Crystal Growth & Design · 2008 · 264 citations · 13 references
Molecular BiologyOrganic ChemistryNew PolymorphChemistryCbz-sac IiChemical BiologyMedicinal ChemistryStructure ElucidationMechanism Of ActionPharmacologyOrganometallic PolymerFunctional SelectivityNatural SciencesCarbamazepine CocrystalsX-ray DiffractionCoordination PolymerMedicineCarbohydrate-protein InteractionDrug Discovery
Cocrystals of carbamazepine with nicotinamide and saccharin are shown to be polymorphic. Two polymorphs of carbamazepine-nicotinamide (CBZ-NCT) cocrystals and two polymorphs of carbamazepine-saccharin (CBZ-SAC) cocrystals were grown from solution in the presence of polymer heteronuclei. The two CBZ-NCT polymorphs, CBZ-NCT I and a polymer nucleated (PN) form of CBZ-NCT, were characterized by Raman spectroscopy and powder X-ray diffraction. CBZ-SAC II, a new polymorph, was found to be in the monoclinic space group C2/c with a = 35.72 Å, b = 6.84 Å, c = 16.11 Å, and β = 98.03°. The unique feature of CBZ-SAC II is the formation of a heterosynthon between the carbamazepine and saccharin. These results are notable because CBZ-NCT and CBZ-SAC are among the most widely studied pharmaceutical cocrystals.
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Adam L. Grzesiak, Meidong Lang, Ki‐Bum Kim et al. · Journal of Pharmaceutical Sciences · 2003 · 504 citations · Full text
Reaction Crystallization of Pharmaceutical Molecular Complexes
Naír Rodríguez‐Hornedo, Sarah J. Nehm, Kurt F. Seefeldt et al. · Molecular Pharmaceutics · 2006 · 310 citations