Single α-particle irradiation permits real-time visualization of RNF8 accumulation at DNA damaged sites.

As well as being a significant source of environmental radiation exposure, α-particles are increasingly considered for use in targeted radiation therapy. A better understanding of α-particle induced damage at the DNA scale can be achieved by following their tracks in real-time in targeted living cells. Focused α-particle microbeams can facilitate this but, due to their low energy (up to a few MeV) and limited range, α-particles detection, delivery, and follow-up observations of radiation-induced damage remain difficult.

Hydroxyl radical production induced by plasma hydrogenated nanodiamonds under X-ray irradiation.

For the first time, overproduction of hydroxyl radicals (HO˙) induced by plasma hydrogenated detonation nanodiamonds (H-NDs) under X-ray irradiation is reported. Using coumarin (COU) as a fluorescent probe, we reveal a significant increase of 40% of the HO˙ production in the presence of H-NDs (6-100 μg ml) compared with water alone. This effect is related to the negative electron affinity of the hydrogenated nanodiamonds and illustrates the ability of H-NDs to produce reactive oxygen species probably via electron emission in water under X-ray irradiation.

Nanoparticle Adhesion and Mobility in Thin Layers: Nanodiamonds As a Model.

Small size and enhanced properties of nanoparticles (NP) are great advantages toward device miniaturization. However, adhesion is essential for the reliability of such NP layer-based devices. In this work, we present some quick tests to investigate the adhesion behavior of the whole NP layer by mimicking several applicative environments: biological buffers and cells, corrosion, and microfabrication processes.