کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8994343 | 1114390 | 2005 | 15 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Structural analysis of polymorphism and solvation in tranilast
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کلمات کلیدی
tranilastSolid state NMR - NMR جامداتThermal analysis - آنالیز حرارتیX‐ray diffractometry - اشعه ماوراء بنفشcrystallography - بلورنگاری، بلورشناسی یا کریستالوگرافیPhysical characterization - خصوصیات فیزیکیFTIR - طیف سنج مادون قرمزRaman spectroscopy - طیف سنجی رامانConformational polymorphism - پلی مورفیسم سازگاریHydrogen bonding - پیوند هیدروژنی
موضوعات مرتبط
علوم پزشکی و سلامت
داروسازی، سم شناسی و علوم دارویی
اکتشاف دارویی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Five polymorphic forms of tranilast were characterized by thermal, diffractometric, and spectroscopic techniques. The crystal structures of the most stable anhydrous form (Form I), a chloroform solvate, and a dichloromethane solvate were determined from singleâcrystal Xâray analysis. Two additional anhydrous forms of tranilast (Forms II and III) were also studied, but were not amenable to SCXRD. All five forms were also analyzed using solidâstate nuclear magnetic resonance, Fourier transform infrared, and Fourier transformâRaman spectroscopy, and thermal methods. From the trends observed in the crystal structures and the spectral data, some conclusions can be made about hydrogen bonding, molecular conformation, and crystal packing differences in the polymorphs and solvates. Form II was found to be a spectroscopically distinctive polymorph that is probably missing an important intramolecular hydrogen bond coupled with a conformational change. In contrast, Form III was found to be more similar to the crystallographically characterized forms, and is more likely a packing and hydrogenâbonding polymorph with a weakened intermolecular hydrogenâbonding interaction relative to the other forms. From a pharmaceutical development perspective, it is shown that although the anhydrous forms of tranilast have similar thermal properties, they can be reliably distinguished by spectroscopic methods. © 2005 WileyâLiss, Inc. and the American Pharmacists Association J Pharm Sci 94:651-665, 2005
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Pharmaceutical Sciences - Volume 94, Issue 3, March 2005, Pages 651-665
Journal: Journal of Pharmaceutical Sciences - Volume 94, Issue 3, March 2005, Pages 651-665
نویسندگان
Frederick G. Vogt, Dawn E. Cohen, Joshua D. Bowman, Grant P. Spoors, Gary E. Zuber, Gudrun A. Trescher, Philip C. Dell'Orco, Lee M. Katrincic, Charles W. Debrosse, R. Curtis Haltiwanger,