Viktor Suitchmezian
University of Kiel
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Featured researches published by Viktor Suitchmezian.
Journal of Pharmaceutical Sciences | 2008
Viktor Suitchmezian; Inke Jeß; Christian Näther
Hydrocortisone was investigated for polymorphism and pseudopolymorphism and three different polymorphic modifications (I-III) and one 2-propanol solvate were found. Forms I and III crystallize in the orthorhombic space group P2(1)2(1)2(1), whereas form II and the 2-propanol solvate crystallize monoclinic in space group P2(1). In all the modifications the molecules are connected by intermolecular O--H...O hydrogen bonding. In the 2-propanol solvate, channels are formed in which the solvent molecules are embedded. Solvent-mediated conversion experiments reveal that the commercially available form I represents the thermodynamically most stable modification at room temperature, whereas forms II and III are metastable. On heating, form III transforms into form II in an endothermic reaction, which shows that an enantiotropic relationship exists between these forms. Form I exhibits the highest melting point and the highest heat of fusion and thus represents the thermodynamically most stable form over the whole temperature range. DSC measurements indicate that form I behaves monotropic to forms II and III. Desolvation of the 2-propanol solvate at higher temperatures results in a transformation into form II, whereas the removal of 2-propanol at room temperature and in vacuum reduced pressure leads to the formation of form III.
Journal of Pharmaceutical Sciences | 2008
Viktor Suitchmezian; Inke Jeß; Christian Näther
Hydrocortisone was investigated for polymorphism and pseudopolymorphism and three different polymorphic modifications (I-III) and one 2-propanol solvate were found. Forms I and III crystallize in the orthorhombic space group P2(1)2(1)2(1), whereas form II and the 2-propanol solvate crystallize monoclinic in space group P2(1). In all the modifications the molecules are connected by intermolecular O--H...O hydrogen bonding. In the 2-propanol solvate, channels are formed in which the solvent molecules are embedded. Solvent-mediated conversion experiments reveal that the commercially available form I represents the thermodynamically most stable modification at room temperature, whereas forms II and III are metastable. On heating, form III transforms into form II in an endothermic reaction, which shows that an enantiotropic relationship exists between these forms. Form I exhibits the highest melting point and the highest heat of fusion and thus represents the thermodynamically most stable form over the whole temperature range. DSC measurements indicate that form I behaves monotropic to forms II and III. Desolvation of the 2-propanol solvate at higher temperatures results in a transformation into form II, whereas the removal of 2-propanol at room temperature and in vacuum reduced pressure leads to the formation of form III.
Crystal Growth & Design | 2008
Viktor Suitchmezian; Inke Jess; Jan Sehnert; Lena Seyfarth; Jürgen Senker; Christian Näther
Crystal Growth & Design | 2007
Viktor Suitchmezian; Inke Jess; Christian Näther
International Journal of Pharmaceutics | 2006
Viktor Suitchmezian; Inke Jeß; Christian Näther
Crystal Growth & Design | 2009
Viktor Suitchmezian; Inke Jess; Christian Näther
Solid State Sciences | 2006
Viktor Suitchmezian; Inke Jeß; Christian Näther
Acta Crystallographica Section E-structure Reports Online | 2007
Viktor Suitchmezian; Inke Jess; Christian Näther
Acta Crystallographica Section E: Crystallographic Communications | 2006
Viktor Suitchmezian; Inke Jess; Christian Näther
Zeitschrift für anorganische und allgemeine Chemie | 2008
Viktor Suitchmezian; Inke Jeß; Christian Näther