Rapid mixed mode solid phase extraction method for the determination of acrylamide in roasted coffee by HPLC-MS/MS

被引:81
作者
Bortolomeazzi, Renzo [1 ]
Munari, Marina [1 ]
Anese, Monica [1 ]
Verardo, Giancarlo [2 ]
机构
[1] Univ Udine, Dept Food Sci, I-33100 Udine, Italy
[2] Univ Udine, Dept Chem Phys & Environm, I-33100 Udine, Italy
关键词
Acrylamide; Roasted coffee; Solid phase extraction (SPE); Mixed mode SPE; Liquid chromatography-tandem mass spectrometry (LC-MS/MS); CHROMATOGRAPHY-MASS-SPECTROMETRY; COLLABORATIVE TRIAL; GAS-CHROMATOGRAPHY; SAMPLE PREPARATION; FOOD-PRODUCTS; LIQUID; VALIDATION;
D O I
10.1016/j.foodchem.2012.07.057
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In this work, a rapid and reliable purification method based on a single mixed solid phase extraction (SPE) column, for the determination of acrylamide in roasted coffee by liquid chromatography-tandem mass spectrometry, was developed. Deuterium labelled d(3)-acrylamide was used as internal standard. Acrylamide was extracted by 10 mL of water and the extract purified by a single SPE column consisting of 0.5 g of an in-house prepared mixture of C18, strong cation (SCX) and anion exchange (SAX) sorbents in the ratio 2/1.5/1.5 (w/w/w). The amount of the three sorbents was optimised in order to eliminate the main interfering compounds present in coffee extracts, such as melanoidins, trigonelline, chlorogenic acids and caffeine. The SPE procedure was very simple and consisted of pushing 1 mL of an aqueous coffee extract through the SPE column followed by 1 mL of water which was collected for the analysis. The method was tested on six samples of roasted coffee of different composition and roasting level. The repeatability of the method, expressed as relative standard deviation (n = 6), was lower than 5%. The recovery of acrylamide at three spiked levels ranged from 92% to 95%. The limits of detection (LOD) and quantitation (LOQ) were 5 and 16 mu g kg(-1), respectively. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2687 / 2693
页数:7
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