Carbamates target site interactions

The major difference between OPs and carbamates is in their metabolic fate. This strongly indicates that metabolism and detoxification are the most important factors in resistance evolution. The current emphasis on target site interactions and their associated resistance mechanisms reflects their perceived practical importance, the importance of their study for the development of new insecticidal molecules, and the fundability of such research. But detailed studies of the biochemical characteristics and physiological behavior of the enzymes involved in insecticide metabolism and detoxification are still very important. 

Carbary I (1-naphthyl methylcarbamate) is a chemical in the carbamate family used chiefly as an insecticide. It is a colorless white crystalline solid. Carbaryl disrupts the nervous system by adding a carbamyl moiety to the active site of the acetylcholinesterase enzyme, which prevents it from interacting with acetylcholine.1 It is classified as a likely human carcinogen by the EPA. The pesticide is used indiscriminately, so the toxicity has raised public concern about the ecosystem and human health. Carbaryl is lethal to many non-target insects such as the honeybee. Accumulation of the pesticide occurs in many aquatic organisms such as catfish and algae.2 Due to public health and ecosystem concerns a number of analytical procedures have been used to determine carbaryl concentrations. 

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