Yu Huicheng, Ma Zhenzhen, Wu Zhaoyang
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, China; School of Chemistry and Chemical Engineering, Guangxi University for Nationalities, Nanning, 530008, China; School of Chemistry and Chemical Engineering, Guangxi University for Nationalities, Nanning, 530008, China; Key Laboratory of Chemistry and Engineering of Forest Products, Guangxi University for Nationalities, Nanning, 530008, China; Key Laboratory of Guangxi Colleges and Universities for Food Safety and Pharmaceutical Analytical Chemistry, Guangxi University for Nationalities, Nanning, 530008, China.
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, China.
Anal Chim Acta. 2015 Oct 8;896:137-42. doi: 10.1016/j.aca.2015.09.005. Epub 2015 Sep 11.
The preparation of a persistently stable and sensitive biosensor is highly important for practical applications. To improve the stability and sensitivity of glutamate sensors, an electrode modified with glutamate dehydrogenase (GDH)/Ni-Pd/core-shell nanoparticles was developed using the thermal polymerization of acrylamide (AM) to immobilize the synthesized Ni-Pd/core-shell nanoparticles onto a glassy carbon electrode (GCE). The modified electrode was characterized by scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). Electrochemical data showed that the prepared biosensor had remarkably enhanced electrocatalytic activity toward glutamate. Moreover, superior reproducibility and excellent stability were observed (relative average deviation was 2.96% after continuous use of the same sensor for 60 times, and current responses remained at 94.85% of the initial value after 60 d). The sensor also demonstrated highly sensitive amperometric detection of glutamate with a low limit of detection (0.052 μM, S/N = 3), high sensitivity (4.768 μA μM(-1) cm(-2)), and a wide, useful linear range (0.1-500 μM). No interference from potential interfering species such as l-cysteine, ascorbic acid, and l-aspartate were noted. The determination of glutamate levels in actual samples achieved good recovery percentages.
制备一种持久稳定且灵敏的生物传感器对于实际应用至关重要。为了提高谷氨酸传感器的稳定性和灵敏度,利用丙烯酰胺(AM)的热聚合反应,将合成的Ni-Pd核壳纳米颗粒固定在玻碳电极(GCE)上,制备了一种用谷氨酸脱氢酶(GDH)/Ni-Pd核壳纳米颗粒修饰的电极。通过扫描电子显微镜(SEM)、傅里叶变换红外(FTIR)光谱、循环伏安法(CV)和电化学阻抗谱(EIS)对修饰电极进行了表征。电化学数据表明,制备的生物传感器对谷氨酸具有显著增强的电催化活性。此外,还观察到了优异的重现性和稳定性(同一传感器连续使用60次后相对平均偏差为2.96%,60天后电流响应仍保持在初始值的94.85%)。该传感器还展示了对谷氨酸的高灵敏安培检测,检测限低(0.052 μM,S/N = 3)、灵敏度高(4.768 μA μM⁻¹ cm⁻²)以及宽且有用的线性范围(0.1 - 500 μM)。未观察到来自潜在干扰物质如L-半胱氨酸、抗坏血酸和L-天冬氨酸的干扰。实际样品中谷氨酸水平的测定获得了良好的回收率。