紫外分光光度法测定原料药和制剂中硫酸羟氯喹含量的方法建立与验证

Tejaswini P. Masne, Shyam Rangari, K. Gupta, M. Umekar
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引用次数: 0

摘要

目的:设计出原料药和制剂(片剂)硫酸羟氯喹的含量测定方法。因此,该方法可用于常规定量分析和稳定性。以下描述了计划工作的目标和范围:建立一种合适的分光光度法测定片剂硫酸羟氯喹。对方法进行验证。方法:采用曲线下面积法(AUC)和基于吸光度测量的A1%溶液法(method- ii),两种方法均在329.4 nm波长处采用紫外可见分光光度计,配1 cm石英池,以0.01N醋酸水为溶剂。结果:绘制了硫酸羟氯喹在0.01N乙酸中的吸收光谱图。平均最大值为329.4 nm。AUC和1%的相关系数分别为0.9992和0.999 (r2>0.999),在5 ~ 35 g/mL浓度范围内吸光度与药物浓度呈线性关系,表明该方法是线性的。各种方法计算的用药百分率接近100.12%,99.41%的结果与市售片剂配方的标签声明一致。按照ICH要求,完成了验证参数的研究。结论:所建立的方法具有良好的准确度和精密度,降低了检测限和定量限。他们直截了当,值得信赖,而且非常挑剔。由于减少了分析硫酸羟氯喹所需的时间,这些公开的方法对于药物剂型中的常规定量分析是理想的。比昂贵的高效液相色谱技术更省时、低成本的方法是应用分光光度法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Method Development and Validation of UV-Spectrophotometric Estimation of Hydroxychloroquine Sulphate in Bulk and Pharmaceutical Dosage Form
Aims: The devised method for estimating hydroxychloroquine sulphate in bulk and pharmaceutical dose forms (tablets) is the subject of this work. The method can therefore be applied to regular quantitative analysis and stability. The following describes the planned work's goal and scope: To create an appropriate spectrophotometric method for tablet-based hydroxychloroquine sulphate estimation. Carry out the method's validation. Methodology: These techniques include the area under curve (AUC) method-I and the A1% solution method based on absorbance measurement, or method-II, both of which are chosen at wavelengths of 329.4 nm using a UV-visible spectrophotometer with a 1 cm matched quartz cell and 0.01N acetic acid with water as a solvent. Results: Plots of the hydroxychloroquine sulphate absorption spectra in 0.01N acetic acid were made. 329.4 nm was found to be the average maximum. With correlation coefficients of 0.9992 and 0.999 (r2>0.999) for AUC and 1%, respectively, and a linear connection between the absorbance and drug concentration in concentration ranges of 5-35 g/mL, it is clear that the method is linear. The percentage of medication calculated by various methods was close to 100.12, and 99.41% of the results were consistent with the label claim of the commercially available tablet formulation. As per ICH requirements, the validation parameter research was completed. Conclusion: The described UV methods offer good accuracy and precision with reduced limits of detection and quantification. They are straightforward, trustworthy, and highly selective. These disclosed methods are ideal for routine quantitative analysis in pharmaceutical dosage forms due to the decreased time required for analysis of hydroxychloroquine sulphate. The time-saving, low-cost alternative to the expensive high-performance liquid chromatographic technology is the applied spectrophotometric approaches.
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