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Formulation and characterization of amphotericin B–chitosan–dextran sulfate nanoparticles
- Source :
- International Journal of Pharmaceutics. 329:142-149
- Publication Year :
- 2007
- Publisher :
- Elsevier BV, 2007.
-
Abstract
- A new nanoparticulate delivery system for amphotericin B (AmB) has been developed by means of the polyelectrolyte complexation technique. Two opposite charged polymers were used to form nanoparticles through electrostatic interaction, chitosan (CH) as a positively charged polymer and dextran sulfate (DS) as a polymer with a negative charge, together with zinc sulfate as a crosslinking and hardening agent. The AmB nanoparticles obtained possessed a mean particle size of 600-800 nm with a polydispersity index of 0.2, indicating a narrow size distribution. The measured zeta potential of the nanoparticle surface was approximately -32 mV indicating a strong negative charge at the particle's surface. Scanning electron microscopy revealed spherical particles with a smooth surface. Drug association efficacy of up to 65% was achieved. Dissolution studies demonstrated a fast release behavior suggesting that AmB exhibits only moderate interaction with the weakly crosslinked polymers of the nanoparticles. Although, electronic absorbance spectra showed that the aggregation state of AmB was modified within the nanoparticles, a reduction of nephrotoxicity was observed in an in vivo renal toxicity study.
- Subjects :
- Male
chemistry.chemical_classification
Chitosan
Mice, Inbred ICR
Chromatography
Chemistry
Dextran Sulfate
Dispersity
technology, industry, and agriculture
Pharmaceutical Science
Nanoparticle
Polymer
Polyelectrolyte
Mice
chemistry.chemical_compound
Drug Delivery Systems
Nanomedicine
Dextran
Chemical engineering
Amphotericin B
Zeta potential
Animals
Nanoparticles
Particle size
Microparticle
Subjects
Details
- ISSN :
- 03785173
- Volume :
- 329
- Database :
- OpenAIRE
- Journal :
- International Journal of Pharmaceutics
- Accession number :
- edsair.doi.dedup.....66fd4bfc340069d90d17d4443442054f
- Full Text :
- https://doi.org/10.1016/j.ijpharm.2006.08.013