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Evaluation of (–)-borneol derivatives against the Zika vector, Aedes aegypti and a non-target species, Artemia sp
Ist Teil von
Environmental science and pollution research international, 2018-11, Vol.25 (31), p.31165-31174
Ort / Verlag
Berlin/Heidelberg: Springer Berlin Heidelberg
Erscheinungsjahr
2018
Quelle
Springer Online Journals【Remote access available】
Beschreibungen/Notizen
Zika, dengue, and chikungunya are vector-borne diseases of pronounced concern transmitted by the mosquito
Aedes aegypti
Linn. (Diptera: Culicidae). The most important method to avoid outbreaks is to control mosquito spreading by the employment of insecticides and larvicides. Failure to control mosquito dispersal is mostly accounted to
Ae. aegypti
resistance to currently available larvicides and insecticides, encouraging the development of novel pesticides. In addition, the excessive use of larvicides poses serious threats to human health and the environment. Evaluation of natural products as larvicides in an attempt to overcome this situation is often found in the literature because products originated from nature are considered less toxic to non-target species and more eco-friendly. (–)-Borneol is a bicyclic monoterpene present in essential oils with moderate larvicidal activity. On account of these facts, it was of our interest to synthesize (–)-borneol ester derivatives aiming to study its structure-activity relationships against
Ae. aegypti
larvae. With the goal to estimate toxicity to a non-target species, evaluation of the lethal concentration 50% (LC
50
) on
Artemia
sp. (Artemiidae) and calculation of selectivity towards
Ae. aegypti
were carried out. The most potent derivative, (–)-Bornyl chloroacetate, exhibited the highest suitability index, demonstrating lower environmental toxicity than other borneol ester derivatives. A parabolic relationship between (–)-borneol esters larvicidal activity and partition coefficient (Log P) was achieved and a correlation equation obtained, validating the importance of lipophilicity to the larvicidal activity of these compounds.