Self-Immolative Photosensitizers for Self-Reported Cancer Phototheranostics

Wang，Chunfei1; Sun，Yongjie1; Huang，Shaojuan1; Wei，Zixiang1; Tan，Jingyun1; Wu，Changfeng2; Chen，Qiang1,3; Zhang，Xuanjun1,3

2023-06-21

10.1021/jacs.3c01666

Journal of the American Chemical Society   影响因子和分区

0002-7863

1520-5126

Photosensitizers to precise target and change fluorescence upon light illumination could accurately self-report where and when the photosensitizers work, enabling us to visualize the therapeutic process and precisely regulate treatment outcomes, which is the unremitting pursuit of precision and personalized medicine. Here, we report self-immolative photosensitizers by adopting a strategy of light-manipulated oxidative cleavage of C═C bonds that can generate a burst of reactive oxygen species, to cleave to release self-reported red-emitting products and trigger nonapoptotic cell oncosis. Strong electron-withdrawing groups are found to effectively suppress the C═C bond cleavage and phototoxicity via studying the structure-activity relationship, allowing us to elaborate NG1-NG5 that could temporarily inactivate the photosensitizer and quench the fluorescence by different glutathione (GSH)-responsive groups. Thereinto, NG2 with 2-cyano-4-nitrobenzene-1-sulfonyl group displays excellent GSH responsiveness than the other four. Surprisingly, NG2 shows better reactivity with GSH in weakly acidic condition, which inspires the application in weakly acidic tumor microenvironment where GSH elevates. To this end, we further synthesize NG-cRGD by anchoring integrin αβ binding cyclic pentapeptide (cRGD) for tumor targeting. In A549 xenografted tumor mice, NG-cRGD successfully deprotects to restore near-infrared fluorescence because of elevated GSH in tumor site, which is subsequently cleaved upon light irradiation releasing red-emitting products to report photosensitizer working, while effectively ablating tumors via triggered oncosis. The advanced self-immolative organic photosensitizer may accelerate the development of self-reported phototheranostics in future precision oncology.

SCI ; EI ; IC

英语

NI论文

通讯

Science and Technology Development Fund, Macau SAR["0114/2019/A2","0085/2020/A2","0058/2022/A1","0087/2022/A2"] ; Guangdong Basic and Applied Basic Research Foundation["2022A1515010616","2023A1515012524"] ; Shenzhen Science and Technology Program["KQTD20170810111314625","JCYJ20210324115807021"] ; Research Grant of University of Macau["SRG2021-00008-FHS","MYRG2020-00130-FHS","MYRG2022-00036-FHS"]

Chemistry

Chemistry, Multidisciplinary

WOS:001011864500001

AMER CHEMICAL SOC

20232514271929

Fluorescence ; Infrared devices ; Mammals ; Tumors

Biological Materials and Tissue Engineering:461.2 ; Light/Optics:741.1

2-s2.0-85162000362

Scopus

1.Faculty of Health Sciences,University of Macau,999078,Macao
2.Department of Biomedical Engineering,Southern University of Science and Technology,Shenzhen,518055,China
3.MOE Frontiers Science Centre for Precision Oncology,University of Macau,999078,Macao

Wang，Chunfei,Sun，Yongjie,Huang，Shaojuan,et al. Self-Immolative Photosensitizers for Self-Reported Cancer Phototheranostics[J]. Journal of the American Chemical Society,2023,145(24):13099-13113.

Wang，Chunfei.,Sun，Yongjie.,Huang，Shaojuan.,Wei，Zixiang.,Tan，Jingyun.,...&Zhang，Xuanjun.(2023).Self-Immolative Photosensitizers for Self-Reported Cancer Phototheranostics.Journal of the American Chemical Society,145(24),13099-13113.

Wang，Chunfei,et al."Self-Immolative Photosensitizers for Self-Reported Cancer Phototheranostics".Journal of the American Chemical Society 145.24(2023):13099-13113.