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Details

Autor(en) / Beteiligte
Titel
A sensitive and selective method for the determination of selected pesticides in fruit by gas chromatography/mass spectrometry with negative chemical ionization
Ist Teil von
  • Journal of Chromatography A, 2012-11, Vol.1264, p.110-116
Ort / Verlag
Netherlands: Elsevier B.V
Erscheinungsjahr
2012
Link zum Volltext
Quelle
MEDLINE
Beschreibungen/Notizen
  • ► Selective and sensitive method for determination of multi-class pesticides. ► GC–MS with a triple stage quadrupole analyzer (GC–TSQ–MS). ► Working in negative chemical ionization mode using methane as reactive gas. ► Analysis of real samples intended for baby food. ► Extraction method: liquid extraction using ethyl acetate as extraction solvent. Multiresidue methods (MRMs) for pesticides residues determination in fruit and vegetables, based on GC–MS, are mainly performed in electron impact ionization mode. However an important group of them provide much better response working in negative chemical ionization mode due to the elimination of a high percentage of background signal. Considering that a selective and sensitive method has been developed for the determination of multiclass pesticide residues in different commodities by GC–MS with a triple stage quadrupole analyzer (GC–TSQ–MS); the pesticide signal has been optimized in MS–MS whilst working in negative chemical ionization mode using methane as the reagent gas. The proposed method was fully validated for 53 compounds in tomato, apple and orange matrices. The obtained limits of determination were lower than 0.1μg/kg for more than 50% of the pesticides studied, and lower than 1μg/kg for all pesticides studied, except for cypermethrin, boscalid, bifenthrin and deltamethrin. Linearity was studied in the 0.5–50μg/kg range and a linear response was obtained for all pesticides in all matrices. Recoveries were evaluated at two different levels (1 and 50μg/kg) and recoveries were ranged between 70 and 120% in tomato, apple and orange, except in the cases of chlorfenapyr, ofurace, chlozolinate, chlorothalonil, tolylfluanid and dichlofluanid with recovery values close to 60% at 1μg/kg fortification levels. Repetitivity was evaluated and the relative standard deviation (RSD%) was lower than 10% in all cases. The developed method was employed in the analysis of real samples intended for baby food and the obtained results showed that 50% of the samples were positive for different pesticide residues. The concentration range detected was between 5 and 100μg/kg. The positive detection of OCs was particularly noticeable; these included chlorothalonil, fenhexamide, clorpyrifos and lambda cyhalothrin, which are very persistent and toxic with low acute reference dose. Endosulfan sulfate, which is not approved, was detected at a low concentration.

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