Pesavento M, Merli D, Biesuz R, Alberti G, Marchetti S, Milanese C
Department of Chemistry, University of Pavia, Italy.
Department of Chemistry, University of Pavia, Italy.
Anal Chim Acta. 2021 Jan 15;1142:201-210. doi: 10.1016/j.aca.2020.10.059. Epub 2020 Nov 3.
There is an increasing interest in determining the concentration of furanic compounds naturally formed in food aqueous matrices, by in situ, fast and low-cost methods. A sensor presenting such characteristics is here proposed, and characterized. It is based on a molecularly imprinted polymer (MIP) as a receptor with electrochemical transduction on a screen printed cell (SPC). The molecularly imprinted polymer has been developed for a particular furanic derivative, 2-furaldehyde (2-FAL). The detection bases on the reduction of 2-FAL selectively adsorbed on the polymer layer in contact with the working electrode. The polymer layer is simply formed by in situ polymerization, directly over the SPC and it was characterized by IR, SEM and electrochemical methods. Even if based on an easy and fast preparation procedure, the layer sufficiently adheres to the cell surface giving a reusable sensor. Square wave voltammetry (SWV) was applied as the signal acquisition method. The sensor performance in aqueous solution (NaCl 0.1 M) was tested, obtaining that the dose-response curve is fitted by the Langmuir adsorption isotherm. The sensitivity, and so the limit of detection, were noticeably improved by a chemometric approach based on the Design of experiment method. (optimized conditions: E = 0.03 V, E = 0.066 V, f = 31 s). In water solution at pH around neutrality the dynamic range was from about 50 μM to 20 mM. Similar results were obtained for a white wine containing 12% ethanol, which has been considered as a typical example of beverage possibly containing furhaldehydes. The higher limit of quantification can be modulated by the amount of MIP deposited, while the lower detection limit by the conditions of the electrochemical measurement.
人们越来越关注通过原位、快速且低成本的方法来测定食品水性基质中天然形成的呋喃类化合物的浓度。本文提出并表征了一种具有此类特性的传感器。它基于分子印迹聚合物(MIP)作为受体,并在丝网印刷电极(SPC)上进行电化学转换。该分子印迹聚合物是针对特定的呋喃衍生物2-呋喃甲醛(2-FAL)开发的。检测基于选择性吸附在与工作电极接触的聚合物层上的2-FAL的还原。聚合物层通过原位聚合直接在SPC上简单形成,并通过红外光谱、扫描电子显微镜和电化学方法对其进行了表征。即使基于简单快速的制备过程,该层也能充分粘附在电极表面,从而得到可重复使用的传感器。采用方波伏安法(SWV)作为信号采集方法。测试了该传感器在水溶液(0.1M NaCl)中的性能,结果表明剂量-响应曲线符合朗缪尔吸附等温线。基于实验设计方法的化学计量学方法显著提高了灵敏度以及检测限。(优化条件:E = 0.03V,E = 0.066V,f = 31s)。在pH接近中性的水溶液中,动态范围约为50μM至20mM。对于含有12%乙醇的白葡萄酒也得到了类似结果,该白葡萄酒被视为可能含有呋喃醛的典型饮料示例。较高的定量限可通过沉积的MIP量进行调节,而较低的检测限则受电化学测量条件的影响。