Taste masking and rheology improvement of drug complexed with beta-cyclodextrin and hydroxypropyl-β-cyclodextrin by hot-melt extrusion

Carbohydr Polym. 2018 Apr 1:185:19-26. doi: 10.1016/j.carbpol.2018.01.011. Epub 2018 Jan 4.

Abstract

This study aimed to mask fluconazole (FLU) taste and improve its rheological properties by an efficient process of cyclodextrin complexation. For this, hot-melt extrusion (HME) was used to obtain extrudates composed of FLU, hydroxypropylcellulose, and one of two different cyclodextrins (β-cyclodextrin or hydroxypropyl-β-cyclodextrin) maintaining the drug:cyclodextrin molar ratio at 1:0.3 or 1:0.2, respectively. Samples were characterized by physicochemical tests, palatability using e-tongue and antifungal assays. Drug stability was preserved after HME, according to spectroscopy test (correlation coefficient >0.9) and HPLC-assay (100-107%). Flowability was improved in HME systems with compressibility of <12%. Similarly, floodability exhibited significant enhancement (dispersibility <10%). Whereas extrudates of FLU containing only the polymeric matrix led to a slow drug dissolution efficiency (18.6%) and a partial drug taste masking; extrudates containing cyclodextrin accelerated FLU dissolution (dissolution efficiency approx. 30%) and provided a complete drug taste masking. Moreover, HME process could produce drug complexes with high complexation efficiency and preserve its antifungal activity.

Keywords: Antifungal assay; Cyclodextrin; E-tongue; Hot-melt extrusion; Palatability; Rheology.

MeSH terms

  • Antifungal Agents / chemistry*
  • Antifungal Agents / pharmacology
  • Candida / drug effects
  • Electronic Nose
  • Fluconazole / chemistry*
  • Fluconazole / pharmacology
  • Rheology
  • Solubility
  • Taste*
  • beta-Cyclodextrins / chemistry*
  • beta-Cyclodextrins / pharmacology

Substances

  • Antifungal Agents
  • beta-Cyclodextrins
  • Fluconazole
  • betadex