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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Utility of formazans and cetylpyridinium chloride in rapid spectrophotometric determination of zinc in biological materials and pharmaceutical formulations.
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Utility of formazans and cetylpyridinium chloride in rapid spectrophotometric determination of zinc in biological materials and pharmaceutical formulations.

机译:甲maz和十六烷基氯化吡啶用于快速分光光度法测定生物材料和药物制剂中的锌。

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摘要

A facile, rapid and sensitive spectrophotometric method for the determination of zinc is performed, based on complexation reaction between the metal ion and 1,5-diphenyl-3-acetylformazan (I) 1-(o-carboxyphenyl)-3-acetyl-5-acetylformazan (II), 1-(o-carboxyphenyl)-3-acetyl-5-phenylformazan (III), and 1-(o-carboxyphenyl)-3-acetyl-5-m-tolylformazan (IV) in the presence of cationic surfactant cetylpyridinium chloride (CPC). The important analytical parameters and their effects on the reported system are investigated. Zinc reacts with the reagents (I-IV) and CPC in the ratio 1:1:2 (metal:reagent:CPC) in the pH range 8.5, 7.5, 5.5 and 6.5 to form a ternary complex with an absorption maximum 616, 656, 672 and 599 nm, respectively. The reaction was extremely rapid at room temperature, and the absorbance value remains unchanged for at least 1 week. The apparent stability constant of the complex were found to be 13.1 9.2, 11.4 and 12.3, and adheres to Beer's law for 0.05-3.50 &mgr;g per 10 ml of zinc. For more accurate analysis, Ringbom optimum concentration range was found from 0.08 to 3.20 &mgr;g per 10 ml of zinc. The apparent molar absorptivity, Sandell sensitivity, detection and quantification limits are also calculated. Taking a constant concentration of metal ion and determining its concentration in the presence of large number of foreign ions tested the effect of foreign ions. The method was applied for determination of zinc in serum, human hair and pharmaceutical formulations, where excellent agreements between reported and obtained results were achieved. The relative standard deviation was better than 1.67%.
机译:基于金属离子与1,5-二苯基-3-乙酰基甲酰胺(I)1-(邻羧基苯基)-3-乙酰基-5之间的络合反应,进行了快速,灵敏的分光光度法测定锌-乙酰基甲a(II),1-(邻-羧基苯基)-3-乙酰基-5-苯基甲a(III)和1-(邻-羧基苯基)-3-乙酰基-5-间甲苯基甲zan(IV)阳离子表面活性剂十六烷基吡啶鎓氯化物(CPC)。研究了重要的分析参数及其对报告系统的影响。锌在8.5、7.5、5.5和6.5的pH范围内与试剂(I-IV)和CPC的比例为1:1:2(金属:试剂:CPC)形成三元络合物,吸收最大值为616、656分别为672和599 nm。该反应在室温下非常快,并且吸光度值至少保持1周不变。发现该复合物的表观稳定常数为13.1、9.2、11.4和12.3,并且遵守比尔定律,每10ml锌为0.05-3.50mg。为了进行更准确的分析,发现林宝的最佳浓度范围是每10毫升锌0.08至3.20微克。还计算了表观摩尔吸收率,Sandell灵敏度,检测和定量极限。采取恒定浓度的金属离子并在存在大量外来离子的情况下确定其浓度,测试了外来离子的效果。该方法用于测定血清,人发和药物制剂中的锌,在报告和获得的结果之间取得了极好的一致性。相对标准偏差优于1.67%。

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