Chemistry Group, Birla Institute of Technology and Science, Pilani-Goa Campus, Zuarinagar Goa, PIN 403726, India.
Sensors (Basel). 2010;10(7):6377-94. doi: 10.3390/s100706377. Epub 2010 Jun 28.
A highly sensitive and specific enzyme inhibition assay based on alcohol oxidase (AlOx) and horseradish peroxidase (HRP) for determination of mercury Hg(II) in water samples has been presented. This article describes the optimization and miniaturization of an enzymatic assay using a chemiluminescence reaction. The analytical performance and detection limit for determination of Hg(II) was optimized in 96 well plates and further extended to 384 well plates with a 10-fold reduction in assay volume. Inhibition of the enzyme activity by dissolved Hg(II) was found to be linear in the range 5-500 pg·mL(-1) with 3% CV in inter-batch assay. Due to miniaturization of assay in 384 well plates, Hg(II) was measurable as low as 1 pg·mL(-1) within 15 min. About 10-fold more specificity of the developed assay for Hg(II) analysis was confirmed by challenging with interfering divalent metal ions such as cadmium Cd(II) and lead Pb(II). Using the proposed assay we could successfully demonstrate that in a composite mixture of Hg(II), Cd(II) and Pb(II), inhibition by each metal ion is significantly enhanced in the presence of the others. Applicability of the proposed assay for the determination of the Hg(II) in spiked drinking and sea water resulted in recoveries ranging from 100-110.52%.
本文提出了一种基于醇氧化酶(AlOx)和辣根过氧化物酶(HRP)的高灵敏度和高特异性的酶抑制分析方法,用于测定水样中的汞(Hg(II))。本文描述了使用化学发光反应对酶分析进行优化和小型化的过程。在 96 孔板中优化了分析性能和检测限,进一步将检测限扩展到 384 孔板,使检测体积减少了 10 倍。发现溶解的 Hg(II)对酶活性的抑制在 5-500 pg·mL(-1)范围内呈线性,批间测定的 CV 为 3%。由于在 384 孔板中进行了小型化测定,因此在 15 分钟内可以检测到低至 1 pg·mL(-1)的 Hg(II)。通过用干扰二价金属离子(如镉(Cd(II))和铅(Pb(II))挑战,证实了开发的分析方法对 Hg(II)分析具有约 10 倍的更高特异性。使用所提出的测定方法,我们可以成功地证明,在 Hg(II)、Cd(II)和 Pb(II)的复合混合物中,在其他金属离子存在的情况下,每种金属离子的抑制作用显著增强。所提出的测定方法在测定加标饮用水和海水中的 Hg(II)的应用中,回收率范围为 100-110.52%。