化学
内吞作用
荧光
细胞内
生物物理学
免疫原性细胞死亡
佐剂
药品
赫拉
细胞
细胞生物学
程序性细胞死亡
免疫系统
癌细胞
DNA
微量注射
细胞膜
三磷酸腺苷
癌症研究
药物输送
全身给药
毒品携带者
光动力疗法
雷达51
适体
分子生物学
荧光素
转染
作者
Caixia Wang,Siqi Zhang,Yuxin Xie,Jifu Du,Zhicong Chao,Huangxian Ju,Ying Liu
标识
DOI:10.1021/acs.analchem.5c07267
摘要
Immune adjuvants are essential components in chemo-immunotherapy; however, determining the optimal administration timing to synchronize them with recruited immune cells is challenging due to the difficulty in in vivo tracing of immunogenic cell death (ICD). Current ex vivo ICD assessment methodologies delay reporting and are thus incapable of guiding in situ chemo-immunotherapy. Here, we develop a cell Membrane-Anchored NIR-II Fluorescent Timer-Embedded Drug (MANTED) to real-time track ICD and guide adjuvant administration timing. MANTED is constructed by conjugating a DNA NIR-II ATP reporter to rare earth nanoparticles (RENPs), loading with chemotherapy drugs to the DNA helix, and anchoring to a 4T1 cell membrane via a biorthogonal click reaction, which prevents endocytosis and intracellular ATP interference. The ATP reporter is functionalized with the quencher FD1080 to quench NIR-II fluorescence of RENPs and is blocked with a photocleavable complementary strand to suppress tumor microenvironment ATP interference before the ICD process. Upon 980 nm laser irradiation, the UV upconversion emission of RENPs cleaves the PC linker, releasing the drug for chemotherapy and activating MANTED. Subsequent 808 nm laser irradiation induces RENPs’ downconversion NIR-II fluorescence recovery upon ATP recognition, which is monitored in real time. The optimal timing for adjuvant administration is chosen when the fluorescence intensity is saturated. MANTED-guided chemo-immunotherapy enhances therapeutic efficiency.
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