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A simple HPLC method for determination of permethrin residues in wine

机译:一种简单的HPLC法测定葡萄酒中的苄氯菊酯残留量

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摘要

An isocratic High Performance Liquid Chromatographic (HPLC) method was optimized for 3-phenoxybenzyl (1RS)-cis-trans-3-(2,2-dichlorovinyl)-2,2-dimethyl-cyclopropanecarboxylate (permethrin) residues identification and quantification in wine matrix. Analytical reverse phase (RP) C-18 column was used (25 cm × 4 mm i.d., 5 μ m) with mobile phase consisting of acetonitrile and water in ratio 70 %/30 % (v v−1), flow-rate 2.0 mL min−1, UV-detection at 215 nm and controlled oven temperature at 25°C. The peaks of isomers were identified with the retention times as compared to standard cis-/trans- mixture and confirmed with characteristic spectra using photodiode array detector. Under these conditions, permethrin isomers were well separated with resolution 2.8 and no interference with the naturally present wine compounds was observed. The method was validated for linearity, precision, accuracy, limit of detection (LOD) and limit of quantification (LOQ). Linear regression analysis data proved a good linear relationship (correlation coefficients, r2, for cis- and trans-isomer are: 0.9995 and 0.9997, respectively) between response of the detector and concentration of permethrin isomers over a wide concentration range for both isomers (0.55 mg L−1 −4.40 mg L−1). Experimental data showed mean recoveries between 93.95% and 96.58% with RSD values in range: 0.89% −3.69%. The effect of ethanol content in the solvent on permethrin isomers peak areas was also studied and 60% v v−1 ethanol was found to be optimal for sample preparation. The method was successfully tested on 20 commercial wine samples from the market in which no permethrin was detected. Thus, it was proved that it is suitable for routine permethrin residues analysis. The proposed method is suitable for routine analysis because of the simple sample preparation, acceptable run-time, low cost and its applicability with conventional instruments.
机译:优化了等度高效液相色谱(HPLC)方法用于葡萄酒中3-苯氧基苄基(1RS)-顺-反式-3-(2,2-二氯乙烯基)-2,2-二甲基-环丙烷羧酸酯(氯菊酯)残留物的鉴定和定量矩阵。使用反相(RP)C-18色谱柱(25 cm×4 mm内径,5 µm),流动相由乙腈和水组成,比率为70%/ 30%(vv →1 < / sup>),流速2.0 mL min -1 ,在215 nm处进行UV检测,并在25°C下控制烤箱温度。与标准的顺式/反式混合物相比,可通过保留时间确定异构体的峰,并使用光电二极管阵列检测器通过特征光谱进行确认。在这些条件下,苄氯菊酯异构体的分离度为2.8,并且未观察到对天然存在的葡萄酒化合物的干扰。验证了该方法的线性,精密度,准确性,检测限(LOD)和定量限(LOQ)。线性回归分析数据证明检测器的响应与氯氰菊酯同分异构体在一个样品中的浓度之间具有良好的线性关系(顺式和反式异构体的相关系数r 2 分别为0.9995和0.9997)。两种异构体的浓度范围很广(0.55 mg L -1> s )。实验数据显示,RSD值在0.89%–3.69%范围内,平均回收率在93.95%和96.58%之间。还研究了溶剂中乙醇含量对氯菊酯异构体峰面积的影响,发现60%v v 乙醇最适合样品制备。该方法已成功在市场上未检测到苄氯菊酯的20种商业葡萄酒样品上进行了测试。因此,证明适用于常规苄氯菊酯残留分析。所提出的方法由于样品制备简单,运行时间可接受,成本低并且适用于常规仪器而适合常规分析。

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    Institute for Public Health of the Republic of Macedonia, Department for Medicines Quality Control, Skopje, Republic of Macedonia;

    Institute of Chemistry, St's Cyril and Methodius University, Skopje, Republic of Macedonia;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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