A dummy molecularly imprinted solid-phase extraction coupled with liquid chromatography-tandem mass spectrometry for selective determination of four pyridine carboxylic acid herbicides in milk

被引:25
作者
Tan, Sijia [1 ,2 ]
Yu, Hailong [1 ]
He, Yahui [1 ]
Wang, Miao [1 ]
Liu, Guiqiao [2 ]
Hong, Sihui [1 ]
Yan, Feiyan [3 ]
Wang, Yanli [3 ]
Wang, MengQiang [1 ]
Li, Tengfei [2 ]
Wang, Jing [1 ]
Abd El-Aty, A. M. [4 ,5 ]
Haclmuftuoglu, Ahmet [1 ,5 ]
She, Yongxin [1 ]
机构
[1] Chinese Acad Agr Sci, Inst Qual Stand & Testing Technol Agroprod, Beijing 100081, Peoples R China
[2] Hebei Engn Univ, Food Coll, Handan 056038, 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
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2019年 / 1108卷
基金
中国国家自然科学基金;
关键词
Molecularly imprinted polymers; Pyridine carboxylic acid herbicides; Solid-phase extraction; Milk; Residue determination; POLYMERS; SAMPLES; RESIDUES; WATER; FOOD;
D O I
10.1016/j.jchromb.2019.01.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We aim to develop a solid-phase extraction (SPE) based on a dummy molecularly imprinted polymer (MIP) and liquid chromatography-tandem quadrupole mass spectrometry (LC-MS/MS) for selective determination of four pyridine carboxylic acid herbicides (aminopyralid, picloram, fluroxypyr, and clopyralid) in milk samples. Using picloram as the dummy template, MIP nanocomposites with highly selective recognition and adsorption for the target molecule and its structural analogs were successfully synthesized by precipitation polymerization. Adsorption isotherms and kinetics were used to determine the adsorption performance and specific recognition mechanism of both MIPs and non-molecularly imprinted polymers (NIP). The Scatchard plot analysis revealed that two different binding sites were formed in the MIP with maximum binding capacity (Q(max)) of 1171.8 mu g.g(-1) and 3022.5 mu g.g -1 , respectively. Recovery at three spiking levels of 10, 20, and 50 mu g.L-I ranged between 75.3 and 89.8% with relative standard deviations (RSDs) < 14.3%.The limit of detection (LOD) was estimated to be 0.124 mu g.L-1. Finally, the feasibility of the proposed methodology was successfully applied to quantify aminopyralid and another three pyridine carboxylic acid herbicides in milk.
引用
收藏
页码:65 / 72
页数:8
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