Research and Development Centre, Bharathiar University, Coimbatore 641 014, Tamilnadu, India.
Research and Development Centre, Bharathiar University, Coimbatore 641 014, Tamilnadu, India; Electrochemistry Research Group, Department of Chemistry, St. Joseph's College, Autonomous, Lalbagh Road, Bangalore 560 027, Karnataka, India.
Mater Sci Eng C Mater Biol Appl. 2017 Jul 1;76:114-122. doi: 10.1016/j.msec.2017.03.082. Epub 2017 Mar 12.
The fabrication of differential pulse voltametry (DPV) sensor for the effective detection of Quercetin (QR) was achieved by modifying carbon paste electrode (CPE) with Iron decorated multi walled carbon nano tubes (Fe-MWCNTs) followed by drop casting of hexadecyltrimethylammonium bromide onto the surface for optimal results. Cyclic voltammetry and DPV techniques were used for qualitative and quantitative analysis of QR (Quercetin) respectively. The sensor revealed impressive electro-catalytic behavior towards oxidation of QR with almost 6.4 times increase in current compared to bare carbon paste electrode CPE and also decrease in the energetics. Under optimum conditions, a wide linear dynamic range of 0.06 to 3000μM, with a lower limit of detection, 1.20nM with S/N=3 was observed. Absence of peak for the interfering molecules such as Folic acid and Ascorbic acid makes it a unique sensor with significant analytical advantage. The quantification of QR at this sensor was not affected by the presence of 1000 fold Uric Acid implying that the sensor is capable of specifically identifying QR in a mixture of interfering molecules. In this paper, we demonstrate that with minimal use of modifiers and simple procedures of fabrication, the fabricated sensor exhibits excellent stability, reproducibility and swift responses. Application of the developed electrode was demonstrated by detecting QR in wine and coconut water samples with satisfactory recoveries.
通过在碳糊电极(CPE)表面修饰铁修饰的多壁碳纳米管(Fe-MWCNTs),并滴铸十六烷基三甲基溴化铵,成功制备了用于有效检测槲皮素(QR)的差分脉冲伏安法(DPV)传感器。循环伏安法和 DPV 技术分别用于 QR(槲皮素)的定性和定量分析。与裸碳糊电极 CPE 相比,该传感器对 QR 的氧化表现出令人印象深刻的电催化行为,电流增加了近 6.4 倍,同时能量也降低了。在最佳条件下,观察到 0.06 至 3000μM 的宽线性动态范围,检测限为 1.20nM,S/N=3。干扰分子如叶酸和抗坏血酸不存在峰,这使其成为具有显著分析优势的独特传感器。在该传感器上对 QR 的定量不受 1000 倍尿酸存在的影响,这意味着传感器能够在干扰分子混合物中特异性识别 QR。在本文中,我们证明了,通过最小化使用修饰剂和简单的制造程序,所制造的传感器表现出优异的稳定性、重现性和快速响应。通过对葡萄酒和椰子水中的 QR 进行检测,展示了所开发电极的应用,回收率令人满意。