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Rapid determination of emerging contaminants in water and herbal infusions by in situ derivatization and gas chromatography-tandem mass spectrometry

机译:原位衍生化和气相色谱-串联质谱法快速测定水和草药浸膏中的新兴污染物

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摘要

A simple and rapid method is proposed for the determination of fourteen emerging contaminants (ibuprofen, salicylic acid, fenoprofen, carbamazepine, diclofenac, hexestrol, dienestrol, diethylstilbestrol, estrone, mestranol, progesterone, 4-androstene-3,17-dione, 17 alpha-ethinylestradiol and propylparaben) in water and different herbal infusions (tea, chamomile, linden-blossom and pennyroyal). This procedure is based on the derivatization of the target analytes with ethyl chloroformate and ultrasound-assisted dispersive liquid-liquid microextraction with 100 mu L of chloroform followed by gas chromatography-tandem mass spectrometry. The limits of detection of the target compounds ranged from 0.01 to 0.03 ng mL(-1) in water and from 0.06 to 0.15 ng mL(-1) in the different herbal infusions. The developed method was applied to water samples from different sources (well, river and dam) and herbal infusions and estrone was found in herbal infusions and five of the target compounds were detected in water at levels below 0.50 ng mL(-1).
机译:提出了一种简单而快速的方法来测定14种新出现的污染物(布洛芬,水杨酸,非诺洛芬,卡马西平,双氯芬酸,己烯雌酚,己烯雌酚,己烯雌酚,雌酮,甲雌醇,孕酮,4-雄烯酮-3,17-二酮,17α -乙炔雌二醇和对羟基苯甲酸丙酯)和不同草药注入液(茶,洋甘菊,菩提树花和薄荷油)。该步骤基于目标分析物与氯甲酸乙酯的衍生化,以及超声辅助的分散液-液微萃取与100μL氯仿的混合,然后进行气相色谱-串联质谱分析。在不同的草药输注水中,目标化合物的检出限范围为0.01到0.03 ng mL(-1),从0.06到0.15 ng mL(-1)。所开发的方法适用于来自不同来源(井,河和大坝)的水样品和草药浸液,在草药浸液中发现了雌酮,并且在水中的0.50 ng mL(-1)以下检测到了五种目标化合物。

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