Capture and stimulated release of circulating tumor cells on polymer-grafted silicon nanostructures

Adv Mater. 2013 Mar 20;25(11):1547-51. doi: 10.1002/adma.201203185. Epub 2012 Dec 17.

Abstract

A platform for capture and release of circulating tumor cells is demonstrated by utilizing polymer grafted silicon nanowires. In this platform, integration of ligand-receptor recognition, nanostructure amplification, and thermal responsive polymers enables a highly efficient and selective capture of cancer cells. Subsequently, these captured cells are released upon a physical stimulation with outstanding cell viability.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylic Resins / chemistry
  • Antibodies / chemistry
  • Antibodies / immunology
  • Antigens, Neoplasm / chemistry
  • Antigens, Neoplasm / immunology
  • Biotin / chemistry
  • Biotin / metabolism
  • Cell Adhesion Molecules / chemistry
  • Cell Adhesion Molecules / immunology
  • Cell Line, Tumor
  • Cell Separation / instrumentation
  • Cell Separation / methods*
  • Epithelial Cell Adhesion Molecule
  • Humans
  • MCF-7 Cells
  • Nanowires / chemistry*
  • Neoplastic Cells, Circulating*
  • Polymers / chemistry
  • Silicon / chemistry*
  • Streptavidin / chemistry
  • Streptavidin / metabolism

Substances

  • Acrylic Resins
  • Antibodies
  • Antigens, Neoplasm
  • Cell Adhesion Molecules
  • Epithelial Cell Adhesion Molecule
  • Polymers
  • poly-N-isopropylacrylamide
  • Biotin
  • Streptavidin
  • Silicon