Albendazole-Related Drug Residues in Milk and Their Fate during Cheesemaking, Ripening, and Storage

1998 ◽  
Vol 61 (11) ◽  
pp. 1484-1488 ◽  
Author(s):  
DIMITRIOS J. FLETOURIS ◽  
NICKOS A. BOTSOGLOU ◽  
IOANNIS E. PSOMAS ◽  
ANTONIOS I. MANTIS

The level and nature of the albendazole residues in milk of treated cows were determined as a function of the time of milking (12-h intervals), and the fate of those residues during cheesemaking, ripening, and storage was examined when the obtained milk was used for making Teleme cheese. Ion-pair liquid chromatographic analysis with fluorescence detection showed that the albendazole sulfoxide metabolite reached its maximum (523 ± 199 μg/kg) at the lst milking and declined below the detection limit by the 4th milking. The sulfone metabolite attained its highest level (812 ± 99 μg/kg) more slowly (at the 2nd milking) and declined below detection limit by the 13th milking. The 2-aminosulfone metabolite, which was present in the milk obtained at the lst milking, reached its maximum (128 ± 36 μg/kg) at the 3rd milking, and slowly declined to a level below detection limit by the 15th milking. Whey and cheese analysis revealed that about 70% of each major metabolite initially present in milk could be distributed in the whey. The remaining 30% occurred in the cheese at residue levels higher than those initially present in the milk of the 1st or 2nd milking (688 versus 445 or 450 versus 230 μg/kg for albendazole sulfoxide; 890 versus 608 or 1502 versus 783 μg/kg for albendazole sulfone; 19 versus 15 or 161 versus 105 μg/kg for albendazole 2-aminosulfone). Ripening and storage of the cheeses made from milks from the lst or 2nd milkings results in a decrease of the sulfoxide metabolite (to 225 or 206 μg/kg), an increase of the sulfone metabolite (to 1,181 or 1,893 μg/kg), and no effect on the 2-aminosulfone metabolite.

1976 ◽  
Vol 59 (3) ◽  
pp. 637-640
Author(s):  
James F Lawrence ◽  
Harry A McLeod

Abstract A gas-liquid chromatographic (GLC) method is described for the analysis and confirmation of azodrin (monocrotophos, 3-(dimethoxyphosphinyl)-N-methyl-cis-crotonamide) residues in strawberries. The strawberries are extracted with acetone, and the filtrate is partitioned with a mixture of methylene chloride and petroleum ether followed by further extraction with methylene chloride. The organic phases are combined, dried with anhydrous sodium sulfate, and concentrated to a small volume for GLC analysis on a 3% OV-210 column with flame photometric detection. Identity of the compound is confirmed by chromatography on the same column after trifluoroacetylation of an aliquot of the strawberry extract. The detection limit is about 2 ppb. The types of strawberry samples analyzed were fresh, frozen, pureed, and jam.


1985 ◽  
Vol 8 (8) ◽  
pp. 1489-1500 ◽  
Author(s):  
Robert J. Y. Shi ◽  
Winnie L. Gee ◽  
Roger L. Williams ◽  
Leslie Z. Benet ◽  
Emil T. Lin

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