Literature DB >> 19540323

The effect of temperature and moisture on the amorphous-to-crystalline transformation of stavudine.

Schalk Strydom1, Wilna Liebenberg, Lian Yu, Melgardt de Villiers.   

Abstract

Stavudine is a nucleoside reverse transcriptase inhibitor active against HIV, and is known to exist in two polymorphic forms designated as forms I and II, and a hydrate form III. An amorphous solid of stavudine was successfully prepared and characterized during this investigation. A comprehensive evaluation of the stability of this amorphous solid showed that the amorphous solid transforms to either form II (anhydrous) or form III (hydrate) when exposed to temperature, in the absence or presence of moisture, respectively. The amorphous-to-hydrate transformation occurred at relatively low RH (>32%) and led to the formation of crystal aggregates of the hydrated form. Steady state growth rate analyses also showed that the amorphous-to-crystalline transformation occurs at a greater rate in the presence of moisture, compared to the transformation at the same temperature in a dry environment. Crystal growth studies showed that it is possible to stabilize the amorphous solid of stavudine against crystal transformations in the absence of moisture by coating it with poly(methyl methacrylate). However, this polymer coating could not prevent crystal growth from the amorphous solid during exposure to moisture.

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Year:  2009        PMID: 19540323     DOI: 10.1016/j.ijpharm.2009.06.012

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


  3 in total

1.  Influence of microenvironment pH, humidity, and temperature on the stability of polymorphic and amorphous forms of clopidogrel bisulfate.

Authors:  Dhara K Raijada; Saranjit Singh; Arvind K Bansal
Journal:  AAPS PharmSciTech       Date:  2010-01-29       Impact factor: 3.246

2.  Physicochemical properties of amorphous roxithromycin prepared by quench cooling of the melt or desolvation of a chloroform solvate.

Authors:  Marique Aucamp; Wilna Liebenberg; Schalk J Strydom; Elsa C van Tonder; Melgardt M de Villiers
Journal:  AAPS PharmSciTech       Date:  2012-03-06       Impact factor: 3.246

3.  Disintegration mediated controlled release supersaturating solid dispersion formulation of an insoluble drug: design, development, optimization, and in vitro evaluation.

Authors:  Sanjay Verma; Varma S Rudraraju
Journal:  AAPS PharmSciTech       Date:  2014-09-05       Impact factor: 3.246

  3 in total

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