Magnetic mesoporous nanospheres anchored with LyP-1 as an efficient pancreatic cancer probe

Biomaterials. 2017 Jan:115:9-18. doi: 10.1016/j.biomaterials.2016.11.006. Epub 2016 Nov 11.

Abstract

Immobilization of a ligand that selectively interacts with cancer cells to nanomaterials can enhance their diagnostic and therapeutic efficiency. In this study, we firstly demonstrate the high expression of receptor for cyclic nine-amino acid peptide LyP-1 (Cys-Gly-Asn-Lys-Arg-Thr-Arg-Gly-Cys) in both mouse and human pancreatic cancer. Based on these findings, sub-50 nm multifunctional superparamagnetic mesoporous nanospheres with surface modified with LyP-1 are rationally designed. Theses nanospheres have a core of silica-protected magnetite nanoparticle and a shell of FITC-labeled mesoporous silica, and they are able to specifically recognize and conjugate with the pancreatic cancer cell in vitro, as verified by the combined techniques of fluorescent imaging and T2 weight magnetic resonance imaging. After systematic administration, these LyP-1 immobilized nanospheres are found to actively target to mouse orthotopic xenograft of pancreatic cancer, which opens up the door for applications in early probing and diagnosis of pancreatic cancer by the multimodal imaging.

Keywords: LyP-1; Magnetic resonance imaging; Molecular imaging; Pancreatic cancer; Superparamagnetic nanospheres.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Contrast Media / chemistry
  • Female
  • Magnetite Nanoparticles / chemistry*
  • Magnetite Nanoparticles / ultrastructure
  • Mice
  • Mice, Inbred BALB C
  • Molecular Probe Techniques*
  • Molecular Probes / chemistry
  • Multimodal Imaging / methods
  • Nanocapsules / chemistry
  • Nanocapsules / ultrastructure
  • Nanoconjugates / chemistry
  • Nanoconjugates / ultrastructure
  • Nanospheres / chemistry*
  • Nanospheres / ultrastructure
  • Pancreatic Neoplasms / diagnostic imaging*
  • Pancreatic Neoplasms / metabolism*
  • Pancreatic Neoplasms / pathology
  • Peptides, Cyclic / chemistry
  • Peptides, Cyclic / pharmacokinetics*
  • Porosity
  • Reproducibility of Results
  • Sensitivity and Specificity

Substances

  • Contrast Media
  • LyP-1 peptide
  • Magnetite Nanoparticles
  • Molecular Probes
  • Nanocapsules
  • Nanoconjugates
  • Peptides, Cyclic