B Kanthappa, Manjunatha J G, Osman Sameh Mohamed, Ataollahi Narges
Department of Chemistry, FMKMC College, Constituent College of Mangalore University, Madikeri, Karnataka, India, 571201.
Chemistry Department, College of Science, King Saud University, P.O. Box 2455, 11451, Riyadh, Saudi Arabia.
Sci Rep. 2024 Dec 28;14(1):30950. doi: 10.1038/s41598-024-82011-8.
In this study, DL-phenylalanine modified with a multiwall carbon nanotube paste electrode is used as advanced electrochemical sensor for analysing of 0.1 mM caffeic acid (CFA) with simultaneous detection of riboflavin (RFN). The developed sensors include electrochemically polymerized DL-phenylalanine (DL-PA) modified multiwall carbon nanotube paste electrode [DL-PAMMCNTPE] and bare multiwall carbon nanotube paste electrode [BMCNTPE]. The increasing stability in the developed electrochemical sensor for the quantification of CFA is highlighted in detail, along with its characterization using voltammetric techniques such as electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), differential pulse voltammetry (DPV), and linear Sweep Voltammetry (LSV). Scanning electron microscopy (SEM) technique was used to studied the structural analysis of BMCNTPE and DL-PAMMCNTPE surface. The investigation of 0.1 mM CFA in 0.2 M phosphate buffered solution (PBS) using a 7.0 pH at 0.1 V/s scan rate was highlighted using DL-PAMMCNTPE, which shows good electrochemical responses compared to BMCNTPE. This work characterizes the voltammetric responses by inspecting the pH effect, scan rate effect, and concentration difference of CFA at the DL-PAMMCNTPE surface. The CFA responses specify that the scan rate progress is adsorption controlled. The concentration of CFA detection was started from 20 μM to 600 μM using DPV method, with lower limit of detection (LOD) of 0.280 μM and limit of quantification (LOQ) of 0.936 μM. And for CV method concentration range 20 to 550 μM, with LOD of 0.198 μM and LOQ of 0.702 μM. Furthermore, the developed electrochemical sensor responses are shows good stability, repeatability, and reproducibility, for CFA. The analytical applicability of CFA in apple juice and coffee powder samples was also evaluated.
在本研究中,用多壁碳纳米管糊电极修饰的DL-苯丙氨酸被用作先进的电化学传感器,用于分析0.1 mM的咖啡酸(CFA)并同时检测核黄素(RFN)。所开发的传感器包括电化学聚合的DL-苯丙氨酸(DL-PA)修饰的多壁碳纳米管糊电极[DL-PAMMCNTPE]和裸多壁碳纳米管糊电极[BMCNTPE]。详细突出了所开发的用于定量CFA的电化学传感器中不断提高的稳定性,以及使用伏安技术(如电化学阻抗谱(EIS)、循环伏安法(CV)、差分脉冲伏安法(DPV)和线性扫描伏安法(LSV))对其进行的表征。扫描电子显微镜(SEM)技术用于研究BMCNTPE和DL-PAMMCNTPE表面的结构分析。使用DL-PAMMCNTPE突出了在0.2 M磷酸盐缓冲溶液(PBS)中,pH为7.0、扫描速率为0.1 V/s时对0.1 mM CFA的研究,与BMCNTPE相比,其显示出良好的电化学响应。这项工作通过检查pH效应、扫描速率效应以及DL-PAMMCNTPE表面CFA的浓度差异来表征伏安响应。CFA响应表明扫描速率的变化是吸附控制的。使用DPV方法检测CFA的浓度范围从20 μM到600 μM,检测下限(LOD)为0.280 μM,定量限(LOQ)为0.936 μM。对于CV方法,浓度范围为20至550 μM,LOD为0.198 μM,LOQ为0.702 μM。此外,所开发的电化学传感器对CFA的响应显示出良好的稳定性、重复性和再现性。还评估了CFA在苹果汁和咖啡粉样品中的分析适用性。