Design and characterization of chitosan/citrate films as carrier for oral macromolecule delivery

Eur J Pharm Sci. 2020 Apr 15:146:105270. doi: 10.1016/j.ejps.2020.105270. Epub 2020 Feb 19.

Abstract

The oral delivery of biopharmaceuticals requires the including of absorption enhancer, protease inhibitor and a suitable carrier system. The aim of the present work was to formulate and characterize chitosan solutions/films incorporating citric acid (CA) as potential excipient in comparison to the well-known acetic acid (AA)-based films as a reference. Films were made by the solvent casting method with/without glycerol (G), propylene glycol (PG) and polyethylene glycol (PEG-400) as plasticizers. The minimum film forming temperature (MFFT) of the prepared solutions, film thickness, hardness/deformation, mucoadhesivity, moisture content, FT-IR spectra and surface free energy (SFE) were investigated. Chitosan has been reported as a safe and effective paracellular absorption enhancer for hydrophilic macromolecules, therefore there would be more rationale for incorporating CA as a solubility enhancer, a permeation enhancer and an enzyme inhibitor. CA shows good cross-linking, an ideal plasticizing property and increases both tensile strength and mucoadhesivity, thus its incorporation simplifies the formulation while improving effectiveness. We concluded that CA (3.5, 4 and 5 w/v %)-based chitosan solution could be used as a novel coating/subcoating polymer for oral macromolecule delivery, or as oral mucoadhesive films.

Keywords: Chitosan; Citric acid; FT-IR; Mechanical properties; Mucoadhesion; Plasticizer; Surface characteristics.

MeSH terms

  • Administration, Oral
  • Chitosan / chemistry*
  • Citrates / chemistry*
  • Drug Carriers*
  • Spectroscopy, Fourier Transform Infrared
  • Surface Properties

Substances

  • Citrates
  • Drug Carriers
  • Chitosan