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利用微波辅助萃取-中空纤维-液/固相微萃取快速测定鱼样中的54种药品及个人护理用品。

Rapid determination of 54 pharmaceutical and personal care products in fish samples using microwave-assisted extraction-Hollow fiber-Liquid/solid phase microextraction.

作者信息

Zhang Yi, Guo Wen, Yue Zhenfeng, Lin Li, Zhao Fengjuan, Chen Peijin, Wu Weidong, Zhu Hong, Yang Bo, Kuang Yanyun, Wang Jiong

机构信息

Food Inspection and Quarantine Technology Center, Shenzhen Entry-Exit Inspection and Quarantine Bureau of China, Shenzhen, Guangdong, PR China.

Food Inspection and Quarantine Technology Center, Shenzhen Entry-Exit Inspection and Quarantine Bureau of China, Shenzhen, Guangdong, PR China; School of Chemistry and Environment Engineering Shenzhen University, Shenzhen, Guangdong, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Apr 15;1051:41-53. doi: 10.1016/j.jchromb.2017.01.026. Epub 2017 Jan 21.

Abstract

In this paper, a simple, rapid, solvent-less and environmental friendliness microextraction method, microwave-assisted extraction-hollow fiber-liquid/solid phase microextraction (MAE-HF-L/SME), was developed for simultaneous extraction and enrichment of 54 trace hydrophilic/lipophilic pharmaceutical and personal care products (PPCPs) from fish samples. A solid-phase extraction material, solid-phase microextraction (SPME) fiber, was synthesized. The SPME fiber had a homogeneous, loose structure and good mechanical properties, and they exhibited a good adsorption capacity for most PPCPs selected. The material formed the basis for the method of MAE-HF-L/SME. A method of liquid chromatography-high resolution mass spectroscopy (LC-HRMS) for analysis of 54 PPCPs. Under optimal synthesis and extraction conditions, the limits of detection (LODs, n=3) and the limits of quantitation (LOQs, n=10) for the 54 PPCPs were between 0.01-0.50μg·kg and 0.052.00μg·kg, respectively. Percent recoveries and the relative standard deviations (RSDs) in spiked fish samples (n=6) were between 56.3%-119.9% and 0.3%-17.1%, respectively. The microextraction process of 54 PPCPs in MAE-HF-L/SME took approximately 12min. The method has a low matrix interference and high enrichment factor and may be applicable for determination of 54 different PPCPs in fish samples.

摘要

本文开发了一种简单、快速、无溶剂且环境友好的微萃取方法——微波辅助萃取-中空纤维液/固相微萃取(MAE-HF-L/SME),用于同时从鱼样中萃取和富集54种痕量亲水性/亲脂性药物及个人护理用品(PPCPs)。合成了一种固相萃取材料——固相微萃取(SPME)纤维。该SPME纤维结构均匀、疏松,具有良好的机械性能,对所选的大多数PPCPs表现出良好的吸附能力。该材料构成了MAE-HF-L/SME方法的基础。建立了一种用于分析54种PPCPs的液相色谱-高分辨质谱(LC-HRMS)方法。在最佳合成和萃取条件下,54种PPCPs的检测限(LODs,n=3)和定量限(LOQs,n=10)分别在0.01 - 0.50μg·kg和0.05 - 2.00μg·kg之间。加标鱼样(n=6)中的回收率和相对标准偏差(RSDs)分别在56.3% - 119.9%和0.3% - 17.1%之间。MAE-HF-L/SME中54种PPCPs的微萃取过程约需12分钟。该方法具有低基质干扰和高富集倍数,可适用于鱼样中54种不同PPCPs的测定。

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