摘要
基于头孢噻肟钠在0.3 mol/L NaOH溶液中沸水浴降解产物具有还原性,在酸性介质中可将Fe(Ⅲ)还原为Fe(Ⅱ),邻菲啰啉能与所生成的Fe(Ⅱ)显色生成红色络合物,最大吸收波长λ=508 nm;表观摩尔吸光系数ε=1.1×10^4L.mol^-1.cm^-1;头孢噻肟钠在0.4~80μg/mL范围内呈良好的线性关系;线性回归方程为A=-0.00204+0.01989ρ(μg/mL);线性相关系数r=0.9998;检出限为0.18μg/mL;RSD为1.2%(5.0μg/mL,n=11);平均回收率为99%。初步探讨了反应机理,并优化了对头孢噻肟钠的测定条件。
A simple and sensitive spectrophotometric method is described for the determination of cefotaxime. The method is based on the degradation of cefotaxime which was carried out in 0.3 mol/L NaOH solution at 100℃, and can be oxidized by Fe(Ⅲ) in acidic solution. Fe(Ⅱ ) can form a complex with o-phenanthroline hydrate, of which the maximum absorption wavelength is at 508nm, ε= 1.1×10^4 L(mol·cm). The Beer's law is obeyed in the range of 0.4 ~ 80μg/mL for cefotaxime. The linear regression equation is A = - 0.00204 + 0.01989C (μg/mL), with a linear correlation coefficient of 0.9998. The detection limit is 0.18 μg/mL. RSD is 1.2% (5.0μg/mL, n = 11), and average recovery is 99%. The reaction mechanism is studied intensively. This proposed method has been successfttlly applied to the determination of cefotaxime with satisfactory results.
出处
《分析试验室》
CAS
CSCD
北大核心
2007年第11期42-44,共3页
Chinese Journal of Analysis Laboratory
基金
河南省自然科学基金(2000150034)
河南省高校环境科学与工程重点学科实验室项目资助