Rose Andrew L, Moffett James W, Waite T David
Centre for Water and Waste Technology, School of Civil and Environmental Engineering, The University of New South Wales, Sydney, Australia.
Anal Chem. 2008 Feb 15;80(4):1215-27. doi: 10.1021/ac7018975. Epub 2008 Jan 18.
Superoxide, the one-electron reduced form of dioxygen, is known to be generated in marine environments by photochemical and biological processes. Because of its selective reaction with only a few commonly occurring compounds, superoxide is expected to approach concentrations in the high picomolar or low nanomolar range in seawater. Most currently existing methods do not have both the necessary sensitivity and selectivity to measure naturally occurring concentrations. In contrast, we demonstrate here that the chemiluminescence reagent 2-methyl-6-(4-methoxyphenyl)-3,7-dihydroimidazo[l,2-a]pyrazin-3(7H)-one (MCLA) is selective for superoxide in seawater and can be used with a detection limit of around 50 pM. Although a wide range of potential interferences were shown not to react with MCLA directly, some care must be taken when analyzing samples containing nanomolar concentrations of Fe(II), Cu(I), Mo(V), V(III), or V(IV), since these compounds can react with oxygen to produce superoxide during analysis that is subsequently detected. We describe two methods for calibrating the system, one employing photochemically generated superoxide standards and the other employing the superoxide-generating xanthine/xanthine oxidase system and discuss limitations on the use of each. The method was successfully used in the field to determine steady-state superoxide concentrations in the water column in the eastern equatorial Pacific Ocean.
超氧阴离子是氧气的单电子还原形式,已知其在海洋环境中通过光化学和生物过程产生。由于它仅与少数常见化合物发生选择性反应,预计超氧阴离子在海水中的浓度接近高皮摩尔或低纳摩尔范围。目前大多数现有方法都没有同时具备测量自然存在浓度所需的灵敏度和选择性。相比之下,我们在此证明化学发光试剂2-甲基-6-(4-甲氧基苯基)-3,7-二氢咪唑并[1,2-a]吡嗪-3(7H)-酮(MCLA)对海水中的超氧阴离子具有选择性,并且可以在检测限约为50 pM的情况下使用。尽管已表明多种潜在干扰物不会直接与MCLA反应,但在分析含有纳摩尔浓度的Fe(II)、Cu(I)、Mo(V)、V(III)或V(IV)的样品时必须小心,因为这些化合物在分析过程中可与氧气反应生成随后被检测到的超氧阴离子。我们描述了两种校准该系统的方法,一种采用光化学产生的超氧阴离子标准品,另一种采用产生超氧阴离子的黄嘌呤/黄嘌呤氧化酶系统,并讨论了每种方法的使用局限性。该方法已成功应用于现场,以测定赤道东太平洋水柱中的稳态超氧阴离子浓度。