Formulation and Evaluation of Novel Solid Lipid Microparticles for the Sustained Release of Ofloxacin

Pharm Nanotechnol. 2017;5(4):329-341. doi: 10.2174/2211738506666171226121720.

Abstract

Objective: The aim of this study was to prepare solid lipid microparticles (SLM) with incorporated ofloxacin, suitable for oral delivery.

Methods: Ofloxacin-loaded SLM were prepared using stearic acid and chloroform as lipid matrix and Tween-80 as surfactant, by high shear homogenization technique and followed by lyophilization. The physiochemical characterization of SLMs were investigated by scanning electron microscopy, transmission electron microscopy, zeta potential, zone of inhibition, in-vitro study, ex-vivo study and stability study.

Results: The result demonstrated that the entrapment efficiency, particle size and zeta potential of microparticles were 86.02%, 203.7nm and -32.68mv, respectively. The in-vitro and ex-vivo studies showed sustained release of drug from formulation.

Conclusion: These results indicate that SLM might be a promising delivery system to enhance the pharmacological activity of ofloxacin.

Keywords: High shear homogenization technique; Tween-80; ofloxacin; solid lipid microparticles; stearic acid.

MeSH terms

  • Anti-Bacterial Agents / chemistry*
  • Anti-Bacterial Agents / pharmacology
  • Chemistry, Pharmaceutical
  • Delayed-Action Preparations
  • Drug Carriers / chemistry*
  • Drug Liberation
  • Drug Stability
  • Excipients / chemistry
  • Humans
  • Lipids / chemistry*
  • Microbial Sensitivity Tests
  • Microspheres
  • Ofloxacin / chemistry*
  • Ofloxacin / pharmacology
  • Particle Size
  • Polysorbates / chemistry
  • Stearic Acids / chemistry

Substances

  • Anti-Bacterial Agents
  • Delayed-Action Preparations
  • Drug Carriers
  • Excipients
  • Lipids
  • Polysorbates
  • Stearic Acids
  • stearic acid
  • Ofloxacin