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 and 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 the generation of singlet oxygen-triggered reactive oxygen species. The in vivo studies with the representative conjugate 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 and with iodine incorporation exhibit favorable and superior photophysical and photobiological aspects and demonstrate thereby their potential applications in imaging and PDT of cancer.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373210PMC
http://dx.doi.org/10.1021/acsomega.3c02416DOI Listing

Publication Analysis

Top Keywords

photodynamic therapy
8
biocompatible aza-bodipy-biotin
4
aza-bodipy-biotin conjugates
4
conjugates photodynamic
4
therapy cancer
4
cancer objective
4
objective develop
4
develop efficient
4
efficient photosensitizers
4
photosensitizers cancerous
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!