Regan F B, Meaney M P, Lunte S M
Center for Bioanalytical Research, University of Kansas, Lawrence 66047.
J Chromatogr B Biomed Appl. 1994 Jul 15;657(2):409-17. doi: 10.1016/0378-4347(94)00098-0.
Co2+, Fe2+, Cu2+ and Zn2+ were separated and detected following derivatization with 4-(2-pyridylazo)resorcinol by capillary electrophoresis with UV-Vis detection. Parameters which were examined include both on-column and pre-column complexation, limit of detection, capillary loadability, linear dynamic range and reproducibility. A sample stacking technique was investigated in order to obtain better detection limits and greater sensitivity. Detection limits of 1 x 10(-8) M were achieved for Co2+, Fe2+ and Zn2+ and 4 x 10(-7) M for Cu2+. Mass detection limits were 0.2 fmol for Co2+, Fe2+ and Zn2+ and 7.0 fmol for Cu2+. The use of this method for the determination of metals in vitamin tablets and a pond water sample is presented.
采用紫外可见检测的毛细管电泳法,在4-(2-吡啶偶氮)间苯二酚衍生化后,对Co2+、Fe2+、Cu2+和Zn2+进行分离和检测。所考察的参数包括柱上和柱前络合、检测限、毛细管负载能力、线性动态范围和重现性。研究了一种样品堆积技术,以获得更好的检测限和更高的灵敏度。Co2+、Fe2+和Zn2+的检测限为1×10(-8) M,Cu2+的检测限为4×10(-7) M。Co2+、Fe2+和Zn2+的质量检测限为0.2 fmol,Cu2+的质量检测限为7.0 fmol。介绍了该方法用于测定维生素片中的金属和池塘水样中的金属。