No abstract

Blast waves generated by improvised explosive devices (IEDs) cause traumatic brain injury (TBI) in soldiers and civilians. In vivo animal models that use shock tubes are extensively used in laboratories to simulate field conditions, to identify mechanisms of injury, and to develop injury thresholds. In this article, we place rats in different locations along the length of the shock tube (i.e., inside, outside, and near the exit), to examine the role of animal placement location (APL) in the biomechanical load experienced by the animal. We found that the biomechanical load on the brain and internal organs in the thoracic cavity (lungs and heart) varied significantly depending on the APL. When the specimen is positioned outside, organs in the thoracic cavity experience a higher pressure for a longer duration, in contrast to APL inside the shock tube. This in turn will possibly alter the injury type, severity, and lethality. We found that the optimal APL is where the Friedlander waveform is first formed inside the shock tube. Once the optimal APL was determined, the effect of the incident blast intensity on the surface and intracranial pressure was measured and analyzed. Noticeably, surface and intracranial pressure increases linearly with the incident peak overpressures, though surface pressures are significantly higher than the other two. Further, we developed and validated an anatomically accurate finite element model of the rat head. With this model, we determined that the main pathway of pressure transmission to the brain was through the skull and not through the snout; however, the snout plays a secondary role in diffracting the incoming blast wave towards the skull.

Stereolithography (SLA) is an interesting manufacturing technology to overcome limitations of commercially available particulated biomaterials dedicated to intra-oral bone regeneration applications. The purpose of this study was to evaluate the in vitro and in vivo biocompatibility and osteoinductive properties of two calcium-phosphate (CaP)-based scaffolds manufactured by SLA three-dimensional (3D) printing. Pellets and macro-porous scaffolds were manufactured in pure hydroxyapatite (HA) and in biphasic CaP (HA:60-TCP:40). Physico-chemical characterization was performed using micro X-ray fluorescence, scanning electron microscopy (SEM), optical interferometry, and microtomography (μCT) analyses. Osteoblast-like MG-63 cells were used to evaluate the biocompatibility of the pellets in vitro with MTS assay and the cell morphology and growth characterized by SEM and DAPI-actin staining showed similar early behavior. For in vivo biocompatibility, newly formed bone and biodegradability of the experimental scaffolds were evaluated in a subperiosteal cranial rat model using μCT and descriptive histology. The histological analysis has not indicated evidences of inflammation but highlighted close contacts between newly formed bone and the experimental biomaterials revealing an excellent scaffold osseointegration. This study emphasizes the relevance of SLA 3D printing of CaP-based biomaterials for intra-oral bone regeneration even if manufacturing accuracy has to be improved and further experiments using biomimetic scaffolds should be conducted. K E Y W O R D Sbone regeneration, bone scaffold, histology, microtomography, stereolithography

Aegagropiles are round-shaped conglomerations of Posidonia oceanica debris commonly found along the coasts of the Mediterranean Sea. This study presents a detailed description of the composition of aegagropiles in terms of their internal organisation in different layers (and the orientation of the fibres in these layers), the proportion of constituent elements (fibres and minerals) and the histological (by way of microscopic observations) nature of all of these aegagropiles elements. The aim of this work is to take a detailed interest in the structure of the aegagropiles of Posidonia oceanica and to determine the process that forms them. Aegagropiles are an assemblage of two types of debris from the P. oceanica meadow: (1) plantbased: fibres more or less degraded from P. oceanica shoots (leaves and rhizomes) and ( 2) mineral particles such as silicates and biotic Ca-carbonate debris. On the basis of structural and compositional observations, we proposed an elucidation of the cycle in several phases: initiation of a "roll" by aggregation of litter fibres and sand in the ripple marks, growth, breakdown of the roll into small balls (microbial and mechanical degradation) and export of aegagropiles down (into the abyss) or on to the beaches. Calculations estimate that considering its density of 0.2 g/cm 3 , an aegagropile represents the accumulation of fibres from approximately 25 shoots of P. oceanica.

No abstract

No abstract

is an open access repository that collects the work of Arts et Métiers ParisTech researchers and makes it freely available over the web where possible. AbstractA dynamic crash loading experiment is performed on polypropylene foam which is used in composite sandwich structures for safety applications. Several interrupted shocks are conducted, in between which, microtomographic acquisitions are made showing the change of the sample during its compression. These data can help construct and validate predictive models, although, because this material is multi-scale (constitutive beads at the mesoscopic scale are made of microscopic closed cells), image processing is required to extract useful quantitative measurements. Such processing is described here, so as to determine a representative volume for each bead of the sample, to associate values such as bead density to each bead and to each stage of the compression. This can help build a predictive model at the mesoscopic scale.

Multiple myeloma (MM)-associated osteolytic bone disease is a major cause of morbidity and mortality in MM patients and the development of new therapeutic strategies is of great interest. The proto-oncogene SRC is an attractive target for such a strategy. In the current study, we investigated the effect of treatment with the SRC inhibitor saracatinib (AZD0530) on osteoclast and osteoblast differentiation and function, and on the development of MM and its associated bone disease in the 5TGM.1 and 5T2MM murine MM models. In vitro data showed an inhibitory effect of saracatinib on osteoclast differentiation, polarization and resorptive function. In osteoblasts, collagen deposition and matrix mineralization were affected by saracatinib. MM cell proliferation and tumor burden remained unaltered following saracatinib treatment and we could not detect any synergistic effects with drugs that are part of standard care in MM. We observed a marked reduction of bone loss after treatment of MM-bearing mice with saracatinib as reflected by a restoration of trabecular bone parameters to levels observed in naive control mice. Histomorphometric analyses support that this occurs through an inhibition of bone resorption. In conclusion, these data further establish SRC inhibition as a promising therapeutic approach for the treatment of MM-associated osteolytic bone disease.