Determination of organophosphorus pesticides in bovine tissue by an on-line coupled matrix solid-phase dispersion–solid phase extraction–high performance liquid chromatography with diode array detection method

A miniaturized method based on matrix solid-phase dispersion coupled to solid phase extraction and high performance liquid chromatography with diode array detection (MSPD–SPE–HPLC/DAD) was developed for the trace simultaneous determination of the following organophosphorus pesticides (OPPs) in bovin...

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Published inJournal of Chromatography A Vol. 1218; no. 39; pp. 6869 - 6877
Main Authors GUTIERREZ VALENCIA, Tania M, GARCIA DE LLASERA, Martha P
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 28.09.2011
Elsevier
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Abstract A miniaturized method based on matrix solid-phase dispersion coupled to solid phase extraction and high performance liquid chromatography with diode array detection (MSPD–SPE–HPLC/DAD) was developed for the trace simultaneous determination of the following organophosphorus pesticides (OPPs) in bovine tissue: parathion-methyl, fenitrothion, parathion, chlorfenvinphos, diazinon, ethion, fenchlorphos, chlorpyrifos and carbophenothion. To perform the coupling between MSPD and SPE, 0.05 g of sample was dispersed with 0.2 g of C 18 silica sorbent and packed into a stainless steel cartridge containing 0.05 g of silica gel in the bottom. After a clean-up of high and medium polarity interferences with water and an acetonitrile:water mixture, the OPPs were desorbed from the MSPD cartridge with pure acetonitrile and directly transferred to a dynamic mixing chamber for dilution with water and preconcentration into an SPE 20 mm × 2.0 mm I.D. C 18 silica column. Subsequently, the OPPs were eluted on-line with the chromatographic mobile phase to the analytical column and the diode array detector for their separation and detection, respectively. The method was validated and yielded recovery values between 91% and 101% and precision values, expressed as relative standard deviations (RSD), which were less than or equal to 12%. Linearity was good and ranged from 0.5 to 10 μg g −1 , and the limits of detection of the OPPs were in the range of 0.04–0.25 μg g −1. The method was satisfactorily applied to the analysis of real samples and is recommended for food control, research efforts when sample amounts are limited, and laboratories that have ordinary chromatographic instrumentation.
AbstractList A miniaturized method based on matrix solid-phase dispersion coupled to solid phase extraction and high performance liquid chromatography with diode array detection (MSPD-SPE-HPLC/DAD) was developed for the trace simultaneous determination of the following organophosphorus pesticides (OPPs) in bovine tissue: parathion-methyl, fenitrothion, parathion, chlorfenvinphos, diazinon, ethion, fenchlorphos, chlorpyrifos and carbophenothion. To perform the coupling between MSPD and SPE, 0.05 g of sample was dispersed with 0.2 g of C(18) silica sorbent and packed into a stainless steel cartridge containing 0.05 g of silica gel in the bottom. After a clean-up of high and medium polarity interferences with water and an acetonitrile:water mixture, the OPPs were desorbed from the MSPD cartridge with pure acetonitrile and directly transferred to a dynamic mixing chamber for dilution with water and preconcentration into an SPE 20 mm × 2.0 mm I.D. C(18) silica column. Subsequently, the OPPs were eluted on-line with the chromatographic mobile phase to the analytical column and the diode array detector for their separation and detection, respectively. The method was validated and yielded recovery values between 91% and 101% and precision values, expressed as relative standard deviations (RSD), which were less than or equal to 12%. Linearity was good and ranged from 0.5 to 10 μg g(-1), and the limits of detection of the OPPs were in the range of 0.04-0.25 μg g(-1). The method was satisfactorily applied to the analysis of real samples and is recommended for food control, research efforts when sample amounts are limited, and laboratories that have ordinary chromatographic instrumentation.
A miniaturized method based on matrix solid-phase dispersion coupled to solid phase extraction and high performance liquid chromatography with diode array detection (MSPD-SPE-HPLC/DAD) was developed for the trace simultaneous determination of the following organophosphorus pesticides (OPPs) in bovine tissue: parathion-methyl, fenitrothion, parathion, chlorfenvinphos, diazinon, ethion, fenchlorphos, chlorpyrifos and carbophenothion. To perform the coupling between MSPD and SPE, 0.05 g of sample was dispersed with 0.2 g of C sub(18 silica sorbent and packed into a stainless steel cartridge containing 0.05 g of silica gel in the bottom. After a clean-up of high and medium polarity interferences with water and an acetonitrile:water mixture, the OPPs were desorbed from the MSPD cartridge with pure acetonitrile and directly transferred to a dynamic mixing chamber for dilution with water and preconcentration into an SPE 20 mm x 2.0 mm I.D. C) sub(1)8 silica column. Subsequently, the OPPs were eluted on-line with the chromatographic mobile phase to the analytical column and the diode array detector for their separation and detection, respectively. The method was validated and yielded recovery values between 91% and 101% and precision values, expressed as relative standard deviations (RSD), which were less than or equal to 12%. Linearity was good and ranged from 0.5 to 10 mu g g super(-1) sub(,) and the limits of detection of the OPPs were in the range of 0.04-0.25 mu g g super(-1. The method was satisfactorily applied to the analysis of real samples and is recommended for food control, research efforts when sample amounts are limited, and laboratories that have ordinary chromatographic instrumentation.)
