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ORAL PRESENTATION / SÖZLÜ SUNUM



                               Investigation of Some Neonicotinoids in Honey by LC-MS/MS

                                   Halil ERGÜN  1,*                    Levent ALTINTAŞ
                                                                                        2

                    1 Republic of Türkiye Ministry of Agriculture and Forestry, Veterinary Control Central
                              Research Institute, Department of Toxicology, Ankara, TÜRKIYE

                   2 Ankara University, Faculty of Veterinary Medicine, Department of Pharmacology and

                                                Toxicology, Ankara, TÜRKIYE

               *Correspound Author: hergun84@msn.com


                     Honey is a natural substance that is susceptible to contamination by environmental

               pollutants. The presence of contaminants in honey is an indicator of environmental pollution.

               Furthermore,  it  may  pose  risks  to  consumer  health.  This  research  aimed  to  optimise  a
               method  for  the  detection  of  residual  quantities  of  the  pesticides  acetamiprid  (ACE),

               clothianidin (CLO), imidacloprid (IMI), thiamethoxam (TMX) and thiacloprid (THI) in honey,
               and subsequently to apply this optimised method to an investigation into the prevalence of

               neonicotinoidal  contamination.  The  QuEChERS  (quick,  easy,  cheap,  effective,  robust  and
               safe)  method,  in  conjunction  with  liquid  chromatography-mass  spectrometry/mass

               spectrometry  (LC-MS/MS),  was  employed  for  the  determination  of  five  neonicotinoid  in

               honey. The method was optimized and validated in accordance with European Commission
               guidelines (2002/657/EC). The method demonstrated a linear correlation with R² values

               exceeding 0.99 for all investigated compounds. Mean recoveries ranged between 70% and
               110% (99% on average), and relative standard deviations (RSDs) were generally below 20%.

               The method's CCα (decision limit) and CCβ (detection capability) both ranged from 5 to 20
               ng/g and 5-21 ng/g, respectively. Following method validation, the concentrations of IMI,

               ACE, TMX, CLO, and THI in all honey samples (flower, pine, and chestnut honey) available for
               retail in Ankara, Türkiye were determined to be ˂LOD based on the analytical results. It was

               concluded that the proposed method is usable and advantageous because it is effective,
               reliable, sensitive, and reproducible and can be used for the simultaneous analysis of more

               than one analyte in a short time using a few reagents.

               Keywords: Honey, LC-MS/MS, Neonicotinoid, Residue, Validation.


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