posted on 2022-07-19, 16:07authored byDaniel B. Patience, Erwin Irdam, Nicole Madden, Liang Chen, Min He, Frederick Osei-Yeboah
Three simple methods are presented for predicting particle
size
distribution (PSD) percentiles when subjecting a pharmaceutical crystallization
wet-milled slurry to a single temperature cycle for two of Biogen’s
drug substances. The methods are (I) a mathematical manipulation of
the wet-milled PSD based on particle death during dissolution; (II)
a linear empirical model fit of product PSD percentiles as a function
of the wet-milled PSD percentiles and the amount of material dissolved;
and (III) a nonlinear model fit to the change in PSD as a function
of the amount of material dissolved and the particle surface area/volume
ratio. The three methods were verified on production scale batches.
Method II’s approach was also used for particle size control
during manufacture by implementing a temperature solved from the model
using the batch’s wet-milled particle size percentiles and
a final target size. Method III was found to be the most accurate
at prediction because it models particle surface area to volume ratio
influencing crystal dissolution and growth rates. Method II was found
to be not as accurate as method III; however, it was easily implementable
during process control at the production scale. Method I provided
the quickest estimate of final particle size using only the initial
PSD and a solubility expression. Method III was recommended for best
particle size prediction.