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首页> 外文期刊>Журнал прикладной спектроскопии >SIMPLE AND SENSITIVE SPECTROPHOTOMETRIC METHODS FOR DETERMINATION OF AMANTADINE HYDROCHLORIDE
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SIMPLE AND SENSITIVE SPECTROPHOTOMETRIC METHODS FOR DETERMINATION OF AMANTADINE HYDROCHLORIDE

机译:简单而灵敏的分光光度法测定盐酸金刚烷胺

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摘要

Three simple and sensitive spectrophotometric methods (A-C) for determination of amantadine hydro-chloride have been developed and validated. The first method (A) is based on the oxidation of the drug by ammonium mofybdate. The second method (B) was bused on the charge-transfer complexation reaction between the amantadine base as an electron donor and iodine as a a-acceptor. The third method (C) is based on the reaction of N-alkylvinylamine formed from the interaction of the free amino group in amantadine molecide and acetalde-hyde with chloranil to give colored vinylamino-substituted benzoquinone. The colored products of these reactions were measured at their corresponding maximum absorption peaks. Different variables affecting the reactions were carefully studied and optimized. Under the optimum conditions, linear relationships with good correlation coefficients 0.9993-0.9998 were found between the reading and the corresponding concentration of the drug in the range 2-90 fig- mf1. The limits of detection ranged from 0.16 to 1.91 ug- mf1. The precision of the methods was satisfactory: the values of relative standard deviation did not exceed 1.63 %. The proposed methods were successfully applied to the analysis of amantadine HCl in its capsules with good accuracy; and precisions; the label claim percentages ranged from 99.8 to 100.5 ± (0.52-1.22) %. The results obtained by the proposed spectrophotometric methods were comparable with those obtained by the official method.
机译:已开发并验证了三种简单而灵敏的分光光度法测定盐酸金刚烷胺的方法。第一种方法(A)是基于钼酸铵对药物的氧化。第二种方法(B)用于金刚烷胺碱作为电子供体与碘作为α受体的电荷转移络合反应。第三种方法(C)是基于由金刚烷胺分子内的游离氨基和乙醛与氯代苯胺相互作用形成的N-烷基乙烯基胺反应,得到有色的乙烯基氨基取代的苯醌。这些反应的有色产物在其相应的最大吸收峰处测量。仔细研究和优化了影响反应的不同变量。在最佳条件下,在读数和相应浓度范围为2-90 fig-mf1的药物之间发现具有良好相关系数0.9993-0.9998的线性关系。检测限范围为0.16至1.91 ugmf1。方法的精密度令人满意:相对标准偏差的值不超过1.63%。所提出的方法已成功地用于胶囊中盐酸金刚烷胺的分析,具有良好的准确度。和精度;标签索赔百分比范围为99.8至100.5±(0.52-1.22)%。通过提议的分光光度法获得的结果与通过官方方法获得的结果相当。

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