首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Flow-injection spectrophotometric determination of ascorbic acid in pharmaceutical products with the Prussian Blue reaction
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Flow-injection spectrophotometric determination of ascorbic acid in pharmaceutical products with the Prussian Blue reaction

机译:普鲁士蓝反应流动注射分光光度法测定药品中的抗坏血酸

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摘要

A lot of modern analytical strategies for exploiting chemistries have been developed by using flow-injection analysis. However, even after 20 years of flow-injection evolution, there still are new quantitative procedures being established using old qualitative assays. The formation of Prussian Blue is a classical test to detect Fe2+ using hexacyanoferrate(III) as a precipitating reagent. This reaction was evaluated for spectrophotometric determination of ascorbic acid employing Fe3+ and hexacyanoferrate(III) as chromogenic reagents. An excess of the complexing anion avoids the formation of precipitate and forms a deep blue solution when Fe3+ is reduced to Fe2+ by ascorbic acid. The maximum absorbance of the colored complex occurs at 700 nm and the molar absorptivity is 3.0 × 104 1 mol~(-1) cm~(-1). Under flow-injection conditions the Prussian Blue reaction was employed with an intermittent flow of an oxalate alkaline solution for removing the colored product adsorbed on tube and flow-cell walls. Reference solutions containing 5.0 × 10?6-1.0 × 10~(-4) M of ascorbic acid were employed to obtain the analytical curve (r = 0.9999). For all solutions the relative standard deviation was lower than 1.0% (n=10). Results obtained for ascorbic acid determination in pharmaceutical products (Cewin, Redoxon and Cebion) are in good agreement with those obtained by using a flow-injection procedure involving the reaction between triiodide and ascorbic acid. The sampling frequency is 140 h~(-1) and only 430 μ1 of reagents is consumed in each determination.
机译:通过使用流动注射分析,已经开发出许多用于化学开发的现代分析策略。然而,即使经过20年的流动注射发展,仍使用旧的定性分析方法建立了新的定量程序。普鲁士蓝的形成是使用六氰合铁酸盐(III)作为沉淀剂检测Fe2 +的经典测试。使用Fe3 +和六氰合铁酸盐(III)作为显色剂,评估了该反应的分光光度法测定抗坏血酸。当Fe3 +被抗坏血酸还原为Fe2 +时,过量的络合阴离子可避免形成沉淀并形成深蓝色溶液。有色配合物的最大吸收在700 nm处发生,摩尔吸收率为3.0×104 1 mol〜(-1)cm〜(-1)。在流动注射条件下,将普鲁士蓝反应与草酸盐碱性溶液的间歇流一起使用,以除去吸附在管壁和流通池壁上的有色产物。用含5.0×10-6-1.0×10〜(-4)M抗坏血酸的参考溶液获得分析曲线(r = 0.9999)。对于所有溶液,相对标准偏差均低于1.0%(n = 10)。药品(Cewin,Redoxon和Cebion)中抗坏血酸的测定结果与使用涉及三碘化物和抗坏血酸反应的流动注射程序获得的结果吻合良好。采样频率为140 h〜(-1),每次测定仅消耗430μ1试剂。

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