Deng Hao-Hua, Wu Gang-Wei, He Dong, Peng Hua-Ping, Liu Ai-Lin, Xia Xing-Hua, Chen Wei
Department of Pharmaceutical Analysis, Fujian Medical University, Fuzhou 350004, China and Higher Educational Key Laboratory for Nano Biomedical Technology of Fujian Province, Fujian Medical University, Fuzhou 350004, China.
Department of Pharmaceutical Analysis, Fujian Medical University, Fuzhou 350004, China and Department of Pharmacy, Fujian Provincial Hospital, Fuzhou 350001, China.
Analyst. 2015 Nov 21;140(22):7650-6. doi: 10.1039/c5an01284h.
Given the importance of hydrogen peroxide (H2O2) in many biological processes and its wide application in various industries, the demand for sensitive, accurate, and economical H2O2 sensors is high. In this study, we used Fenton reaction-stimulated fluorescence quenching of N-acetyl-L-cysteine-protected gold nanoclusters (NAC-AuNCs) as a reporter system for the determination of H2O2. After the experimental conditions were optimized, the sensing platform enabled the analysis of H2O2 with a limit of detection (LOD) as low as 0.027 μM. As the glucose oxidase cascade leads to the generation of H2O2 and catalase catalyzes the decomposition of H2O2, these two biocatalytic procedures can be probed by the Fenton reaction-mediated quenching of NAC-AuNCs. The LOD for glucose was found to be 0.18 μM, and the linear range was 0.39-27.22 μM. The LOD for catalase was 0.002 U mL(-1), and the linear range was 0.01-0.3 U mL(-1). Moreover, the proposed sensing methods were successfully applied for human serum glucose detection and the non-invasive determination of catalase activity in human saliva, demonstrating their great potential for practical applications.
鉴于过氧化氢(H2O2)在许多生物过程中的重要性及其在各行业的广泛应用,对灵敏、准确且经济的H2O2传感器需求很高。在本研究中,我们利用芬顿反应刺激的N-乙酰-L-半胱氨酸保护的金纳米簇(NAC-AuNCs)荧光猝灭作为测定H2O2的报告系统。优化实验条件后,该传感平台能够分析H2O2,检测限(LOD)低至0.027 μM。由于葡萄糖氧化酶级联反应会产生H2O2,而过氧化氢酶催化H2O2分解,这两个生物催化过程可以通过芬顿反应介导的NAC-AuNCs猝灭来探测。发现葡萄糖的LOD为0.18 μM,线性范围为0.39 - 27.22 μM。过氧化氢酶的LOD为0.002 U mL(-1),线性范围为0.01 - 0.3 U mL(-1)。此外,所提出的传感方法成功应用于人体血清葡萄糖检测和人体唾液中过氧化氢酶活性的无创测定,证明了它们在实际应用中的巨大潜力。