Karadas Nurgul, Ozkan Sibel A
Ankara University, Faculty of Pharmacy, Department of Analytical Chemistry, 06100 Ankara, Turkey; Hitit University, Faculty of Science and Arts, Department of Chemistry, Corum, Turkey.
Ankara University, Faculty of Pharmacy, Department of Analytical Chemistry, 06100 Ankara, Turkey.
Talanta. 2014 Feb;119:248-54. doi: 10.1016/j.talanta.2013.10.065. Epub 2013 Nov 11.
Electrochemical oxidation of pemetrexed (PMX) was studied on bare, carboxylic acid functionalized multi-walled carbon nanotubes and over-oxidized polypyrrole modified (oo-PPy/MWCNTs-COOH/GCE) glassy carbon electrodes by cyclic and adsorptive stripping differential pulse voltammetric techniques. The oo-PPy/MWCNTs-COOH/GCE is very sensitive to the oxidation of PMX. The results proved that the over-oxidation of the PPy film gave a negative charge density on porous layer that improved the adsorption for PMX. The effects of pH, concentrations of MWCNTs and monomer, the number of cycles for the electropolymerization and the scan rate for sensor preparation were optimized. The MWCNTs-COOH and oo-PPy based sensor showed an excellent recognition capacity toward PMX. The linear responses have been obtained in the range from 8.00 × 10(-7)M to 1.00 × 10(-4)M with 2.04 × 10(-7)M detection limit for the bare GCE and from 1.00 × 10(-8)M to 1.00 × 10(-7)M with 3.28 × 10(-9)M detection limit for the modified GCE. The oxidation of PMX was controlled by the adsorption process on both types of electrode surfaces. The proposed methods were compared with the literature on UV spectrophotometric assay, which was carried out at an absorption maximum of 225 nm. The proposed method and the designed sensors have been successfully applied for the determination of PMX in pharmaceuticals.
采用循环伏安法和吸附溶出差分脉冲伏安法,研究了培美曲塞(PMX)在裸玻碳电极、羧酸功能化多壁碳纳米管修饰玻碳电极以及过氧化聚吡咯修饰(oo-PPy/MWCNTs-COOH/GCE)玻碳电极上的电化学氧化行为。oo-PPy/MWCNTs-COOH/GCE对PMX的氧化非常敏感。结果表明,聚吡咯膜的过氧化使多孔层带上负电荷密度,提高了对PMX的吸附。优化了pH值、多壁碳纳米管和单体浓度、电聚合循环次数以及传感器制备扫描速率等因素的影响。基于MWCNTs-COOH和oo-PPy的传感器对PMX表现出优异的识别能力。裸玻碳电极在8.00×10⁻⁷M至1.00×10⁻⁴M范围内获得线性响应,检测限为2.04×10⁻⁷M;修饰玻碳电极在1.00×10⁻⁸M至1.00×10⁻⁷M范围内获得线性响应,检测限为3.28×10⁻⁹M。两种电极表面上PMX的氧化均受吸附过程控制。将所提出的方法与文献中在225nm最大吸收波长处进行的紫外分光光度法测定进行了比较。所提出的方法和设计的传感器已成功应用于药物中PMX的测定。