Design and evaluation of a novel nanoparticulate-based formulation encapsulating a HIP complex of lysozyme

Pharm Dev Technol. 2013 May-Jun;18(3):752-9. doi: 10.3109/10837450.2012.737806. Epub 2012 Nov 9.

Abstract

Formulation development of protein therapeutics using polymeric nanoparticles has found very little success in recent years. Major formulation challenges include rapid denaturation, susceptibility to lose bioactivity in presence of organic solvents and poor encapsulation in polymeric matrix. In the present study, we have prepared hydrophobic ion pairing (HIP) complex of lysozyme, a model protein, using dextran sulfate (DS) as a complexing polymer. We have optimized the process of formation and dissociation of HIP complex between lysozyme and DS. The effect of HIP complexation on enzymatic activity of lysozyme was also studied. Nanoparticles were prepared and characterized using spontaneous emulsion solvent diffusion method. Furthermore, we have also investigated release of lysozyme from nanoparticles along with its enzymatic activity. Results of this study indicate that nanoparticles can sustain the release of lysozyme without compromising its enzymatic activity. HIP complexation using a polymer may also be employed to formulate sustained release dosage forms of other macromolecules with enhanced encapsulation efficiency.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Chemistry, Pharmaceutical / methods*
  • Drug Carriers / administration & dosage
  • Drug Carriers / chemical synthesis*
  • Drug Design*
  • Drug Evaluation, Preclinical / methods
  • Drug Stability
  • Hydrophobic and Hydrophilic Interactions*
  • Macromolecular Substances / administration & dosage
  • Macromolecular Substances / chemical synthesis
  • Micrococcus / drug effects
  • Micrococcus / enzymology
  • Muramidase / administration & dosage
  • Muramidase / chemical synthesis*
  • Nanoparticles / administration & dosage
  • Nanoparticles / chemistry*
  • Static Electricity
  • Thermodynamics

Substances

  • Drug Carriers
  • Macromolecular Substances
  • Muramidase