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Directly thiolated modification onto the surface of detonation nanodiamonds
Journal article   Peer reviewed

Directly thiolated modification onto the surface of detonation nanodiamonds

Ming-Hua Hsu, Hong Chuang, Fong-Yu Cheng, Ying-Pei Huang, Chien-Chung Han, Jiun-Yu Chen, Su-Chin Huang, Jen-Kun Chen, Dian-Syue Wu, Hsueh-Liang Chu, …
ACS Applied Materials and Interfaces, Vol.6(10), pp.7198-7203
28/05/2014

Abstract

detonation nanodiamond functionalized nanodiamond nanodiamond surface modification thiolated thiolated nanodiamond
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. © 2014 American Chemical Society.

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