Abstract

The efficacy of color sorting on reducing aflatoxin levels in shelled apricot kernels was assessed. Naturally-contaminated kernels were submitted to an electronic optical sorter or blanched, peeled, and manually sorted to visually identify and sort discolored kernels (dark and spotted) from healthy ones. The samples obtained from the two sorting approaches were ground, homogenized, and analysed by HPLC-FLD for their aflatoxin content. A mass balance approach was used to measure the distribution of aflatoxins in the collected fractions. Aflatoxin B1 and B2 were identified and quantitated in all collected fractions at levels ranging from 1.7 to 22,451.5 µg/kg of AFB1 + AFB2, whereas AFG1 and AFG2 were not detected. Excellent results were obtained by manual sorting of peeled kernels since the removal of discolored kernels (2.6%–19.9% of total peeled kernels) removed 97.3%–99.5% of total aflatoxins. The combination of peeling and visual/manual separation of discolored kernels is a feasible strategy to remove 97%–99% of aflatoxins accumulated in naturally-contaminated samples. Electronic optical sorter gave highly variable results since the amount of AFB1 + AFB2 measured in rejected fractions (15%–18% of total kernels) ranged from 13% to 59% of total aflatoxins. An improved immunoaffinity-based HPLC-FLD method having low limits of detection for the four aflatoxins (0.01–0.05 µg/kg) was developed and used to monitor the occurrence of aflatoxins in 47 commercial products containing apricot kernels and/or almonds commercialized in Italy. Low aflatoxin levels were found in 38% of the tested samples and ranged from 0.06 to 1.50 μg/kg for AFB1 and from 0.06 to 1.79 μg/kg for total aflatoxins.

Highlights

  • The main production areas of apricots (Prunus armeniaca) are the Mediterranean and MiddleEast

  • High values of limit of detection (LOD) and limit of quantitation (LOQ) were observed for discolored apricot kernels because of the low amount of matrix equivalent injected into the HPLC system and the absence of immuonoaffinity cleanup

  • Found in for the aflatoxin initial apricot kernels, andininthese the two fractions collected the1 e‐sorter from each in of the 2 levels found in the initial apricot kernels, and in the two fractions collected from the e‐sorter from each of the three samples. Statistical analysis of these results showed the absence of significant differences the three samples. Statistical analysis of these results showed the absence of significant differences apricot kernels before e-sorting, and in the fractions collected from the e-sorter machine

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Summary

Introduction

The main production areas of apricots (Prunus armeniaca) are the Mediterranean and MiddleEast. The top five producers of apricots (fresh fruit) in 2013 were Turkey (811,609 tonnes), Iran (457,308 tonnes), Uzbekistan (430,000 tonnes), Algeria (319,784 tonnes), and Italy (198,290 tonnes) [1]. A significant portion of apricots are used to produce apricot stone/pit and its kernel. Apricot kernels are byproducts of the apricot processing industry [2]. In Turkey, 10% of the apricots are used as fresh product, the rest of the product is traditionally stored in sacks with a 20% moisture level after harvesting, sulphuring, drying and stone/pit separation processes [3]. Apricot stones/pits are separated from apricot pulp and processed into shells, mainly used as fuel, and kernels that are exported worldwide, mainly to European countries [4]. Two main varieties of apricot kernels can be differentiated, sweet and bitter. Apricot kernels can be of interest as a food or feed ingredient because of their high crude protein content

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