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Spectrophotometric determination of methoxamine hydrochloride using NQS and brucine metaperiodate

机译:用NQS和偏高庚氨酸分光光度法测定盐酸甲氧胺。

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Two simple and sensitive extractive visible spectro photometric methods (A and B) for the assay of Methoxamine hydrochloride (MHC), in pure and pharmaceutical formulations, The method-A is based on the condensation reaction of MHC reduced with sodium 1,2-naphthaquinone-4-sulfonate (NQS) in an alkaline medium to form an orange-red colored Schiff's base of maximum absorption peak (λmax) at 445 nm,The method-B is based on the formation coloured complexes with the dimethoxy benzene nucleus of brucine is attacked by Per Iodate with the formation of o-quinone (bruciquinone) which in turn undergoes nucleophilic attack on the most electron rich position of the coupler i.e., proton bearing amino group (primary amine), to give 1-mono substituted bruciquinone derivative. The reaction mechanism in both methods were discussed. The absorbance of colored complex is gound at 520nm. Beer's law is obeyed in the concentration range 5-30 μg/Ml,50-500 μg/Ml, the molar absorptivity values are1.9652 x 105, 1.4797 x 104L/mol.cm, Sandell sensitivity are1.2605 x 10-3,1.6741x10-2ng/cm2 (For methods A&B).The methods proposed gave reproducible results with the percentage recoveries in the formulations found to be 99.800 to 99.772 (Method A) and 99.812 to 99.749 (Method B).
机译:两种简单而灵敏的萃取可见光分光光度法(A和B),用于测定纯制剂和药物制剂中的甲氧胺盐酸盐(MHC),方法A是基于MHC与1,2-萘萘醌钠的缩合反应在碱性介质中用-4-磺酸盐(NQS)形成桔红色的席夫氏碱,在445 nm处具有最大吸收峰(λmax),方法B是基于与浅紫红色的二甲氧基苯核形成有色配合物在碘酸盐的作用下,形成邻醌(溴醌),邻苯醌(bruciquinone)继而在成色剂的电子最多的位置(即带有质子的氨基)(伯胺)上经历亲核性攻击,从而生成1-mono取代的Bruciquinone衍生物。讨论了两种方法的反应机理。有色配合物的吸光度在520nm处。在5-30μg/ Ml,50-500μg/ Ml的浓度范围内遵守比尔定律,摩尔吸光度值为1.9652 x 105、1.4797 x 104L / mol.cm,Sandell灵敏度为1.2605 x 10-3, 1.6741x10-2ng / cm2(对于方法A&B)。所提出的方法可再现的结果是,制剂中的回收率百分比分别为99.800至99.772(方法A)和99.812至99.749(方法B)。

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