Determination of Diflubenzuron and Hexaflumuron in Fruits by High Performance Liquid Chromatography with Online Polymeric Monolithic Column Solid phase Extraction
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Determination of Diflubenzuron and Hexaflumuron in Fruits by High Performance Liquid Chromatography with Online Polymeric Monolithic Column Solid phase Extraction
Vol. 37, Issue 8, Pages: 900-905(2018)
作者机构:
1. 华北理工大学公共卫生学院
2. 华北理工大学药学院
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Determination of Diflubenzuron and Hexaflumuron in Fruits by High Performance Liquid Chromatography with Online Polymeric Monolithic Column Solid phase Extraction. [J]. 37(8):900-905(2018)
DOI:
Determination of Diflubenzuron and Hexaflumuron in Fruits by High Performance Liquid Chromatography with Online Polymeric Monolithic Column Solid phase Extraction. [J]. 37(8):900-905(2018)DOI:
Determination of Diflubenzuron and Hexaflumuron in Fruits by High Performance Liquid Chromatography with Online Polymeric Monolithic Column Solid phase Extraction
A method based on high performance liquid chromatography(HPLC) with online monolithic column solid phase extraction was developed for the determination of diflubenzuron and hexa flumuron in fruits. The polymer(poly(2 ethylhexyl methacrylate co ethylene dimethacrylate)) monolithic column(10 mm×46 mm,id.) was prepared by using 2 ethylhexyl methacrylate(EHMA) as monomer and ethylene dimethacrylate(EDMA) as crosslinker,which exhibited a porous structure with a specific surface area of 16401 m2·g-1. Using polymer monolithic column as online solid phase extraction sorbent,the extracted fruit sample solution was loaded into the monolithic column using 5 mmol·L-1 NH4OAc at a flow rate of 01 mL·min-1. The adsorbed analytes were transferred from monolithic column to the analytical column using acetonitrile-water(65∶35,by volume) as mobile phase at a flow rate of 10 mL·min-1. Under the optimized conditions,there was a good linearty for the method in the range of 01-500 mg·L-1(r≥0998). The limits of detection and quantitation for diflubenzuron and hexaflumuron were 0007 2 mg·kg-1 and 0009 mg·kg-1,and 0024 mg·kg-1 and 0030 mg·kg-1,respectively. The recoveries at three spiked levels of 003,03 and 15 mg·kg-1 were in the range of 895%-102% with intra day and inter day relative standard deviations not more than 68%.
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