Wu Zai-Sheng, Zhang Song-Bai, Guo Meng-Meng, Chen Chen-Rui, Shen Guo-Li, Yu Ru-Qin
State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, PR China.
Anal Chim Acta. 2007 Feb 12;584(1):122-8. doi: 10.1016/j.aca.2006.11.003. Epub 2006 Nov 10.
An unmodified gold nanoparticle-based colorimetric assay system in homogeneous format has been developed using hydrogen peroxide (H(2)O(2)) as a model analyte. H(2)O(2) is added to o-phenylenediamine/horseradish peroxidase solution, and allowed to react for 10 min. Then, unmodified gold nanoparticles that serve as "reaction indicators" are added to the reaction solution. The resulting mixture color changes dramatically from red to blue. The reason is that azoaniline, a horseradish peroxidase-catalyzed oxidation product, induces the nanoparticle aggregation. Using this approach, H(2)O(2) can be semiquantitatively determined over the concentration range of approximately 4 orders of magnitude by the naked eye. If the observed peak intensity at 420 nm is used for the construction of the calibration plot, hydrogen peroxide can be accurately determined down to concentration levels of 1.3 x 10(-6) M. Compared with the conventional electrochemical protocol, this sensing system offers several important advantages: (1) ability to be monitored by the naked eye, (2) avoiding the need of surface modification of electrodes or gold nanoparticles and (3) detection in homogeneous solution. It is worthy of note that this efficient and convenient strategy is also suitable for the detection of other species, such as glucose and cholesterol.
已开发出一种基于未修饰金纳米颗粒的均相比色测定系统,该系统使用过氧化氢(H₂O₂)作为模型分析物。将H₂O₂加入邻苯二胺/辣根过氧化物酶溶液中,反应10分钟。然后,将用作“反应指示剂”的未修饰金纳米颗粒加入反应溶液中。所得混合物的颜色从红色急剧变为蓝色。原因是辣根过氧化物酶催化氧化产物偶氮苯胺会诱导纳米颗粒聚集。使用这种方法,通过肉眼可在约4个数量级的浓度范围内对H₂O₂进行半定量测定。如果将在420nm处观察到的峰值强度用于构建校准曲线,则可准确测定低至1.3×10⁻⁶ M浓度水平的过氧化氢。与传统的电化学方法相比,该传感系统具有几个重要优点:(1)可通过肉眼监测;(2)无需对电极或金纳米颗粒进行表面修饰;(3)在均相溶液中进行检测。值得注意的是,这种高效便捷的策略也适用于检测其他物质,如葡萄糖和胆固醇。