Abstract
Designing nanoparticles with desired properties is a challenging endeavor, due to the large combinatorial space
and complex structure-function relationships. High throughput methodologies and machine learning
approaches are attractive and emergent strategies to accelerate nanoparticle composition design. To date, how
to combine nanoparticle formulation, screening, and computational decision-making into a single effective
workflow is underexplored. In this study, we showcase the integration of three key technologies, namely
microfluidic-based formulation, high content imaging, and active machine learning. As a case study, we apply
our approach for designing PLGA-PEG nanoparticles with high uptake in human breast cancer cells. Starting
from a small set of nanoparticles for model training, our approach led to an increase in uptake from ~5-fold to
~15-fold in only two machine learning guided iterations, taking one week each. To the best of our knowledge,
this is the first time that these three technologies have been successfully integrated to optimize a biological
response through nanoparticle composition. Our results underscore the potential of the proposed platform for
rapid and unbiased nanoparticle optimization.
Supplementary materials
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