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首页> 外文期刊>Journal of separation science. >Development of multi-response optimization and quadratic calibration curve for determination of ten pesticides in complex sample matrices using QuEChERS dispersive liquid-liquid microextraction followed by gas chromatography
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Development of multi-response optimization and quadratic calibration curve for determination of ten pesticides in complex sample matrices using QuEChERS dispersive liquid-liquid microextraction followed by gas chromatography

机译:用QueChers色散液 - 液微萃取,用气相色谱法测定复合样品基质中十种农药的多响应优化和二次校准曲线的开发

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In this study, QuEChERS combined with dispersive liquid-liquid microextraction is developed for extraction of ten pesticides in complex sample matrices of water and milk. In this regard, effective factors of proposed extraction technique combined with gas chromatography with flame ionization detector were designed, modeled, and optimized using central composite design, multiple linear regression, and Nelder-Mead simplex optimization. Later, univariate calibration model for ten pesticides was developed in concentration range of 0.5-100 ng/mL. Surprisingly, quadratic calibration behavior was observed for some of the pesticides. In this regard, Mandel's test was used for evaluating linearity and types of calibration equation. Finally, four pesticides followed linear calibration curve with sensitivity (0.23-0.66 mL/ng), analytical sensitivity (0.20-0.32), regression coefficient (0.988-0.995), limit of detection (0.39-1.83 ng/mL), and limit of quantitation (1.30-6.10 ng/mL) and six of them followed quadratic calibration curve with sensitivity (0.18-0.93 mL/ng), analytical sensitivity (0.25-0.86), regression coefficient (0.944-0.999), limit of detection (0.59-1.92 ng/mL), and limit of quantitation (1.96-6.40 ng/mL). The calculated limits of detection were below the maximum residue limits according to European Union pesticides database of European Commission. Finally, the proposed analytical method was used for determination of ten pesticides in water and milk samples.
机译:在该研究中,QueChers与分散液 - 液微萃取结合用于提取10种杀虫剂的水和牛奶的复杂样品基质中。在这方面,采用中央复合设计,多元线性回归和NELDER-MED单纯X优化设计,建模和优化了所提出的提取技术的有效因素与火焰电离检测器的气相色谱。后来,十种杀虫剂的单变量校准模型在0.5-100ng / ml的浓度范围内开发。令人惊讶的是,对于一些农药,观察到二次校准行为。在这方面,Mandel的测试用于评估校准方程的线性度和类型。最后,四种农药遵循具有灵敏度的线性校准曲线(0.23-0.66ml / ng),分析敏感性(0.20-0.32),回归系数(0.988-0.995),检测限(0.39-1.83ng / ml)和限制它们的定量(1.30-6.10ng / ml)和六个遵循具有灵敏度的二次校准曲线(0.18-0.93ml / ng),分析灵敏度(0.25-0.86),回归系数(0.944-0.999),检测限(0.59- 1.92 ng / ml)和定量限制(1.96-6.40ng / ml)。根据欧盟委员会的欧洲联盟杀虫剂数据库,计算的检测限优于最大的残留限制。最后,所提出的分析方法用于测定水和牛奶样品中的十种农药。

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