TY - JOUR
T1 - Investigation of the Particle Growth of Fenofibrate following Antisolvent Precipitation and Freeze-Drying
AU - Tierney, Teresa B.
AU - Guo, Yina
AU - Beloshapkin, Sergey
AU - Rasmuson, Åke C.
AU - Hudson, Sarah P.
N1 - Publisher Copyright:
© 2015 American Chemical Society.
PY - 2015/10/13
Y1 - 2015/10/13
N2 - Submicron to small-micron-sized particles of the hydrophobic drug, fenofibrate, were prepared by controlled crystallization in order to influence its dissolution behavior. An antisolvent precipitation process successfully generated particles (200-300 nm) which matched the size and dissolution behavior of a commercial wet-milled formulation of the drug. Although the preparation of submicron-sized particles was straightforward, retaining their size in suspension and during isolation was a challenge. Additives were employed to temporarily stabilize the suspension, and extend the time window for isolation of the submicron particles. Precipitated particles were isolated primarily by immediate freeze-drying, but drying stresses were found to destabilize the fragile submicron system. The growth pathway of particles in suspension and during oven and freeze-drying were compared. Although the growth pathways appeared considerably different from a visual morphological perspective, an investigation of the electron diffraction patterns and the inner-particle surfaces showed that the growth pathways were the same: molecular addition by Ostwald ripening. The observed differences in the time-resolved particle morphologies were found to be a result of the freeze-drying process.
AB - Submicron to small-micron-sized particles of the hydrophobic drug, fenofibrate, were prepared by controlled crystallization in order to influence its dissolution behavior. An antisolvent precipitation process successfully generated particles (200-300 nm) which matched the size and dissolution behavior of a commercial wet-milled formulation of the drug. Although the preparation of submicron-sized particles was straightforward, retaining their size in suspension and during isolation was a challenge. Additives were employed to temporarily stabilize the suspension, and extend the time window for isolation of the submicron particles. Precipitated particles were isolated primarily by immediate freeze-drying, but drying stresses were found to destabilize the fragile submicron system. The growth pathway of particles in suspension and during oven and freeze-drying were compared. Although the growth pathways appeared considerably different from a visual morphological perspective, an investigation of the electron diffraction patterns and the inner-particle surfaces showed that the growth pathways were the same: molecular addition by Ostwald ripening. The observed differences in the time-resolved particle morphologies were found to be a result of the freeze-drying process.
UR - http://www.scopus.com/inward/record.url?scp=84946430347&partnerID=8YFLogxK
U2 - 10.1021/acs.cgd.5b00662
DO - 10.1021/acs.cgd.5b00662
M3 - Article
AN - SCOPUS:84946430347
SN - 1528-7483
VL - 15
SP - 5213
EP - 5222
JO - Crystal Growth and Design
JF - Crystal Growth and Design
IS - 11
ER -