Determination of 22 alternative plasticizers in wrap film by solid phase extraction and ultra-high performance supercritical fluid chromatography-tandem mass spectrometry

被引:7
|
作者
He, Pei-xia [1 ,2 ]
Ling, Yun [1 ]
Yong, Wei [1 ]
Yao, Mei-yi [1 ]
Zhang, Yu-jia [1 ]
Feng, Xue-song [2 ]
Zhang, Yuan [3 ]
Zhang, Feng [1 ]
机构
[1] Chinese Acad Inspect & Quarantine, Inst Food Safety, 11 Ronghua South Rd, Beijing 100176, Peoples R China
[2] China Med Univ, Sch Pharm, Shenyang 110122, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, Canc Hosp, Natl Clin Res Ctr Canc, Dept Pharm,Natl Canc Ctr, Beijing 100021, Peoples R China
关键词
Ultra-high performance supercritical fluid; chromatography-tandem mass spectrometry; Alternative plasticizers; Wrap film; Solid phase extraction; ORGANOPHOSPHORUS FLAME RETARDANTS; LIQUID-CHROMATOGRAPHY; MATRIX; MICROEXTRACTION; IONIZATION; DISPERSION; ESTERS; ION;
D O I
10.1016/j.chroma.2022.462916
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A rapid, accurate and novel analytical method based on ultra-high performance supercritical fluid chromatography-tandem mass spectrometry for determination of 22 alternative plasticizers in wrap film was developed. Instrumental analysis and sample preparation procedures were systematically optimized. The targets were separated on Torus 1-AA column (100 mm x 3 mm, 1.7 mu m). Mobile phase A was supercritical carbon dioxide, and mobile phase B was ethanol/methanol (7:3, v/v) containing 0.1% formic acid and 0.5 mM ammonium acetate. Gradient elution was performed. The analytes were extracted by 10 mL n-hexane/dichloromethane (1:1, v/v), and further purified on silica solid phase extraction cartridges. The analytes were quantified by ultra-high performance supercritical fluid chromatography tandem mass spectrometry with electrospray ionization source, and detection was performed on multiple reaction monitoring mode. Two commercially available isotopically-labelled internal standards were used for quantification calibration, and analytes were divided into two groups according to the more appropriate internal standards (chemistry similarity, closeness of retention time).Method validation was performed in terms of recovery, repeatability, linearity, sensitivity and matrix effect. Linearity was assessed using matrix-matched standard calibration. Satisfactory linearity (r 2 > 0.995), intra-day precision (RSDs < 9.6%), inter-day precision (RSDs < 10.9%), recovery (75.6-124.5%) as well as good selectivity was observed. The limits of detection were 0.04-10 mu g/kg, while the limits of quantification were 1.0-50 mu g/kg. Most targets did not show significant matrix effect. Validation results verified that the proposed method was efficient, rapid and sensitive. Eventually it was successfully applied to food wrap film analysis, and results indicated that DEHA, ATBC, DBA and TnBP were the most frequently detected plasticizers in wrap film samples,which was worthy of attention.(c) 2022 Published by Elsevier B.V.
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页数:13
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