posted on 2024-03-29, 13:09authored byWaleed Mustafa, Sarah Hall, Laura Huynh, Rachel Mannasse, Serter Luleburgaz, Eli Vlaisavljevich, Yasemin Yuksel Durmaz
Nanocone clusters (NCCs) have been developed as clusters
with inclusion
complexes of FDA-approved β-cyclodextrin (βCD) and perfluorocarbons
(PFC) (i.e., perfluoropentane (PFP) and perfluorohexane (PFH)) and
have shown promise in nanoparticle-mediated histotripsy (NMH) applications
owing to their lowered cavitation threshold, ease of production, and
fluorocarbon quantification. However, there is still a lack of information
on the best conditions of the synthesis of NCCs as a product that
can have a maximum determinable fluorocarbon content and maintain
the stability of the NCC during synthesis and when used as histotripsy
agents or exposed to physiological conditions. These concerns about
the stability of the clusters and the best possible formulation are
investigated in the current work. The cluster formation potential
was tested taking into consideration the nature of both PFCs and βCD
by employing different synthesis conditions in terms of solution and
environmental parameters such as concentration of solvent, stoichiometry
between βCD and PFCs, temperature, pH, solvent type, etc. The
best route of synthesis was then translated into various batch sizes
and investigated in terms of the PFC loading and yield. These studies
revealed that preparing NCCs in double-distilled water in an ice bath
at the optimized solution concentration gave the highest yields and
optimal PFC loading, as determined from gas chromatography. Furthermore,
the stability of the clusters with different stoichiometries was scrutinized
in varying concentrations, mechanical disruption times, pH levels,
and temperature conditions, showing effects on each cluster’s
particle size in dynamic light scattering, visualized in transmission
electron microscopy, and cavitation behavior in agarose gel tissue
phantoms. These studies revealed stable clusters for all formulations,
with PFH-containing NCCs emerging to be the most stable in terms of
their cluster size and bubble formation potential in histotripsy.
Finally, the shelf life of these clusters was investigated using DLS,
which revealed a stable cluster. In conclusion, NCCs have shown high
stability in terms of both synthesis, which can be replicated in gram-level
production, and the cluster itself, which can be exposed to harsher
conditions and still form stable bubbles in histotripsy.