The determination of patulin from food samples using dual-dummy molecularly imprinted solid-phase extraction coupled with LC-MS/MS
文献类型: 外文期刊
作者: Zhao, Minjuan 1 ; Shao, Hua 1 ; He, Yahui 1 ; Li, Hui 1 ; Yan, Mengmeng 1 ; Jiang, Zejun 1 ; Wang, Jing 1 ; Abd El-Aty, A 1 ;
作者机构: 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
关键词: Patulin; Molecularly imprinted polymers; Food; Solid-phase extraction; High-performance liquid chromatography - tandem mass spectrometry
期刊名称:JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES ( 影响因子:3.205; 五年影响因子:3.068 )
ISSN: 1570-0232
年卷期: 2019 年 1125 卷
页码:
收录情况: SCI
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.
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