Development of procedures for the triazole fungicides determination in fruits and liquid samples using microextraction techniques and chromatographic separation
Abstract
Agricultural crops can be damaged by funguses, insects, worms and other
organisms that cause diseases and decrease the yield of production. The effect of
these damaging agents can be reduced using pesticides. Among them, triazole
compounds are effective substances against fungus; for example, Oidium.
Nevertheless, it has been detected that the residues of these fungicides in foods as
well as in derivate products can affect the health of the consumers. Therefore, the
European Union has established several regulations fixing the maximum residue of
pesticide levels in a wide range of foods trying to assure the consumer safety.
Hence, it is very important to develop adequate methods to determine these
pesticide compounds. In most cases, gas or liquid chromatographic (GC, LC)
separations are used in the analysis of the samples. But firstly, it is necessary to use
proper sample treatments in order to preconcentrate and isolate the target analytes.
To reach this aim, microextraction techniques are very effective tools; because allow
to do both preconcentration and extraction of the analytes in one simple step that
considerably reduces the source of errors.
With these objectives, two remarkable techniques have been widely used
during the last years: solid phase microextraction (SPME) and liquid phase
microextraction (LPME) with its different options. Both techniques that avoid the use
or reduce the amount of toxic solvents are convenient coupled to chromatographic
equipments providing good quantitative results in a wide number of matrices and
compounds.
In this work simple and reliable methods have been developed using SPME and
ultrasound assisted emulsification microextraction (USAEME) coupled to GC or LC for
triazole fungicides determination. The proposed methods allow confidently determine
triazole concentrations of μg L‐1 order in different fruit samples.
Chemometric tools have been used to accomplish successful determinations.
Firstly, in the selection and optimization of the variables involved in the
microextraction processes; and secondly, to overcome the problems related to the
overlapping peaks. Different fractional factorial designs have been used for the screening of the experimental variables; and central composite designs have been
carried out to get the best experimental conditions. Trying to solve the overlapping
peak problems multivariate calibration methods have been used. Parallel Factor
Analysis 2 (PARAFAC2), Multivariate Curve Resolution (MCR) and Parallel Factor
Analysis with Linear Dependencies (PARALIND) have been proposed, the adequate
algorithms have been used according to data characteristics, and the results have been
compared.
Because its occurrence in Basque Country and its relevance in the production of
cider and txakoli regional wines the grape and apple samples were selected. These
crops are often treated with triazole compounds trying to solve the problems caused
by the funguses. The peel and pulp from grape and apple, their juices and some
commercial products such as musts, juice and cider have been analysed showing the
adequacy of the developed methods for the triazole determination in this kind of fruit
samples.