A Carbon‐Caged Rhodamine Generating Nitrosoperoxycarbonate for Photoimmunotherapy

Author:

Yin Lei1,Zhao Bei2,Zhou Jie3,Huang Yunxia1,Ma Hao4,Zhou Ting5,Mou Jie5,Min Peiru4,Chen Jinquan3,Ge Guangbo2,Qian Xuhong16,Luo Xiao6,Yang Youjun1ORCID

Affiliation:

1. State Key Laboratory of Bioreactor Engineering Shanghai Key Laboratory of Chemical Biology School of Pharmacy East China University of Science and Technology Shanghai 200237 China

2. Shanghai Frontiers Science Center of TCM Chemical Biology Institute of Interdisciplinary Integrative Medicine Research Shanghai University of Traditional Chinese Medicine Shanghai 201203 China

3. State Key Laboratory of Precision Spectroscopy East China Normal University Shanghai 200241 China

4. Department of Plastic and Reconstructive Surgery Shanghai Ninth People's Hospital affiliated to Shanghai Jiao Tong University School of Medicine Shanghai 200011 China

5. Jiangsu Key Laboratory of New drug and Clinical Pharmacy Xuzhou Medical University Xuzhou 221004 Jiangsu China

6. Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development School of Chemistry and Molecular Engineering East China Normal University Shanghai 200241 China

Abstract

AbstractPhotoimmunotherapy is a promising cancer treatment modality. While potent 1‐e oxidative species are known to induce immunogenic cell death (ICD), they are also associated with unspecific oxidation and collateral tissue damage. This difficulty may be addressed by post‐generation radical reinforcement. Namely, non‐oxidative radicals are first generated and subsequently activated into powerful oxidative radicals to induce ICD. Here, we developed a photo‐triggered molecular donor (NPCD565) of nitrosoperoxycarbonate (ONOOCO2), the first of its class to our knowledge, and further evaluated its feasibility for immunotherapy. Upon irradiation of NPCD565 by light within a broad spectral region from ultraviolet to red, ONOOCO2 is released along with a bright rhodamine dye (RD565), whose fluorescence is a reliable and convenient build‐in reporter for the localization, kinetics, and dose of ONOOCO2 generation. Upon photolysis of NPCD565 in 4T1 cells, damage‐associated molecular patterns (DAMPs) indicative of ICD were observed and confirmed to exhibit immunogenicity by induced maturation of dendritic cells. In vivo studies with a bilateral tumor‐bearing mouse model showcased the potent tumor‐killing capability of NPCD565 of the primary tumors and growth suppression of the distant tumors. This work unveils the potent immunogenicity of ONOOCO2, and its donor (NPCD565) has broad potential for photo‐immunotherapy of cancer.

Funder

Key Technologies Research and Development Program

National Natural Science Foundation of China

Program of Shanghai Academic Research Leader

Publisher

Wiley

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