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首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Automated solid-phase extraction hyphenated to voltammetry for the determination of quercetin using magnetic nanoparticles and sequential injection lab-on-valve approach
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Automated solid-phase extraction hyphenated to voltammetry for the determination of quercetin using magnetic nanoparticles and sequential injection lab-on-valve approach

机译:伏安法自动固相萃取-伏安法使用磁性纳米颗粒和顺序进样的实验室方法测定槲皮素

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摘要

In this study, an automated sequential injection lab-on-valve (SI-LOV) system was designed for the on-line matrix removal and preconcentration of quercetin. Octadecyl functionalized magnetic silica nanoparticles were prepared and packed into the microcolumn of the LOV as adsorbents. After being adsorbed through hydrophobic interaction, the analyte was eluted and subsequently introduced into the electrochemical flow cell by voltammetric quantification. The main parameters affecting the performance of solid-phase extraction, such as sample pH and flow rate, eluent solution and volume, accumulation potential and accumulation time were investigated in detail. Under the optimum experimental conditions, a linear calibration curve was obtained in the range of 1.0 × 10~(?8) to 1 × 10~(?5) mol L~(?1) with R~2 = 0.9979. The limit of detection (LOD) and limit of quantitation (LOQ) were 1.3 × 10~(?9) and 4.3 × 10~(?9) mol L~(?1), respectively. The relative standard deviation (RSD) for the determination of 1.0 × 10~(?6) mol L~(?1) quercetin was found to be 2.9% (n = 11) along with a sampling frequency of 40 h~(?1). The applicability and reliability of the automated method described here had been applied to the determination of quercetin in human urine and red wine samples through recovery experiments, and the obtained results were in good agreement with those obtained by the HPLC method.
机译:在这项研究中,设计了一种自动顺序进样阀实验室(SI-LOV)系统,用于槲皮素的在线基质去除和预浓缩。制备了十八烷基官能化的磁性二氧化硅纳米粒子,并将其包装到LOV的微柱中作为吸附剂。通过疏水相互作用被吸附后,洗脱分析物,然后通过伏安定量将其引入电化学流动池。详细研究了影响固相萃取性能的主要参数,例如样品的pH和流速,洗脱液和体积,累积电位和累积时间。在最佳实验条件下,线性校正曲线的取值范围为1.0×10〜(?8)至1×10〜(?5)mol L〜(?1),R〜2 = 0.9979。检出限(LOD)和定量限(LOQ)分别为1.3×10〜(?9)mol L〜(?1)。测定1.0×10〜(?6)mol L〜(?1)槲皮素的相对标准偏差(RSD)为2.9%(n = 11),采样频率为40 h〜(?1 )。通过回收率实验,将本文所述的自动化方法的适用性和可靠性应用于人尿和红酒样品中槲皮素的测定,所得结果与HPLC法结果吻合良好。

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