TY - JOUR
T1 - Physical stability enhancement and pharmacokinetics of a lithium ionic cocrystal with glucose
AU - Duggirala, Naga Kiran
AU - Smith, Adam J.
AU - Wojtas, Łukasz
AU - Shytle, R. Douglas
AU - Zaworotko, Michael J.
N1 - Publisher Copyright:
© 2014 American Chemical Society.
PY - 2014/11/5
Y1 - 2014/11/5
N2 - (Chemical Equation Presented). Current lithium drugs are plagued with a narrow therapeutic window and tend to be hygroscopic. However, they remain the gold standard for treating manic episodes in bipolar disorder. In this contribution, we report a crystal engineering study aimed at the preparation and characterization of ionic cocrystals (ICCs) of lithium chloride (LIC) and lithium bromide (LIB) with glucose (GLU). The structure of LIBGLU was studied by single-crystal X-ray diffraction and found to be isostructural with related sodium chloride-glucose ICCs. The physical stability of LICGLU was compared to that of LIC at 50% RH and 25 °C and through dynamic vapor sorption analysis. The blood and brain pharmacokinetics of LICGLU were compared to those of LIC in rat models and revealed little change in performance. This study reveals that ICCs can modestly improve the solid-form stability of lithium salts without impacting in vivo performance, a step toward enabling the development of the next generation of lithium therapeutics.
AB - (Chemical Equation Presented). Current lithium drugs are plagued with a narrow therapeutic window and tend to be hygroscopic. However, they remain the gold standard for treating manic episodes in bipolar disorder. In this contribution, we report a crystal engineering study aimed at the preparation and characterization of ionic cocrystals (ICCs) of lithium chloride (LIC) and lithium bromide (LIB) with glucose (GLU). The structure of LIBGLU was studied by single-crystal X-ray diffraction and found to be isostructural with related sodium chloride-glucose ICCs. The physical stability of LICGLU was compared to that of LIC at 50% RH and 25 °C and through dynamic vapor sorption analysis. The blood and brain pharmacokinetics of LICGLU were compared to those of LIC in rat models and revealed little change in performance. This study reveals that ICCs can modestly improve the solid-form stability of lithium salts without impacting in vivo performance, a step toward enabling the development of the next generation of lithium therapeutics.
UR - http://www.scopus.com/inward/record.url?scp=84908676106&partnerID=8YFLogxK
U2 - 10.1021/cg501310d
DO - 10.1021/cg501310d
M3 - Article
AN - SCOPUS:84908676106
SN - 1528-7483
VL - 14
SP - 6135
EP - 6142
JO - Crystal Growth and Design
JF - Crystal Growth and Design
IS - 11
ER -