Calibration of NO sensors for in-vivo voltammetry: laboratory synthesis of NO and the use of UV-visible spectroscopy for determining stock concentrations

被引:44
作者
Brown, FO
Finnerty, NJ
Bolger, FB
Millar, J
Lowry, JP [1 ]
机构
[1] Univ Coll Dublin, Dept Pharmacol, Conway Inst Biomol & Biomed Res, Dublin 4, Ireland
[2] Natl Univ Ireland, Sensors Dev Unit, Bioelectroanal Lab, Dept Chem, Maynooth, Kildare, Ireland
[3] Queen Mary Univ London, Dept Neurosci, London E1 4NS, England
基金
英国工程与自然科学研究理事会;
关键词
nitric oxide; laboratory synthesis; UV-visible spectroscopy; in-vivo voltammetry; electrochemical sensors; calibrations;
D O I
10.1007/s00216-004-2964-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The increasing scientific interest in nitric oxide (NO) necessitates the development of novel and simple methods of synthesising NO on a laboratory scale. In this study we have refined and developed a method of NO synthesis, using the neutral Griess reagent, which is inexpensive, simple to perform, and provides a reliable method of generating NO gas for in-vivo sensor calibration. The concentration of the generated NO stock solution was determined using UV-visible spectroscopy to be 0.28+/-0.01 mmol L-1. The level of NO2- contaminant, also determined using spectroscopy, was found to be 0.67+/-0.21 mmol L-1. However, this is not sufficient to cause any considerable increase in oxidation current when the NO stock solution is used for electrochemical sensor calibration over physiologically relevant concentrations; the NO sensitivity of bare Pt-disk electrodes operating at +900 mV (vs. SCE) was 1.08 nA mumol(-1) L, while that for NO2- was 5.9x10(-3) nA mumol(-1) L. The stability of the NO stock solution was also monitored for up to 2 h after synthesis and 30 min was found to be the time limit within which calibrations should be performed.
引用
收藏
页码:964 / 971
页数:8
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