Monitoring Pesticide Residues in Olive Products: Organophosphorus Insecticides in Olives and Oil

1994 ◽  
Vol 77 (5) ◽  
pp. 1096-1100 ◽  
Author(s):  
Chaido Lentza-Rizos

Abstract A simple and efficient gas-liquid chromatographic method was used to screen and quantitate residues of azinphos ethyl, chlorpyrifos, diazinon, di-methoate, fenthion, fenthion sulfoxide, methi-dathion, parathion ethyl, and parathion methyl in olive fruit and olive oil. Most olive fruit samples analyzed during 1991-1992 either contained no detectable residues of the insecticides or contained low concentrations of fenthion, dimethoate, and chlorpyrifos. One sample contained fenthion sulfoxide at a level exceeding FAO/WHO Codex Ali-mentarius maximum residue levels (MRL) for total fenthion. Commercially packed oil samples either contained no detectable residues of the insecticides or contained low concentrations of fenthion, fenthion sulfoxide, and chlorpyrifos. More than half of the virgin oil samples collected from individual growers contained no detectable residues. The others contained mostly fenthion and its sulfoxide metabolite. Of the samples analyzed, 13% exceeded Codex MRL for total fenthion residues. These samples were from a monitoring program targeted at produce most likely to contain residues. Refining procedures seem to act as a decontamination technique for oil containing fenthion residues.

1990 ◽  
Vol 73 (3) ◽  
pp. 365-367
Author(s):  
Lyse Larocque ◽  
Germain Carignan ◽  
Stephen Sved

Abstract A survey on the presence of sulfamethazine (sulfadimidine) residues In consumer milk has been conducted In 10 cities across Canada. In each city, homogenized milk was purchased at 3 different retail outlets, each supplied by different processing plants. A total of 30 samples was analyzed by a liquid chromatographic method. The limit of quantitation was 5 ppb. In addition to automatic integration, visual inspection of the chromatograms was required to distinguish between low concentrations of sulfamethazine and 2 unknown interfering peaks. Two samples, from different cities, contained 11.4 and 5.24 ppb of the drug. Drug Identity was confirmed by mass spectrometry. All other samples appeared to be free of the drug.


1985 ◽  
Vol 68 (4) ◽  
pp. 665-671
Author(s):  
Agnes I Macintosh ◽  
Ginette Lauriault ◽  
George A Neville

Abstract A liquid chromatographic method was used to monitor a depletion study of carbadox (and its most important metabolite, desoxycarbadox) in young pigs fed carbadox-treated rations for 1 week. Carbadox was found in blood (20 ppb), blood serum (26 ppb), and muscle tissue 24 h after withdrawal from treated ration; residues were reduced to a trace (< 2 ppb) in 48 h, and eliminated by 72 h. Desoxycarbadox, although not detected in blood, was found in muscle (17 ppb) 24 h after withdrawal; it was reduced to 9 ppb at 48 h and to a trace by 72 h. Although no carbadox was detected in liver 24 h after withdrawal, appreciable desoxycarbadox (125 ppb) was found in liver 24 h after withdrawal; it was reduced to 17 ppb at 48 h and to a trace by 72 h. Whereas only a trace of carbadox was found in kidney 24 h after withdrawal, 186 ppb desoxycarbadox was found in kidney at 24 h, 34 ppb at 48 h, and a trace at 72 h. No metabolite of carbadox other than desoxycarbadox was found in extracts of swine tissues during this medicated feed trial, and no metabolite was found in blood extracts by using the established 'methodology. The effect of tissue storage (aging) at - 20°C on levels of the drug and its metabolite was a modest alteration of residue levels. The inadvertent use of feed adulterated with furazolidone and initially medicated with chlortetracycline, sulfamethazine, and penicillin G, did not affect the uptake of carbadox in this depletion study or interfere ) with the analytical methodology.


2010 ◽  
Vol 22 (2) ◽  
pp. 281-296 ◽  
Author(s):  
M. Mašković ◽  
B. Jančić-Stojanović ◽  
A. Malenović ◽  
D. Ivanović ◽  
M. Medenica

Sign in / Sign up

Export Citation Format

Share Document