Automated and manual luminescent assay of antioxidant capacity: analytical features by comparison.

The analytical performances of a manual and a partially automated chemiluminescent (CL) assay, of total antioxidant capacity (TAC) were assessed. In both cases the light emitting reaction involved luminol, horseradish peroxidase and hydrogen peroxyde, but the emission kinetics and the parameters taken into account to calculate TAC values were completely different. The major characteristics expressing the quality of the two analytical methods, i.e. inaccuracy, repeteability and reproducibility, sensitivity, time required for the analysis and detection limit, were estimated by using standard solutions of Trolox. The reliability of the automated method, in comparison with the more validated manual one, was demonstrated testing food samples such as honey, wine and dietary supplements and performing a statistical analysis of the results. The comparison of the two series of data by t-test resulted in p values in the range 0.1-0.01. The time required for the analysis of each sample was reduced to one third using the automated method.

Determination of organophosphorus pesticides in honeybees after solid-phase microextraction.

A method based on solid-phase microextraction (SPME) followed by gas chromatography with nitrogen-phosphorus detection was developed for the purpose of determining 18 organophosphorus pesticide residues in honeybee samples (Apis mellifera). The extraction capacities of polyacrylate and poly(dimethylsiloxane) fibers were compared. The main factors affecting the SPME process, such as the absorption time profile, salt, and temperature, were optimized. The method involved honeybee sample homogenization, elution with an acetone:water solution (1:1) and dilution in water prior to fiber extraction. Moreover, the matrix effect on the extraction was evaluated. In samples spiked at the 0.2 mg kg(-1) level, the coefficient variation was between 1 and 13% and the detection limits were below 10 microg kg(-1). The SPME procedure was found to be quicker and more cost-effective than the solvent extraction method commonly used. The method was applied successfully to environmental screening. Parathion methyl was detected and confirmed in the real samples analyzed.

Multiresidual method for the gas chromatographic analysis of pesticides in honeybees cleaned by gel permeation chromatography.

The analysis of several organophosphorus and carbamate pesticide residues in the bodies of honeybees using gas chromatography (GC) and gel permeation chromatography (GPC) clean-up is described. Freeze-dried or lyophilized insect samples were blended with diatomaceous earth (Extrelut) then underwent elution with methylene chloride. This extraction method has shown good recovery on various spike standard levels. Samples are cleaned up by GPC with a Bio Beads SX 3 column and a cyclohexane-ethylacetate (1:1) eluant. Organophosphorus and carbamate compounds are quantified using capillary gas chromatography. Good linearity ranges were observed for all compounds. The extraction process was rapid and results were good, despite the complexity of the matrix on which it was applied. It allowed a reduction both in cost and the consumption of solvents, thereby safeguarding the health of the analyst and the environment. Environmental monitoring using bees was confirmed to be a valid procedure.

[Residues of chlororganic and phosphorganic phitodrugs in samples of honey produced in Emilia-Romagna (author's transl)]. / Ricerca di residui di fitofarmaci clororganici e fosforganici in campioni di miele dell'Emilia-Romagna

Forty-five samples of honey produced in Emilia-Romagna between June and September 1974 have been subjected to gaschromatography to check for the presence of residues of chlororganic and phosphorganic phytodrugs. Residues of chlororganic phytodrugs in appreciable amounts have been found to be present in 11 samples only, more precisely lindane has been reported in 6 samples, aldrin in 4 samples, DDT in 4 samples, DDD and dieldrin respectively in one sample only. The higher concentration for DDT has been 0,04 ppm. No residues of phosphorganic phytodrugs have been found to be present in any of the samples examined. As the presence of residue has been observed only in a small number of samples and low concentration have been found, we belive that the problem of honey pollution by phytodrug residues is a minor one, even when related to the situation of foods in general.