4.5 Article

Human Exposures to Neonicotinoids in Kumasi, Ghana

Journal

ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY
Volume 40, Issue 8, Pages 2306-2318

Publisher

WILEY
DOI: 10.1002/etc.5065

Keywords

Pesticide risk assessment; Pesticides; Biomonitoring; Neonicotinoid; Imidacloprid equivalent; Chronic reference dose

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan [16H0177906, 18K1984708, 18KK028708, JPMXS0420100620, 17K2003807, 18H0413208, 17KK0009]
  2. JSPS Bilateral Open Partnership Joint Research Projects [JPJSBP120209902]
  3. Environment Research and Technology Development Fund of the Environmental Restoration and Conservation Agency of Japan [SII-1/3-2, 4RF-1802/18949907]
  4. Soroptimist Japan Foundation
  5. Nakajima Foundation
  6. Sumitomo Foundation
  7. Nihon Seimei Foundation
  8. Japan Prize Foundation
  9. Japan Science and Technology Agency/Japan International Cooperation Agency's Science and Technology Research Partnership for Sustainable Development [JPMJSA1501]
  10. Hokkaido University School of Veterinary Medicine Wise/Leading Travel and Subsistence grant

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The study evaluated neonicotinoid exposures in the consumer population of Kumasi, Ghana, and found that the majority of subjects were exposed to multiple neonicotinoids simultaneously, with females having significantly higher daily intakes compared to males.
Neonicotinoid insecticides (NNIs) are now popular in many agricultural systems across Africa; however, the extent of human exposures to NNIs in African countries is scarcely reported. The present study evaluates neonicotinoid exposures in the consumer population of Kumasi, a cosmopolitan city in Ghana. A total of 75 human urine samples were collected from healthy volunteers (nonfarmers, aged 13-80 yr) and analyzed with a liquid chromatography electrospray ionization tandem mass spectrometry system. Seven NNIs and 3 NNI metabolites were detected in the following pattern (frequency, median concentration, maximum concentration): N-dm-acetamiprid (94.7%, 0.41 mu g/L, 8.79 mu g/L) > imidacloprid (70.7%, 0.15 mu g/L, 211.62 mu g/L) > N-(6-chloro-3-pyridylmethyl)-N-ethyl-N '-methylformamidine (62.2%, 0.43 mu g/L, 53.85 mu g/L) > 2-[N-(6-chloro-3-pyridylmethyl)-N-ethylamino]-2-(methylimino)acetic acid (56.8%, 0.10 mu g/L, 3.53 mu g/L) > clothianidin (40%, >limit of quantification [LOQ], 0.45 mu g/L) > nitenpyram (18.7%, >LOQ, 0.14 mu g/L) approximate to thiamethoxam (18.7%, >LOQ, 0.21 mu g/L) > dinotefuran (12.0%, >LOQ, 1.01 mu g/L) > acetamiprid (2.7%, >LOQ, 0.08 mu g/L) approximate to thiacloprid (2.7%, >LOQ, 0.14 mu g/L). Approximately 92% of the subjects were found to be exposed to multiple neonicotinoids simultaneously. The mean, median, and maximum imidacloprid equivalent of the relative potency factor of NNIs were found to be 1.6, 0.5, and 22.52, respectively. The median estimated daily intakes of acetamiprid, imidacloprid, and nitenpyram were 0.47, 1.27, and 0.02 mu g/kg/d for females and 0.91, 0.66, and 0.08 mu g/kg/d for males, respectively. The maximum daily intakes of all the NNIs were <1% of their chronic reference doses (cRfDs), except for imidacloprid and thiacloprid which recorded maximum daily intakes corresponding to 17.97 and 8.28% of cRfDs, respectively. To the best of our knowledge, the present study is the first biomonitoring report on neonicotinoid insecticides in Africa. Environ Toxicol Chem 2021;00:1-13. (c) 2021 SETAC

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