posted on 2021-08-24, 14:05authored byKurt D. Ristroph, Jenna A. Ott, Luqman A. Issah, Brian K. Wilson, Amila Kujović, Madeleine Armstrong, Sujit S. Datta, Robert K. Prud’homme
Nanoformulating poorly water-soluble
drugs is attractive for improving
oral dissolution kinetics, but concentrating and drying dilute nanoparticle
(NP) suspensions is a barrier to translation. This work describes
a reversible, pH-driven flocculation technique for concentrating NPs
stabilized with a carboxylic acid-bearing cellulose polymer. Lumefantrine
NPs 150 nm in diameter stabilized by anionic hydroxypropylmethylcellulose
acetate succinate, a Food and Drug Administration-approved pharmaceutical
polymer excipient, are prepared using flash nanoprecipitation. Particles
are then concentrated 50-fold by acid-induced flocculation at pH 2.0,
separation (either filtration or centrifugation), and base-induced
redispersion at pH 6.9, reducing the drying time 50-fold. Dried powders
retain enhanced lumefantrine dissolution kinetics. Filtration efficiency
is assessed, and flocculation is found to improve NP retention from
3 to 85% on a 2.5 μm filter. The kinetics of flocculation and
the fractal nature of the flocs are studied using confocal microscopy
and agree closely with a diffusion-limited aggregation model. These
results demonstrate a proof of concept that reversible flocculation
is a facile method for separating amphiphilic polyelectrolyte-coated
NPs from suspension for advanced processing.