导数分光光度法测定片剂中美西多的含量

L. L. Kvachakhiya, V. K. Shormanov, Elena V. Maksina
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引用次数: 0

摘要

Mexidol(3-羟基-6-甲基-2-乙基琥珀酸吡啶)是一种具有神经保护、抗缺氧、抗缺血、促智、抗应激和老年保护作用的药物,可以抑制或减缓氧化反应。Оbjective:建立一种选择性、简便的测定片剂中美西多含量的方法。材料和方法。研究对象为墨西多(3-羟基-6-甲基-2-乙基琥珀酸吡啶)和0.125 g墨西多片。采用导数分光光度法进行分析。结果。揭示了墨西多在石英紫外区强烈吸收电磁辐射的能力。这种现象是由于分析物分子中含有多个发色团:吡啶环的共轭芳键体系、氮原子上的未配对电子和与芳体系共轭的烯醇羟基。在292 nm区域,墨西多比吸收系数的二阶导数与光度溶液中分析物的量呈线性关系(范围为2.5 ~ 50.0 μg/ml)。构造了标定图,并用最小二乘法计算了标定图的方程。相关系数超过0.999。检测限为1.25µg/ml,定量限为2.5µg/ml。该技术的特点是必要的再现性和正确性。使用建议的方法测定分析物的标准偏差和相对标准偏差的值(n=6;P=0.95),片剂质量分别为1.16、0.012,片剂质量分别为0.125 g、1.32、0.013。结论。建立了一种基于二阶导数计算的简便、选择性测定0.125 g片剂中墨西多定量含量的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of Mexidol in tablets by the method of derivative spectrophotometry
Mexidol (3-hydroxy-6-methyl-2-ethylpyridine succinate) is a drug that exhibits neuroprotective, antihypoxic, anti-ischemic, nootropic, anti-stress and geroprotective effects and can suppress or slow down oxidation reactions. Оbjective: to develop a selective and simple method for assessing the content of mexidol in tablets. Materials and methods. The objects of the study were mexidol (3-hydroxy-6-methyl-2-ethylpyridine succinate) and Mexidol tablets 0.125 g. Derivative spectrophotometry was used as an analysis method. Results. The ability of mexidol to intensively absorb electromagnetic radiation in the quartz ultraviolet region was revealed. This phenomenon is due to the fact that the analyte molecule contains a number of chromophore groups: a system of conjugated aromatic bonds of the pyridine ring, unpaired electrons at the nitrogen atom, and an enol hydroxyl conjugated with the aromatic system In the region of 292 nm, there is a linear dependence of the derivatives of the 2nd order of the specific absorption coefficient of mexidol on the amount of analyte in the photometric solution (range 2.5-50.0 μg/ml). A calibration graph has been constructed, and its equation has been calculated by the least-squares method. The correlation coefficient exceeds 0.999. The limits of detection and quantification are 1.25 and 2.5 µg/ml, respectively. The technique is characterized by the necessary reproducibility and correctness. The values of the standard deviation and relative standard deviation in the determination of the analyte using the proposed method (n=6; P=0.95) in the tablet mass are 1.16 and 0.012, respectively, in tablets of 0.125 g, 1.32 and 0.013, respectively. Conclusion. A simple and selective method has been developed for estimating the quantitative content of mexidol in 0.125 g tablets based on the calculation of second-order derivatives of spectra.
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