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首页> 外文期刊>Journal of trace elements in medicine and biology: Organ of the Society for Minerals and Trace Elements (GMS) >Trace determination of cobalt in biological fluids based on preconcentration with a new competitive ligand using dispersive liquid-liquid microextraction combined with slotted quartz tube-flame atomic absorption spectrophotometry
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Trace determination of cobalt in biological fluids based on preconcentration with a new competitive ligand using dispersive liquid-liquid microextraction combined with slotted quartz tube-flame atomic absorption spectrophotometry

机译:采用分散液 - 液体微萃取与开槽石英管 - 火焰原子吸收分光光度法基于新竞争性配体的基于前浓缩配体的生物流体中钴的谱测定

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摘要

A new competitive ligand has been synthesized for the preconcentration to obtain lower detection limits by using dispersive liquid-liquid microextraction combined with slotted quartz tube-flame atomic absorption spectrophotometry (DLLME-SQT-FAAS). The proposed method is simple, eco-friendly and has high sensitivity. The preconcentration procedure was optimized on the basis of various parameters affecting the complex formation and extraction efficiency such as pH and volume of buffer solution, volume of ligand solution, mixing period, volume and type of extraction solvent, volume and type of dispersive solvent, and salt effect. Instrumental parameters were also optimized to get higher sensitivity. Under the optimum conditions, the calibration graph was linear in the range of 10-250 ng mL(-1) land the resulted limits of detection and quantification (LOD and LOQ) for combined method were 4.7 and 15.7 ng(-1) mL(-1), respectively. The detection power was improved 48-fold using DLLME-SQT-FAAS method compared to conventional FAAS. The precision of the method was found to be high with a relative standard deviation of 2.5%. The accuracy of method was evaluated by recovery experiments using matrix matching study on spiked urine and blood samples. The recoveries for urine and blood samples ranged from 99.8 to 108.9% and 102.5 to 110.0%, respectively.
机译:已经合成了一种新的竞争性配体,用于预浓缩,通过使用分散液 - 液微萃取与开槽石英管 - 火焰原子吸收分光光度法(DLLME-SQT-FAAS)组合获得较低的检测限值。所提出的方法简单,环保,灵敏度高。基于影响复杂形成和提取效率的各种参数进行优化的预浓缩过程,例如pH和缓冲溶液的pH和体积,配体溶液的体积,混合期,萃取溶剂的体积,体积和类型的分散溶剂,以及盐效果。仪器参数也被优化以获得更高的灵敏度。在最佳条件下,校准图在10-250 ng ml(-1)的范围内为LAND,所产生的检测和定量(LOD和LOQ)的限制为4.7和15.7ng(-1)ml( -1)分别。与传统FAAS相比,使用DLLME-SQT-FAAS方法改善了48倍的检测功率。发现该方法的精度高,相对标准偏差为2.5%。通过使用掺入尿液和血液样品的基质匹配研究,通过恢复实验评估方法的准确性。尿液和血液样品的回收率分别为99.8至108.9%和102.5至110.0%。

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