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肿瘤微环境中内源性HO敏感且弱酸性pH触发的氮掺杂石墨烯纳米颗粒(N-GNMs)作为模拟过氧化物酶的纳米酶用于肿瘤特异性治疗。

Endogenous HO-Sensitive and Weak Acidic pH-Triggered Nitrogen-Doped Graphene Nanoparticles (N-GNMs) in the Tumor Microenvironment Serve as Peroxidase-Mimicking Nanozymes for Tumor-Specific Treatment.

作者信息

Liang Danyang, Yang Yongzhen, Li Gongjian, Wang Qin, Chen Heting, Deng Xiaoyuan

机构信息

MOE Key Laboratory of Laser Life Science & Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China.

Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China.

出版信息

Materials (Basel). 2021 Apr 13;14(8):1933. doi: 10.3390/ma14081933.

Abstract

Nanozymes are emerging as a promising strategy for the treatment of tumors. Herein, to cope with the tumor microenvironment (TME), weak acidity (pH 5.6 to 6.8) and trace amounts of overexpressed hydrogen peroxide (HO) (100 µM-1 mM), we report nitrogen-doped graphene nanomaterials (N-GNMs), which act as highly efficient catalytic peroxidase (POD)-mimicking nanozymes in the TME for tumor-specific treatment. N-GNMs exhibit POD catalytic properties triggered by a weakly acidic TME and convert HO into highly toxic hydroxyl radicals (•OH) thus causing the death of tumor cells while in the neutral pH surroundings of normal tissues, such catalysis is restrained and leaves normal cells undamaged thereby achieving a tumor-specific treatment. N-GNMs also display a high catalytic activity and can respond to the trace endogenous HO in the TME resulting in a high efficiency of tumor therapy. Our in vitro chemical and cell experiments illustrated the POD-like activity of N-GNMs and in vivo tumor model experiments confirmed the significant inhibitory effect of N-GNMs on tumor growth.

摘要

纳米酶正成为一种很有前景的肿瘤治疗策略。在此,为应对肿瘤微环境(TME)的弱酸性(pH 5.6至6.8)和痕量过表达的过氧化氢(HO)(100 µM - 1 mM),我们报道了氮掺杂石墨烯纳米材料(N-GNMs),其在TME中作为高效催化过氧化物酶(POD)模拟纳米酶用于肿瘤特异性治疗。N-GNMs表现出由弱酸性TME触发的POD催化特性,并将HO转化为高毒性的羟基自由基(•OH),从而导致肿瘤细胞死亡,而在正常组织的中性pH环境中,这种催化作用受到抑制,正常细胞不受损害,从而实现肿瘤特异性治疗。N-GNMs还表现出高催化活性,并且可以对TME中的痕量内源性HO作出反应,从而实现高效的肿瘤治疗。我们的体外化学和细胞实验证明了N-GNMs的类POD活性,体内肿瘤模型实验证实了N-GNMs对肿瘤生长具有显著的抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a110/8070265/82c7abdf64bd/materials-14-01933-sch001.jpg

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