Headspace Solid-phase Microextraction Combines with Gas Chromatography Mass Spectrometry for Determination of Organochlorine Pesticides in Pork Sample
Yongning Wu
Abstract
Yongning Wu
Abstract
Objective Headspace solid-phase microextraction (HS-SPME) was used as a clean-up and pre-concentration procedure for the simultaneous determination of organochlorine pesticides(OCPs)in pork samples. Method Two stable isotopic compounds, 13C labeled mirex and 13C labeled hexachlorobenzene, were used as internal standard. Gas chromatographic analysis with mass spectrometry (GC-MS) facilitates sensitive detection of the selected pesticides. Several parameters controlling SPME were studied and optimised: choice of SPME fiber, extraction temperature, extraction time, desorption time, desorption temperature and content of salt. Result Under optimal conditions, detection limits obtained were in the range of 1 to 100 ng/g depending on pesticide. Good recoveries (range from 90% to 120% in most cases) were achieved. Conclision The result showed that the HS-SPME/GC-MS method is suitable for the analysis of multi-residue OCPs in pork sample.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective Headspace solid-phase microextraction (HS-SPME) was used as a clean-up and pre-concentration procedure for the simultaneous determination of organochlorine pesticides(OCPs)in pork samples. Method Two stable isotopic compounds, 13C labeled mirex and 13C labeled hexachlorobenzene, were used as internal standard. Gas chromatographic analysis with mass spectrometry (GC-MS) facilitates sensitive detection of the selected pesticides. Several parameters controlling SPME were studied and optimised: choice of SPME fiber, extraction temperature, extraction time, desorption time, desorption temperature and content of salt. Result Under optimal conditions, detection limits obtained were in the range of 1 to 100 ng/g depending on pesticide. Good recoveries (range from 90% to 120% in most cases) were achieved. Conclision The result showed that the HS-SPME/GC-MS method is suitable for the analysis of multi-residue OCPs in pork sample.
Key concepts: Solid-phase microextraction, Chromatography, Chemistry, Mass spectrometry, Hexachlorobenzene, Gas chromatography–mass spectrometry, Detection limit, Gas chromatography