Graphene oxide-based dispersive solid-phase extraction combined with in situ derivatization and gas chromatography-mass spectrometry for the determination of acidic pharmaceuticals in water

被引:42
作者
Naing, Nyi Nyi [1 ,2 ]
Li, Sam Fong Yau [1 ,2 ]
Lee, Hian Kee [1 ,2 ]
机构
[1] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
[2] Natl Univ Singapore, Environm Res Inst, T Lab 0201, Singapore 117411, Singapore
基金
新加坡国家研究基金会;
关键词
Dispersive solid phase extraction; Amine functionalized graphene; In situ derivatization; Acidic pharmaceuticals; ASSISTED EMULSIFICATION MICROEXTRACTION; PERFORMANCE LIQUID-CHROMATOGRAPHY; MULTI-RESIDUE ANALYSIS; WASTE-WATER; CARBAMATE PESTICIDES; BASIC DRUGS; WHOLE-BLOOD; SAMPLES; REDUCTION; SORBENT;
D O I
10.1016/j.chroma.2015.11.070
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A fast and low-cost sample preparation method of graphene based dispersive solid-phase extraction combined with gas chromatography-mass spectrometric (GC-MS) analysis, was developed. The procedure involves an initial extraction with water-immiscible organic solvent, followed by a rapid clean-up using amine functionalized reduced graphene oxide as sorbent Simple and fast one-step in situ derivatization using trimethylphenylammonium hydroxide was subsequently applied on acidic pharmaceuticals serving as model analytes, ibuprofen, gemfibrozil, naproxen, ketoprofen and diclofenac, before GC-MS analysis. Extraction parameters affecting the derivatization and extraction efficiency such as volume of derivatization agent, effect of desorption solvent, effect of pH and effect of ionic strength were investigated. Under the optimum conditions, the method demonstrated good limits of detection ranging from 1 to 16 ng L-1, linearity (from 0.01 to 50 and 0.05 to 50 mu g L-1, depending on the analytes) and satisfactory repeatability of extractions (relative standard deviations, below 13%, n = 3). (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:69 / 76
页数:8
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