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Real-time monitoring of ROS secreted by Ana-1 mouse Macrophages by nanomaterial sensitized Electrochemiluminescence

机译:纳米材料敏化电化学发光的ANA-1小鼠巨噬细胞分泌ROS的实时监测

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摘要

Reactive oxygen species (ROS) are closely related to numerous physiological and pathological processes, but the real-time monitoring of ROS is still a challenge because of their rapid diffusion, low concentration, and short half-life in biological systems. Herein, two excellent electrochemiluminescent (ECL) cytosensors were developed for the real-time detection of ROS. Using poly-L-lysine (PLL) to promote cell adhesion, based on the prefunctionalization with gold nanoparticles (AuNPs) or AuNPs/titania nanotubes (TiO2NTs) nanocomposites for indium-doped tin oxide (ITO)-coated glass, two sensors are acquired. For AuNP-functionalized one (Sensor 1), the result for the H2O2 assay demonstrated a good linear response from 0.01 ?M to 0.2 ?M and a limit of detection down to 8.9 nM. After capitalizing on the synergetic effect of AuNPs and TiO2NTs, the AuNP/TiO2NT-based biosensor (Sensor 2) displayed better sensitivity toward H2O2 detection with a linear response from 5 nM to 0.1 ?M and a lower limit of detection (LOD) of 2 nM. On this basis, we changed the cell density and stimulated cells with different drugs to detect the production of ROS, indicating the good applicability of the biosensors.
机译:活性氧(Reactive oxygen species,ROS)与许多生理和病理过程密切相关,但由于其在生物系统中扩散快、浓度低、半衰期短,因此对其进行实时监测仍然是一个挑战。在此,我们开发了两种优秀的电化学发光(ECL)细胞传感器,用于实时检测活性氧。利用聚L-赖氨酸(PLL)促进细胞粘附,基于金纳米粒子(AuNPs)或AuNPs/二氧化钛纳米管(TiO2NTs)纳米复合物对掺铟氧化锡(ITO)涂层玻璃的预功能化,获得了两个传感器。对于AuNP功能化的一个(传感器1),H2O2分析的结果显示,从0.01?到0.01?的线性响应良好?M到0.2?M,检测限降至8.9 nM。在利用了AuNP和TiO2纳米颗粒的协同效应后,基于AuNP/TiO2纳米颗粒的生物传感器(传感器2)对H2O2的检测显示出更好的灵敏度,线性响应范围为5 nM到0.1 nM?M,检测下限(LOD)为2 nM。在此基础上,我们改变了细胞密度,用不同的药物刺激细胞来检测活性氧的产生,表明该生物传感器具有良好的适用性。

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