Laboratory of Integrated Systems, EPFL - École Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland; Biosensors Laboratory, Department of Chemistry Drug Technologies, Sapienza University of Rome, P.le Aldo Moro, 5-00185 Roma, Italy.
Laboratory of Integrated Systems, EPFL - École Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland.
Methods. 2017 Oct 1;129:89-95. doi: 10.1016/j.ymeth.2017.06.005. Epub 2017 Jun 13.
In this work, we have developed for the first time a method to make novel gold and platinum hybrid bimetallic nanostructures differing in shape and size. Au-Pt nanostructures were prepared by electrodeposition in two simple steps. The first step consists of the electrodeposition of nanocoral Au onto a gold substrate using hydrogen as a dynamic template in an ammonium chloride solution. After that, the Pt nanostructures were deposited onto the nanocoral Au organized in pores. Using Pt (II) and Pt (IV), we realized nanocoral Au decorated with Pt nanospheres and nanocoral Au decorated with Pt nanoflowers, respectively. The bimetallic nanostructures showed better capability to electrochemically oxidize hydrogen peroxide compared with nanocoral Au. Moreover, Au-Pt nanostructures were able to lower the potential of detection and a higher performance was obtained at a low applied potential. Then, glucose oxidase was immobilized onto the bimetallic Au-Pt nanostructure using cross-linking with glutaraldehyde. The biosensor was characterized by chronoamperometry at +0.15V vs. Ag pseudo-reference electrode (PRE) and showed good analytical performances with a linear range from 0.01 to 2.00mM and a sensitivity of 33.66µA/mMcm. The good value of K (2.28mM) demonstrates that the hybrid nanostructure is a favorable environment for the enzyme. Moreover, the low working potential can minimize the interference from ascorbic acid and uric acid as well as reducing power consumption to effect sensing. The simple procedure to realize this nanostructure and to immobilize enzymes, as well as the analytical performances of the resulting devices, encourage the use of this technology for the development of biosensors for clinical analysis.
在这项工作中,我们首次开发了一种方法来制备形状和尺寸不同的新型金铂混合双金属纳米结构。采用两步电化学沉积法制备 Au-Pt 纳米结构。第一步是在氯化铵溶液中以氢气为动态模板,在金基底上电沉积纳米珊瑚 Au。之后,Pt 纳米结构沉积在多孔组织的纳米珊瑚 Au 上。分别使用 Pt(II)和 Pt(IV),我们实现了纳米珊瑚 Au 上修饰 Pt 纳米球和纳米珊瑚 Au 上修饰 Pt 纳米花。与纳米珊瑚 Au 相比,双金属纳米结构具有更好的电化学氧化过氧化物的能力。此外,Au-Pt 纳米结构能够降低检测电位,并在较低的应用电位下获得更高的性能。然后,用过氧化氢酶通过戊二醛交联固定在双金属 Au-Pt 纳米结构上。通过计时安培法在 +0.15V 对 Ag 伪参比电极(PRE)进行了生物传感器的特征描述,并表现出良好的分析性能,线性范围为 0.01 至 2.00mM,灵敏度为 33.66µA/mMcm。良好的 K 值(2.28mM)表明,该混合纳米结构是酶的理想环境。此外,低工作电位可以最小化抗坏血酸和尿酸的干扰以及降低功耗以进行感应。实现这种纳米结构和固定酶的简单程序以及由此产生的器件的分析性能,鼓励将该技术用于开发用于临床分析的生物传感器。