Charles University, Faculty of Science, Department of Analytical Chemistry, UNESCO Laboratory of Environmental Electrochemistry, Hlavova 2030/8, 128 43 Prague 2, Czech Republic; J. Heyrovský Institute of Physical Chemistry of the Czech Academy of Sciences, Dolejškova 2155/3, 182 23 Prague 8, Czech Republic.
J. Heyrovský Institute of Physical Chemistry of the Czech Academy of Sciences, Dolejškova 2155/3, 182 23 Prague 8, Czech Republic.
Anal Chim Acta. 2019 Dec 9;1087:44-50. doi: 10.1016/j.aca.2019.08.062. Epub 2019 Aug 31.
A new method for the simultaneous determination of two tumour biomarkers, homovanillic (HVA) and vanillylmandelic acid (VMA), using flow injection analysis (FIA) with amperometric detection (AD) at a commercially available boron doped diamond electrode (BDDE) was developed. It was found that this method is suitable for the determination of HVA (in the presence of VMA) and VMA (in the presence of HVA) in optimum medium of Britton-Robinson buffer (0.04 mol L, pH 3.0). Calibration dependences consist of two linear parts for both biomarkers, the first one being in the concentration range from 1 to 10 μmol L and the second one from 10 to 100 μmol L (with obtained LODs 0.44 μmol L for HVA and 0.34 μmol L for VMA, respectively). To minimize any negative effects related to the passivation of the working electrode, suitable cleaning pulses (+2.4 V for 30 s) were imposed on the working electrode after each measurement. An attempt to use FIA with multiple pulse amperometric detection to determine both analytes in one run was not successful. Changing potentials in short intervals in multiple pulse detection probably results in mutual interaction of analytes and/or products of their electrochemical oxidation, thus preventing the application of this approach.
采用安培检测的流动注射分析(FIA),在市售的掺硼金刚石电极(BDDE)上,建立了一种同时测定两种肿瘤生物标志物——高香草酸(HVA)和香草扁桃酸(VMA)的新方法。结果发现,该方法适用于在最佳 Britton-Robinson 缓冲介质(0.04 mol/L,pH 3.0)中测定 HVA(VMA 存在时)和 VMA(HVA 存在时)。两种生物标志物的校准曲线均由两个线性部分组成,第一个线性部分的浓度范围为 1 至 10 μmol/L,第二个线性部分的浓度范围为 10 至 100 μmol/L(HVA 的检出限为 0.44 μmol/L,VMA 的检出限为 0.34 μmol/L)。为了尽量减少工作电极钝化带来的任何负面影响,在每次测量后,对工作电极施加合适的清洗脉冲(+2.4 V,持续 30 s)。尝试在一次运行中使用多脉冲安培检测的 FIA 同时测定这两种分析物,但并未成功。在多脉冲检测中短时间内改变电位可能会导致分析物及其电化学氧化产物之间的相互作用,从而阻止了这种方法的应用。