Dipartimento di Scienze Agrarie, degli Alimenti e dell'Ambiente, CSRA- Centro Servizi di Ricerca Applicata, Università degli Studi di Foggia, Via Napoli, 25, 71100 Foggia, Italy.
Dipartimento di Scienze Agrarie, degli Alimenti e dell'Ambiente, CSRA- Centro Servizi di Ricerca Applicata, Università degli Studi di Foggia, Via Napoli, 25, 71100 Foggia, Italy.
Anal Chim Acta. 2015 Sep 24;894:1-6. doi: 10.1016/j.aca.2015.05.057. Epub 2015 Jul 9.
In this work, the application of a new pulsed amperometric detection (PAD) waveform at a glassy carbon electrode, operating in typical chromatographic mobile phases, is proposed for the sensitive and reproducible determination of arylethanolaminic and phenolic moiety based compounds (e.g. beta-agonists and polyphenols). Preliminary experiments by cyclic voltammetry were carried out to investigate the electrochemical behaviour and to select the detection and cleaning electrode potentials. The proposed potential-time profile was designed to prevent the carbon electrode fouling under repeated analyses, thus ensuring a reproducible and sensitive quantitative determination, without the need of any mechanical or chemical electrode cleaning procedure. The waveform electrochemical parameters, including detection and delay times, were optimized in terms of sensitivity, limit of detection and response stability. The optimized waveform allowed the sensitive and stable detection of model compounds, such as clenbuterol and caffeic acid, that showed detection limits of 0.1 μg L(-1) and 14 μg L(-1), quantification limits of 0.4 μg L(-1) and 46 μg L(-1), and linearity up to 100 μg L(-1) (r = 0.9993) and 10 mg L(-1) (r = 0.9998), respectively. Similar results were obtained for other compounds of the same classes, with precision values under repeatability conditions ranging from 3.0 to 5.9%. The proposed method can be then considered as an excellent alternative to the post-column detection of beta-agonists, phenols and polyphenols.
在这项工作中,提出了在玻碳电极上应用新的脉冲安培检测(PAD)波形,在典型的色谱流动相中运行,用于灵敏和可重现地测定芳基乙醇胺和酚部分化合物(例如β-激动剂和多酚)。通过循环伏安法进行了初步实验,以研究电化学行为并选择检测和清洗电极电位。所提出的电位-时间曲线旨在防止碳电极在重复分析下发生污垢,从而确保可重现和灵敏的定量测定,而无需任何机械或化学电极清洗程序。该波形电化学参数,包括检测和延迟时间,根据灵敏度、检测限和响应稳定性进行了优化。优化后的波形允许对模型化合物(如克伦特罗和咖啡酸)进行灵敏和稳定的检测,其检测限分别为 0.1μg/L 和 14μg/L,定量限分别为 0.4μg/L 和 46μg/L,线性范围分别高达 100μg/L(r=0.9993)和 10mg/L(r=0.9998)。对于同一类别的其他化合物也得到了类似的结果,在重复性条件下的精密度值范围为 3.0 至 5.9%。因此,该方法可以被认为是替代β-激动剂、酚类和多酚类化合物的柱后检测的一种极好的方法。