In vivo imaging and biodistribution of near infrared dye loaded brain-metastatic-breast-cancer-cell-membrane coated polymeric nanoparticles

Nanotechnology. 2019 Jun 28;30(26):265101. doi: 10.1088/1361-6528/ab0f46. Epub 2019 Mar 13.

Abstract

Brain metastatic breast cancer is challenging to treat due to the presence of the blood-brain barrier (BBB) and a lack of ability to target precisely. Most drugs fail to cross the BBB limiting their effectiveness. To combat this problem, a brain metastatic breast cancer cell (MDA-MB-831) membrane-coated polymeric nanoparticle (CCNP) was synthesized. The small size (∼70 nm) and anionic surface charge (-20 mV) achieved during formulation allowed for high penetration and retention in the brain when compared to the PEGylated polymeric nanoparticle alone (mPEG-PLGA or NP). Doxorubicin-loaded CCNP showed high preferential cytotoxicity in vitro. Live (4-120 h) and ex vivo near-infrared imaging in nude mice showed extended circulation and retention of CCNP compared to uncoated nanoparticles. These data indicate that drug/dye-loaded CCNPs demonstrate excellent potential for cancer theranostics of brain metastatic breast tumors.

MeSH terms

  • Animals
  • Blood-Brain Barrier
  • Brain Neoplasms / drug therapy*
  • Brain Neoplasms / secondary*
  • Breast Neoplasms / drug therapy*
  • Cell Line, Tumor
  • Doxorubicin / administration & dosage*
  • Doxorubicin / chemistry
  • Doxorubicin / pharmacokinetics
  • Female
  • Humans
  • Mice
  • Mice, Nude
  • Nanoconjugates / chemistry
  • Particle Size
  • Polymers / chemistry*
  • Spectroscopy, Near-Infrared
  • Theranostic Nanomedicine
  • Tissue Distribution
  • Xenograft Model Antitumor Assays

Substances

  • Nanoconjugates
  • Polymers
  • Doxorubicin