Diselenide-crosslinked carboxymethyl chitosan nanoparticles for doxorubicin delivery: Preparation and in vivo evaluation

Carbohydr Polym. 2022 Sep 15:292:119699. doi: 10.1016/j.carbpol.2022.119699. Epub 2022 Jun 6.

Abstract

In this paper, we report a simple approach to fabricate diselenide-crosslinked carboxymethyl chitosan nanoparticles (DSe-CMC NPs) for doxorubicin (DOX) delivery, with disulfide analogs (DS-CMC NPs) as control. DS-CMC NPs and DSe-CMC NPs featured a spherical morphology and narrow size distribution with the average size about 200 nm. Carboxymethyl chitosan (CMC) as the starting material not only improved the biocompatibility of the nanocarriers but also enhanced physiological stability. Due to electrostatic interactions between DOX and CMC, the nanoparticles had high drug encapsulation efficiency (∼25 %). The nanoparticles disintegration and drug release were accelerated by the cleavage of diselenide bonds through oxidation by H2O2 or reduction by GSH. In vitro cell experiments revealed that DOX-loaded DSe-CMC NPs possessed the highest drug accumulation and cytotoxicity in tumor cells. Moreover, DOX-loaded DSe-CMC NPs performed the enhanced growth inhibition in vivo than that of DS-CMC NPs. Thus, the diselenide-crosslinked nanoparticles possess great potentials for DOX delivery.

Keywords: Carboxymethyl chitosan; Diselenide; Disulfide; Drug delivery; Nanoparticles.

MeSH terms

  • Chitosan* / chemistry
  • Cytotoxins / chemistry
  • Cytotoxins / toxicity
  • Doxorubicin / chemistry
  • Doxorubicin / pharmacology
  • Drug Carriers / chemistry
  • Drug Carriers / toxicity
  • Drug Delivery Systems
  • Drug Liberation
  • Hydrogen Peroxide
  • Nanoparticles* / chemistry
  • Oxidation-Reduction

Substances

  • Cytotoxins
  • Drug Carriers
  • Doxorubicin
  • Chitosan
  • Hydrogen Peroxide