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首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >A combination of solid-phase extraction and dispersive solid-phase extraction effectively reduces the matrix interference in liquid chromatography-ultraviolet detection during pyraclostrobin analysis in perilla leaves
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A combination of solid-phase extraction and dispersive solid-phase extraction effectively reduces the matrix interference in liquid chromatography-ultraviolet detection during pyraclostrobin analysis in perilla leaves

机译:固相萃取和分散固相萃取相结合可有效减少紫苏叶中唑菌酯分析过程中液相色谱-紫外检测中的基质干扰

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摘要

Perilla leaves contain many interfering substances; thus, it is difficult to protect the analytes during identification and integration. Furthermore, increasing the amount of sample to lower the detection limit worsens the situation. To overcome this problem, we established a new method using a combination of solid-phase extraction and dispersive solid-phase extraction to analyze pyraclostrobin in perilla leaves by liquid chromatography with ultraviolet absorbance detection. The target compound was quantitated by external calibration with a good determination coefficient (R-2 = 0.997). The method was validated (in triplicate) with three fortification levels, and 79.06- 89.10% of the target compound was recovered with a relative standard deviation <4. The limits of detection and quantification were 0.0033 and 0.01 mg/kg, respectively. The method was successfully applied to field samples collected from two different areas at Gwangju and Muan. The decline in the resiudue concentrations was best ascribed to a first-order kinetic model with half-lives of 5.7 and 4.6 days. The variation between the patterns was attributed to humidity. Copyright (c) 2015 John Wiley & Sons, Ltd.
机译:紫苏叶中含有许多干扰物质。因此,在鉴定和整合过程中很难保护分析物。此外,增加样品量以降低检测限会使情况恶化。为了克服这个问题,我们建立了一种固相萃取与分散固相萃取相结合的新方法,通过液相色谱-紫外吸收法分析紫苏叶中的吡菌酯。通过外部校准以良好的测定系数对目标化合物进行定量(R-2 = 0.997)。对该方法进行了三次强化验证(一式三份),并回收了79.06- 89.10%的目标化合物,相对标准偏差<4。检出限和定量限分别为0.0033和0.01 mg / kg。该方法已成功应用于从光州和务安两个不同地区采集的野外样品。残留浓度的下降最好归因于一阶动力学模型,其半衰期为5.7天和4.6天。图案之间的变化归因于湿度。版权所有(c)2015 John Wiley&Sons,Ltd.

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