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Updated: May 23, 2025

An In Vitro Enzymatic Assay to Measure Transcription Inhibition by GalliumIII and H3 5,10,15-trispentafluorophenylcorroles
Published on: March 18, 2015
Glycosylated Phosphorous(V) Corrole as effective Photosensitizers for Cancer Photodynamic Therapy via Enhancing
Qiu-Juan Xie1, Jing-He Cen2, Feng Li2
1School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou, Guangdong, 511442, China.
Abstract:
Developing effective photosensitizers (PSs) is the most important for cancer photodynamic therapy (PDT) treatment. Phosphrous corrole complex is a kind of promising photosensitizer. Herein, we report the synthesis and anticancer activity of a novel glycosylated phosphorous(V) corrole PS 5,15-bis(pentafuorophenyl)-10-(4-glycosyl phenyl) corrole phosphorous(V) complex (2-P) which was prepared from the glycosylation of phosphorous(V) 5,15-bis(pentafuorophenyl)-10-(4-oxhydryl phenyl) corrole (1-P). Experimental results indicate that 2-P exhibits significantly higher uptake in cancer cells than 1-P, leading to an enhanced photo-cytotoxicity toward tumor cells while maintaining low dark or phototoxicity to normal cells such as HEK293T. Upon light exposure, 2-P may remarkably increase the reactive oxygen species (ROS) level of tumor cells, a key factor for enhancing the PDT efficacy. This study demonstrates the potential of 2-P as an effective PS for PDT, highlighting the glycosylation modification is an effective strategy for the design of new phosphorous corrole PDT drugs.
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