一阶导数光谱法同时测定合成混合物中美沙拉嗪和利福昔明的含量

Krishna V. Prajapati, H. Raj, V. Jain, Neelam S. Prajapati
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引用次数: 1

摘要

目的:建立一种简便、灵敏、快速、准确、精确、经济的一阶导数分光光度法同时测定合成混合物中美沙拉嗪(MESA)和利福昔明(Rifaximin)的含量。方法:采用导数分光光度法测定两种药物的零交叉点(ZCP)。在0.01 N NaOH溶液中获得一阶导数光谱,分别在329.20 nm (RIFA的ZCP)和292.80 nm (MESA的ZCP)处测定。琥珀酸盐在MESA 10 ~ 50 μg/ml和RIFA 10 ~ 50 μg/ml浓度范围内呈线性关系。结果:MESA和RIFA的检出限分别为0.321 μg/ml和0.301 μg/ml。MESA和RIFA的定量限分别为0.974 μg/ml和0.912 μg/ml。MESA和RIFA的平均回收率分别为100.20%和99.52%。该方法简便、灵敏、准确、精密度高,适用于合成混合物中MESA和RIFA的同时测定。分析结果已通过统计和恢复研究得到验证。结论:该方法成功地应用于已批准专利的药物合成混合物中,无干扰。分析结果已通过统计和恢复研究得到验证。因此,这种方法准确、精密、坚固、坚固、经济。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First derivative spectroscopic method for simultaneous estimation of mesalazine and rifaximin in synthetic mixture
Objective: The present study was aimed to describe a simple, sensitive, rapid, accurate, precise and economical first derivative spectrophotometric method for the simultaneous determination of Mesalazine (MESA) and Rifaximin (RIFA) in synthetic mixture. Methods: The derivative spectrophotometric method was based on the determination of both the drugs at their respective zero crossing point (ZCP). The first order derivative spectra were obtained in 0.01 N NaOH and the determinations were made at 329.20 nm (ZCP of RIFA) for MESA and 292.80 nm (ZCP of MESA) for RIFA. The linearity was obtained in the concentration range of succinate 10-50 μg/ml for MESA and 10-50 μg/ml for RIFA. Results: The limit of determination was 0.321 μg/ml and 0.301 μg/ml for MESA and RIFA, respectively. The limit of quantification was 0.974 μg/ml and 0.912 μg/ml for MESA and RIFA, respectively. The mean recovery was 100.20 and 99.52% for MESA and RIFA, respectively. The method was found to be simple, sensitive, accurate and precise and was applicable for the simultaneous determination of MESA and RIFA in synthetic mixture. The results of analysis have been validated statistically and by recovery studies. Conclusions: The method was successfully applied to pharmaceutical synthetic mixture which is considered in approved patent which show no interference. The result of analysis has been validated statistically and by recovery studies. So, this method accurate, precise, robust, rugged and economic in nature.
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