Ccanccapa-Cartagena Alexander, Masiá Ana, Picó Yolanda
Food and Environmental Safety Research Group (SAMA-UV), Facultat de Farmàcia, Universitat de València, Av. Vicent Andrés Estellés s/n, 46100, Burjassot, Valencia, Spain.
Anal Bioanal Chem. 2017 Aug;409(20):4787-4799. doi: 10.1007/s00216-017-0422-7. Epub 2017 Jun 10.
A simple and environmentally friendly dispersive liquid-liquid microextraction (DLLME) method coupled with electrospray ionization liquid chromatography triple quadrupole mass spectrometry (LC-QqQ-MS/MS) was developed for the simultaneous determination of 17 synthetic and natural pyrethroids. A comparison of solid-phase extraction (SPE) versus DLLME for water samples and only "dilute and shoot" versus the additional extract cleanup by DLLME for sediment samples is reported. Chloroform was the extracting solvent in the DLLME technique for both water and sediment samples. Ultrasonic energy was applied to fully extract the analytes into fine droplets, providing high recoveries in short times. Method detection limits (MDLs) ranged from 0.12 to 0.62 ng L and recoveries from 70 to 119% with RSD values 2-15% (n = 5) for water samples. In sediment samples, MDLs ranged from 0.50 to 2.50 ng g and recoveries from 71 to 112% with RSDs 2-16% (n = 5). The proposed method showed a good linearity within the range of 10-500 ng mL, with coefficients of determination (R ) higher than 0.99. Matrix effects were observed for most compounds in water and sediment (ME% < -10%). The proposed methodology was applied for the analysis of water and sediment samples from Albufera wetland and Turia River. Acrinathrin (48 ng g) and etofenprox (16 ng g) were detected in sediment samples. Graphical abstract Pyrethrins and pyrethroid determination in water and sediments by DLLME and LC-MS/MS.
开发了一种简单且环保的分散液液微萃取(DLLME)方法,并与电喷雾电离液相色谱三重四极杆质谱联用(LC-QqQ-MS/MS),用于同时测定17种合成拟除虫菊酯和天然拟除虫菊酯。报告了水样品中固相萃取(SPE)与DLLME的比较,以及沉积物样品中仅“稀释进样”与通过DLLME进行额外萃取净化的比较。氯仿是DLLME技术中用于水和沉积物样品的萃取溶剂。应用超声能量将分析物充分萃取到细小液滴中,在短时间内提供了高回收率。水样品的方法检测限(MDLs)范围为0.12至0.62 ng/L,回收率为70%至119%,相对标准偏差(RSD)值为2%至15%(n = 5)。在沉积物样品中,MDLs范围为0.50至2.50 ng/g,回收率为71%至112%,RSD为2%至16%(n = 5)。所提出的方法在10 - 500 ng/mL范围内显示出良好的线性,决定系数(R²)高于0.99。在水和沉积物中观察到大多数化合物存在基质效应(ME% < -10%)。所提出的方法应用于分析阿尔布费拉湿地和图里亚河的水和沉积物样品。在沉积物样品中检测到氟丙菊酯(48 ng/g)和醚菊酯(16 ng/g)。图形摘要 通过DLLME和LC-MS/MS测定水和沉积物中的除虫菊素和拟除虫菊酯。