首页> 外文期刊>International journal of analytical chemistry >A New Spectrophotometric Method for Determination of Selenium in Cosmetic and Pharmaceutical Preparations after Preconcentration with Cloud Point Extraction
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A New Spectrophotometric Method for Determination of Selenium in Cosmetic and Pharmaceutical Preparations after Preconcentration with Cloud Point Extraction

机译:浊点萃取预富集分光光度法测定化妆品和药物制剂中的硒

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A simple, rapid, and sensitive spectrophotometric method for the determination of trace amounts of selenium (IV) was described. In this method, all selenium spices reduced to selenium (IV) using 6 M HCl. Cloud point extraction was applied as a preconcentration method for spectrophotometric determination of selenium (IV) in aqueous solution. The proposed method is based on the complexation of Selenium (IV) with dithizone at pH < 1 in micellar medium (Triton X-100). After complexation with dithizone, the analyte was quantitatively extracted to the surfactant-rich phase by centrifugation and diluted to 5 mL with methanol. Since the absorption maxima of the complex (424 nm) and dithizone (434 nm) overlap, hence, the corrected absorbance, Acorr, was used to overcome the problem. With regard to the preconcentration, the tested parameters were the pH of the extraction, the concentration of the surfactant, the concentration of dithizone, and equilibration temperature and time. The detection limit is 4.4 ng mL-1; the relative standard deviation for six replicate measurements is 2.18% for 50 ng mL-1of selenium. The procedure was applied successfully to the determination of selenium in two kinds of pharmaceutical samples.
机译:描述了一种简单,快速,灵敏的分光光度法测定痕量硒(IV)的方法。在这种方法中,所有硒香料都使用6 M HCl还原为硒(IV)。浊点萃取作为分光光度法测定水溶液中硒(IV)的预浓缩方法。所提出的方法是基于胶束介质(Triton X-100)中硒(IV)与双硫zone在pH <1时的络合。与双硫zone络合后,通过离心将分析物定量提取到富含表面活性剂的相中,并用甲醇稀释至5 mL。由于络合物(424 nm)和双硫zone(434 nm)的最大吸收重叠,因此,使用校正后的吸光度Acorr来解决该问题。关于预浓缩,测试的参数是提取液的pH,表面活性剂的浓度,双硫zone的浓度以及平衡温度和时间。检出限为4.4 ng mL-1;对于50μngmL-1的硒,六次重复测量的相对标准偏差为2.18%。该方法成功应用于两种药物样品中硒的测定。

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