Nuñez-Vergara L J, Squella J A, Gonzalez E M
J Assoc Off Anal Chem. 1979 May;62(3):556-9.
A polarographic method has been developed for the quantitative analysis of cephradine and its dosage forms. Direct determinations on capsules are carried out; excipients and coloring matter do not interfere in the determination. The electroactive product is formed by acidic hydrolysis with 5.0N HCl and heating at 80 degrees C for 60 min. Two polarographic waves are obtained: I = -0.46 V and II = -0.78 v vs. SCE. Both reduction waves are diffusion controlled. Wave I is preferred for analytical purposes. The precise chemical identity of the electroactive product has not been determined, but UV spectral data and the TLC Rf value are reported. A linear relation is established for levels of cephradine between 10(-2) and 10(-5)M in 5.0N HCl.
已开发出一种极谱法用于头孢拉定及其剂型的定量分析。对胶囊进行直接测定;辅料和色素不干扰测定。通过用5.0N盐酸进行酸性水解并在80℃加热60分钟形成电活性产物。获得两个极谱波:相对于饱和甘汞电极(SCE),波I = -0.46V,波II = -0.78V。两个还原波均受扩散控制。出于分析目的,优选波I。尚未确定电活性产物的确切化学特性,但报告了紫外光谱数据和薄层色谱比移值(Rf值)。在5.0N盐酸中,头孢拉定浓度在10⁻²至10⁻⁵M之间建立了线性关系。