Chemistry Department, Maynooth University, Maynooth W23 F2H6, County Kildare, Ireland.
Sensors (Basel). 2017 Jul 8;17(7):1596. doi: 10.3390/s17071596.
We detail an extensive characterisation study on a previously described dual amperometric H₂O₂ biosensor consisting of H₂O₂ detection (blank) and degradation (catalase) electrodes. In vitro investigations demonstrated excellent H₂O₂ sensitivity and selectivity against the interferent, ascorbic acid. Ex vivo studies were performed to mimic physiological conditions prior to in vivo deployment. Exposure to brain tissue homogenate identified reliable sensitivity and selectivity recordings up to seven days for both blank and catalase electrodes. Furthermore, there was no compromise in pre- and post-implanted catalase electrode sensitivity in ex vivo mouse brain. In vivo investigations performed in anaesthetised mice confirmed the ability of the H₂O₂ biosensor to detect increases in amperometric current following locally perfused/infused H₂O₂ and antioxidant inhibitors mercaptosuccinic acid and sodium azide. Subsequent recordings in freely moving mice identified negligible effects of control saline and sodium ascorbate interference injections on amperometric H₂O₂ current. Furthermore, the stability of the amperometric current was confirmed over a five-day period and analysis of 24-h signal recordings identified the absence of diurnal variations in amperometric current. Collectively, these findings confirm the biosensor current responds in vivo to increasing exogenous and endogenous H₂O₂ and tentatively supports measurement of H₂O₂ dynamics in freely moving NOD SCID mice.
我们详细描述了之前描述的双安培型 H₂O₂ 生物传感器的广泛特征研究,该传感器由 H₂O₂ 检测(空白)和降解(过氧化氢酶)电极组成。体外研究表明,该传感器对干扰物抗坏血酸具有出色的 H₂O₂ 灵敏度和选择性。在体内部署之前,进行了离体研究以模拟生理条件。暴露于脑组织匀浆中,空白和过氧化氢酶电极在长达七天的时间内均能可靠地进行灵敏度和选择性记录。此外,在离体小鼠脑中,植入前和植入后的过氧化氢酶电极灵敏度没有受到影响。在麻醉小鼠中进行的体内研究证实,H₂O₂ 生物传感器能够检测到局部灌注/输注 H₂O₂ 以及抗氧化剂抑制剂巯基琥珀酸和叠氮化钠后安培电流的增加。在自由活动的小鼠中的后续记录表明,对照生理盐水和抗坏血酸钠干扰注射对安培 H₂O₂ 电流几乎没有影响。此外,还确认了在五天的时间内安培电流的稳定性,并通过对 24 小时信号记录的分析,确定了安培电流没有昼夜变化。总的来说,这些发现证实了生物传感器电流在体内对增加的外源性和内源性 H₂O₂有反应,并初步支持在自由活动的 NOD SCID 小鼠中测量 H₂O₂ 动力学。