Engineering Asymmetric D-π-A BODIPYs as High-Performance Photosensitizers for Photodynamic Therapy

Abstract

Asymmetric D-π-A BODIPY photosensitizer 5c, based-on a mono-naphtho[b]-fused BODIPY core substituted with 8-trifluoromethylphenyl, 3-(4-methylthiopheneethylene), and 2-iodine groups, adopts a distorted structure. This design yields red-visible absorption at 661 nm, achieving a 38% ¹O₂ yield alongside the concurrent generation of O₂•─. Incorporated into nanoparticles, 5c demonstrates potent photodynamic activity (IC₅₀ = 3.2 μM) in cancer cells under low-dose laser irradiation, highlighting its potential as a highly efficient PDT agent.

Supplementary files

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Communication
Submitted
23 Aug 2025
Accepted
18 Dec 2025
First published
22 Dec 2025

Chem. Commun., 2026, Accepted Manuscript

Engineering Asymmetric D-π-A BODIPYs as High-Performance Photosensitizers for Photodynamic Therapy

Z. Zhai, C. fangjian, P. Li, C. Qu and Z. Shen, Chem. Commun., 2026, Accepted Manuscript , DOI: 10.1039/D5CC04867B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements