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Kinetic Modelling for the Assay of Nortriptyline Hydrochloride Using Potassium Permanganate as Oxidant

机译:高锰酸钾为氧化剂测定盐酸去甲替林的动力学模型

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摘要

Kinetic methods for accurate determination of nortriptyline hydrochloride have been described. The methods are based on the oxidation of nortriptyline hydrochloride with KMnO4 in acidic and basic media. In acidic medium, the decrease in absorbance at 525.5 nm and in basic medium, the increase in absorbance at 608.5 nm were measured as a function of time. The variables affecting the reactions were carefully investigated and optimised. Kinetic models such as initial rate, rate constant, variable time and fixed time were employed to construct the calibration curves. The initial rate and fixed time methods were selected for quantification of nortriptyline hydrochloride. In acidic medium, the calibration curves showed a linear response over the concentration range 10–50 μg mL−1 for initial rate and 10–60 μg mL−1 for fixed time method (2 min). In basic medium, the calibration graphs were linear over the concentration range 10–100 μg mL−1 for initial rate and fixed time methods (4 min). In acidic medium, the limits of detection for initial rate and fixed time methods (2 min) were 1.02 and 3.26 μg mL−1, respectively. In basic medium, the limits of detection were found to be 1.67 and 1.55 μg mL−1 for initial rate and fixed time methods (4 min), respectively. The initial rate and fixed time methods have been successfully applied to the determination of nortriptyline hydrochloride in commercial dosage form. Statistical comparison of the results of the proposed methods with those of reference method exhibited excellent agreement and there is no significant difference between the compared methods in terms of accuracy and precision.
机译:已经描述了准确测定盐酸去甲替林的动力学方法。该方法基于在酸性和碱性介质中用KMnO4氧化去甲替林盐酸盐。在酸性介质中,测量的是时间随时间变化的525.5 nm处吸光度的降低,在碱性介质中,在608.5 nm处的吸光度增加。仔细研究和优化了影响反应的变量。建立动力学模型,如初始速率,速率常数,可变时间和固定时间,以建立校正曲线。选择初始速率和固定时间方法定量盐酸去甲替林。在酸性介质中,校准曲线在初始浓度范围为10–50μgmL -1 和固定时间为10–60μgmL -1 范围内显示线性响应方法(2分钟)。在基本介质中,对于初始速率和固定时间方法(4分钟),校准曲线在10-100μgmL -1 的浓度范围内是线性的。在酸性介质中,初始速率和固定时间方法(2分钟)的检出限分别为1.02和3.26μgmL -1 。在基本培养基中,初始速率和固定时间方法(4分钟)的检出限分别为1.67和1.55μgmL -1 。初始速率和固定时间方法已成功应用于商业剂型中盐酸去甲替林的测定。所提方法与参考方法结果的统计比较显示出极好的一致性,并且比较方法在准确性和精密度上没有显着差异。

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