Determination of Trichlorfon in Technical and Powder Formulations

1988 ◽  
Vol 71 (2) ◽  
pp. 317-320
Author(s):  
Stephen C Slahck

Abstract A facile procedure is described for the determination of trichlorfon in technical material and an 80% powder formulation by using liquid chromatography with ion-pairing and UV detection. Liquid chromatography allows the direct determination of trichlorfon and detection of any dichlorvos present. This method is applicable to quality control and storage stability analyses and eliminates any need for derivatization to counter the thermal lability of trichlorfon. The average standard deviations for the technical and 80% formulation determinations were 0.51 and 0.37%, respectively.

2016 ◽  
Vol 8 (27) ◽  
pp. 5441-5447 ◽  
Author(s):  
Débora R. S. Lima ◽  
Marcelo Cossenza ◽  
Carlos Gustavo Garcia ◽  
Camila C. Portugal ◽  
Flávia F. de C. Marques ◽  
...  

A HPLC-UV method has been developed and validated for the determination of ascorbic acid in chicken embryo retina.


2006 ◽  
Vol 94 (4) ◽  
pp. 640-650 ◽  
Author(s):  
Giovanna Loredana La Torre ◽  
Marcello Saitta ◽  
Fortunato Vilasi ◽  
Teresa Pellicanò ◽  
Giacomo Dugo

2013 ◽  
Vol 57 (1) ◽  
pp. 25-32 ◽  
Author(s):  
Anna Gajda ◽  
Andrzej Posyniak ◽  
Andrzej Bober ◽  
Tomasz Błądek ◽  
Jan Żmudzki

Summary A liquid chromatography method with UV detection for determination of oxytetracycline (OTC) in honey has been developed. The samples were extracted with the solution of oxalic acid. The clean-up procedure was performed by solid phase extraction (SPE) using polymeric Strata X and carboxylic acid cartridges. Chromatographic separation was carried out on the Luna C8 analytical column with mobile phase consisting of acetonitrile-0.02 M oxalic acid. The method has been successfully validated according to the requirements of the European Decision 2002/657/EC and this method is used in routine control of oxytetracycline in honey samples. The limit of detection (LOD) and limit of quantification (LOQ) of the presented method were 10 and 12.5 μg/kg, respectively. The developed method has also been verified in quantitative determination of oxytetracycline residues in honey after experimental treatment with this product in bee colonies.


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