journal article·2023-02-14

Anthracene-Bridged Photosensitizers for Effective and Safe Photodynamic Therapy

Jucai Gao, Hui Yang, Yaru Lu, Qiankun Shi, Shidang Xu, Wenbo Wu, Fang Hu, Bin Liu

Chemistry of Materials· Volume 35· Issue 3
Publisher page

Abstract

Photodynamic therapy (PDT) is a minimally invasive therapeutic modality. However, the residual photosensitizers (PSs) after PDT can still produce toxic singlet oxygen ( 1 O 2 ) under sunlight to damage normal tissues. The PS that can be switched off after PDT is desirable but rare. Herein, we propose a general strategy to design effective and self-degradable PSs by embedding an anthracene bridge into donor–acceptor (D–A) structures. First, the steric anthracene can regulate the orbital distribution for enhancing the 1 O 2 production capacity. More importantly, the anthracene is responsive to the self-produced 1 O 2 for self-degradation. Besides, the degradation rate can be fine-tuned by the hydrophilicity of PSs. In this way, the PSs can realize a balance between treatment and suicide to ensure PDT and post-treatment safety. This work provides new insights into the design of degradable PSs with a clear mechanism, aiming to improve the post-safety of PDT.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanoplatforms for cancer theranostics · Photodynamic Therapy Research Studies · Luminescence and Fluorescent Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Biomaterials Research Center, School of Biomedical Engineering, Southern Medical University, Guangzhou 510515, China

Institute of Molecular Aggregation Science, Tianjin University, Tianjin 300072, China

Department of Chemical and Biomolecular Engineering, National University of Singapore, Singapore 117585, Singapore

Funding

National University of Singapore · National Natural Science Foundation of China · Guangdong Basic and Applied Basic Research Foundation

References (30)

Show source-provided references
1. 10.1038/nrc107110.1038/nrc1071 ↗
2. 10.1016/j.biopha.2018.07.04910.1016/j.biopha.2018.07.049 ↗
3. 10.1002/jpp.32810.1002/jpp.328 ↗
4. 10.1073/pnas.171755211510.1073/pnas.1717552115 ↗
5. 10.1002/anie.20190871210.1002/anie.201908712 ↗
6. 10.3390/cancers902001910.3390/cancers9020019 ↗
7. 10.1021/acsnano.1c0157710.1021/acsnano.1c01577 ↗
8. 10.2174/1574891x11308999001210.2174/1574891x113089990012 ↗
9. 10.1021/jacs.1c0867910.1021/jacs.1c08679 ↗
10. 10.1016/j.pdpdt.2019.02.02110.1016/j.pdpdt.2019.02.021 ↗
11. 10.1038/nrc189410.1038/nrc1894 ↗
12. 10.1126/sciadv.abb271210.1126/sciadv.abb2712 ↗
13. 10.1021/jacs.1c0737910.1021/jacs.1c07379 ↗
14. 10.5946/ce.2013.46.1.2410.5946/ce.2013.46.1.24 ↗
15. 10.1080/14764172.2018.150245510.1080/14764172.2018.1502455 ↗
16. 10.1016/j.saa.2021.12078310.1016/j.saa.2021.120783 ↗
17. 10.1021/acs.chemmater.1c0117310.1021/acs.chemmater.1c01173 ↗
18. 10.1002/anie.20201247710.1002/anie.202012477 ↗
19. 10.1002/advs.20210410110.1002/advs.202104101 ↗
20. 10.1016/s1572-1000(05)00060-810.1016/s1572-1000(05)00060-8 ↗
21. 10.1002/adhm.20190013210.1002/adhm.201900132 ↗
22. 10.1039/c5cc08606j10.1039/c5cc08606j ↗
23. 10.1016/1010-6030(94)03945-q10.1016/1010-6030(94)03945-q ↗
24. 10.1021/ac502103t10.1021/ac502103t ↗
25. 10.1002/agt2.710.1002/agt2.7 ↗
26. 10.1039/c7mh00469a10.1039/c7mh00469a ↗
27. 10.1002/adma.20180135010.1002/adma.201801350 ↗
28. 10.1021/jacs.1c0821110.1021/jacs.1c08211 ↗
29. 10.1039/c7cc04864e10.1039/c7cc04864e ↗
30. 10.1002/anie.20220433010.1002/anie.202204330 ↗