Fomesafen serves as a widely employed
selective herbicide for addressing
broadleaf weeds, but the short duration of efficacy limits utilization
efficiency. There exists an exigent requirement to extend its efficacy
through controlled release mechanisms. Fomesafen@SiO2-starch
microspheres with α-amylase responsiveness were synthesized
through the direct binding of drug-loaded silica microspheres and
modified starch. This fabrication method capitalizes on the enzymatic
degradation potential of the outer starch layer by amylase. In contrast
with earlier analogous structures that exhibited inferior drug loading
efficacy, the prepared fomesafen@SiO2-starch microspheres
demonstrated a significantly enhanced drug loading capacity of up
to 35.7%. Furthermore, in comparison to fomesafen technical, the prepared
fomesafen@SiO2-starch microspheres exhibited a notable
capacity to mitigate the photolysis of fomesafen through the utilization
of the starch outer layer. Additionally, the fomesafen@SiO2-starch microspheres demonstrated favorable wettability and adhesive
properties. At the recommended dosage, the herbicidal efficacy of
fomesafen@SiO2-starch microspheres against Brassica napus L. and Portulaca oleracea
L. over 14 days was observed to be comparable to that
of the fomesafen technical, concurrently exhibiting a degree of sustained
release. These findings underscore the potential of microspheres in
regulating the release of fomesafen, thereby presenting a promising
avenue for the development of sustainable drug delivery systems in
agriculture.