کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5746226 1618787 2017 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Targeted screening and safety evaluation of 276 agrochemical residues in raisins using buffered ethyl acetate extraction and liquid chromatography-tandem mass spectrometry analysis
ترجمه فارسی عنوان
غربالگری هدفمند و ارزیابی ایمنی از 276 باقیمانده آگرو شیمیایی در کشمش با استفاده از استخراج اتیل استات بافر و تجزیه و تحلیل طیف مایع کروماتوگرافی مایع
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست شیمی زیست محیطی
چکیده انگلیسی


- Quantitation of 276 agrochemical residues in raisins by LC-MS/MS.
- Limits of quantitation ranged between 0.01 and 10 ng/g.
- Precision <15% at 10 ng/g for 93.8% of the compounds.
- Recoveries 70-120% for 93.5% of compounds at regulatory default MRL of 10 ng/g.
- Method allowed comprehensive evaluation of agrochemical residues in raisins from Indian market.

A buffered ethyl acetate extraction method was optimized and validated in raisin matrix to monitor 276 pesticides by liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis. The final method involved homogenization of raisinsalong with water 1:1 raisins: water followed by extraction using ethyl acetate (10 mL/10 g raisins homogenate in presence of 0.1 mL acetic acid, 0.5 g sodium acetate and 10 g sodium sulfate, and cleanup by dispersive solid phase extraction with primary secondary amine sorbent (25 mg/5 mL extract). 276 pesticides were estimated within 20 min of chromatographic run time by retention time dependent 'scheduled multiple reaction monitoring' (sMRM) by LC-MS/MS.The method was validated as per European guideline, DG-SANTE/11945/2015, at 2, 10, and 25 ng/g spiking levels where the method precision in terms of repeatability was <15% at 10 ng/g for 93.8% of the compounds. The Limit of quantification (LOQ) ranged between 0.01 and 10 ng/g with recoveries 70-120% with ≤20% RSD for 93.5% of compounds at regulatory default MRL of 10 ng/g. The matrix induced signal suppressions or enhancement were moderate (60-130% accuracy against solvent standard) for 85% compounds in white raisins and 67% compounds in black raisins. The method was successfully applied for screening of 94 market samples of raisins for the target analytes. The dietaryexposures calculated against the average concentrations detected were wellbelow the maximum permissible intake (MPI) values and the collected raisin samples were considered safe for human consumption without any acute toxicity hazard.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemosphere - Volume 184, October 2017, Pages 1036-1042
نویسندگان
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