Targeted delivery of panitumumab-scaffold bosutinib-encapsulated polycaprolactone nanoparticles for EGFR-overexpressed colorectal cancer

Nanomedicine (Lond). 2023 Apr;18(9):713-741. doi: 10.2217/nnm-2022-0240. Epub 2023 Jun 13.

Abstract

Aims: Panitumumab (anti-Erb)-conjugated polycaprolactone (PCL) nanoparticles loaded with bosutinib (BTNB) were used to develop a targeted drug-delivery system for colon cancer cells. Materials & methods: Using carbodiimide coupling, anti-Erb was conjugated to BTNB-loaded PCL nanoparticles. Dynamic light scattering, scanning electron microscopy, transmission electron microscopy, Fourier-transform infrared spectroscopy, differential scanning calorimetry, x-ray diffraction and thermogravimetric analysis were used to analyze nanoparticles. Results: According to in vitro studies, anti-Erb-BTNB-PCL nanoparticles inhibited HCT116 cells more than BTNB alone. Cell arrest at different phases was examined for apoptotic potential. An in vivo efficacy study showed that anti-Erb-BTNB-PCL nanoparticles could target tumors selectively. Conclusion: Anti-Erb-conjugated BTNB nanoparticles could specifically target colon cancer.

Keywords: CD44; HCT116; apoptosis; bosutinib; cell cycle analysis; colon cancer; polycaprolactone; scanning electron microscopy; thermogravimetric analysis; transmission electron microscopy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Colonic Neoplasms*
  • Colorectal Neoplasms* / drug therapy
  • ErbB Receptors
  • Humans
  • Nanoparticles* / chemistry
  • Panitumumab
  • Polyesters / chemistry

Substances

  • polycaprolactone
  • Panitumumab
  • bosutinib
  • Polyesters
  • ErbB Receptors
  • EGFR protein, human