Wang Nannan, Miller Christopher J, Wang Peng, Waite T David
School of Mechanical Engineering, Beijing Institute of Petrochemical Technology, Beijing 102617, PR China; School of Municipal and Environmental Engineering, Harbin Institute of Technology, Harbin 150090, PR China.
School of Civil and Environmental Engineering, The University of New South Wales, Sydney, NSW 2052, Australia.
Anal Chim Acta. 2017 Apr 22;963:61-67. doi: 10.1016/j.aca.2017.02.033. Epub 2017 Mar 6.
The Amplex Red/horseradish peroxidase (AR/HRP) assay for HO is one of the most sensitive and simple approaches for HO quantification, which is effected by measuring the highly-fluorescent resorufin formed from oxidation of AR by the oxidizing intermediates generated by reaction of HRP and HO. The direct reactions of S(-II) with both HO and resorufin are too slow to be of relevance on analytical timescales, however, the reaction between S(-II) and the HRP/HO oxidizing intermediates is rapid enough to compete with the desired reaction of these oxidizing intermediates with AR, suppressing formation of the resorufin analyte. As this mode of interference can be considered simply a competition between the AR reagent and S(-II) for the intermediate oxidizing species, a simple equation is derived in this work enabling one to correct for this interference and obtain a good estimate of the true HO concentration after measuring the apparent HO concentration and the S(-II) concentration. This mode of interference is general to any compound that can act as a HRP substrate even if not directly reactive with HO. As such, the approach described is widely applicable to many potential reducing interferents and opens up the use of the AR/HRP assay to a much wider range of conditions, as well as demonstrating the utility of explicitly considering the mechanism of the analytical process.
用于血红素加氧酶(HO)的Amplex Red/辣根过氧化物酶(AR/HRP)检测法是HO定量分析中最灵敏且简单的方法之一,该方法通过测量由HRP与HO反应生成的氧化中间体氧化AR所形成的高荧光试卤灵来实现。然而,S(-II)与HO和试卤灵的直接反应太慢,在分析时间尺度上不具有相关性,而S(-II)与HRP/HO氧化中间体之间的反应足够快,能够与这些氧化中间体与AR的预期反应竞争,从而抑制试卤灵分析物的形成。由于这种干扰模式可简单视为AR试剂与S(-II)对中间氧化物种的竞争,因此在本研究中推导出一个简单方程,通过测量表观HO浓度和S(-II)浓度,能够校正这种干扰并获得对真实HO浓度的良好估计。这种干扰模式对于任何可作为HRP底物的化合物都是普遍存在的,即使该化合物不与HO直接反应。因此,所描述的方法广泛适用于许多潜在的还原性干扰物,并将AR/HRP检测法的应用拓展到更广泛的条件范围,同时也证明了明确考虑分析过程机制的实用性。