Experimental characterization and micromechanical modeling of the elastic response of the human humerus under bending impact.

This paper investigates the characterization and numerical modeling of the elastic behavior of the human humerus bone using a recently developed micromechanical approach coupled to nanoindentation measurements. At first, standard three-point bending experiments were conducted under low static loading, using several humerus diaphysis in order to identify the apparent elastic modulus of the bone in static regime. Then, a drop tower impact experiment was used on the same set of humerus diaphysis specimens, in order to assess the elastic modulus in dynamic regime. These measurements will be used as reference bases for comparison purpose. The originality of this work, lies in the coupling between a two-phase micromechanical approach based on Mori-Tanaka homogenization scheme for cylindrical voids and nanoindentation measurements of the elastic modulus of the bone matrix phase. This model has been implemented using a user defined material subroutine VMAT in ABAQUS© Explicit code. The bone mechanical response prediction using the proposed methodology was validated against previous standard experimental data. Finally, it was shown that the numerical predictions are consistent with the physical measurements obtained on human humerus via the good estimation of the ultimate impact load.

Eosin-mediated synthesis of polymer coatings combining photodynamic inactivation and antimicrobial properties.

Polymer coatings exhibiting photodynamic bacterial inactivation properties have been successfully engineered. Such coatings were obtained by photoinduced crosslinking of a PEG-diacrylate monomer associated with the eosin Y dye which was used as both a radical photoinitiator and an antibacterial agent. A dual curing process was followed by combining compatible and solvent-free polymerization mechanisms, i.e. Aza-Michael reaction and free-radical polymerization in the presence of amines. The kinetics evolution of the photopolymerization process was followed using in situ Fourier transform infrared spectroscopy, allowing for the elucidation of the underlying mechanistic pathways. The influence of eosin Y and amines on the thermal and mechanical properties of the films was evidenced and discussed in terms of crosslinking chemistry. The antibacterial properties of the coatings against two different strains (Escherichia coli and Staphylococcus aureus) were evaluated on short and long terms, revealing that eosin confers both photodynamic inactivation and antimicrobial properties to the films. These coatings are therefore particularly promising for disposable medical devices.

Nanobiotechnology and its role in the development of new analytical devices.

Physical methods of molecule observation and manipulation will prove useful, not only as research tools for investigating biomolecular structure and behavior, but also for the creation of nanostructures. Supramolecular and self-assembling structures are able to generate nanostructures, with many such systems being of biological origin. They form the interface between nanotechnology and biotechnology. Whereas biotechnological processes usually involve populations of cells or molecules, nanotechnological methods operate at the level of individual molecule manipulation. This article considers what advances have been made through cross-fertilisation between nanotechnology and biotechnology to develop for the next millennium new analytical tools at the microscale, using nanostructures as the sensitive part and with the ability to detect individual molecules.

Under buffer SFM observation of immunospecies adsorbed on a cyano grafted silicon substrate.

Scanning force microscopy (SFM) in contact mode and in liquid medium has been employed to study immunospecies layers adsorbed on a silicon wafer. The silicon wafer has been grafted with a cyanosilane monolayer in order to create a surface with strong adhesive properties which prevent proteins being swept by the scan of the SFM tip. The force curves reveal that the adhesive force has been increased by a factor six without roughness modification (< 1 nm). After the incubation of the surface in a monoclonal antibody (mouse anti-human alpha-fetoprotein IgG) solution, SFM surface images suggest an homogeneous layer composed by ellipsoidal objects (40-60 nm in diameter, 6-13 nm in height). The substrate was moreover incubated in an antigenic solution (human alpha-fetoprotein): SFM images reveal that proteins have been added onto the antibody layer.