کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2485347 | 1114352 | 2008 | 12 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Structural, Thermodynamic, and Kinetic Aspectsof the Trimorphism of Hydrocortisone
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کلمات کلیدی
PseudopolymorphismThermogravimetric analysis - تجزیه و تحلیل ترموگرافیDesolvation - تخریبCrystal structure - ساختار کریستالیHydrocortisone - هیدروکورتیزونX-ray powder diffractometry - پراش اشعه ایکس پراشPolymorphism - پلی مورفیسمCalorimetry (DSC) - کالریمتری (DSC)Crystals - کریستال هاCocrystals - کوکریستال ها
موضوعات مرتبط
علوم پزشکی و سلامت
داروسازی، سم شناسی و علوم دارویی
اکتشاف دارویی
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
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 P212121, whereas form II and the 2-propanol solvate crystallize monoclinic in space group P21. In all the modifications the molecules are connected by intermolecular OâH···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.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Pharmaceutical Sciences - Volume 97, Issue 10, October 2008, Pages 4516-4527
Journal: Journal of Pharmaceutical Sciences - Volume 97, Issue 10, October 2008, Pages 4516-4527
نویسندگان
Viktor Suitchmezian, Inke JeÃ, Christian Näther,