Literature DB >> 10675701

Preparation and characterisation of a new insoluble polymorphic form of glibenclamide.

A Panagopoulou-Kaplani1, S Malamataris.   

Abstract

A crystalline form of glibenclamide, with higher melting point (218 degrees C) and lower solubility in simulated gastric and intestinal fluids, was arisen during an attempt to elucidate transitional phases by melting, cooling and reheating. The new form was obtained from the glassy state, by applying sublimation at 130-160 degrees C and was characterised by differential scanning calorimetry (DSC), infrared (IR) spectroscopy, scanning electron microscopy (SEM), hot-stage microscopy (HSM), X-ray powder diffraction (XRD) and solubility studies. Formation of the new crystal form is considered as reason of reduction in dissolution and bioavailability of tablets.

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Year:  2000        PMID: 10675701     DOI: 10.1016/s0378-5173(99)00401-9

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  3 in total

1.  The role of molecular structure in the crystal polymorphism of local anesthetic drugs: crystal polymorphism of local anesthetic drugs, part X.

Authors:  Andrea C Schmidt
Journal:  Pharm Res       Date:  2005-11-16       Impact factor: 4.200

2.  Correlation of Solubility Thermodynamics of Glibenclamide with Recrystallization and In Vitro Release Profile.

Authors:  Ravi Maharjan; Junoh Jeong; Ripesh Bhujel; Min-Soo Kim; Hyo-Kyung Han; Nam Ah Kim; Seong Hoon Jeong
Journal:  Molecules       Date:  2022-02-18       Impact factor: 4.411

3.  Preparation and crystallographic analysis of gliclazide polymorphs.

Authors:  A J Rajamma; S B Sateesha; M K Narode; V R S S Prashanth; A M Karthik
Journal:  Indian J Pharm Sci       Date:  2015 Jan-Feb       Impact factor: 0.975

  3 in total

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