Purpose
To recover polymer-stabilized amorphous nanoparticles from aqueous dispersions efficiently by salt flocculation and to show
that the particles redisperse and dissolve rapidly to produce highly supersaturated solutions.
Methods
Nanoparticle dispersions of itraconazole stabilized by nonionic polymers were formed by antisolvent precipitation and immediately
flocculated with sodium sulfate, filtered and dried. The size after redispersion in water, crystallinity, and morphology were
compared with those for particles produced by spray drying and rapid freezing.
Results
Particle drug loading increased to ∼90% after salt flocculation and removal of excess polymer with the filtrate. The formation
of the flocs at constant particle volume fraction led to low fractal dimensions (open flocs), which facilitated redispersion
in water to the original primary particle size of ∼300 nm. Amorphous particles, which were preserved throughout the flocculation–filtration–drying
process, dissolved to supersaturation levels of up to 14 in pH 6.8 media. In contrast, both spray dried and rapidly frozen
nanoparticle dispersions crystallized and did not produce submicron particle dispersions upon addition to water, nor high
supersaturation values.
Conclusions
Salt flocculation produces large yields of high surface area amorphous nanoparticle powders that de-aggregate and dissolve
rapidly upon redispersion in pH 6.8 media, for supersaturation levels up to 14.
KEY WORDS amorphous drug - nanoparticle filtration - nanoparticle recovery - salt flocculation - supersaturation