Literature DB >> 15198535

Influence of moisture on the crystal forms of niclosamide obtained from acetone and ethyl acetate.

Rahul V Manek1, William M Kolling.   

Abstract

The purpose of this study was to elucidate the formation of crystal hydrates of niclosamide and to delineate the effect of relative humidity on the crystal forms obtained from acetone and ethyl acetate. Recrystallization of niclosamide was performed in the presence and absence of moisture. Two hydrates and their corresponding anhydrates were isolated. The hydrates obtained by the process of recrystallization from acetone (Form I) and that obtained from ethyl acetate (Form II) were classified based on differences in their dehydration profile, crystal structure, shape, and morphology. Crystals obtained in the absence of moisture were unstable, and when exposed to the laboratory atmosphere transformed to their corresponding hydrates. Differential scanning calorimetry thermograms indicate that Form I changes to an anhydrate at temperatures below 100 degrees C, while Form II dehydrates in a stepwise manner above 140 degrees C. This finding was further confirmed by thermogravimetric analysis. Dehydration of Form II was accompanied by a loss of structural integrity, demonstrating that water molecules play an important role in maintaining its crystal structure. Form I, Form II, and the anhydrate of Form II showed no significant moisture sorption over the entire range of relative humidity. Although the anhydrate of Form I did not show any moisture uptake at low humidity, it converted to the monohydrate at elevated relative humidity (>95%). All forms could be interconverted depending on the solvent and humidity conditions.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15198535      PMCID: PMC2784847          DOI: 10.1208/pt050114

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  5 in total

1.  Formation of isomorphic desolvates: creating a molecular vacuum.

Authors:  G A Stephenson; E G Groleau; R L Kleemann; W Xu; D R Rigsbee
Journal:  J Pharm Sci       Date:  1998-05       Impact factor: 3.534

2.  Letter: The effect of crystal packing and defects on desolvation of hydrate crystals of caffeine and L-(--)-1,4-cyclohexadiene-1-alanine.

Authors:  S R Byrn; C T Lin
Journal:  J Am Chem Soc       Date:  1976-06-23       Impact factor: 15.419

Review 3.  Pharmaceutical applications of polymorphism.

Authors:  J Haleblian; W McCrone
Journal:  J Pharm Sci       Date:  1969-08       Impact factor: 3.534

4.  Crystal pseudopolymorphism of cephaloglycin and cephalexin.

Authors:  R R Pfeiffer; K S Yang; M A Tucker
Journal:  J Pharm Sci       Date:  1970-12       Impact factor: 3.534

5.  Role of an isomorphic desolvate in dissolution failures of an erythromycin tablet formulation.

Authors:  J F Bauer; W Dziki; J E Quick
Journal:  J Pharm Sci       Date:  1999-11       Impact factor: 3.534

  5 in total
  2 in total

1.  Cation-π interactions drive hydrophobic self-assembly and aggregation of niclosamide in water.

Authors:  Said A H Vuai; Mtabazi G Sahini; Isaac Onoka; Lucy W Kiruri; Daniel M Shadrack
Journal:  RSC Adv       Date:  2021-10-07       Impact factor: 4.036

2.  Interaction Behavior Between Niclosamide and Pepsin Determined by Spectroscopic and Docking Methods.

Authors:  Liuqi Guo; Xiaoli Ma; Jin Yan; Kailin Xu; Qing Wang; Hui Li
Journal:  J Fluoresc       Date:  2015-09-26       Impact factor: 2.217

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.