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通过电化学平台进行时空一氧化氮调节以剖析肿瘤细胞反应

Spatiotemporal Nitric Oxide Modulation via Electrochemical Platform to Profile Tumor Cell Response.

作者信息

Won Chanju, Kim Sojin, Kwak Dongvin, Kim Taemin, Kim Jinhui, Lee Eunjun, Kim Suyeon, Velmurugan Adith Ramakrishnan, Ringe Stefan, Kim Hugh I, Jin Kyoungsuk

机构信息

Department of Chemistry, Korea University, 145, Anam-ro, Seongbuk-gu, Seoul, Republic of, Korea E-mail: and.

Single Cell Analysis Laboratory, Korea University, 145, Anam-ro, Seongbuk-gu, Seoul, Republic of, Korea.

出版信息

Angew Chem Int Ed Engl. 2024 Dec 9;63(50):e202411260. doi: 10.1002/anie.202411260. Epub 2024 Oct 24.

Abstract

Nitric oxide (NO) is a gaseous molecule intricately implicated in oncologic processes, encompassing the modulation of angiogenesis and instigating apoptosis. Investigation of the antitumor effects of NO is currently underway, necessitating a detailed understanding of its cellular-level reactions. Regulating the behavior of radical NO species has been a significant challenge, primarily due to its instability in aqueous environments by rapid O-induced degradation. In this study, we devised an electrochemical platform to investigate the cellular responses to reactive gaseous molecules. Our designed platform precisely controlled the NO flux and diffusion rates of NO to tumor cells. COMSOL Multiphysics calculations based on diffusion and reaction kinetics were conducted to simulate the behavior of electrochemically generated NO. We discerned that the effective radius, NO flux, and electrolysis duration are pivotal factors governing cellular response by NO.

摘要

一氧化氮(NO)是一种气态分子,与肿瘤学过程有着复杂的关联,包括对血管生成的调节和诱导细胞凋亡。目前正在对NO的抗肿瘤作用进行研究,这需要详细了解其细胞水平的反应。调节自由基NO物种的行为一直是一项重大挑战,主要是因为它在水性环境中会因快速的氧诱导降解而不稳定。在本研究中,我们设计了一个电化学平台来研究细胞对反应性气态分子的反应。我们设计的平台精确控制了NO通量以及NO向肿瘤细胞的扩散速率。基于扩散和反应动力学进行了COMSOL Multiphysics计算,以模拟电化学产生的NO的行为。我们发现有效半径、NO通量和电解持续时间是控制NO引起细胞反应的关键因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b27/11609960/96262f32ec54/ANIE-63-e202411260-g003.jpg

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