摘要
报道了安乃近的单扫描示波极谱法测定。样品在酸性条件下用碘将其氧化 ,然后在 p H=1 1 .0的氨 -氯化铵缓冲液中 ,起扫电位 -0 .4 0 V ( vs.SCE )测定 -0 .76V处的二次导数峰高。峰高与安乃近浓度在 0 .0 1~ 3 μg/m L范围内呈线性关系。检出限为 0 .0 0 5μg/m L。同时对该氧化产物的极谱行为和反应机理作了探讨。方法用于测定安乃近的含量 ,结果满意。
A method for the determination of novalgin has been described. Novalgin was oxidized by iodine in acidic solution and a sensitive reduction wave of its oxidation product was obstained at-0.76 V ( vs.SCE ) by single sweep oscillopolarography in NH 3·H 2O NH 4Cl buffer solution (pH=11.0). An excellent linear relationship between the peak height and the concentration of novalgin has been found in the range of 0.01~3 μg/mL. The detection limit was 0.005 μg/mL. Furthermore, the polarographic behaviour and the electrode reaction mechanism of its oxidation product were studied. The methods has been applied to the determination of novalgin in tablet with satisfactory results.
出处
《分析科学学报》
CAS
CSCD
2000年第1期61-64,共4页
Journal of Analytical Science