Abstract

The treatment depth of existing photodynamic therapy (PDT) is limited because of the absorption of visible excitation light in biological tissue. It can be augmented by means of upconversion nanoparticles (UCNPs) transforming deep-penetrating near-infrared (NIR) light to visible light, exciting PDT drugs. We report here a facile strategy to assemble such PDT nanocomposites functionalized for cancer targeting, based on coating of the UCNPs with a silica layer encapsulating the Rose Bengal photosensitizer and bioconjugation to antibodies through a bifunctional fusion protein consisting of a solid-binding peptide linker genetically fused to Streptococcus Protein G′. The fusion protein (Linker-Protein G) mediates the functionalization of silica-coated UCNPs with cancer cell antibodies, allowing for specific target recognition and delivery. The resulting nanocomposites were shown to target cancer cells specifically, generate intracellular reactive oxygen species under 980 nm excitation, and induce NIR-triggered phototoxicity to suppress cancer cell growth in vitro.

Original languageEnglish
Pages (from-to)11945-11953
Number of pages9
JournalACS Applied Materials and Interfaces
Volume8
Issue number19
DOIs
Publication statusPublished - 18 May 2016

Keywords

  • luminescence resonance energy transfer
  • photodynamic therapy
  • solid-binding peptides
  • targeted imaging
  • upconversion nanoparticles

Fingerprint Dive into the research topics of 'Facile assembly of functional upconversion nanoparticles for targeted cancer imaging and photodynamic therapy'. Together they form a unique fingerprint.

  • Cite this