Directly thiolated modification onto the surface of detonation nanodiamonds

ACS Appl Mater Interfaces. 2014 May 28;6(10):7198-203. doi: 10.1021/am500324z. Epub 2014 May 6.

Abstract

An efficient method for modifying the surface of detonation nanodiamonds (5 and 100 nm) with thiol groups (-SH) by using an organic chemistry strategy is presented herein. Thiolated nanodiamonds were characterized by spectroscopic techniques, and the atomic percentage of sulfur was analyzed by elemental analysis and X-ray photoelectron spectroscopy. The conjugation between thiolated nanodiamonds and gold nanoparticles was elucidated by transmission electron microscopy and UV-vis spectrometry. Moreover, the material did not show significant cytotoxicity to the human lung carcinoma cell line and may prospectively be applied in bioconjugated technology. The new method that we elucidated may significantly improve the approach to surface modification of detonation nanodiamonds and build up a new platform for the application of nanodiamonds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Gold / chemistry
  • Humans
  • Metal Nanoparticles / chemistry
  • Metal Nanoparticles / toxicity
  • Microscopy, Electron, Transmission
  • Nanodiamonds / chemistry*
  • Nanodiamonds / toxicity
  • Particle Size
  • Photoelectron Spectroscopy
  • Sulfhydryl Compounds / chemistry*

Substances

  • Nanodiamonds
  • Sulfhydryl Compounds
  • Gold