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Differential pulse voltammetric determination of salbutamol sulfate in syrup pharmaceutical formulation using poly(4-amino-3-hydroxynaphthalene sulfonic acid) modified glassy carbon electrode

机译:聚(4-氨基-3-羟基萘磺酸)修饰玻碳电极微分脉冲伏安法测定糖浆剂中硫酸沙丁胺醇

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摘要

A new method for determination of salbutamol sulfate has been developed using poly(4-amino-3-hydroxynaphthalene sulfonic acid/GCE. Cyclic voltammetric investigation of the electrochemical behavior of salbutamol sulfate at the polymer modified glassy carbon unveiled electrocatalytic activity of the modifier towards irreversible oxidation of salbutamol sulfate. Dependence of peak current predominantly on scan rate than on square root of scan rate, and peak potential shift with pH demonstrated that oxidation of salbutamol sulfate at the polymer modified electrode follows adsorption reaction kinetics with proton participation.Under optimized solution and differential pulse voltammetric parameters, the oxidative peak current showed linear dependence on salbutamol sulfate concentration in the range 0.2 to 8 μM with method detection limit (3s/m) and determination coefficient (R2) of 6.8 × 10−8 M and 0.99786, respectively. Low method detection limit, relatively wide linear range, and recovery results of spiked standard salbutamol sulfate in syrup samples in the range 96.7–98.9% validated the method for determination of salbutamol sulfate in pharmaceutical formulations.Differential pulse voltammetric analysis of salbutamol sulfate syrup formulation for its salbutamol sulfate content revealed 98.8 to 99.3% of the labeled value confirming the applicability of the developed method for determination of salbutamol sulfate in real samples.
机译:聚(4-氨基-3-羟基萘磺酸/ GCE)建立了测定硫酸沙丁胺醇的新方法,循环伏安法研究了硫酸沙丁胺醇在聚合物改性玻璃碳上的电化学行为,揭示了该改性剂对不可逆的电催化活性。峰值电流主要取决于扫描速率,而不是扫描速率的平方根,以及峰电位随pH的变化表明,在聚合物修饰电极上硫酸沙丁胺醇的氧化遵循具有质子参与的吸附反应动力学。差分脉冲伏安法参数时,氧化峰值电流对硫酸沙丁胺醇浓度呈线性依赖关系,范围为0.2至8μM,方法检测极限(3s / m)和测定系数(R 2 )为6.8×10 −8 M和0.99786。方法检测下限低,线性范围较大r范围和糖浆样品中加标标准硫酸沙丁胺醇硫酸盐的回收结果在96.7–98.9%范围内,验证了测定药物制剂中硫酸沙丁胺醇的方法。硫酸沙丁胺醇糖浆制剂中硫酸沙丁胺醇含量的差示脉冲伏安分析显示98.8至9.85。标记值的99.3%证实了所开发方法测定实际样品中硫酸沙丁胺醇的适用性。

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