首页> 外文期刊>Analytica chimica acta >Application of dispersive liquid-liquid microextraction and dispersive micro-solid-phase extraction for the determination of quinolones in swine muscle by high-performance liquid chromatography with diode-array detection
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Application of dispersive liquid-liquid microextraction and dispersive micro-solid-phase extraction for the determination of quinolones in swine muscle by high-performance liquid chromatography with diode-array detection

机译:分散液-液微萃取和分散微固相萃取在高效液相色谱-二极管阵列检测法测定猪肌肉中喹诺酮类药物中的应用

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Dispersive liquid-liquid microextraction (DLLME) and dispersive micro-solid-phase extraction (DMSPE) are two simple and low-cost sample preparation methods for liquid samples. In this work, these two methods were applied to solid tissue sample for the determination of seven quinolones by high-performance liquid chromatography with diode-array detection (HPLC-DAD). After the homogenization of the swine muscle with acetonitrile and salt-promoted partitioning, small amounts of the extract were used for the DLLME and DMSPE methods. In the DLLME approach, the target analytes in the extraction solvent were rapidly extracted into a small volume of dichloromethane for drying and the residue was reconstituted for HPLC-DAD analysis. In the DMSPE approach, the target analytes in the extraction solvent were trapped by dispersive silica-based PSA (primary and secondary amine) sorbents and desorbed into a small amount of desorption solution for HPLC-DAD analysis. Under the optimal conditions, relative recoveries were determined for swine muscle spiked 50-200 μ g kg~(-1) and quantification was achieved by matrix-matched calibration. The calibration curves of seven quinolones showed linearity with a correlation coefficient value above 0.998 for both approaches. Relative recoveries ranged from 93.0 to 104.7% and from 95.5 to 111.0% for DLLME and DMSPE, respectively. Limits of detection (LODs) ranged from 5.6 to 23.8 μ g kg~(-1) and from 7.5 to 26.3 μg kg~(-1) for DLLME and DMSPE, respectively.
机译:分散液-液微萃取(DLLME)和分散微固相萃取(DMSPE)是液体样品的两种简单且低成本的样品制备方法。在这项工作中,将这两种方法应用于实体组织样品,通过高效液相色谱-二极管阵列检测(HPLC-DAD)方法测定七个喹诺酮类药物。用乙腈和盐促进的分区将猪肌肉匀浆后,将少量提取物用于DLLME和DMSPE方法。在DLLME方法中,将萃取溶剂中的目标分析物快速萃取到少量二氯甲烷中进行干燥,然后将残留物重构进行HPLC-DAD分析。在DMSPE方法中,萃取溶剂中的目标分析物被分散的二氧化硅基PSA(伯胺和仲胺)吸附剂截留,并解吸到少量解吸溶液中以进行HPLC-DAD分析。在最佳条件下,测定猪肌肉掺入的50-200μg kg〜(-1)的相对回收率,并通过基质匹配校准实现定量。两种方法的七个喹诺酮的校准曲线均显示线性,相关系数值均高于0.998。 DLLME和DMSPE的相对回收率分别为93.0%至104.7%和95.5%至111.0%。 DLLME和DMSPE的检测限(LOD)分别为5.6至23.8μg kg〜(-1)和7.5至26.3μgkg〜(-1)。

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