Fabrication of Novel Avermectin Nanoemulsion Using
a Polyurethane Emulsifier with Cleavable Disulfide Bonds
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Abstract
In this study, a polyurethane emulsifer
with various functional
groups was prepared from isophorone diisocyanate, avermectin, 2,2-dimethylol
propionic acid, and bis(2-hydroxyethyl) disulfide. The chemical structure
of the polymer was confirmed by Fourier transform infrared spectroscopy,
proton nuclear magnetic resonance, and element analysis. The polymer
exhibited adequate emulsification ability for avermectin after neutralization
with triethylamine. A satisfaying nanoemulsion was obtained, in which
avermectin was encapsulated in nanoparticles with 50 wt % drug loading,
low organic solvent content, and high stability under dilution and
centrifuging treatment in addition to low surface tension, high affinity
to crop leaf, and improved avermectin photostability. The resulting
nanoparticles showed degradability in the presence of dl-dithiothreitol
or inside the insect as a result of the disulfide bonds, promoting
the release of avermectin. As a result, the avermectin nanoparticles
showed higher insecticidal ability compared to both the avermectin
nanoparticles without a disulfide group and the avermectin emulsifiable
concentrate