Comparative assessment of in vitro/in vivo performances of orodispersible electrospun and casting films containing rizatriptan benzoate

Eur J Pharm Biopharm. 2020 Sep:154:283-289. doi: 10.1016/j.ejpb.2020.06.023. Epub 2020 Jul 4.

Abstract

The electrospinning process is a promising approach to produce various drug-loaded orodispersible films (ODFs) with a rapid onset of their actions. However, there is only limited number of studies comparing the pharmacological performances of electrospun ODFs (eODFs) with traditional casting films (CFs). In this study, rizatriptan benzoate (RB), a pain relieving agent was formulated with PVP and PVA into ODFs using electrospinning and casting methods. The ODFs were subsequently characterized with respect to their morphology, solid state properties and mechanical characteristics. The uniformity of the dosage units, disintegration behavior and dissolution patterns of the ODFs were also evaluated prior to the pharmacokinetic study. The obtained CFs and eODFs were semitransparent and white in appearance, respectively. The scanning electron microscopy revealed that the eODFs contained nanoporous structure, while the CFs showed no observable pores. RB was amorphously dispersed in both these films without drug-polymer interactions. The uniformity of dosage units for both eODFs and CFs was complied with European Pharmacopeia. As compared to the CFs, the eODFs were more flexible and lesser rigid in nature and showed faster disintegration and dissolution rates. In addition, the eODFs exhibited a higher bioavailability with a shorter Tmax relative to the CFs and commercial RB tablets. This study demonstrated that eODFs were superior to CFs with respect to in vivo pharmacological effects, which could be attributed to the submicron structure of eODFs obtained through the electrospinning process.

Keywords: Casting films; Electrospinning; Nanofibers; Orodispersible films; Rizatriptan benzoate.

Publication types

  • Comparative Study

MeSH terms

  • Administration, Oral
  • Animals
  • Chemistry, Pharmaceutical / methods*
  • Drug Carriers / administration & dosage
  • Drug Carriers / chemistry
  • Drug Carriers / metabolism*
  • Drug Delivery Systems / methods*
  • Drug Liberation*
  • Male
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Serotonin Receptor Agonists / administration & dosage
  • Serotonin Receptor Agonists / chemistry
  • Serotonin Receptor Agonists / metabolism
  • Triazoles / administration & dosage
  • Triazoles / chemistry
  • Triazoles / metabolism*
  • Tryptamines / administration & dosage
  • Tryptamines / chemistry
  • Tryptamines / metabolism*
  • X-Ray Diffraction / methods

Substances

  • Drug Carriers
  • Serotonin Receptor Agonists
  • Triazoles
  • Tryptamines
  • rizatriptan