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Validated stability indicating methods for determination of nitazoxanide in presence of its degradation products

机译:经验证的稳定性指示方法可在存在其降解产物的情况下测定硝唑尼特

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摘要

Three sensitive, selective and reproducible stability-indicating methods are presented for determination of nitazoxanide (NTZ), a new anti-protozoal drug, in presence of its degradation products. Method A utilizes the first derivative of ratio spectra spectrophotometry by measurement of the amplitude at 364.4 nm using one of the degradation products as a divisor. Method B is a chemometric-assisted spectrophotometry, where principal component regression (PCR) and partial least squares (PLS) were applied. These two approaches were successfully applied to quantify NTZ in presence of degradation products using the information included in the absorption spectra in the range 260–360 nm. Method C is based on the separation of NTZ from its degradation products followed by densitometric measurement of the bands at 254 nm. The separation was carried out on silica gel 60F254, using chloroform–methanol–ammonia solution–glacial acetic acid (95:5:1:1 by volume, pH=5.80) as a developing system. These methods are suitable as stability-indicating methods for the determination of NTZ in presence of its degradation products either in bulk powder or in pharmaceutical formulations. Statistical analysis of the results has been carried out revealing high accuracy and good precision.
机译:提出了三种灵敏,选择性和可重现的稳定性指示方法,用于在存在其降解产物的情况下测定一种新的抗原生动物药物硝唑尼特(NTZ)。方法A利用比率光谱分光光度法的一阶导数,通过使用降解产物之一作为除数来测量364.4 nm处的振幅。方法B是化学计量学分光光度法,其中应用了主成分回归(PCR)和偏最小二乘(PLS)。这两种方法已成功地用于定量分析存在降解产物的NTZ,使用的吸收光谱范围为260-360 nm。方法C基于从降解产物中分离NTZ,然后光密度测量254 nm波段的方法。分离在硅胶60F254上进行,使用氯仿-甲醇-氨溶液-冰醋酸(体积比为95:5:1:1,pH = 5.80)作为展开系统。这些方法适合作为稳定性指示方法,用于测定散装粉末或药物制剂中NTZ降解产物的存在。对结果进行了统计分析,显示出较高的准确性和良好的精度。

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