Department of Chemistry, St. Joseph's College, Bangalore, Karnataka, India.
J Colloid Interface Sci. 2013 Jul 15;402:223-9. doi: 10.1016/j.jcis.2013.03.059. Epub 2013 Apr 11.
An electrochemical sensor for the amperometric determination of L-tryptophan (Trp) was fabricated by modifying the carbon paste electrode (CPE) with multi-walled carbon nanotubes (MWCNTs) using drop cast method. 4.0 μL of the dispersion containing 2.0 mg of MWCNTs in 1.0 mL of ethanol was drop cast onto the electrode surface and dried in hot air oven to form a stable layer of MWCNTs. The electro-catalytic activity of the modified electrode towards the oxidation of Trp was thoroughly investigated. The modification with MWCNTs has greatly improved the current sensitivity of CPE for the oxidation of Trp. A very minimal amount of the modifier was required to achieve such a high sensitivity. The field emission scanning electron microscopy (FESEM) images revealed a uniform coverage of the surface of CPE by MWCNTs. Nyquist plots revealed the least charge transfer resistance for the modified electrode. The analytical performance of the modified electrode was examined using amperometry under hydro-dynamic conditions. The two linear dynamic ranges observed for Trp were 0.6-9.0 μM and 10.0-100.0 μM. The amperometric determination of Trp did not suffer any interference from other biomolecules. The detection limit of Trp at modified electrode was (3.30±0.37)×10(-8)M (S/N=3). The analytical applications of the modified electrode were demonstrated by estimating Trp in the spiked milk and biological fluid such as blood serum. The modified electrode showed good reproducibility, long-term stability and anti-fouling effects.
采用滴涂法将多壁碳纳米管(MWCNTs)修饰到碳糊电极(CPE)上,制备了用于测定 L-色氨酸(Trp)的电化学传感器。将 4.0 μL 分散体滴涂到电极表面,该分散体含有 1.0 mL 乙醇中的 2.0mg MWCNTs,并在热空气烘箱中干燥以形成 MWCNTs 的稳定层。详细研究了修饰电极对 Trp 氧化的电催化活性。MWCNTs 的修饰极大地提高了 CPE 对 Trp 氧化的电流灵敏度。只需少量的修饰剂即可实现如此高的灵敏度。场发射扫描电子显微镜(FESEM)图像显示 MWCNTs 均匀覆盖了 CPE 的表面。奈奎斯特图显示修饰电极的电荷转移电阻最小。在动态水力条件下,采用安培法检查了修饰电极的分析性能。观察到 Trp 的两个线性动态范围分别为 0.6-9.0 μM 和 10.0-100.0 μM。修饰电极对 Trp 的安培测定没有受到其他生物分子的任何干扰。在修饰电极上,Trp 的检测限为(3.30±0.37)×10(-8)M(S/N=3)。通过估计加标牛奶和血清等生物液体中的 Trp,证明了修饰电极的分析应用。修饰电极显示出良好的重现性、长期稳定性和抗污损效果。