Literature DB >> 8123714

Solid-state NMR and IR for the analysis of pharmaceutical solids: polymorphs of fosinopril sodium.

H G Brittain1, K R Morris, D E Bugay, A B Thakur, A T Serajuddin.   

Abstract

The two polymorphic modifications of fosinopril sodium have been characterized as to their differences in melting behaviour, powder X-ray diffraction patterns, Fourier transform infrared spectra (FTIR), and solid-state 31P- and 13C-NMR spectra. The polymorphs were found to be enantiotropically related based upon melting point, heat of fusion, and solution mediated transformation data. Analysis of the solid-state FTIR and 13C-NMR data indicated that the environment of the acetal side chain of fosinopril sodium differed in two polymorphs, and that there might be cis-trans isomerization about the C6-N peptide bond. These conformational differences are postulated as the origin of the observed polymorphism.

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Year:  1993        PMID: 8123714     DOI: 10.1016/0731-7085(93)80083-d

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  2 in total

1.  Modeling and monitoring of polymorphic transformations during the drying phase of wet granulation.

Authors:  Tiffani D Davis; Garnet E Peck; Joseph G Stowell; Kenneth R Morris; Stephen R Byrn
Journal:  Pharm Res       Date:  2004-05       Impact factor: 4.200

2.  Influence of processing-induced phase transformations on the dissolution of theophylline tablets.

Authors:  Smita Debnath; Raj Suryanarayanan
Journal:  AAPS PharmSciTech       Date:  2004-02-12       Impact factor: 3.246

  2 in total

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