Cox J A, Dabek-Zlotorzynska E
Department of Chemistry, Miami University, Oxford, OH 45056.
J Chromatogr. 1991 Apr 26;543(1):226-32. doi: 10.1016/s0021-9673(01)95772-3.
Organic disulfides generally are not oxidized at bare electrodes under conditions that are suited to routine amperometric detection, and thiols are typically oxidized in a manner that leads to partial blockage of the surface. Modification of a carbon electrode with a film of Ru(III,IV) oxide stabilized with cyanocross-links permits the amperometric detection of cystine, cysteine, glutathione, methionine, and glutathione disulfide under conditions compatible with their chromatographic separation on a strong cation-exchange column. Detection limits of 0.2-0.6 microM and linear dynamic ranges of at least 1-50 microM were obtained. The electrode was stable for at least 11 days with a pH 1 citrate, phosphate mobile phase.
在适合常规安培检测的条件下,有机二硫化物通常不会在裸电极上被氧化,而硫醇通常以导致表面部分堵塞的方式被氧化。用氰基交联稳定的氧化钌(III,IV)薄膜修饰碳电极,可在与它们在强阳离子交换柱上进行色谱分离兼容的条件下,对胱氨酸、半胱氨酸、谷胱甘肽、甲硫氨酸和谷胱甘肽二硫化物进行安培检测。检测限为0.2 - 0.6微摩尔,线性动态范围至少为1 - 50微摩尔。使用pH值为1的柠檬酸盐、磷酸盐流动相时,该电极至少可稳定11天。