scholarly journals Residues of Chlormequat and Mepiquat in Grain—Results from the Danish National Pesticide Survey

1999 ◽  
Vol 82 (2) ◽  
pp. 331-336 ◽  
Author(s):  
René K Juhler ◽  
Martin Vahl

Abstract The objective of the present work was to establish information on chlormequat and mepiquat residues in grain for human consumption. Chlormequat (2- chloro-N,N,N-trimethylethylammonium, CAS RN 7003-89-6) and mepiquat (1,1-dimethylpiperid- inium, CAS RN 15302-91-7) are plant growth regulators used to stabilize stalks in cereals. The study was part of the Danish National Pesticide Survey, managed by the Danish Veterinary and Food Administration. Samples were collected in autumn 1997. Residue contents were determined with a newly developed liquid chromatographic- tandem mass spectrometric (LC-MS/MS) method for chlormequat analysis. The method was extended to include mepiquat in the present study. Quantitation was done by the internal standards method, using mass chromatograms of the most intense daughter ions of mepiquat (m/z 98), chlormequat (m/z 58), and [13C]-chlormequat (m/z 61, internal standard). For chlormequat, the overall limit of detection (LD) was 6 μg/kg and the limit of determination (LOD) was 10 μg/kg. For mepiquat, LD was 2 μg/kg and LOD was 3 μg/kg. Of 77 samples analyzed, 51 contained chlormequat and 11 contained mepiquat. The highest levels of chlormequat were found in samples of oatmeal (3.76 mg/kg) and rye (1.08 mg/kg). In 9 rye grain samples containing chlormequat, 5 also contained mepiquat. However, in all samples analyzed, the residues of chlormequat and mepiquat were below maximum residue limits.

2008 ◽  
Vol 91 (4) ◽  
pp. 731-738 ◽  
Author(s):  
Liberato Brum ◽  
Ana Maria Pugens ◽  
Mariely Camila Pritsch ◽  
Patricia Bertuol Mantovani ◽  
Maurício Bedim dos Santos ◽  
...  

Abstract A fast, sensitive, and specific liquid chromatographic/tandem mass spectrometric method was developed and validated for determination of tetracycline in human plasma. Tetracycline and oxytetracycline [internal standard (IS)] were extracted from the plasma by protein precipitation. The mobile phase consisted of acetonitrileformic acid 0.1 (48 + 52, v/v), run at a flow rate of 1 mL/min (split 1:5). Detection was performed by positive electrospray ionization in multiple reaction monitoring mode, monitoring the transitions 444.8 > 410.0 and 461.0 > 426.0 for tetracycline and IS, respectively. The analysis was performed in 3.5 min and the method was linear in the plasma concentration range of 506000 ng/mL. The mean extraction recoveries for tetracycline and IS from plasma were 92.14 and 94.04, respectively. Method validation investigated parameters such as the linearity, precision, accuracy, specificity, and stability, giving results within the acceptable range. The proposed method was successfully applied for determination of tetracycline in human plasma samples to support bioequivalence studies.


2014 ◽  
Vol 6 (18) ◽  
pp. 7407-7414 ◽  
Author(s):  
Pallavi Alegete ◽  
Prasad Kancherla ◽  
Saeed S. Albaseer ◽  
Sathyanarayana Boodida

A rapid and sensitive ultra-performance liquid chromatographic/tandem mass spectrometric assay (LC-MS/MS) was developed to simultaneously quantify fluoxetine and mirtazapine in human plasma using fluoxetine-D5 and olanzapine as internal standards (IS), respectively.


Foods ◽  
2020 ◽  
Vol 9 (10) ◽  
pp. 1368
Author(s):  
Mariana O. Almeida ◽  
Silvia Catarina S. Oloris ◽  
Vanessa Heloisa F. Faria ◽  
Márcia Cassimira M. Ribeiro ◽  
Daniel M. Cantini ◽  
...  

This study aimed to optimize and validate a multi-residue method for identifying and quantifying pesticides in honey by using both gas and liquid chromatographic separation followed by mass spectrometric detection. The proposed method was validated to detect 168 compounds, 127 of them by LC-MS/MS (liquid chromatography tandem mass spectrometric detection) and 41 by GC-MS/MS (gas chromatography tandem mass spectrometric detection). The limit of detection (LOD) and limit of quantification (LOQ) values for the analytes determined by LC-MS/MS were 0.0001–0.0004 mg/kg and 0.0002–0.0008 mg/kg, respectively. For GC-MS/MS analyses, the LOD and LOQ values were 0.001–0.004 mg/kg and 0.002–0.008 mg/kg. In total, 33 samples of commercial honey produced by apiaries in six Brazilian states were analyzed with the validated method. Residual amounts of 15 analytes were detected in 31 samples (93.9%). The method described in the present study was able to detect an extensive and broad range of pesticides with very high sensitivity.


2002 ◽  
Vol 48 (11) ◽  
pp. 2049-2051 ◽  
Author(s):  
Charles A Kroll ◽  
Mark J Magera ◽  
Janice K Helgeson ◽  
Dietrich Matern ◽  
Piero Rinaldo

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