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Dive into the research topics where Viktor Suitchmezian is active.

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Featured researches published by Viktor Suitchmezian.


Journal of Pharmaceutical Sciences | 2008

Structural, Thermodynamic, and Kinetic Aspectsof the Trimorphism of Hydrocortisone

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

Research ArticlesStructural, Thermodynamic, and Kinetic Aspectsof the Trimorphism of Hydrocortisone

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

Structural, Thermodynamic, and Kinetic Aspects of the Polymorphism and Pseudopolymorphism of Prednisolone (11,17α,21-Trihydroxy-1,4-pregnadien-3,20-dion)

Viktor Suitchmezian; Inke Jess; Jan Sehnert; Lena Seyfarth; Jürgen Senker; Christian Näther


Crystal Growth & Design | 2007

Investigations on the polymorphism and pseudopolymorphism of the glucocorticoid triamcinolone : New findings for a well-known drug

Viktor Suitchmezian; Inke Jess; Christian Näther


International Journal of Pharmaceutics | 2006

Investigations on the polymorphism and pseudopolymorphism of triamcinolone diacetate.

Viktor Suitchmezian; Inke Jeß; Christian Näther


Crystal Growth & Design | 2009

Investigations on the Desolvation Reaction of Pseudopolymorphic Forms of Hydrocortisone

Viktor Suitchmezian; Inke Jess; Christian Näther


Solid State Sciences | 2006

Crystal structures and properties of two new pseudopolymorphic modifications of the glucocorticoide triamcinolone diacetate

Viktor Suitchmezian; Inke Jeß; Christian Näther


Acta Crystallographica Section E-structure Reports Online | 2007

Betamethasone-21-pentanoate methanol solvate

Viktor Suitchmezian; Inke Jess; Christian Näther


Acta Crystallographica Section E: Crystallographic Communications | 2006

Triamcinolone diacetate chloro­form solvate

Viktor Suitchmezian; Inke Jess; Christian Näther


Zeitschrift für anorganische und allgemeine Chemie | 2008

Untersuchungen zur Polymorphie von Clobetason Butyrat

Viktor Suitchmezian; Inke Jeß; Christian Näther

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Jan Sehnert

University of Bayreuth

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