稳定性指示HPTLC法测定药物剂型中美他多辛的含量

Neeraj Kaul, Himani Agrawal, Bharat Patil, Abhijit Kakad, S.R. Dhaneshwar
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引用次数: 20

摘要

建立了一种灵敏度高、选择性好、准确度高、稳定性好的高效薄层色谱分析方法,用于原料药和制剂中美他多辛的分析。该方法采用薄层铝板预涂硅胶60F-254作为固定相。溶剂体系为丙酮-氯仿-甲醇-氨(7.0:4.0:3.0:1.2,v/v/v/v)。在315 nm吸光度模式下对美他多辛进行密度分析。该系统检测到的美他多辛斑点紧凑(6个重复的Rf值为0.45±0.02)。对美他多辛进行了酸、碱、中性水解、氧化、干湿热处理、光、紫外降解等实验。这种药物在各种压力条件下都能降解。降解产物在不同Rf值的纯药物中被很好地分离。对方法进行了线性、精密度、鲁棒性、定量限、定量限、特异性和准确性验证。在100 ~ 1500 ng/spot范围内呈线性关系,相关系数r2 = 0.9997±1.02。在200 ~ 700 ng/spot的工作浓度范围内,校正图的线性回归分析结果表明,r2 = 0.9999±0.58呈良好的线性关系。斜率和截距的平均值分别为0.11±0.04和18.73±1.89。检测限为50 ng/点,定量限为100 ng/点。统计分析表明,该方法具有重复性好、专属性强的特点。由于该方法可以有效地将药物与降解产物分离,因此可以作为稳定性指示方法。此外,采用HPTLC方法对酸碱降解过程进行了动力学研究。构建阿伦尼乌斯图,分别计算酸碱降解过程的活化能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Application of stability-indicating HPTLC method for quantitative determination of metadoxine in pharmaceutical dosage form

A sensitive, selective, precise and stability-indicating high-performance thin-layer chromatographic method for analysis of metadoxine both as a bulk drug and in formulations was developed and validated. The method employed TLC aluminium plates precoated with silica gel 60F-254 as the stationary phase. The solvent system consisted of acetone–chloroform–methanol–ammonia (7.0: 4.0: 3.0: 1.2, v/v/v/v). Densitometric analysis of metadoxine was carried out in the absorbance mode at 315 nm. This system was found to give compact spots for metadoxine (Rf value of 0.45 ± 0.02, for six replicates). Metadoxine was subjected to acid, alkali and neutral hydrolysis, oxidation, dry and wet heat treatment and photo and UV degradation. The drug undergoes degradation under all stress conditions. Also, the degraded products were well resolved from the pure drug with significantly different Rf values. The method was validated for linearity, precision, robustness, LOD, LOQ, specificity and accuracy. Linearity was found to be in the range of 100–1500 ng/spot with significantly high value of correlation coefficient r2 = 0.9997 ± 1.02. The linear regression analysis data for the calibration plots showed good linear relationship with r2 = 0.9999 ± 0.58 in the working concentration range of 200–700 ng/spot. The mean value of slope and intercept were 0.11 ± 0.04 and 18.73 ± 1.89, respectively. The limits of detection and quantitation were 50 and 100 ng/spot, respectively. Statistical analysis proves that the method is repeatable and specific for the estimation of the said drug. As the method could effectively separate the drug from its degradation products, it can be employed as a stability-indicating one. Moreover, the proposed HPTLC method was utilized to investigate the kinetics of acid and base degradation process. Arrhenius plot was constructed and activation energy was calculated respectively for acid and base degradation process.

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