Mucoadhesive nanoparticles-based oral drug delivery systems enhance ameliorative effects of low molecular weight heparin on experimental colitis

Carbohydr Polym. 2020 Oct 15:246:116660. doi: 10.1016/j.carbpol.2020.116660. Epub 2020 Jun 17.

Abstract

Low molecular weight heparin (LMWH) is reported to have therapeutic action on ulcerative colitis (UC). To facilitate its oral administration and improve the colon-targeting property, LMWH-loaded nanoparticles (TMC-NPs and SA-TMC-NPs) are prepared and evaluated by a series of studies, including their stabilities, drug release profiles, mucosal permeation, mucoadhesion, cytotoxicities, cellular uptake profiles, anticoagulant and anti-inflammatory activities, mucosal healing properties, biosafety and ameliorative effects on experimental colitis. Consequently, oral administration of LMWH-loaded NPs for 5 days perform significant therapeutic effects on mice, which are manifested as improved body weight gains, colon length, DAI score, MPO activity and histological characteristics. Besides, SA-TMC-NPs show better colon-targeting property than TMC-NPs that is demonstrated by lower oral absorption (ATPP 38.95 s) and stronger mucoadhesion (kcps reduces 36.46 %) to inflamed colon tissues. Therefore, TMC-based NPs are proved to be as promising oral colon-targeting drug delivery systems of LMWH and has potential application in UC treatment.

Keywords: Colon targeting; Low molecular weight heparin; Mucoadhesion; Oral drug delivery; Trimethyl chitosan; Ulcerative colitis.

MeSH terms

  • Administration, Oral
  • Animals
  • Anti-Inflammatory Agents / metabolism
  • Anti-Inflammatory Agents / pharmacology*
  • Biomarkers / metabolism
  • Chitosan / chemistry*
  • Colitis / chemically induced
  • Colitis / drug therapy*
  • Colitis / metabolism
  • Colitis / pathology
  • Colon / drug effects
  • Colon / metabolism
  • Colon / pathology
  • Drug Delivery Systems / methods*
  • Drug Liberation
  • Gene Expression
  • Heparin, Low-Molecular-Weight / metabolism
  • Heparin, Low-Molecular-Weight / pharmacology*
  • Kinetics
  • Male
  • Mice
  • Nanoparticles
  • Peroxidase / genetics
  • Peroxidase / metabolism
  • RAW 264.7 Cells
  • Rats
  • Rats, Sprague-Dawley
  • Treatment Outcome
  • Trinitrobenzenesulfonic Acid / toxicity

Substances

  • Anti-Inflammatory Agents
  • Biomarkers
  • Heparin, Low-Molecular-Weight
  • N-trimethyl chitosan chloride
  • Trinitrobenzenesulfonic Acid
  • Chitosan
  • Peroxidase