Related Experiment Video
Updated: Jul 27, 2026

12:48
PLGA Nanoparticles Formed by Single- or Double-emulsion with Vitamin E-TPGS
Published on: December 27, 2013
66.4K
Long term multiple sclerosis drug delivery using dendritic polyglycerol flower-like microspheres
Priscila Veloso da Silva1, Alvaro Antonio Alencar de Queiroz2
1Materials for Engineering/Biomaterials (CAPES), Physics and Chemistry Institute (IFQ)/Federal University of Itajubá (UNIFEI), Itajubá, Brazil.
Journal of Biomaterials Science. Polymer Edition
|October 15, 2019
Summary
This study developed dendritic polyglycerol microspheres (DPGlyM) for multiple sclerosis treatment, successfully loading dimethyl fumarate (DMF) and curcumin (CUR). The DPGlyM system demonstrated sustained drug release and good biocompatibility.
Area of Science:
- Materials Science
- Nanotechnology
- Pharmacology
Background:
- Multiple sclerosis (MS) is a chronic neurological disease.
- Current treatments for MS have limitations.
- Novel drug delivery systems are needed to improve therapeutic efficacy and patient outcomes.
Purpose of the Study:
- To produce and characterize dendritic polyglycerol microspheres (DPGlyM) as a novel carrier for dimethyl fumarate (DMF) and curcumin (CUR).
- To evaluate the potential of DPGlyM loaded with DMF and CUR for the treatment of multiple sclerosis.
Main Methods:
- Molecular docking (MD) was employed to predict drug-carrier interactions.
- Scanning electron microscopy (SEM) was used to determine microsphere morphology and size.
- Encapsulation and loading efficiencies, zeta potential, cytotoxicity, hemocompatibility, and in vitro drug release were assessed.
Main Results:
- DPGlyM showed spontaneous interactions with DMF and CUR, with high encapsulation (94.1%) and loading (65.3%) efficiencies.
- Microspheres (30-40 μm) formed stable suspensions and exhibited no cytotoxicity or hemolysis.
- In vitro release studies demonstrated sustained release of DMF and CUR over 5 days, following super case II transport kinetics.
Conclusions:
- DPGlyM is a promising biocompatible carrier for DMF and CUR.
- This novel drug delivery system offers sustained release, potentially improving multiple sclerosis treatment.
- Further in vivo studies are warranted to confirm therapeutic efficacy.

