Formation, drug-release kinetics and solution-stability of N-acetyl-Ncarboxymethyl chitosan nanoparticles as potential drug carriers

Authors

  • Helen Priscila Bassani BioPol , Chemistry Department, Federal University of Paraná ă UFPR, P.O. 19081, Curitiba (PR), 81531-980, Brazil.
  • Francine Valenga BioPol , Chemistry Department, Federal University of Paraná ă UFPR, P.O. 19081, Curitiba (PR), 81531-980, Brazil.
  • Maria Rita Sierakowski BioPol , Chemistry Department, Federal University of Paraná ă UFPR, P.O. 19081, Curitiba (PR), 81531-980, Brazil.
  • Rilton Alves de Freitas BioPol , Chemistry Department, Federal University of Paraná ă UFPR, P.O. 19081, Curitiba (PR), 81531-980, Brazil.

Keywords:

N-acetyl-N-carboxymethyl chitosan, nanoaggregation, nanoparticle, light-scattering (dynamic), stability, controlled release

Abstract

Nano-aggregates of N-acetyl-N-carboxymethyl chitosan (NCac) were studied at 0.5 mg.mL-1 using pyrene fluorimetry analysis in 0.1 mol.L-1 phosphate buffer (pH 7.4). The size and morphology of the aggregates were determined by dynamic light scattering and atomic force microscopy. The stability of the particles for periods up to 20 h in buffer was determined. Camptothecin was entrapped in the particles using various methods and the rate constant for drug release (k) was determined. Lower k values indicate strong interactions between the drug and the hydrophobic core of the polymeric micelles

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Published

2013-06-30

How to Cite

Helen Priscila Bassani, Francine Valenga, Maria Rita Sierakowski, & Rilton Alves de Freitas. (2013). Formation, drug-release kinetics and solution-stability of N-acetyl-Ncarboxymethyl chitosan nanoparticles as potential drug carriers. International Journal of Drug Delivery, 5(2), 214–223. Retrieved from https://ijdd.arjournals.org/index.php/ijdd/article/view/199

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Original Research Articles