Design and evaluation of the anticancer activity of paclitaxel-loaded anisotropic-poly(lactic-co-glycolic acid) nanoparticles with PEGylated chitosan surface modifications

Int J Biol Macromol. 2020 Nov 1:162:1064-1075. doi: 10.1016/j.ijbiomac.2020.06.237. Epub 2020 Jun 26.

Abstract

This study aimed to evaluate the anticancer activity of paclitaxel-loaded poly(lactic-co-glycolic acid) (PLGA) nanoparticles (PNPs) based on their shapes and surface modifications in breast cancer cells. We hypothesized that anisotropic-PNPs (AT-PNPs) with PEGylated chitosan (CP) surface modifications and high aspect ratios exhibit higher anticancer activity than PNPs and AT-PNPs with CP surface modifications and low aspect ratios. Six types of PNPs and AT-PNPs with different shapes and surface modifications were successfully prepared. The cellular uptake and cytotoxicity of the AT-PNPs were higher than those of the PNPs, while the cellular uptake and cytotoxicity of the PNPs and AT-PNPs with CP were higher than those of the uncoated PNPs and AT-PNPs. Moreover, all the particles remained stable for 4 months. In conclusion, this study primarily described the preparation of CP-AT-PNPs, and the CP-AT-PNPs2 developed herein are expected to demonstrate promising anticancer effects in animal experiments and clinical studies.

Keywords: Anisotropic-PLGA nanoparticles; Anticancer effects; PEGylated chitosan.

MeSH terms

  • Antineoplastic Agents* / chemistry
  • Antineoplastic Agents* / pharmacokinetics
  • Antineoplastic Agents* / pharmacology
  • Chitosan* / chemistry
  • Chitosan* / pharmacokinetics
  • Chitosan* / pharmacology
  • Drug Design*
  • Drug Screening Assays, Antitumor
  • Humans
  • MCF-7 Cells
  • Nanoparticles* / chemistry
  • Nanoparticles* / therapeutic use
  • Neoplasms* / drug therapy
  • Neoplasms* / metabolism
  • Neoplasms* / pathology
  • Paclitaxel* / chemistry
  • Paclitaxel* / pharmacokinetics
  • Paclitaxel* / pharmacology
  • Polyethylene Glycols* / chemistry
  • Polyethylene Glycols* / pharmacokinetics
  • Polyethylene Glycols* / pharmacology
  • Polylactic Acid-Polyglycolic Acid Copolymer* / chemistry
  • Polylactic Acid-Polyglycolic Acid Copolymer* / pharmacokinetics
  • Polylactic Acid-Polyglycolic Acid Copolymer* / pharmacology

Substances

  • Antineoplastic Agents
  • Polylactic Acid-Polyglycolic Acid Copolymer
  • Polyethylene Glycols
  • Chitosan
  • Paclitaxel