Author/Authors :
Amirahmadi، Maryam نويسنده 2Food and Drug Reference Control Laboratories Center, Food and Drug Organization, MOH & ME, Tehran, Iran,Food and Drug Laboratory Research Center, Food and Drug Organization, MOH & ME, Tehran, Iran , , Shoeibi، Shahram نويسنده 2Food and Drug Reference Control Laboratories Center, Food and Drug Organization, MOH & ME, Tehran, Iran,Food and Drug Laboratory Research Center, Food and Drug Organization, MOH & ME, Tehran, Iran , , Abdollah، Mehdi نويسنده School of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran , , Rastegar، Hossein نويسنده , , Khosrokhavar، Roya نويسنده 1Food and Drug Laboratory Research Center, Food and Drug Organization, MOH & ME, Tehran, IranFood and Drug Reference Control Laboratories Center, Food and Drug Organization, MOH & ME, Tehran, Iran , , Pirali Hamedani، Morteza نويسنده Food and Drug Laboratory Research Center, Food and Drug Organization, MOH & ME, Tehran, Iran Department of Pharmacology, School of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran ,
Abstract :
Tea is an agricultural product of the leaves, leaf buds, and internodes of various cultivars and sub-varieties of the
Camellia sinensis plant, processed and vulcanized using various methods. Tea is a main beverage in Iranian food
basket so should be free from toxic elements such as pesticides residue. There is no data bank on the residue of
pesticides in the consumed black tea in Iran. The present study is the first attempt for monitoring of 25 pesticide
residues from different chemical groups in tea samples obtained from local markets in Tehran, I.R. Iran during the
period 2011. A reliable and accurate method based on spiked calibration curve and QuEChERS sample preparation
was developed for determination of pesticide residues in tea by gas chromatography–mass spectrometry (GC/MS).
The using of spiked calibration standards for constructing the calibration curve substantially reduced adverse
matrix-related effects and negative recovery affected by GCB on pesticides. The recovery of pesticides at 3
concentration levels (n = 3) was in range of 81.4 - 99.4%. The method was proved to be repeatable with RSDr
lower than 20%. The limits of quantification for all pesticides were ?20 ng/g. 53 samples from 17 imported and
manufactured brand were analyzed. Detectable pesticides residues were found in 28.3% (15 samples) of the
samples. All of the positive samples were contaminated with unregulated pesticides (Endosulfan Sulfate or
Bifenthrin) which are established by ISIRI. None of the samples had contamination higher than maximum residue
limit set by EU and India.