The determination of patulin from food samples using dual-dummy molecularly imprinted solid-phase extraction coupled with LC-MS/MS

被引:32
|
作者
Zhao, Minjuan [1 ]
Shao, Hua [1 ]
He, Yahui [1 ,2 ]
Li, Hui [1 ]
Yan, Mengmeng [1 ]
Jiang, Zejun [1 ]
Wang, Jing [1 ]
Abd El-Aty, A. M. [4 ,5 ]
Hacimuftuoglu, Ahmet [5 ]
Yan, Feiyan [3 ]
Wang, Yanli [3 ]
She, Yongxin [1 ]
机构
[1] Chinese Acad Agr Sci, Inst Qual Stand & Testing Technol Agroprod, Beijing 100081, Peoples R China
[2] Beijing Persee Gen Instrument Co Ltd, Beijing 101200, Pinggu County, Peoples R China
[3] Guangxi Acad Agr Sci, Inst Qual Stand & Testing Technol Agroprod, Naning 530000, Peoples R China
[4] Cairo Univ, Fac Vet Med, Dept Pharmacol, Giza 12211, Egypt
[5] Ataturk Univ, Med Fac, Dept Med Pharmacol, TR-25240 Erzurum, Turkey
基金
中国国家自然科学基金;
关键词
Patulin; Molecularly imprinted polymers; Food; Solid-phase extraction; High-performance liquid chromatography - tandem mass spectrometry; APPLE JUICE; POLYMER; PRODUCTS; DEGRADATION;
D O I
10.1016/j.jchromb.2019.121714
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A molecularly imprinted polymer (MIP) with specific adsorption for patulin was successfully polymerized by precipitation polymerization using 2-oxindole (2-oxin) and 6-hydroxynicotinic acid (6-HNA) as dummy template molecules, methylacrylic acid (MAA) as a functional monomer, trimethylolpropane trimethacrylate (TRIM) as a crosslinker, 2,2-azobis-(2-methylpropionitrile) (AIBN) as a initiator, and methanol as a porogen solvent. The molecularly imprinted solid phase extraction (MI-SPE) column was prepared using the polymer as a sorbent and applied for the selective extraction of patulin from real samples. The results showed that the MI-SPE method had high selectivity and specific adsorption towards patulin with mean recoveries ranged between 81.3% and 106.3% and a relative standard deviation (RSD) < 4.5%. Additionally, the developed MI-SPE method coupled with liquid chromatography-tandem mass spectrometry (LC-MS/MS) exhibited good linearity in the range of 1-100 ng mL(-1) with correlation coefficients (R-2) > 0.998. The limits of detection (LODs, S/N = 3) were 0.05-0.2 ng g(-1), and the limits of quantification (LOQs, S/N = 10) were 0.2-0.5 ng g(-1). The developed method showed a better purification and higher patulin recovery for real samples than the quick, easy, cheap, effective, rugged, safe "QuEChERS" method.
引用
收藏
页数:7
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