A miniaturized method based on matrix solid-phase dispersion coupled to solid phase extraction and high performance liquid chromatography with diode array detection (MSPD–SPE–HPLC/DAD) was developed for the trace simultaneous determination of the following organophosphorus pesticides (OPPs) in bovine tissue: parathion-methyl, fenitrothion, parathion, chlorfenvinphos, diazinon, ethion, fenchlorphos, chlorpyrifos and carbophenothion. To perform the coupling between MSPD and SPE, 0.05g of sample was dispersed with 0.2g of C₁₈ silica sorbent and packed into a stainless steel cartridge containing 0.05g of silica gel in the bottom. After a clean-up of high and medium polarity interferences with water and an acetonitrile:water mixture, the OPPs were desorbed from the MSPD cartridge with pure acetonitrile and directly transferred to a dynamic mixing chamber for dilution with water and preconcentration into an SPE 20mm×2.0mm I.D. C₁₈ silica column. Subsequently, the OPPs were eluted on-line with the chromatographic mobile phase to the analytical column and the diode array detector for their separation and detection, respectively. The method was validated and yielded recovery values between 91% and 101% and precision values, expressed as relative standard deviations (RSD), which were less than or equal to 12%. Linearity was good and ranged from 0.5 to 10μgg⁻¹ , and the limits of detection of the OPPs were in the range of 0.04–0.25μgg⁻¹. The method was satisfactorily applied to the analysis of real samples and is recommended for food control, research efforts when sample amounts are limited, and laboratories that have ordinary chromatographic instrumentation.
A miniaturized method based on matrix solid-phase dispersion coupled to solid phase extraction and high performance liquid chromatography with diode array detection (MSPD–SPE–HPLC/DAD) was developed for the trace simultaneous determination of the following organophosphorus pesticides (OPPs) in bovine tissue: parathion-methyl, fenitrothion, parathion, chlorfenvinphos, diazinon, ethion, fenchlorphos, chlorpyrifos and carbophenothion. To perform the coupling between MSPD and SPE, 0.05 g of sample was dispersed with 0.2 g of C 18 silica sorbent and packed into a stainless steel cartridge containing 0.05 g of silica gel in the bottom. After a clean-up of high and medium polarity interferences with water and an acetonitrile:water mixture, the OPPs were desorbed from the MSPD cartridge with pure acetonitrile and directly transferred to a dynamic mixing chamber for dilution with water and preconcentration into an SPE 20 mm × 2.0 mm I.D. C 18 silica column. Subsequently, the OPPs were eluted on-line with the chromatographic mobile phase to the analytical column and the diode array detector for their separation and detection, respectively. The method was validated and yielded recovery values between 91% and 101% and precision values, expressed as relative standard deviations (RSD), which were less than or equal to 12%. Linearity was good and ranged from 0.5 to 10 μg g −1 , and the limits of detection of the OPPs were in the range of 0.04–0.25 μg g −1. The method was satisfactorily applied to the analysis of real samples and is recommended for food control, research efforts when sample amounts are limited, and laboratories that have ordinary chromatographic instrumentation.
Author Gutiérrez Valencia, Tania M.
García de Llasera, Martha P.
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Issue 39
Keywords Matrix solid-phase dispersion
Organophosphorus pesticides
On-line coupling analysis
Solid-phase extraction
HPLC
Bovine tissues
Solid phase extraction
Chemical analysis
Liver
Lung
HPLC chromatography
Chemical enrichment
Tissue
Sample preparation
Diode array
Muscle
Beef
Ungulata
Quantitative analysis
Matrix Solid Phase Dispersion extraction
Trace analysis
Validation
Farming animal
Bovine
Offals
Coupled method
Pesticides
Contamination
Vertebrata
Reversed phase chromatography
Mammalia
Ultraviolet detector
Residue
Animal
Organophosphorus compounds
Artiodactyla
Language English
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CC BY 4.0
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Snippet A miniaturized method based on matrix solid-phase dispersion coupled to solid phase extraction and high performance liquid chromatography with diode array...
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SubjectTerms acetonitrile
Animal productions
Animals
Biological and medical sciences
Bovine tissues
carbophenothion
Cattle
chlorfenvinphos
chlorpyrifos
Chromatography, High Pressure Liquid - instrumentation
Chromatography, High Pressure Liquid - methods
detection limit
diazinon
ethion
fenitrothion
Food industries
food safety
Fundamental and applied biological sciences. Psychology
high performance liquid chromatography
HPLC
instrumentation
Liver - chemistry
Lung - chemistry
Matrix solid-phase dispersion
Meat and meat product industries
Methanol - chemistry
Miniaturization
mixing
Muscles - chemistry
On-line coupling analysis
Organophosphorus pesticides
Organothiophosphorus Compounds - analysis
Organothiophosphorus Compounds - isolation & purification
parathion
parathion-methyl
Pesticide Residues - analysis
Pesticide Residues - isolation & purification
Reproducibility of Results
Sensitivity and Specificity
silica gel
Solid Phase Extraction - methods
Solid-phase extraction
stainless steel
Terrestrial animal productions
Tissue Distribution
Vertebrates
Title Determination of organophosphorus pesticides in bovine tissue by an on-line coupled matrix solid-phase dispersion–solid phase extraction–high performance liquid chromatography with diode array detection method
URI https://dx.doi.org/10.1016/j.chroma.2011.08.011
https://www.ncbi.nlm.nih.gov/pubmed/21872255
https://www.proquest.com/docview/1635022468
https://www.proquest.com/docview/1694500089
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