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基于联合调控酶的近红外荧光探针用于缺氧检测:设计、合成及在活细胞和小鼠中的应用。

Near-Infrared Fluorescent Probes for Hypoxia Detection via Joint Regulated Enzymes: Design, Synthesis, and Application in Living Cells and Mice.

机构信息

Shaanxi Engineering Laboratory for Food Green Processing and Safety Control, College of Food Engineering and Nutritional Science , Shaanxi Normal University , Xi'an 710062 , China.

Ministry of Education Key Laboratory of Medicinal Resources and Natural Pharmaceutical Chemistry, National Engineering Laboratory for Resource Developing of Endangered Chinese Crude Drugs in Northwest of China, College of Life Sciences , Shaanxi Normal University , Xi'an 710062 , China.

出版信息

Anal Chem. 2018 Nov 20;90(22):13759-13766. doi: 10.1021/acs.analchem.8b04249. Epub 2018 Nov 8.

Abstract

Hypoxia detection is emphasized with attention due to tumor and related diseases diagnosis, which could provide useful methods for exploring the mechanism of hypoxic tumor. Herein, we report two unprecedented hypoxia-sensitive probes that specifically switch-on their near-infrared fluorescence signals in the presence of hypoxia up-regulated enzymes (nitroreductase and cytochrome P450 reductase). The probes were designed by featuring the decomposition of IR-780 coupled to hypoxia activatable p-nitrobenzyl or azo moiety, which exhibit near-infrared fluorescence emission, high sensitivity, selectivity, stable photostability, and low cytotoxicity. Besides, the joint use of two probes could differentiate the 4T1 and HepG2 cells lines through fluorescence signals successfully. More importantly, applied to monitor hypoxia in 4T1 tumor-bearing BALB/c mice, the two probes have ideal biodistribution with passive accumulation and fast clearance, and there is negligible organ damage by hematoxylin and eosin staining analysis. To the best of our knowledge, there is no fluorescent probe for hypoxia detection via joint hypoxia regulated enzymes reported so far. This method may be of great potential use in cancer and other relevant diseases diagnosis.

摘要

由于肿瘤和相关疾病的诊断需要强调缺氧检测,这为探索缺氧肿瘤的机制提供了有用的方法。在这里,我们报告了两个前所未有的缺氧敏感探针,它们在缺氧上调酶(硝基还原酶和细胞色素 P450 还原酶)存在下特异性地开启近红外荧光信号。这些探针通过将 IR-780 与缺氧激活的对硝基苄基或偶氮部分偶联来设计,具有近红外荧光发射、高灵敏度、选择性、稳定的光稳定性和低细胞毒性。此外,联合使用两种探针可以通过荧光信号成功地区分 4T1 和 HepG2 细胞系。更重要的是,将两种探针应用于监测荷 4T1 肿瘤的 BALB/c 小鼠的缺氧情况,探针具有理想的组织分布,具有被动积累和快速清除的特点,并且通过苏木精和伊红染色分析,器官损伤可忽略不计。据我们所知,目前还没有通过联合缺氧调节酶检测缺氧的荧光探针。这种方法在癌症和其他相关疾病的诊断中可能具有很大的应用潜力。

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