首页> 外文期刊>Journal of Environmental Science and Health, Part B: Pesticides, Food Contaminants, and Agricultural Wastes >Rapid resolution liquid chromatography-tandem mass spectrometry method for the determination of endocrine disrupting chemicals (EDCs), pharmaceuticals and personal care products (PPCPs) in wastewater irrigated soils
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Rapid resolution liquid chromatography-tandem mass spectrometry method for the determination of endocrine disrupting chemicals (EDCs), pharmaceuticals and personal care products (PPCPs) in wastewater irrigated soils

机译:快速分离液相色谱-串联质谱法测定废水灌溉土壤中的内分泌干扰物(EDC),药品和个人护理产品(PPCP)

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摘要

A multiresidue analytical method was developed for the determination of 9 endocrine disrupting chemicals (EDCs) and 19 pharmaceuticals and personal care products (PPCPs) including acidic and neutral pharmaceuticals in water and soil samples using rapid resolution liquid chromatography-tandem mass spectrometry (RRLC-MS/MS). Solid phase extraction (SPE), and ultrasonic extraction combined with silica gel purification were applied as pretreatment methods for water and soil samples, respectively. The extracts of the EDCs and PPCPs in water and soil samples were then analyzed by RRLC-MS/MS in electrospray ionization (ESI) mode in three independent runs. The chromatographic mobile phases consisted of Milli-Q water and acetonitrile for EDCs and neutral pharmaceuticals, and Milli-Q water containing 0.01 % acetic acid (v/v) and acetonitrile: methanol (1:1, v/v) for acidic pharmaceuticals at a flow rate of 0.3 mL/min. Most of the target compounds exhibited signal suppression due to matrix effects. Measures taken to reduce matrix effects included use of isotope-labeled internal standards, and application of matrix-match calibration curves in the RRLC-MS/MS analyses. The limits of quantitation ranged between 0.15 and 14.08 ng/L for water samples and between 0.06 and 10.64 ng/g for solid samples. The recoveries for the target analytes ranged from 62 to 208 % in water samples and 43 to 177 % in solid samples, with majority of the target compounds having recoveries ranging between 70-120 %. Precision, expressed as the relative standard deviation (RSD), was obtained less than 7.6 and 20.5 % for repeatability and reproducibility, respectively. The established method was successfully applied to the water and soil samples from four irrigated plots in Guangzhou. Six compounds namely bisphenol-A, 4-nonylphenol, triclosan, triclocarban, salicylic acid and clofibric acid were detected in the soils.
机译:开发了一种多残留分析方法,使用快速分辨率液相色谱-串联质谱(RRLC-MS)测定水和土壤样品中的9种内分泌干扰物(EDC)和19种药物和个人护理产品(PPCP),包括酸性和中性药物/多发性硬化症)。固相萃取(SPE)和超声萃取结合硅胶纯化分别用作水和土壤样品的预处理方法。然后通过RRLC-MS / MS以电喷雾电离(ESI)模式在三个独立的运行中分析水和土壤样品中EDC和PPCP的提取物。色谱流动相包括用于EDC和中性药物的Milli-Q水和乙腈,以及用于酸性药物的Milli-Q水,其中0.01%的乙酸(v / v)和乙腈:甲醇(1:1,v / v)用于流速为0.3 mL / min。由于基质效应,大多数目标化合物均表现出信号抑制作用。为减少基质效应而采取的措施包括使用同位素标记的内标,以及在RRLC-MS / MS分析中应用基质匹配校准曲线。水样品的定量下限为0.15至14.08 ng / L,固体样品的定量下限为0.06至10.64 ng / g。在水样品中目标分析物的回收率为62%至208%,在固体样品中目标分析物的回收率为43%至177%,大多数目标化合物的回收率在70%至120%之间。对于重复性和再现性,精度分别表示为相对标准偏差(RSD)小于7.6和20.5%。所建立的方法已成功应用于广州四个灌溉小区的水和土壤样品。在土壤中检测到六种化合物,即双酚A,4-壬基酚,三氯生,三氯卡班,水杨酸和氯纤维酸。

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    State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China;

  • 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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  • 入库时间 2022-08-18 00:57:59

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