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首页> 外文期刊>Food analytical methods >Evaluation of Quantification Methods to Compensate for Matrix Effects in the Analysis of Benzalkonium Chloride and Didecyldimethylammonium Chloride in Fruits and Vegetables by LC-ESI-MS/MS
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Evaluation of Quantification Methods to Compensate for Matrix Effects in the Analysis of Benzalkonium Chloride and Didecyldimethylammonium Chloride in Fruits and Vegetables by LC-ESI-MS/MS

机译:LC-ESI-MS / MS法分析水果和蔬菜中苯扎氯铵和十二烷基二甲基氯化铵的定量分析方法以补偿基质效应

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Given the extensive presence of some toxic quaternary ammonium compound residues in foodstuffs arriving into the EU during 2012, the Food Authority Control of Geneva decided to implement a monitoring plan to investigate the presence of these contaminants in food: a method based on quick, easy, cheap, effective, rugged, and safe (QuEChERS) extraction and liquid chromatography electrospray tandem mass spectrometry was developed for analyzing didecyldimethylammonium chloride and four benzalkonium chloride homologue residues in fruits and vegetables. An in-house method validation, based on the SANCO guidelines (Document SANCO No. 12571/2013), was conducted using three independent series in orange, lettuce, and avocado composite samples spiked at three levels (10, 100, 500 mu g/kg). Trueness and precision were calculated by pooling all results at each concentration level to account for the variability among fruits and vegetables. To avoid matrix effects on quantitative results, five quantification strategies were investigated: (i) solvent calibration, (ii) matrix-matched calibration prepared on samples and (iii) on sample extract aliquots, and (iv) standard addition prepared on samples and (v) on sample extract aliquots. Due to the nonlinear instrumental response for the large concentration range investigated, a quadratic calibration model was mandatory for all approaches. Solvent calibration gave very poor recoveries due to the high signal suppression caused by matrix effects. Smaller biases were observed for matrix-matched calibrations; however, these results exhibited relatively low precision. Both of the standard addition methods compensated for matrix effects and provided accurate analytical results. Due to the ease of its implementation, the matrix standard addition method, where analytes are added to sample extract aliquots, was preferred over the classical standard addition in samples. Nonlinear extrapolations appeared to be particularly effective in obtaining good results for both standard addition methods when the calibration curve was convex or very slightly concave. The resulting validated method was used to monitor 108 fruit and vegetable commercial samples in May 2013.
机译:鉴于2012年内进入欧盟的食品中大量存在有毒季铵化合物残留物,日内瓦食品管理局控制部门决定实施一项监测计划,以调查食品中这些污染物的存在:一种基于快速,简便,开发了一种廉价,有效,坚固且安全的(QuEChERS)萃取和液相色谱电喷雾串联质谱法,用于分析水果和蔬菜中的二癸基二甲基氯化铵和四种苯扎氯铵同系物残留。根据SANCO准则(SANCO编号12571/2013),使用三个独立系列的橙汁,生菜和鳄梨复合样品加标为三个水平(10、100、500μg/ g,进行内部方法验证)公斤)。通过汇总每个浓度水平下的所有结果以计算水果和蔬菜之间的变异性,计算出真实性和精密度。为避免基质对定量结果的影响,研究了五种定量策略:(i)溶剂校准,(ii)对样品进行的基质匹配校准和(iii)对样品提取物的等分试样,以及(iv)对样品进行的标准添加和( v)提取样品等分试样。由于在较大浓度范围内都存在非线性仪器响应,因此所有方法都必须使用二次校准模型。由于基质效应引起的高信号抑制,溶剂校准的回收率非常差。对于基质匹配的校准,观察到较小的偏差;但是,这些结果显示出相对较低的精度。两种标准添加方法均能补偿基质效应并提供准确的分析结果。由于易于实施,与将标准分析物添加到样品中的等分试样相比,将基质分析物添加到样品提取等分试样中的方法更可取。当校准曲线是凸的或非常微凹的时,对于两种标准添加方法,非线性外推似乎都对获得良好的结果特别有效。经过验证的结果方法于2013年5月用于监测108个水果和蔬菜的商业样本。

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