Alpha-fetoprotein mediated targeting of polymeric nanoparticles to treat solid tumors

Nanomedicine (Lond). 2022 Aug;17(18):1217-1235. doi: 10.2217/nnm-2022-0097. Epub 2022 Sep 22.

Abstract

Background: Serious side effects caused by paclitaxel formulation, containing toxic solubilizer Cremophor® EL, and its nonspecific accumulation greatly limit clinical paclitaxel application. Aim: To design paclitaxel-loaded copolymer of lactic and glycolic acids nanoparticles decorated with alpha-fetoprotein third domain (rAFP3d-NP) to increase paclitaxel safety profile. Methods: rAFP3d-NP was obtained via carbodiimide technique. Results: The particles were characterized with high paclitaxel loading content of 5% and size of 280 nm. rAFP3d-NP revealed biphasic profile with 67% release of paclitaxel during 220 h. Increased area under the curveinf and mean residence time values after rAFP3d-NP administration confirmed prolonged blood circulation compared with paclitaxel. rAFP3d-NP demonstrated significant tumor growth inhibition at 4T1 and SKOV-3 models. Conclusion: rAFP3d-NP is a promising delivery system for paclitaxel and can be applied similarly for delivery of other hydrophobic drugs.

Keywords: PLGA; alpha-fetoprotein; antitumor efficacy; nanoparticles; paclitaxel; pharmacokinetics.

MeSH terms

  • Cell Line, Tumor
  • Drug Carriers / chemistry
  • Humans
  • Nanoparticles* / chemistry
  • Neoplasms* / drug therapy
  • Paclitaxel / chemistry
  • Polylactic Acid-Polyglycolic Acid Copolymer / chemistry
  • Polymers / chemistry
  • alpha-Fetoproteins

Substances

  • Polylactic Acid-Polyglycolic Acid Copolymer
  • alpha-Fetoproteins
  • Paclitaxel
  • Polymers
  • Drug Carriers