Preparation and Solid-State Characterization of Nonstoichiometric Cocrystals of a Phosphodiesterase-IV Inhibitor and l-Tartaric Acid

Evidence for a series of nonstoichiometric, isostructural, cocrystalline complexes of L-883555, a phosphodiesterase-IV inhibitor, and l-tartaric acid with stoichiometries ranging from 0.3:1 to 0.9:1 is reported here. The free base form of this compound had insufficient bioavailability and, hence, could not be developed as a candidate for safety assessment studies. Several l-tartaric acid complexes were produced during an attempted salt-formation process, with the objective of increasing the bioavailability. It was found that the amount of l-tartaric acid incorporated in the cocrystalline complexes could be controlled by adjusting the acid:base ratio in the reaction mixture without accompanying proton transfer between acid and base. Spectroscopic techniques were employed to locate the site of intermolecular interaction between the acid and base as the N-oxide group in the base and the carboxylic acid of l-tartaric acid. Thermal and spectroscopic analysis of the degradation behavior for the various complexe...

[1]  W. F. Claussen,et al.  Suggested Structures of Water in Inert Gas Hydrates , 1951 .

[2]  Susan J. Bogdanowich,et al.  Spectral Methods for Determination of Water , 1988 .

[3]  J. Ripmeester Crystalline β-cyclodextrin hydrate is non-stoichiometric with 10.5–12 waters per cyclodextrin molecule , 1993 .

[4]  Kiyotaka Sato Crystallization behaviour of fats and lipids — a review , 2001 .

[5]  K. Miki,et al.  Inclusion Crystals of Cholic Acid and Cholanamide with Alcohols: Importance of Hydrogen Bond "Double Hooks" , 1994 .

[6]  W. Saenger,et al.  Crystalline β-cyclodextrin · 12 H2O reversibly dehydrates to β-cyclodextrin · 10.5 H2O under ambient conditions☆ , 1992 .

[7]  C. Vicent,et al.  Molecular Recognition in the Solid State: Hydrogen-Bonding Control of Molecular Aggregation , 1994 .

[8]  Kiyotaka Sato,et al.  Crystallization kinetics of polymorphic forms of a molecular compound constructed by SOS (1,3-distearoyl-2-oleoyl-sn-glycerol) and SSO (1,2-distearoyl-3-oleoyl-rac-glycerol) , 2002 .

[9]  Kiyotaka Sato,et al.  Phase behavior of mixed systems of SOS and OSO , 1992 .

[10]  Orn Almarsson,et al.  Crystal engineering of novel cocrystals of a triazole drug with 1,4-dicarboxylic acids. , 2003, Journal of the American Chemical Society.

[11]  T. Steiner,et al.  Crystalline .beta.-Cyclodextrin Hydrate at Various Humidities: Fast, Continuous, and Reversible Dehydration Studied by X-ray Diffraction , 1994 .

[12]  A. Beatty,et al.  Organic Assemblies of 2-pyridones with Dicarboxylic Acids , 2000 .

[13]  C. Kennard,et al.  Molecular Cocrystals of Carboxylic Acids. XXXIII ⁄ The Crystal Structure of the 1 : 1 Adduct of Indole-2-carboxylic Acid with 5-Nitroquinoline , 1998 .

[14]  W. Tong,et al.  In situ salt screening--a useful technique for discovery support and preformulation studies. , 1998, Pharmaceutical development and technology.