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Published on: January 22, 2015
Gum ghatti-chitosan polyelectrolyte nanoparticles: preparation and characterization
Shelly1, Munish Ahuja, Ashok Kumar
1Drug Delivery Research Laboratory, Department of Pharmaceutical Sciences, Guru Jambheshwar University of Science and Technology, Hisar 125 001, India.
International Journal of Biological Macromolecules
|August 9, 2013
Summary
Gum ghatti and chitosan form optimized polyelectrolyte nanoparticles for ofloxacin delivery. These nanoparticles show comparable antibacterial activity and sustained drug release via diffusion.
Area of Science:
- Materials Science
- Pharmaceutical Sciences
- Biotechnology
Background:
- Gum ghatti and chitosan are natural polymers with potential for drug delivery applications.
- Polyelectrolyte nanoparticles offer advantages in drug encapsulation and controlled release.
- Ofloxacin is a broad-spectrum antibiotic requiring effective delivery systems.
Purpose of the Study:
- To optimize the formulation of gum ghatti-chitosan polyelectrolyte nanoparticles for ofloxacin.
- To investigate the impact of polymer and drug concentrations on nanoparticle characteristics.
- To evaluate the antibacterial efficacy and drug release kinetics of the prepared nanoparticles.
Main Methods:
- Central composite experimental design was employed to optimize nanoparticle formulation.
- Particle size and entrapment efficiency were key parameters analyzed.
- Antibacterial activity and in vitro drug release studies were conducted.
Main Results:
- Optimized concentrations yielded nanoparticles of 121.6 nm size with 94.49% ofloxacin entrapment.
- The prepared polyelectrolyte nanoparticles exhibited antibacterial activity comparable to ofloxacin solution.
- Drug release followed Higuchi's square-root kinetics, indicating diffusion-controlled release.
Conclusions:
- Gum ghatti and chitosan can be effectively combined to create stable polyelectrolyte nanoparticles for ofloxacin.
- The optimized formulation demonstrates potential for effective antibiotic delivery.
- The diffusion-controlled release mechanism suggests suitability for sustained drug delivery applications.

