Fluorescent single-digit detonation nanodiamond for biomedical applications.

Detonation nanodiamonds (DNDs) have emerged as promising candidates for a variety of biomedical applications, thanks to different physicochemical and biological properties, such as small size and reactive surfaces. In this study, we propose carbon dot decorated single digit (4-5 nm diameter) primary particles of detonation nanodiamond as promising fluorescent probes. Due to their intrinsic fluorescence originating from tiny (1-2 atomic layer thickness) carbonaceous structures on their surfaces, they exhibit brightness suitable for in vitro imaging. Moreover, this material offers a unique, cost effective alternative to sub-10 nm nanodiamonds containing fluorescent nitrogen-vacancy color centers, which have not yet been produced at large scale. In this paper, carbon dot decorated nanodiamonds are characterized by several analytical techniques. In addition, the efficient cellular uptake and fluorescence of these particles are observed in vitro on MDA-MD-231 breast cancer cells by means of confocal imaging. Finally, the in vivo biocompatibility of carbon dot decorated nanodiamonds is demonstrated in zebrafish during the development. Our results indicate the potential of single-digit detonation nanodiamonds as biocompatible fluorescent probes. This unique material will find application in correlative light and electron microscopy, where small sized NDs can be attached to antibodies to act as a suitable dual marker for intracellular correlative microscopy of biomolecules.

Surface Analysis of Nanocomplexes by X-ray Photoelectron Spectroscopy (XPS).

Self-assembled nanocomplexes composed of individual molecules that spontaneously connect via noncovalent interactions have recently emerged as versatile alternatives to conventional controlled drug delivery systems because of their unique bioinspired properties (responsiveness, dynamics, etc.). Characterization of such nanocomplexes typically includes their size distribution, surface charge, morphology, drug entrapment efficiency, and verification of the coexistence of labeled components within the nanocomplexes using a colocalization study. Less common is the direct examination of the molecular interactions between the different components in the coassembled nanocomplex, especially in nanocomplexes composed of hygroscopic components, because convenient methods are still lacking. Here, we present a detailed experimental protocol for determining the surface composition and the chemical bonds by X-ray photoelectron spectroscopy (XPS) after drying the deposit hygroscopic sample overnight under UHV. We applied this method to investigate the surface chemistry of binary Ca2+-siRNA nanocomplexes and ternary nanocomplexes of hyaluronan-sulfate (HAS)-Ca2+-siRNA, deposited on a wafer. Notably, we showed that the protocol can be implemented to study the surface composition and interactions of the deposited nanocomplexes with a traditional XPS instrument, and it requires only a relatively small amount of the nanocomplex suspension.

Structure and Bonding in Chlorine-Functionalized Nanodiamond--Nuclear Magnetic Resonance and X-Ray Photoelectron Spectroscopy Study.

We report on investigation of detonation nanodiamond annealed at 800C°in chlorine atmosphere by means of 1H, 13C and 35Cl nuclear magnetic resonance and X-ray photoelectron spectroscopy. The results of these methods are found to be consistent with each other and evidence formation of chlorine-carbon groups and sp2 carbon shell on the nanodiamond surface. The data obtained provide detailed information about the structure and bonding in this diamond nanoparticle. Interaction of nuclear spins with unpaired electron spins of dangling bonds results in fast 13C nuclear spin-lattice relaxation.

Nanostructure synthesis at the solid-water interface: spontaneous assembly and chemical transformations of tellurium nanorods.

Bottom-up synthesis offers novel routes to obtain nanostructures for nanotechnology applications. Most self-assembly processes are carried out in three dimensions (i.e. solutions); however, the large majority of nanostructure-based devices function in two dimensions (i.e. on surfaces). Accordingly, an essential and often cumbersome step in bottom-up applications involves harvesting and transferring the synthesized nanostructures from the solution onto target surfaces. We demonstrate a simple strategy for the synthesis and chemical transformation of tellurium nanorods, which is carried out directly at the solid-solution interface. The technique involves binding the nanorod precursors onto amine-functionalized surfaces, followed by in situ crystallization/oxidation. We show that the surface-anchored tellurium nanorods can be further transformed in situ into Ag2Te, Cu2Te, and SERS-active Au-Te nanorods. This new approach offers a way to construct functional nanostructures directly on surfaces.

Transparent, conductive gold nanowire networks assembled from soluble Au thiocyanate.

Extremely long gold nanowires spontaneously assemble in a water-dimethylsulfoxide (DMSO) solution of Au(SCN)4(-). The Au nanowires were crystalline, exhibited a very high aspect ratio, and, importantly, were produced without co-addition of reducing agents. Transparent conductive films were formed by surface deposition of the nanowires and plasma treatment.