Charged nanoparticles as protein delivery systems

A feasibility study using lysozyme as model protein

Cuifang Cai, Udo Bakowsky, Erik Rytting, Andreas K. Schaper, Thomas Kissel

Research output: Contribution to journalArticle

74 Citations (Scopus)

Abstract

The aim of this study was to investigate the feasibility of negatively charged nano-carriers (nanoparticles), consisting of polymer blends of poly(lactide-co-glycolide) (PLGA) and poly(styrene-co-4-styrene-sulfonate) (PSS), to improve the loading capacity and release properties of a positively charged model protein, lysozyme, through an adsorption process. Nanoparticles were prepared by a solvent displacement method and characterized in terms of size, ζ-potential, morphology, as well as loading capacity of model protein lysozyme. Morphology of these particles was investigated using transmission electron microscopy (TEM), scanning electron microscopy (SEM) and atomic force microscopy (AFM). The loading capacity of lysozyme was evaluated as a function of polymer blend ratio, protein concentration, pH, and ionic strength; in vitro release profiles were also studied. The results show that negatively charged nanoparticles were obtained using polymer blends of PLGA and PSS, characterized by increased net negative surface charge with increasing ratios of PSS. Moreover, protein loading capacity increased as function of PSS/PLGA ratio. Increased pH facilitated the adsorption process and improved the loading capacity. Maximum loading efficiency was achieved at salt concentrations of 50 mM. In vitro release of lysozyme from the polymer blend nanoparticles was dependent on drug loading and full bioactivity of lysozyme was preserved throughout the process. These findings suggest that this is a feasible method to prepare nanoparticles with high surface charge density to efficiently adsorb oppositely charged protein through electrostatic interactions.

Original languageEnglish (US)
Pages (from-to)31-42
Number of pages12
JournalEuropean Journal of Pharmaceutics and Biopharmaceutics
Volume69
Issue number1
DOIs
StatePublished - May 2008
Externally publishedYes

Fingerprint

Feasibility Studies
Muramidase
Nanoparticles
Polymers
Styrene
Proteins
Adsorption
Polyglactin 910
Atomic Force Microscopy
Static Electricity
Transmission Electron Microscopy
Electron Scanning Microscopy
Osmolar Concentration
Salts
Pharmaceutical Preparations
polylactic acid-polyglycolic acid copolymer
In Vitro Techniques

Keywords

  • Charge density
  • Charged nanoparticles
  • Electrostatic interaction
  • Lysozyme
  • Protein delivery

ASJC Scopus subject areas

  • Biotechnology
  • Pharmaceutical Science

Cite this

Charged nanoparticles as protein delivery systems : A feasibility study using lysozyme as model protein. / Cai, Cuifang; Bakowsky, Udo; Rytting, Erik; Schaper, Andreas K.; Kissel, Thomas.

In: European Journal of Pharmaceutics and Biopharmaceutics, Vol. 69, No. 1, 05.2008, p. 31-42.

Research output: Contribution to journalArticle

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