Development of a Broad-Specificity Monoclonal Antibody-Based Immunoaffinity Chromatography Cleanup for Organophosphorus Pesticide Determination in Environmental Samples

被引:27
作者
Xu, Zhen-Lin [1 ,2 ]
Deng, Hao [1 ]
Lei, Hong-Tao [1 ]
Jiang, Yue-Ming [2 ]
Campbell, Katrina [3 ]
Shen, Yu-Dong [1 ]
Yang, Jin-Yi [1 ]
Wang, Hong [1 ]
Sun, Yuan-Ming [1 ]
机构
[1] S China Agr Univ, Guangdong Prov Key Lab Food Qual & Safety, Guangzhou 510642, Guangdong, Peoples R China
[2] Chinese Acad Sci, S China Bot Garden, Key Lab Plant Resources Conservat & Sustainable U, Guangzhou 510650, Guangdong, Peoples R China
[3] Queens Univ Belfast, Sch Biol Sci, Inst Agri Food & Land Use, Belfast BT9 5AG, Antrim, North Ireland
关键词
organophosphorus pesticides; immunoaffinity chromatography; HPLC-MS/MS; environmental samples; SOLID-PHASE EXTRACTION; COLUMN CLEANUP; LIQUID-CHROMATOGRAPHY; RESIDUES; WATER; DRINKING; IMMUNOASSAY; VEGETABLES; ONLINE; FOOD;
D O I
10.1021/jf300896z
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
An immunoaffinity chromatographic (IAC) method for the selective extraction and concentration of 13 organophosphorus pesticides (OPs, including coumaphos, parathion, phoxim, quinalphos, dichlofenthion, triazophos, azinphos-ethyl, phosalone, isochlorthion, parathion-methyl, cyanophos, disulfoton, and phorate) prior to analysis by high-performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS) was developed. The IAC column was prepared by covalently immobilizing a monoclonal antibody with broad specificity for OPs on CNBr-activated Sephrose 4B. The column capacity ranged from 884 to 2641 ng/mL of gel. The optimum elution solvent was 0.01 M phosphate-buffered saline containing 80% methanol. The breakthrough volume of the IAC column was found to be 400 inL. Recoveries of OPs from spiked environmental samples by IAC cleanup and HPLC-MS/MS analysis ranged from 60.2 to 107.1%, with a relative standard deviation below 11.1%. The limit of quantitation for 13 OPs ranged from 0.01 to 0.13 ng/mL (ng/g). The application of IAC cleanup coupled to HPLC-MS/MS in real environmental samples demonstrated the potential of this method for the determination of OP residues in environmental samples at trace levels.
引用
收藏
页码:5847 / 5852
页数:6
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