Affiliations 

  • 1 Department of Chemistry and Industrial Chemistry, Faculty of Pure and Applied Sciences, Kwara State University Malete, P. M. B. 1530, Ilorin, Nigeria; Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia. Electronic address: abdulrauf.bola@kwasu.edu.ng
  • 2 Department of Chemistry and Industrial Chemistry, Faculty of Pure and Applied Sciences, Kwara State University Malete, P. M. B. 1530, Ilorin, Nigeria; Department of Chemistry, School of Science, Kwara State College of Education, P. M. B. 1525, Ilorin, Nigeria. Electronic address: abibatmonisola@yahoo.com
  • 3 Department of Plant and Environmental Biology, Faculty of Pure and Applied Sciences, Kwara State University Malete, P. M. B. 1530, Ilorin, Nigeria. Electronic address: amudalat.lawal@kwasu.edu.ng
  • 4 Department of Integrated Science, School of Sciences, Kwara State College of Education, P. M. B. 1525, Ilorin, Nigeria. Electronic address: yurisibi44@gmail.com
  • 5 Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia. Electronic address: ghtan@um.edu.my
Food Chem, 2025 Jan 15;463(Pt 4):141464.
PMID: 39369599 DOI: 10.1016/j.foodchem.2024.141464

Abstract

The use of pesticides has led to environmental pollution and posed a global health risk, since they remain as residues on foods. Beans one of the most widely cultivated crop in Africa, and susceptible to attack by insects both on field and during storage, leading to the application of pesticides to control pests' infestation. However, misuse of these chemicals by farmers on beans has resulted in the rejection of beans exported to European countries, due to the presence of pesticide residues at concentrations higher than the maximum residues levels (MRLs). In this study, the effectiveness of the Association Official Analytical Chemists (AOAC) Official Method and the European Committee of Standardization (CEN) Standard Method, were determined using multivariate approach for the analysis of organochlorine pesticide residues in 6 varieties of beans samples. The significance of factors (mass of sample, volume of acetonitrile, mass of magnesium sulphate, sample pH, centrifugation time and speed) affecting the efficiency of extraction was estimated using Plackett-Burman design, while central composite design was used to optimize the significant factors. The following optimum factors were subsequently used for method validation, recovery tests, and real sample analysis: 4 g of sample sludge (1:1 v/v), 10 mL of acetonitrile, 4.45 g of MgSO4, and 5 min of centrifugation at 5000 rpm. The figure of merit of analytical methodology estimated using matrix-matched internal standard calibration method gave linearity ranging from 0.25 to 500 μg/kg, with correlation coefficient (R2) greater than 0.99, the recovery ranged from 75.55 to 110.41 (RSD = 0.70-16.65), with LOD and LOQ of 0.23-1.77 μg/kg and 0.76-5.88 μg/kg, respectively.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.