Departamento de Química Analítica e Físico-Química, Centro de Ciências, Universidade Federal do Ceará, Bloco 940, Campus do Pici, 60455-970 Fortaleza, CE, Brazil.
Talanta. 2010 Mar 15;80(5):1730-6. doi: 10.1016/j.talanta.2009.10.014. Epub 2009 Oct 14.
The influence of the boron-doping levels in boron-doped diamond film electrodes on the electrochemical response of nitrofurantoin (NFT) and the development of an electroanalytical procedure for NFT determination were investigated. The investigations were carried out using the techniques of cyclic voltammetry and square wave voltammetry on diamond film electrodes with different boron-doping levels (i.e., 5000, 10,000 and 20,000 mg L(-1)). The level of boron-doping in the diamond film electrodes influenced the electrochemical reduction of NFT. The appropriate cyclic voltammetric response of NFT was obtained with Britton-Robinson buffer at pH 4 and for diamond films doped with 10,000 and 20,000 mg L(-1) of boron. These two films were selected for the development of the electroanalytical procedure. The use of square wave voltammetry with the optimized parameters demonstrated a good linear relationship between the peak current and the NFT concentration for a wide range of concentration. The lower limit of detection for the electrodes doped with 10,000 and 20,000 mg L(-1) of boron were 2.69 x 10(-8) mol L(-1) (6.40 microg L(-1)) and 8.15 x 10(-9) mol L(-1) (1.94 microg L(-1)), respectively, while the lower limits of quantification were 8.96 x 10(-8) mol L(-1) (21.33 microg L(-1)) and 2.72 x 10(-8) mol L(-1) (6.47 microg L(-1)), respectively. The applicability of the proposed procedure was tested using a commercial pharmaceutical formulation of NFT, and the results were compared with the procedure recommended by the British Pharmacopeia. The proposed procedure was sensitive, accurate and precise for analysis of NFT and did not require complex preparations or renovations of the electrode surface. This presents the advantage of eliminating mercury waste and minimizing the adsorptive problems related to the use of other electrodic solid surfaces.
采用循环伏安法和方波伏安法,研究了不同硼掺杂水平(5000、10000 和 20000mg/L)的硼掺杂金刚石薄膜电极对呋喃妥因(NFT)电化学响应的影响,并建立了 NFT 的电化学测定方法。硼掺杂水平影响 NFT 的电化学还原。在 pH 4 的 Britton-Robinson 缓冲液中,对于硼掺杂浓度为 10000 和 20000mg/L 的金刚石薄膜电极,可获得合适的 NFT 循环伏安响应。选用这两种薄膜电极用于建立电化学分析方法。采用优化参数的方波伏安法,对于宽浓度范围,峰电流与 NFT 浓度之间呈现良好的线性关系。硼掺杂浓度为 10000 和 20000mg/L 的电极的检测下限分别为 2.69×10(-8)mol/L(6.40μg/L)和 8.15×10(-9)mol/L(1.94μg/L),定量下限分别为 8.96×10(-8)mol/L(21.33μg/L)和 2.72×10(-8)mol/L(6.47μg/L)。采用所建立的方法对市售 NFT 药物制剂进行了分析,并与英国药典推荐的方法进行了比较。该方法对 NFT 的测定具有较高的灵敏度、准确性和精密度,无需对电极表面进行复杂的预处理。该方法避免了汞废物的产生,并最大程度地减少了使用其他电极固体表面所带来的吸附问题。