Use of whole blood for spectrophotometric determination of cholinesterase activity in dogs

Whole blood has been compared with erythrocytes and plasma for spectrophotometric cholinesterase determination in the dog. Cholinesterase activity was characterized using two substrates: acetylthiocholine and butyrylthiocholine. Acetylcholinesterase was the only form of cholinesterase present on erythrocytes and hydrolysed only acetylthiocholine. Butyrylcholinesterase (pseudocholinesterase) was predominant in plasma, hydrolysing mainly butyrylthiocholine. Based on these results, a method based on the use of two substrates (acetylthiocholine for monitoring acetylcholinesterase and butyrylthiocholine for determining butyrylcholinesterase) in the same whole blood sample is recommended for canine cholinesterase analysis. This way of monitoring both enzymes can be easily automated, yielding good within (CVs < 5%) and between-run (CVs < 7%) precision.     

Use of a field-scale biofilter for the degradation of the organophosphate insecticide coumaphos in cattle dip wastes

Insecticide wastes generated from livestock dipping operations are well suited for biodegradation processes since these wastes are concentrated, contained, and have no other significant toxic components. A field-scale biofilter capable of treating 15000-litre batches of dip waste containing the acaricide coumaphos was used to reduce the coumaphos concentration in two successive 11000-litre batch trials from 2000 mg litre^-1 to 10 mg litre^-1 in approximately 14 days at 25–29°C. Removal of coumaphos from the biofilter effluent is a function of both physical filtration and biodegradation by the biofilter. However, stoichiometric increases in chloride levels in the effluent as coumaphos concentrations decreased confirmed that coumaphos was being degraded by the biofilter rather than just being filtered out. In subsequent 5500-litre batch experiments, the addition of a vitamin supplement to the biofilter-treated dip resulted in a further decrease in coumaphos concentration to approximately 1 mg litre^-1. Results from incubations of two representative Texas soils with biofilter-treated dip spiked with [benzo-U-¹⁴C] coumaphos revealed that 32–36% of the spiked [¹⁴C] coumaphos was mineralized in the soils after 110 days at 30°C. © 1998 SCI.     

Biodegradation of the Organophosphate Insecticide Coumaphos in Highly Contaminated Soils and in Liquid Wastes

Approximately 400000 litres of cattle dip wastes containing approximately 1500 mg litre⁻¹ of the organophosphate insecticide coumaphos are generated yearly along the Mexican border from a USDA program designed to control disease-carrying cattle ticks. Use of unlined evaporation pits for the disposal of these wastes has resulted in highly contaminated soils underlying these sites. Previous work has shown that microbial consortia present in selected dip wastes can be induced to mineralize coumaphos. Our results demonstrate that similar microbial consortia are present in coumaphos-contaminated soils from eight waste sites and that these organisms are capable of mineralizing cou-maphos in these soils using soil slurries to less than 1 mg litre⁻¹ in 7–10 days at 28°C. In addition, our results show that these consortia are able to colonize pea gravel in trickling gravel filters and can be used in these filters to metabolize coumaphos from dip wastes to less than 0·1 mg litre⁻¹ in 7–10 days at 28°C. These simple systems offer potential low cost means to detoxify coumaphos-containing wastes and to bioremediate soils contaminated with this organophosphate compound.     

Obidoxime reactivation of organophosphate-inhibited cholinesterase activity in pigs

The ability of obidoxime to reactivate organophosphate-inhibited cholinesterases was studied in pigs treated with either trichlorfon, dichlorvos or coumaphos. In 6 pigs Cholinesterase activity was measured in the blood samples both before and after in vitro reactivation with obidoxime. Three pigs were treated with obidoxime 6 h after administration of the organophosphates in order to study the possibility of in vivo reactivation.The results show a close correlation between the ability of obidoxime to reactivate the inhibited cholinesterases in vitro and in vivo. However, there was a marked difference in the possibility of reactivation between the 3 organophosphates. Thus no reactivation was possible after treatment with dichlorvos, while reactivation could be achieved for at least 6 h after administration of trichlorfon. After coumaphos treatment reactivation with obidoxime was possible for more than 24 h.     

Residue distribution of the acaricide coumaphos in honey following application of a new slow-release formulation

Acaricide used in beehives for the control of varroa often leaves residues in bee products. The behaviour and distribution of the acaricide coumaphos in honey following the application of a new slow-release strip formulation (CheckMite+) was assessed. The bee colonies were allowed to build new combs without foundation, and two strips were hung in the brood chamber of each colony for a period of 42 days. The distribution of coumaphos residues in honey in relation to the position of the frame and the duration of treatment was examined by collecting samples from each comb at various time intervals up to 145 days after treatment. In the brood chamber, coumaphos was incorporated into honey from the first day of application, and residues accumulated mainly in combs placed next to strips. In the adjacent combs, residues remained at low concentrations with slight variations. In the honey chamber, residue concentrations on the day of strip removal ranged between 0.006 and 0.020 mg kg(-1), while 79 days after application the concentration of coumaphos residues was below 0.020 mg kg(-1). Residues above the EC fixed maximum residue limit (MRL) of 0.1 mg kg(-1) were measured only in brood chamber honey obtained from those combs placed next to strips. In these samples, 0.060-0.111 mg kg(-1) of coumaphos was detected up to 103 days after strip removal. Coumaphos residues in honey extracted from combs that were placed at the edge of the brood chamber were found below the MRL value, even during the 42 day period of CheckMite+ strip treatment.