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Micellar extractions with anionic surfactant SDS and the mixture of SDS/OSAS for determination lovastatin in river samples

机译:阴离子表面活性剂SDS和SDS / OSAS混合物的胶束萃取法测定河流样品中的洛伐他汀

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摘要

The potential of the micellar extractions techniques for the preconcentration of lovastatin (LOV) was studied. The analyte has created micelle with anionic surfactant sodium dodecyl sulfate (SDS). Moreover, we have noticed that it is possible to isolate LOV using a binary mixture of SDS and 1-octanesulfonic acid sodium salt (OSAS). Therefore, two independent procedures were described in this study. Here we demonstrate the optimum analytical conditions for LOV assay such as pH of solution, concentration of surfactants, centrifugation time and electrolyte type. The linear calibration curves were obtained. The method range for LOV-SDS was of 10~(- 6) mol??L~(- 1) to 5 × 10~(- 5) mol??L~(- 1) with detection and quantification limits of 0.69 × 10~(- 6) mol??L~(- 1) and 1.11 × 10~(- 6) mol??L~(- 1), respectively, and the range for LOV-SDS/OSAS was of 10~(- 6) mol??L~(- 1) to 6 × 10~(- 5) mol??L~(- 1), with detection and quantification limits of 1.38 × 10~(- 6) and 2.10 × 10 ~(- 6) mol??L~(- 1). The recoveries of the method using SDS surfactant were 93.5-101% and for the mixture of SDS/OSAS were 85-107.5%. The proposed preconcentration methods after validation were successfully applied to spectrophotometric and chromatographic determination of LOV in water samples from the local river.
机译:研究了胶束提取技术对洛伐他汀(LOV)的预浓缩的潜力。分析物与阴离子表面活性剂十二烷基硫酸钠(SDS)形成胶束。此外,我们注意到可以使用SDS和1-辛烷磺酸钠盐(OSAS)的二元混合物分离LOV。因此,本研究描述了两个独立的程序。在这里,我们展示了LOV分析的最佳分析条件,例如溶液的pH值,表面活性剂的浓度,离心时间和电解质类型。获得了线性校准曲线。 LOV-SDS的方法范围为10〜(-6)mol ?? L〜(-1)至5×10〜(-5)mol?L〜(-1),检测和定量限为0.69× LOV-SDS / OSAS的范围分别为10〜(-6)molΔL〜(-1)和1.11×10〜(-6)molΔL〜(-1),LOV-SDS / OSAS的范围为10〜( -6)mol ?? L〜(-1)至6×10〜(-5)mol ?? L〜(-1),检测和定量限分别为1.38×10〜(-6)和2.10×10〜 (-6)molΔL〜(-1)。使用SDS表面活性剂的方法的回收率为93.5-101%,对于SDS / OSAS的混合物为85-107.5%。经验证的拟议的预浓缩方法已成功应用于分光光度法和色谱法测定当地河流水样中的LOV。

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