(149c) Modeling, Screening and PAT: The Development of a Pharmaceutical Crystallization | AIChE

(149c) Modeling, Screening and PAT: The Development of a Pharmaceutical Crystallization

Authors 

Zarkadas, D. - Presenter, Merck and Co. Inc.


Modeling, Screening and PAT: The Development of a Pharmaceutical
Crystallization.

Crystallization is
a critical unit operation in pharmaceutical processing because it determines
the crystal form, particle size distribution and purity of the drug substance.
Maintaining a consistent process upon scale-up requires an understanding of
growth and nucleation kinetics, relevant mixing time-scales, and local shear
forces in varying geometries.  The
development of a robust crystallization process for an HCl salt of Compound 1
had been particularly difficult due to polymorphism issues, purity and particle
size/shape concerns and poor bulk density in existing processes. Form control
was particularly difficult due to several undesirable hydrates and
solvates.  A previous process produced a
mixture of crystal forms, solids with bulk density was less than 0.1 g/cm3,
and required two processing steps.  The
requirements for optimal drug product formulation were crystals smaller than 20
microns, aspect ratios between 1:5 and 1:3 and maximum obtainable bulk density.

A new single-step process was developed, which made use of
synergistic solubility in a binary system, and desupersaturated
in a ternary solvent system which consistently controlled crystal form.  Single solvent screens failed to yield an
acceptable solvent, but an optimal mixture of toluene/methanol was indentified
in binary screens.  Extensive process
modeling using commercially available software and de novo algorithms enabled processing parameters for mixing, acid
addition rate, and filtration rate to be accurately estimated, leading to a
well-controlled growth-dominated crystallization.  Process performance was further optimized by
on-line particle size tracking and HPLC monitoring.  Using this comprehensive approach, a robust
crystallization was developed for a challenging salt form of Compound 1, producing
over 90% yield, consistently meeting particle size specifications, doubling
bulk density to 0.17 g/cm3, and improving purity from ~96 to >99%.