On-chip electrocatalytic NO sensing using ruthenium oxide nanorods

被引:11
|
作者
Tanumihardja, E. [1 ]
Rodriguez, A. Paradelo [2 ]
Loessberg-Zahl, J. T. [1 ]
Mei, B. [2 ]
Olthuis, W. [1 ]
van den Berg, A. [1 ]
机构
[1] Univ Twente, MESA Inst Nanotechnol, BIOS Lab Chip Grp, Enschede, Netherlands
[2] Univ Twente, Fac Sci & Technol, Photocatalyt Synth Grp, Enschede, Netherlands
来源
SENSORS AND ACTUATORS B-CHEMICAL | 2021年 / 334卷 / 334期
基金
欧洲研究理事会;
关键词
Ruthenium oxide; Electrocatalytic; Nitric oxide; Amperometric sensing; Real-time mass-spectrometry; Endothelial cells; NITRIC-OXIDE; ELECTROCHEMICAL DETECTION; RELEASE; DYSFUNCTION; ELECTRODES; PLATINUM;
D O I
10.1016/j.snb.2021.129631
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Online, on-chip measurement of nitric oxide (NO) in organ-on-chip devices is desired to study endothelial (dys) function under dynamic conditions. In this work, ruthenium oxide (RuOx) is explored as an amperometric NO sensor and its suitability for organ-on-chip applications. For testing purposes, diethylamine NONOate was used as chemical NO donor. The NONOate's NO generation and electrochemical oxidation of generated NO were confirmed by real-time electrochemical/mass-spectrometry. Using RuOx nanorods electrodes, we show that NO oxidation occurred at a lower onset potential (+675 mV vs. Ag/AgCl) than on bare Pt electrode (+800 mV vs. Ag/AgCl). Due to NO adsorption on the RuOx surface, NO oxidation also delivered a higher current density (33.5 nA.mu M-1. cm(-2)) compared to bare Pt (19.6 nA.mu M-1. cm(-2)), making RuOx nanorods a favourable electrode for NO sensing applications. The RuOx electrode's suitability for organ-on-chip applications was successfully tested by using the electrode to detect a few micromolar concentration of NO generated by endothelial cell culture. Overall, the RuOx nanorods proved to be suitable for organ-on-chip studies due to their high sensitivity and selectivity. Our chip-integrated electrode allows for online NO monitoring in biologically relevant in vitro experiments.
引用
收藏
页数:10
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