Improving lithium therapeutics by crystal engineering of novel ionic cocrystals

Mol Pharm. 2013 Dec 2;10(12):4728-38. doi: 10.1021/mp400571a. Epub 2013 Nov 18.

Abstract

Current United States Food and Drug Administration (FDA)-approved lithium salts are plagued with a narrow therapeutic window. Recent attempts to find alternative drugs have identified new chemical entities, but lithium's polypharmacological mechanisms for treating neuropsychiatric disorders are highly debated and are not yet matched. Thus, re-engineering current lithium solid forms in order to optimize performance represents a low cost and low risk approach to the desired therapeutic outcome. In this contribution, we employed a crystal engineering strategy to synthesize the first ionic cocrystals (ICCs) of lithium salts with organic anions. We are unaware of any previous studies that have assessed the biological efficacy of any ICCs, and encouragingly we found that the new speciation did not negatively affect established bioactivities of lithium. We also observed that lithium ICCs exhibit modulated pharmacokinetics compared to lithium carbonate. Indeed, the studies detailed herein represent an important advancement in a crystal engineering approach to a new generation of lithium therapeutics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / drug effects
  • Cell Line
  • Cell Line, Tumor
  • Glycogen Synthase Kinase 3 / metabolism
  • Glycogen Synthase Kinase 3 beta
  • Hippocampus / drug effects
  • Hippocampus / metabolism
  • Ions / chemistry*
  • Ions / pharmacokinetics
  • Ions / pharmacology*
  • Lithium / chemistry*
  • Lithium / pharmacokinetics
  • Lithium / pharmacology*
  • Mice
  • Microglia / drug effects
  • Microglia / metabolism
  • Neural Stem Cells / drug effects
  • Neural Stem Cells / metabolism
  • Nitric Oxide / metabolism
  • Phosphorylation / drug effects
  • Rats
  • Technology, Pharmaceutical / methods

Substances

  • Ions
  • Nitric Oxide
  • Lithium
  • Glycogen Synthase Kinase 3 beta
  • Glycogen Synthase Kinase 3