Chemical kinetics and aqueous degradation pathways of a new class of synthetic ozonide antimalarials

Christine S. Perry, Susan A. Charman, Richard J. Prankerd, Francis C.K. Chiu, Yuxiang Dong, Jonathan L Vennerstrom, William N. Charman

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

Chemical stability of a new class of ozonide (1,2,4 trioxolanes) antimalarial compounds was investigated. The effects of pH, ionic strength, dielectric constant and cyclodextrin-complexation on the chemical stability and degradation product formation of selected compounds were examined. The mechanism of degradation in aqueous solution was probed using 18O-labelled water and kinetic solvent isotope effect studies. The effect of stereochemistry was investigated using selected pairs of stereoisomers. The degradation of the ozonides in aqueous solution followed apparent first-order kinetics, with no effect of ionic strength and no indication of any direct involvement of water in the degradation mechanism. All major degradation products were identified and mass balance was confirmed. Stereochemistry had a significant effect on degradation rate; trans isomers degrading approximately four-fold faster than the corresponding cis isomers. The degradation rates were essentially independent of pH above pH 2; however, an additional specific acid catalysed pathway was dominant below pH 2. Solvent dielectric constant had a significant effect on the degradation rate. It is proposed that the degradation observed in aqueous solution occurred through a concerted heterolytic scission of the central ozonide ring, with chemical substituents on the cyclohexyl ring having only a minor influence on degradation rate.

Original languageEnglish (US)
Pages (from-to)737-747
Number of pages11
JournalJournal of Pharmaceutical Sciences
Volume95
Issue number4
DOIs
StatePublished - Jan 1 2006

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Antimalarials
Reaction kinetics
Degradation
Osmolar Concentration
Stereoisomerism
Water
Cyclodextrins
Stereochemistry
Isotopes
Chemical stability
Ionic strength
Isomers
Permittivity
Acids
1,2,4-trioxane
Kinetics
Complexation

Keywords

  • 1,2,4 Trioxolane
  • Antiinfectives
  • Antimalarial
  • Chemical stability
  • Cyclodextrins
  • Degradation
  • Kinetics
  • Mass spectrometry
  • Ozonide
  • Peroxide

ASJC Scopus subject areas

  • Pharmaceutical Science

Cite this

Chemical kinetics and aqueous degradation pathways of a new class of synthetic ozonide antimalarials. / Perry, Christine S.; Charman, Susan A.; Prankerd, Richard J.; Chiu, Francis C.K.; Dong, Yuxiang; Vennerstrom, Jonathan L; Charman, William N.

In: Journal of Pharmaceutical Sciences, Vol. 95, No. 4, 01.01.2006, p. 737-747.

Research output: Contribution to journalArticle

Perry, Christine S. ; Charman, Susan A. ; Prankerd, Richard J. ; Chiu, Francis C.K. ; Dong, Yuxiang ; Vennerstrom, Jonathan L ; Charman, William N. / Chemical kinetics and aqueous degradation pathways of a new class of synthetic ozonide antimalarials. In: Journal of Pharmaceutical Sciences. 2006 ; Vol. 95, No. 4. pp. 737-747.
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