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 in | Journal of Chromatography A Vol. 1218; no. 39; pp. 6869 - 6877 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
28.09.2011
Elsevier |
Subjects | |
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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. |
Author_xml | – sequence: 1 givenname: Tania M surname: GUTIERREZ VALENCIA fullname: GUTIERREZ VALENCIA, Tania M organization: Facultad de Quimica, Departamento de Quimica Analítica, Universidad Nacional Autónoma de México, México, D.F., 04510, Mexico – sequence: 2 givenname: Martha P surname: GARCIA DE LLASERA fullname: GARCIA DE LLASERA, Martha P organization: Facultad de Quimica, Departamento de Quimica Analítica, Universidad Nacional Autónoma de México, México, D.F., 04510, Mexico |
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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 |
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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 |
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