Design & Synthesis of A Few Pharmaceutical Cocrystals/Salts by Crystal Engineering Approach and Study of Their Physicochemical Properties
Date
2018
Authors
N, Sunil Kumar
Journal Title
Journal ISSN
Volume Title
Publisher
National Institute of Technology Karnataka, Surathkal
Abstract
The pharmaceutical cocrystal of an active pharmaceutical ingredient with
GRAS or non-GRAS compounds offers an opportunity to develop a new drug product
with improved physicochemical properties. Pharmaceutical cocrystal exhibits better
physicochemical properties such as solubility, stability, dissolution, melting point,
crystal habit, compressibility, friability etc. without altering the biological activity of
drug compounds. In the last two decades, numerous research activities have been
carried out to develop the new drug products of BCS Class II and BCS Class IV drug
ingredients by cocrystallization techniques. The result showed remarkable increment in
the solubility and dissolution rate of BCS Class II and IV drug ingredients.
In this context, a series of active pharmaceutical ingredients have been chosen
for the present work which is having poor or high aqueous solubility and permeability.
All the active ingredients chosen in the study are screened for salt/cocrystallization
experiments by crystal engineering approach with various GRAS and non-GRAS
compounds. Solution crystallization and liquid-assisted grinding approach are followed
for the cocrystallization experiments. The newly synthesized salts/cocrystals were
characterized by various spectroscopic (FT-IR, NMR, and UV-Vis), thermal (DSC and
TGA), and PXRD techniques. The crystal structure of the synthesized salts/cocrystals
were determined by SC-XRD techniques. Aqueous solubility (equilibrium solubility)
was measured for the cocrystal/salt of BCS class II drug by UV-Vis spectroscopy and
compared the results with API alone. In all the five series, the stability of the
synthesized salts/cocrystals were evaluated. In some cases, hygroscopicity study at
accelerated humidity condition was performed to demonstrate the non-hygroscopicity
of the synthesized cocrystal/salt. In few cases, isostructurality of the synthesized
salt/cocrystal was described based on the SC-XRD analysis. Further, in one chapter
DFT calculations were performed for the synthesized salt/cocrystal to support the
crystal structure data determined from the SC-XRD analysis.
Description
Keywords
Department of Chemistry, Crystal Engineering, Pharmaceutical cocrystal, cocrystal, salts, supramolecular synthon, isostructurality, stability