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Engineering Oxaliplatin Prodrug Nanoparticles for Second Near‐Infrared Fluorescence Imaging‐Guided Immunotherapy of Colorectal Cancer
Author(s) -
Zhu Qiurong,
Sun Fang,
Li Tianliang,
Zhou Mengxue,
Ye Jiayi,
Ji Aiyan,
Wang Hui,
Ding Chunyong,
Chen Hao,
Xu Zhiai,
Yu Haijun
Publication year - 2021
Publication title -
small
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.785
H-Index - 236
eISSN - 1613-6829
pISSN - 1613-6810
DOI - 10.1002/smll.202007882
Subject(s) - prodrug , oxaliplatin , immunotherapy , cancer research , photothermal therapy , chemotherapy , immunogenic cell death , colorectal cancer , cancer , materials science , medicine , pharmacology , nanotechnology
Colorectal cancer (CRC) ranks as the third common and the fourth lethal cancer type worldwide. Immune checkpoint blockade therapy demonstrates great efficacy in a subset of metastatic CRC patients, but precise activation of the antitumor immune response at the tumor site is still challenging. Here a versatile prodrug nanoparticle for second near‐infrared (NIR‐II) fluorescence imaging‐guided combinatory immunotherapy of CRC is reported. The prodrug nanoparticles are constructed with a polymeric oxaliplatin prodrug (PBOXA) and a donor–spacer–acceptor–spacer–donor type small molecular fluorophore TQTCD. The later displays large Stokes shift (>300 nm), fluorescence emission over 1000 nm, and excellent photothermal conversion performance for NIR‐II fluorescence imaging‐guided photothermal therapy (PTT). The prodrug nanoparticles show seven times higher intratumoral OXA accumulation than free oxaliplatin. TQTCD‐based PTT and PBOXA‐induced chemotherapy trigger immunogenic cell death of the tumor cells and elicit antitumor immune response in a spatiotemporally controllable manner. Further combination of the prodrug nanoparticle‐based PTT/chemotherapy with programmed death ligand 1 blockade significantly promotes intratumoral infiltration of the cytotoxic T lymphocytes and eradicates the CRC tumors. The NIR‐II fluorescence imaging‐guided immunotherapy may provide a promising approach for CRC treatment.

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