Development and validation of a method for fipronil residue determination in ovine plasma using 96-well plate solid-phase extraction and gas chromatography–tandem mass spectrometry

• Published in: Journal of Chromatography A 2008-08, Vol.1201 (1), p.91-99
• Main Authors: Bichon, E., Richard, C.A., Le Bizec, B.
• Format: Article
• Language: English
• Subjects: Analysis; Animal productions; Animals; Biological and medical sciences; blood plasma; European Union - organization & administration; Fipronil; Food Contamination - analysis; Fundamental and applied biological sciences. Psychology; gas chromatography; Gas Chromatography-Mass Spectrometry - methods; Gas Chromatography-Mass Spectrometry - standards; GC–MS/MS; insecticide residues; Life Sciences; mass spectrometry; Pesticide Residues - chemistry; Plasma; Plasma - chemistry; Pyrazoles - chemistry; Reference Standards; Sensitivity and Specificity; Sheep; solid phase extraction; Solid Phase Extraction - methods; tandem mass spectrometry; Terrestrial animal productions; Validation; Vertebrates
• ISSN: 0021-9673; 1873-3778
• DOI: 10.1016/j.chroma.2008.06.024

Fipronil, a phenylpyrazole insecticide introduced for pest control on a broad range of crops, undergoes a reinforcement of the regulation within the European Union (2007/52/EC directive) due to its potential effects on environment and human health. In order to assess the plasmatic concentrations of fipronil residues (sulfone, sulfide, fipronil, desulfinyl and amide) in ovine, a methodology based on gas chromatography coupled with tandem mass spectrometry (GC–MS/MS) was developed and validated according to the European standard (2002/657/EC). The proposed method allows a large number of samples to be treated concurrently ( n = 80) using a reduced sample amounts (0.2 mL), and consents to reach a level of quantification of 0.1 pg μL −1. The sample preparation consisted of a single solid-phase extraction (SPE) purification on a 96-well plate filled with a styrene-divinyl-benzene phase. Linearity was demonstrated all along the investigated range of concentrations, i.e. from 0.25 to 2000 pg μL −1, with coefficient of determination ( R 2) from 0.977 to 0.994, depending on target analytes. Calculated decision limit (CCα) and detection capability (CCβ) for fipronil, sulfone and sulphide were in the range 0.05–0.16 and 0.28–0.73 pg μL −1 respectively.