Imidacloprid belongs to a major new class of insecticides, called neonicotinoids, which are accounting for 11–15% of the total
insecticide market. The binding characteristics of insecticide imidacloprid with hemoglobin (Hb) have been studied by employing
different spectroscopic techniques. The results proved the formation of complex between imidacloprid and Hb. Hydrophobic interaction
and hydrogen bond dominated in the association reaction. Hydrophobic probe 8-anilino-1-naphthalenesulfonic acid (ANS) competitive
experiments indicated that the binding of imidacloprid to Hb primarily took place in hydrophobic regions. The distance between
Hb donor and acceptor imidacloprid was 4.88 nm as derived from Förster’s theory. Alternations of Hb secondary structure in
the presence of imidacloprid were confirmed by synchronous fluorescence, circular dichroism (CD) and three-dimensional fluorescence
spectra. This study enriches our understanding of toxic effect of imidacloprid to the physiologically important protein Hb.
Keywords Imidacloprid - Hemoglobin - Binding site - Fluorescence spectroscopy - Circular dichroism