Literature DB >> 18365695

Polymorphism and pseudopolymorphism of acyclovir.

Young Taek Sohn1, Sang Hee Kim.   

Abstract

Four crystal modifications of acyclovir were isolated by recrystallization and characterized by powder X-ray diffractometry, differential scanning calorimetry, and thermogravimetric analysis. It was confirmed that Form 3 is a hydrate and Form 4 is an acetic acid solvate. The dissolution patterns of three crystal forms of acyclovir were studied in water at 37 +/- 0.5 degrees C, 90 rpm for 120 minutes. The amount dissolved at 120 minutes was highest for Form 1, followed by Form 2 and Form 3. After storage of 25 hours at 0% RH (silica gel, 20 degrees C) Form 3 was transformed to Form 2.

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Year:  2008        PMID: 18365695     DOI: 10.1007/s12272-001-1146-x

Source DB:  PubMed          Journal:  Arch Pharm Res        ISSN: 0253-6269            Impact factor:   4.946


  3 in total

1.  Polymorphs and hydrates of acyclovir.

Authors:  Katie M Lutker; Rosalynn Quiñones; Jiadi Xu; Ayyalusamy Ramamoorthy; Adam J Matzger
Journal:  J Pharm Sci       Date:  2010-11-04       Impact factor: 3.534

2.  Preparation of intravenous stealthy acyclovir nanoparticles with increased mean residence time.

Authors:  Amany O Kamel; Gehanne A S Awad; Ahmed S Geneidi; Nahed D Mortada
Journal:  AAPS PharmSciTech       Date:  2009-12-01       Impact factor: 3.246

3.  Conformational analysis, molecular structure and solid state simulation of the antiviral drug acyclovir (zovirax) using density functional theory methods.

Authors:  Margarita Clara Alvarez-Ros; Mauricio Alcolea Palafox
Journal:  Pharmaceuticals (Basel)       Date:  2014-06-06
  3 in total

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