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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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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. |
format | Online Article Text |
id | pubmed-10373210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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