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采用 HPLC-FLD 法对 SPE 进行系统优化,用于废水中氟喹诺酮类药物的检测。

Systematic optimization of an SPE with HPLC-FLD method for fluoroquinolone detection in wastewater.

机构信息

University of Maryland Baltimore County, Department of Chemical, Biochemical and Environmental Engineering, 1000 Hilltop Circle, Engineering 314, Baltimore, MD 21250, United States.

University of Maryland Baltimore County, Department of Chemical, Biochemical and Environmental Engineering, 1000 Hilltop Circle, Engineering 314, Baltimore, MD 21250, United States.

出版信息

J Hazard Mater. 2015 Jan 23;282:96-105. doi: 10.1016/j.jhazmat.2014.08.027. Epub 2014 Aug 27.

Abstract

This paper describes a selective and ultra-sensitive analytical method for simultaneous determination of 11 fluoroquinolone (FQ) antibiotics in environmental and wastewater samples. The method employs offline solid-phase extraction (SPE) and reversed-phase high performance liquid chromatography with fluorescence detection (HPLC-FLD). A weak cation exchange SPE protocol was developed with a novel loading volume optimization algorithm and a methanol cleanup step to remove background organic matter. Various parameters were optimized to recover FQs from water/wastewater and analyte recovery was generally greater than 80%. Chromatographic separation of the 11 FQs was achieved on a 150 mm pentafluorophenyl column using a gradient elution scheme with methanol, acetonitrile, and 20mM phosphate buffer (pH=2.4). Excitation and emission wavelengths were individually optimized for each FQ using fluorescence spectroscopy; the excitation and emission wavelengths were 276-296 nm and 444-506 nm, respectively. Instrumental quantitation limits were 20-100 pg of mass injected. Of the 11 FQs investigated, seven (i.e., ciprofloxacin, difloxacin, enrofloxacin, fleroxacin, norfloxacin, moxifloxacin, and ofloxacin) were detected during a four-month sampling campaign of wastewater and wastewater-impacted surface water. Concentrations of FQs in raw wastewater, wastewater effluent, and wastewater-impacted surface water were 5-1292, 2-504, and 4-187ng/L, respectively.

摘要

本文描述了一种用于同时测定环境和废水中 11 种氟喹诺酮(FQ)抗生素的选择性和超灵敏分析方法。该方法采用离线固相萃取(SPE)和反相高效液相色谱-荧光检测(HPLC-FLD)。建立了一种新型弱阳离子交换 SPE 方案,采用负载体积优化算法和甲醇清洗步骤去除背景有机物。优化了各种参数以从水/废水中回收 FQ,分析物回收率通常大于 80%。在 150mm 五氟苯基柱上,采用甲醇、乙腈和 20mM 磷酸盐缓冲液(pH=2.4)梯度洗脱方案实现了 11 种 FQ 的色谱分离。使用荧光光谱分别对每种 FQ 进行了激发和发射波长的单独优化;激发和发射波长分别为 276-296nm 和 444-506nm。仪器定量限为 20-100pg 质量注入。在所研究的 11 种 FQ 中,在对废水和受废水影响的地表水进行的为期四个月的采样活动中,检测到了七种(即环丙沙星、二氟沙星、恩诺沙星、氟罗沙星、诺氟沙星、莫西沙星和氧氟沙星)。原废水、废水处理厂出水和受废水影响的地表水的 FQ 浓度分别为 5-1292、2-504 和 4-187ng/L。

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