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用于铁死亡过程中实时细胞内铁测量的电化学纳米探针的研制。

Development of electrochemical nanoprobe for real-time intracellular measurements of Fe during ferroptosis.

作者信息

Ma Yanmei, Li Xinhao, Hu Weikang, Ruan Muyang, Yang Ming, Chang Lingqian, Gu Hongri, Hu Chengzhi

机构信息

Shenzhen Key Laboratory of Biomimetic Robotics and Intelligent Systems, Department of Mechanical and Energy Engineering, Southern University of Science and Technology, Shenzhen, China.

Department of Biomedical Engineering, City University of Hong Kong, Hong Kong, China.

出版信息

Microsyst Nanoeng. 2025 Jul 7;11(1):134. doi: 10.1038/s41378-025-00930-6.

Abstract

Ferroptosis is an iron-dependent form of regulated cell death driven by phospholipid peroxidation and the accumulation of reactive oxygen species (ROS), holding significant importance for therapeutic applications via its induction or inhibition. Accurate detection of intracellular Fe and ROS is essential, as these molecules play essential roles in initiating and propagating ferroptosis. In this study, we present a novel electrochemical nanoprobe for real-time, highly selective detection of intracellular Fe. The nanoprobes are prepared by coating gold nanoparticles (AuNPs) and poly(3,4-ethylenedioxythiophene) (PEDOT) onto silicon carbide nanowires (SiC NWs), which are subsequently functionalized with ferrocenyl endoperoxide carboxylic acid (FDCA) and integrated with a liquid metal-filled glass nanopipette. FDCA is specifically synthesized to enable precise electrochemical detection of Fe with high selectivity (0.1 nM to 1 µM) and exceptional specificity. PEDOT and AuNPs can improve electrical conductivity and provide a versatile interface for further FDCA decoration. We use the nanoprobes to evaluate the intracellular change of Fe in MCF-7 breast cancer cells during erastin-induced ferroptosis. We observe a significant increase in intracellular Fe levels in MCF-7 cells undergoing ferroptosis, accompanied by a notable rise in ROS levels. These findings underscore the potential of this nanoprobe to enhance our understanding of the mechanism of ferroptosis in tumor development and as a potential treatment target.

摘要

铁死亡是一种由磷脂过氧化和活性氧(ROS)积累驱动的铁依赖性调节性细胞死亡形式,通过诱导或抑制铁死亡对治疗应用具有重要意义。准确检测细胞内的铁和ROS至关重要,因为这些分子在启动和传播铁死亡过程中发挥着关键作用。在本研究中,我们提出了一种新型电化学纳米探针,用于实时、高选择性地检测细胞内的铁。该纳米探针是通过将金纳米颗粒(AuNPs)和聚(3,4-乙撑二氧噻吩)(PEDOT)涂覆在碳化硅纳米线(SiC NWs)上制备而成,随后用二茂铁基内过氧化物羧酸(FDCA)进行功能化,并与填充有液态金属的玻璃纳米移液器集成。FDCA是专门合成的,能够以高选择性(0.1 nM至1 μM)和卓越的特异性实现对铁的精确电化学检测。PEDOT和AuNPs可以提高电导率,并为进一步的FDCA修饰提供通用界面。我们使用该纳米探针评估了在埃拉司亭诱导的铁死亡过程中MCF-7乳腺癌细胞内铁的变化。我们观察到正在经历铁死亡的MCF-7细胞内铁水平显著增加,同时ROS水平也显著上升。这些发现强调了这种纳米探针在增强我们对肿瘤发展中铁死亡机制的理解以及作为潜在治疗靶点方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad37/12234944/373e939ab5a6/41378_2025_930_Fig1_HTML.jpg

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