Inclusion complex of amiodarone hydrochloride with cyclodextrins: preparation, characterization and dissolution rate evaluation

Authors

  • Alexandre Machado Rubim Franciscan University Center; Laboratory Drug Quality Control
  • Jaqueline Bandeira Rubenick Federal University of Santa Maria; Postgraduate Program in Pharmaceutical Sciences
  • Marcela Maurer Franciscan University Center; Laboratory Drug Quality Control
  • Luciane Varini Laporta Franciscan University Center; Laboratory Drug Quality Control
  • Clarice Madalena Bueno Rolim Federal University of Santa Maria; Postgraduate Program in Pharmaceutical Sciences

DOI:

https://doi.org/10.1590/s2175-97902017000216083

Keywords:

Amiodarone HCl/evaluation, Amiodarone HCl/solubility, Cyclodextrins/inclusion complexes, Cyclodextrins /thermodynamic studies, Dissolution rate

Abstract

This study aimed to improve the water solubility of amiodarone hydrochloride (AMH) via inclusion complexes with β-cyclodextrin, methyl-β-cyclodextrin and 2-hydroxypropyl-β-cyclodextrin. Inclusion complexes were developed by physical mixture, coevaporation, spray-drying and freeze-drying. Solid state analysis was performed using X-ray powder diffraction, differential scanning calorimetry and scanning electronic microscopy. Thermodynamic studies demonstrate that the inclusion complexes of drug into different cyclodextrins were an exothermic process that occurred spontaneously. Water solubility and drug dissolution rates were significantly increased after the formation of inclusion complexes with the cyclodextrins evaluated in relation to the physical mixture and pure drug. The present study provides useful information for the potential application of complexation with amiodarone HCl. This may be a good strategy for the development of solid pharmaceutical dosage forms.

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Published

2017-01-01

Issue

Section

Articles

How to Cite

Inclusion complex of amiodarone hydrochloride with cyclodextrins: preparation, characterization and dissolution rate evaluation. (2017). Brazilian Journal of Pharmaceutical Sciences, 53(2), e16083-. https://doi.org/10.1590/s2175-97902017000216083