Preparation of letrozole dispersed pHEMA/AAm-g-LDPE drug release system: In-vitro release kinetics for the treatment of endometriosis

Colloids Surf B Biointerfaces. 2019 Jul 1:179:445-452. doi: 10.1016/j.colsurfb.2019.04.014. Epub 2019 Apr 8.

Abstract

This paper focuses on the development of a drug delivery system for systemically controlled release of a poorly soluble drug, letrozole. The work meticulously describes the preparation and characterizations of 2-hydroxyethyl methacrylate (HEMA) polymerization onto hydrophilic acrylamide grafted low-density polyethylene (AAm-g-LDPE) surface for targeted drug release system. The surface morphology and thickness measurement of coated pHEMA layer were measured using scanning electron microscopy (SEM). The swelling study was done in deionized (DI) water and simulated uterine fluid (SUF, pH = 7.6). In vitro release of letrozole from the system was performed in SUF. Further, the release kinetics of letrozole from the system was studied using different mathematical models. The results, suggest that the rate of drug release can be altered by varying the concentrations of cross-linker in pHEMA. The optimized sample released 72% drug at the end of 72 h of measurement.

Keywords: Drug release system; Endometriosis; Letrozole; pHEMA/AAm-g-LDPE.

MeSH terms

  • Acrylamide / chemistry*
  • Animals
  • Cell Death / drug effects
  • Cell Survival / drug effects
  • Drug Liberation*
  • Endometriosis / drug therapy*
  • Female
  • Kinetics
  • Letrozole / pharmacology
  • Letrozole / therapeutic use*
  • Mice
  • NIH 3T3 Cells
  • Polyethylene / chemistry*
  • Polyhydroxyethyl Methacrylate / chemistry*
  • Polymerization
  • Porosity

Substances

  • Acrylamide
  • Polyhydroxyethyl Methacrylate
  • Letrozole
  • Polyethylene