Bermejo E, Zapardiel A, Pérez J A, Huerta A, Hernández L
Department of Analytical Chemistry and Instrumental Analysis, Autonoma University, 28049 Madrid, Spain.
Talanta. 1993 Nov;40(11):1649-56. doi: 10.1016/0039-9140(93)80080-b.
The adsorption behaviour of flunitrazepam at the hanging mercury drop electrode was studied by staircase voltammetry and by adsorptive stripping differential pulse voltammetry. Flunitrazepam is adsorbed in the whole potential range, from the most positive values up to the reduction potential. Flunitrazepam reduction product is also adsorbed. The time dependence of the voltammetric response proves that a diffusion-controlled adsorption takes place. Flunitrazepam can be determined (down to nanomolar levels) by using adsorptive preconcentration prior to the differential pulse voltammetric scan. An application of such a method to flunitrazepam determination in human urine is described. The detection limit was 30 ng per milliliter of urine with a 20-sec accumulation time; the mean relative standard deviation was lower than 3.2% and the mean recovery 97.8%.
采用阶梯伏安法和吸附溶出微分脉冲伏安法研究了氟硝西泮在悬汞滴电极上的吸附行为。氟硝西泮在整个电位范围内都有吸附,从最正的值到还原电位。氟硝西泮的还原产物也有吸附。伏安响应的时间依赖性证明发生了扩散控制的吸附。在微分脉冲伏安扫描之前,通过吸附预富集可以测定氟硝西泮(低至纳摩尔水平)。描述了该方法在人尿中氟硝西泮测定中的应用。在20秒的积累时间下,检测限为每毫升尿液30纳克;平均相对标准偏差低于3.2%,平均回收率为97.8%。