Krzyczmonik Paweł, Klisowska Marta, Leniart Andrzej, Ranoszek-Soliwoda Katarzyna, Surmacki Jakub, Beton-Mysur Karolina, Brożek-Płuska Beata
Department of Inorganic and Analytical Chemistry, Faculty of Chemistry, University of Lodz, Tamka 12, 91-403 Lodz, Poland.
Department of Materials Technology and Chemistry, Faculty of Chemistry, University of Lodz, Pomorska 163 Street, 90-236 Lodz, Poland.
Materials (Basel). 2023 Jul 20;16(14):5113. doi: 10.3390/ma16145113.
The described research aimed to develop the properties of the conductive composite /poly(3,4-ethylenedioxy-thiophene-poly(4-lithium styrenesulfonic acid)/chitosan-AuNPs-glutaraldehyde/ (/PEDOT-PSSLi/chit-AuNPs-GA/) and to develop an electrochemical enzyme sensor based on this composite material and glassy carbon electrodes (GCEs). The composite was created via electrochemical production of an /EDOT-PSSLi/ layer on a glassy carbon electrode (GCE). This layer was covered with a glutaraldehyde cross-linked chitosan and doped with AuNPs. The influence of AuNPs on the increase in the electrical conductivity of the chitosan layers and on facilitating the oxidation of polyphenols in these layers was demonstrated. The enzymatic sensor was obtained via immobilization of the laccase on the surface of the composite, with glutaraldehyde as the linker. The investigation of the surface morphology of the GCE/PEDOT-PSSLi/chit-AuNPs-GA/Laccase sensor was carried out using SEM and AFM microscopy. Using EDS and Raman spectroscopy, AuNPs were detected in the chitosan layer and in the laccase on the surface of the sensor. Polyphenols were determined using differential pulse voltammetry. The biosensor exhibited catalytic activity toward the oxidation of polyphenols. It has been shown that laccase is regenerated through direct electron transfer between the sensor and the enzyme. The results of the DPV tests showed that the developed sensor can be used for the determination of polyphenols. The peak current was linearly proportional to the concentrations of catechol in the range of 2-90 μM, with a limit of detection (LOD) of 1.7 μM; to those of caffeic acid in the range of 2-90 μM, LOD = 1.9 μM; and to those of gallic acid in the range 2-18 μM, LOD = 1.7 μM. Finally, the research conducted in order to determine gallic acid in a natural sample, for which white wine was used, was described.
上述研究旨在开发导电复合材料/聚(3,4 - 乙撑二氧噻吩 - 聚(4 - 锂苯乙烯磺酸))/壳聚糖 - 金纳米粒子 - 戊二醛/(/PEDOT - PSSLi/壳聚糖 - 金纳米粒子 - 戊二醛/)的性能,并基于这种复合材料和玻碳电极(GCE)开发一种电化学酶传感器。该复合材料是通过在玻碳电极(GCE)上电化学制备/EDOT - PSSLi/层而制成的。该层覆盖有戊二醛交联的壳聚糖并掺杂有金纳米粒子。证明了金纳米粒子对壳聚糖层电导率增加以及促进这些层中多酚氧化的影响。通过以戊二醛为连接剂将漆酶固定在复合材料表面获得了酶传感器。使用扫描电子显微镜(SEM)和原子力显微镜(AFM)对GCE/PEDOT - PSSLi/壳聚糖 - 金纳米粒子 - 戊二醛/漆酶传感器的表面形态进行了研究。使用能谱仪(EDS)和拉曼光谱在壳聚糖层和传感器表面的漆酶中检测到了金纳米粒子。使用差分脉冲伏安法测定多酚。该生物传感器对多酚的氧化表现出催化活性。结果表明,漆酶通过传感器与酶之间的直接电子转移得以再生。差分脉冲伏安法(DPV)测试结果表明,所开发的传感器可用于测定多酚。峰电流与邻苯二酚浓度在2 - 90μM范围内呈线性比例关系,检测限(LOD)为1.7μM;与咖啡酸浓度在2 - 90μM范围内呈线性比例关系,LOD = 1.9μM;与没食子酸浓度在2 - 18μM范围内呈线性比例关系,LOD = 1.7μM。最后,描述了为测定天然样品中的没食子酸而进行的研究,该天然样品使用的是白葡萄酒。