Diethanolamine-modified pectin based core-shell composites as dual working gastroretentive drug-cargo

Int J Biol Macromol. 2018 Mar:108:1053-1062. doi: 10.1016/j.ijbiomac.2017.11.019. Epub 2017 Nov 6.

Abstract

The current study aimed at developing diethonolamine-modified high-methoxyl pectin (DMP)-alginate (ALG) based core-shell composites for controlled intragastric delivery of metformin HCl (MFM) by combined approach of floating and bioadhesion. DMP with degree of amidation of 48.72% was initially accomplished and characterized by FTIR, DSC and XRD analyses. MFM-loaded core matrices were then fabricated by ionotropic gelation technique employing zinc acetate as cross-linker. The core matrices were further coated by fenugreek gum (FG)-ALG gel membrane via diffusion-controlled interfacial complexation method. Various formulations demonstrated excellent drug encapsulation efficiency (DEE, 51-70%) and sustained drug eluting behavior (Q8h, 72-96%), which were extremely influenced by polymer-blend (ALG:DMP) ratios, low density additives (olive oil/magnesium stearate) and FG-ALG coating inclusion. The drug release profile of the core-shell matrices (F-7) was best fitted in zero-order kinetic model with case-II transport driven mechanism. It also portrayed outstanding gastroretentive characteristics. Moreover, the composites were analyzed for surface morphology, drug-excipients compatibility, thermal behavior and drug crystallinity. Thus, the developed composites are appropriate for controlled stomach-specific delivery of MFM for type 2 diabetes management.

Keywords: Alginate; Fenugreek gum; High-methoxyl pectin.

MeSH terms

  • Adhesiveness
  • Alginates / chemistry
  • Diffusion
  • Drug Carriers / chemistry*
  • Drug Liberation
  • Ethanolamines / chemistry*
  • Gastric Mucosa / metabolism*
  • Metformin / chemistry
  • Metformin / metabolism
  • Pectins / chemistry*

Substances

  • Alginates
  • Drug Carriers
  • Ethanolamines
  • Pectins
  • Metformin
  • diethanolamine