Shen Man, Dai Xianling, Ning Dongni, Xu Hanqing, Zhou Yang, Chen Gangan, Ren Zhangyin, Chen Ming, Gao Mingxuan, Bao Jing
Department of Clinical Laboratory Medicine, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
College of Pharmacy and Laboratory Medicine, Third Military Medical University (Army Medical University), Chongqing, China.
Front Immunol. 2024 Jul 17;15:1392259. doi: 10.3389/fimmu.2024.1392259. eCollection 2024.
The treatment of wound inflammation is intricately linked to the concentration of reactive oxygen species (ROS) in the wound microenvironment. Among these ROS, HO serves as a critical signaling molecule and second messenger, necessitating the urgent need for its rapid real-time quantitative detection, as well as effective clearance, in the pursuit of effective wound inflammation treatment. Here, we exploited a sophisticated 3D Cu Se/GO nanostructure-based nanonzymatic HO electrochemical sensor, which is further decorated with evenly distributed Pt nanoparticles (Pt NPs) through electrodeposition. The obtained Cu Se/GO@Pt/SPCE sensing electrode possesses a remarkable increase in specific surface derived from the three-dimensional surface constructed by GO nanosheets. Moreover, the localized surface plasma effect of the Cu Se nanospheres enhances the separation of photogenerated electron-hole pairs between the interface of the Cu Se NPs and the Pt NPs. This innovation enables near-infrared light-enhanced catalysis, significantly reducing the detection limit of the Cu Se/GO@Pt/SPCE sensing electrode for HO (from 1.45 μM to 0.53μM) under NIR light. Furthermore, this biosensor electrode enables real-time monitoring of HO released by cells. The NIR-enhanced Cu Se/GO@Pt/SPCE sensing electrode provide a simple-yet-effective method to achieve a detection of ROS (HO、-OH) with high sensitivity and efficiency. This innovation promises to revolutionize the field of wound inflammation treatment by providing clinicians with a powerful tool for accurate and rapid assessment of ROS levels, ultimately leading to improved patient outcomes.
伤口炎症的治疗与伤口微环境中活性氧(ROS)的浓度密切相关。在这些ROS中,HO作为一种关键的信号分子和第二信使,在寻求有效的伤口炎症治疗过程中,迫切需要对其进行快速实时定量检测以及有效清除。在此,我们开发了一种基于复杂的三维Cu Se/GO纳米结构的纳米酶HO电化学传感器,该传感器通过电沉积进一步用均匀分布的铂纳米颗粒(Pt NPs)进行修饰。所获得的Cu Se/GO@Pt/SPCE传感电极具有由GO纳米片构建的三维表面所带来的显著比表面积增加。此外,Cu Se纳米球的局域表面等离子体效应增强了Cu Se NPs与Pt NPs界面之间光生电子 - 空穴对的分离。这一创新实现了近红外光增强催化,在近红外光下显著降低了Cu Se/GO@Pt/SPCE传感电极对HO的检测限(从1.45 μM降至0.53μM)。此外,这种生物传感器电极能够实时监测细胞释放的HO。近红外增强的Cu Se/GO@Pt/SPCE传感电极提供了一种简单而有效的方法,以高灵敏度和高效率实现对ROS(HO、 - OH)的检测。这一创新有望通过为临床医生提供一个用于准确快速评估ROS水平的强大工具,彻底改变伤口炎症治疗领域,最终改善患者预后。