranjal, Ramaiah, Danaboyina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373210/
https://www.ncbi.nlm.nih.gov/pubmed/37521632
http://dx.doi.org/10.1021/acsomega.3c02416
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author Dutta, Dhiraj
Nair, Rajshree R.
Mangalath, Sreejith
Nair, S. Asha
Joseph, Joshy
Gogoi, Pranjal
Ramaiah, Danaboyina
author_facet Dutta, Dhiraj
Nair, Rajshree R.
Mangalath, Sreejith
Nair, S. Asha
Joseph, Joshy
Gogoi, Pranjal
Ramaiah, Danaboyina
author_sort Dutta, Dhiraj
collection PubMed
description [Image: see text] With an objective to develop efficient photosensitizers to cancerous tissues, we synthesized two novel biocompatible sensitizers based on aza-BODIPYs incorporated with heavy atoms and biotin moieties. The bioconjugates DPR2a and DPR2b exhibited a favorable absorption range (600–750 nm) with excellent triplet-state quantum yields (up to 79%) and singlet oxygen generation yields (up to 75%). In vitro photobiological investigations employing MDA-MB-231 breast cancer cell lines exhibited rapid cellular uptake, negligible dark toxicity, and high photocytotoxicity. The mechanism of cell death of these systems was predominantly due to the mitochondrial damage, leading to apoptosis mediated via the generation of singlet oxygen-triggered reactive oxygen species. The in vivo studies with the representative conjugate DPR2a employing female NOD/SCID mice models showed inhibition in tumor growth and significantly decreased tumor volume post photodynamic therapy (PDT) treatment. Our results validate that both DPR2a and DPR2b with iodine incorporation exhibit favorable and superior photophysical and photobiological aspects and demonstrate thereby their potential applications in imaging and PDT of cancer.
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spelling pubmed-103732102023-07-28 Biocompatible Aza-BODIPY-Biotin Conjugates for Photodynamic Therapy of Cancer Dutta, Dhiraj Nair, Rajshree R. Mangalath, Sreejith Nair, S. Asha Joseph, Joshy Gogoi, Pranjal Ramaiah, Danaboyina ACS Omega [Image: see text] With an objective to develop efficient photosensitizers to cancerous tissues, we synthesized two novel biocompatible sensitizers based on aza-BODIPYs incorporated with heavy atoms and biotin moieties. The bioconjugates DPR2a and DPR2b exhibited a favorable absorption range (600–750 nm) with excellent triplet-state quantum yields (up to 79%) and singlet oxygen generation yields (up to 75%). In vitro photobiological investigations employing MDA-MB-231 breast cancer cell lines exhibited rapid cellular uptake, negligible dark toxicity, and high photocytotoxicity. The mechanism of cell death of these systems was predominantly due to the mitochondrial damage, leading to apoptosis mediated via the generation of singlet oxygen-triggered reactive oxygen species. The in vivo studies with the representative conjugate DPR2a employing female NOD/SCID mice models showed inhibition in tumor growth and significantly decreased tumor volume post photodynamic therapy (PDT) treatment. Our results validate that both DPR2a and DPR2b with iodine incorporation exhibit favorable and superior photophysical and photobiological aspects and demonstrate thereby their potential applications in imaging and PDT of cancer. American Chemical Society 2023-06-21 /pmc/articles/PMC10373210/ /pubmed/37521632 http://dx.doi.org/10.1021/acsomega.3c02416 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Dutta, Dhiraj
Nair, Rajshree R.
Mangalath, Sreejith
Nair, S. Asha
Joseph, Joshy
Gogoi, Pranjal
Ramaiah, Danaboyina
Biocompatible Aza-BODIPY-Biotin Conjugates for Photodynamic Therapy of Cancer
title Biocompatible Aza-BODIPY-Biotin Conjugates for Photodynamic Therapy of Cancer
title_full Biocompatible Aza-BODIPY-Biotin Conjugates for Photodynamic Therapy of Cancer
title_fullStr Biocompatible Aza-BODIPY-Biotin Conjugates for Photodynamic Therapy of Cancer
title_full_unstemmed Biocompatible Aza-BODIPY-Biotin Conjugates for Photodynamic Therapy of Cancer
title_short Biocompatible Aza-BODIPY-Biotin Conjugates for Photodynamic Therapy of Cancer
title_sort biocompatible aza-bodipy-biotin conjugates for photodynamic therapy of cancer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373210/
https://www.ncbi.nlm.nih.gov/pubmed/37521632
http://dx.doi.org/10.1021/acsomega.3c02416
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