首页> 外文期刊>Bulletin of the Korean Chemical Society >Highly Sensitive Luminescence Assessment of Bile Acid Using a Balofloxacin-Europium(IH) Probe in Micellar Medium
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Highly Sensitive Luminescence Assessment of Bile Acid Using a Balofloxacin-Europium(IH) Probe in Micellar Medium

机译:在胶束介质中使用Balofloxacin-Europium(IH)探针对胆汁酸进行高灵敏的发光评估

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摘要

A novel and simple method of luminescence enhancement effect for the determination of trace amounts of bile acid was proposed. The procedure was based on the luminescence intensity of the balofloxacin-europium(III) complex that could be strongly enhanced by bile acid in the presence of sodium dodecyl benzene sulfonate (SDBS). Under the optimum conditions, the enhanced luminescence intensity of the system exhibited a good linear relationship with the bile acid concentration in the range 5.0 × 10~(-9) - 7.0 × 10~(-7) mol L~(-1) with a detection limit of 1.3 × 10~(-9) mol L~(-1) (3a). The relative standard deviation (RSD) was 1.7% (n= 11) for 5.0 × 10~(-8) mol L~(-1) bile acid. The applicability of the method to the determination of bile acid was demonstrated by investigating the effect of potential interferences and by analyzing human serum and urine samples. The possible enhancement mechanism of luminescence intensity in balofloxacin-europium(III)-bile acid-SDBS system was also discussed briefly.
机译:提出了一种新颖,简便的发光增强作用测定痕量胆汁酸的方法。该程序基于巴洛沙星-eur(III)配合物的发光强度,在十二烷基苯磺酸钠(SDBS)的存在下胆汁酸可增强该复合物的发光强度。在最佳条件下,系统的增强发光强度与胆汁酸浓度在5.0×10〜(-9)-7.0×10〜(-7)mol L〜(-1)范围内具有良好的线性关系。检测限为1.3×10〜(-9)mol L〜(-1)(3a)。对于5.0×10〜(-8)mol L〜(-1)胆汁酸,相对标准偏差(RSD)为1.7%(n = 11)。通过研究潜在干扰的影响以及分析人的血清和尿液样品,证明了该方法在测定胆汁酸中的适用性。还简要讨论了巴洛沙星-(III)-胆汁酸-SDBS系统中发光强度增强的可能机制。

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