Analysis of pesticide residues in fruits and vegetables using gas chromatography-mass spectrometry: a case from West Omo and Bench-Sheko Zone, Southwest Ethiopia

Author(s):  
Jafer Siraj ◽  
Fikadu Ejeta
2020 ◽  
Vol 4 (2) ◽  
pp. 365-370
Author(s):  
F. Suleiman ◽  
A. A. Nuhu ◽  
K. I. Omoniyi ◽  
Z. I. Yashim

The concentrations of organochlorine pesticide residues were analysed in some vegetables and fruit (spinach, lettuce, cabbage, tomatoes, carrots and onions)  grown at Dagachi farming areas along River Galma of Zaria in Kaduna State, Nigeria. Sample collection and preparation were carried out using standard procedures. The concentrations of all the pesticides in the fruits and vegetables samples were analysed using quick easy cheap effective rugged and safe (QuEChERS) multi- residue extraction and clean up techniques, followed by gas chromatography – mass spectrometry (GC – MS). The most commonly detected organochlorine pesticide residues in the entire samples analysed are lindane, delta – BHC, heptachlor epoxide (B), endosulfan I, dieldrin, and endosulfan II. Furthermore, the results of the study shows that the mean concentration of these organochlorines pesticide detected were higher in onion and spinach with heptachlor epoxide (B) having concentrations 2.303 mg/kg and 2.011 mg/kg respectively. Likewise, endosulfan II (1.433 mg/kg) in lettuce was observed. Heptachlor epoxide (B) detected were also very high in other samples such as carrot, cabbage, and tomatoes and with values 0.600 mg/kg, 0.716 mg/kg, and 0.524 mg/kg respectively. Indeed, these concentrations of all the organochlorine pesticides detected in the fruit and vegetables samples analysed were observed to be at alarming levels, much higher than the maximum residue limits (MRLs) by the Codex 2009 (WHO and FAO) except for lindane with values 0.007 mg/kg and 0.01 mg/kg in carrot and onions respectively 


Foods ◽  
2020 ◽  
Vol 9 (6) ◽  
pp. 746
Author(s):  
Kunho An ◽  
Inhwan Kim ◽  
Chan Lee ◽  
Joon-Kwan Moon ◽  
Hee-Jae Suh ◽  
...  

Morpholine salts of fatty acids have been used in wax coatings on the surfaces of fruit and vegetable commodities in China and the United States, etc. However, morpholine usage was prohibited in many other countries because of safety concerns. We optimized analytical methods to determine morpholine in the peel and pulp of fruits and vegetables by gas chromatography-mass spectrometry (GC-MS). This morpholine analysis method was applied to real samples of apples, citrus fruits, and vegetables from Korea, China, and the U.S. The method was validated using apple and citrus fruit peels and pulp. The method detection limit (MDL) was 1.3–3.3 µg/kg. The recovery rates of morpholine were 88.6–107.2% over a fortified level of 10–400 µg/kg. Intra-day and inter-day precisions were 1.4–9.4% and 1.5–2.8%, respectively. The morpholine concentrations were n.d. (not detected)–11.19 and n.d. (not detected)–12.82 µg/kg in apple and citrus peels, respectively. Morpholine was not detected in citrus or apple pulp samples or in vegetable samples.


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