12 research outputs found

    Analysis of spatial resolution in phase-sensitive compression optical coherence elastography

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    Funding: Australian Research Council; the Cancer Council Western Australia; OncoRes Medical; William and Marlene Schrader Trust of the University of Western Australia scholarship.Optical coherence elastography (OCE) is emerging as a method to image the mechanical properties of tissue on the microscale. However, the spatial resolution, a main advantage of OCE, has not been investigated and is not trivial to evaluate. To address this, we present a framework to analyze resolution in phase-sensitive compression OCE that incorporates the three main determinants of resolution: mechanical deformation of the sample, detection of this deformation using optical coherence tomography (OCT), and signal processing to estimate local axial strain. We demonstrate for the first time, through close correspondence between experiment and simulation of structured phantoms, that resolution in compression OCE is both spatially varying and sample dependent, which we link to the discrepancies between the model of elasticity and the mechanical deformation of the sample. We demonstrate that resolution is dependent on factors such as feature size and mechanical contrast. We believe that the analysis of image formation provided by our framework can expedite the development of compression OCE.Publisher PDFPeer reviewe

    Three-dimensional imaging of cell and extracellular matrix elasticity using quantitative micro-elastography

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    Funding: Australian Research Council; Cancer Council Western Australia; Industrial Transformation Training Centre; The William and Marlene Schrader Trust of the University of Western Australia.Recent studies in mechanobiology have revealed the importance of cellular and extracellular mechanical properties in regulating cellular function in normal and disease states. Although it is established that cells should be investigated in a three-dimensional (3-D) environment, most techniques available to study mechanical properties on the microscopic scale are unable to do so. In this study, for the first time, we present volumetric images of cellular and extracellular elasticity in 3-D biomaterials using quantitative micro-elastography (QME). We achieve this by developing a novel strain estimation algorithm based on 3-D linear regression to improve QME system resolution. We show that QME can reveal elevated elasticity surrounding human adipose-derived stem cells (ASCs) embedded in soft hydrogels. We observe, for the first time in 3-D, further elevation of extracellular elasticity around ASCs with overexpressed TAZ; a mechanosensitive transcription factor which regulates cell volume. Our results demonstrate that QME has the potential to study the effects of extracellular mechanical properties on cellular functions in a 3-D micro-environment.Publisher PDFPeer reviewe

    Enhancing resistance of silk fibroin material to enzymatic degradation by cross-linking both crystalline and amorphous domains

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    Silk fibroin (SF) membranes are finding widespread use as biomaterial scaffolds in a range of tissue engineering applications. The control over SF scaffold degradation kinetics is usually driven by the proportion of SF crystalline domains in the formulation, but membranes with a high ÎČ-sheet content are brittle and still contain amorphous domains, which are highly susceptible to enzymatic degradation. In this work, photo-cross-linking of SF using a ruthenium-based method, and with the addition of glycerol, was used to generate robust and flexible SF membranes for long-term tissue engineering applications requiring slow degradation of the scaffolds. The resulting mechanical properties, protein secondary structure, and degradation rate were investigated. In addition, the cytocompatibility and versatility of porous micropatterning of SF films were assessed. The photo-cross-linking reduced the enzymatic degradation of SF in vitro without interfering with the ÎČ-sheet content of the SF material, while adding glycerol to the composition grants flexibility to the membranes. By combining these methods, the membrane resistance to protease degradation was significantly enhanced compared to either method alone, and the SF mechanical properties were not impaired. We hypothesize that photo-cross-linking protects the SF amorphous regions from enzymatic degradation and complements the natural protection offered by ÎČ-sheets in the crystalline region. Overall, this approach presents broad utility in tissue engineering applications that require a long-term degradation profile and mechanical support.PostprintPeer reviewe

    In Situ Characterization of Melt–Electrowritten Scaffolds in 3D Using Optical Coherence Tomography

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    Recent developments in melt electrowriting (MEW), a high-resolution additive manufacturing technology, have led to increases in scaffold complexity. However, MEW scaffolds are currently characterized ex situ, which causes time–consuming iterations of characterization and fabrication that limit scaffold throughput and more widespread use of the technology. For the first time, an in situ method to characterize the 3D microstructure of MEW scaffolds using optical coherence tomography (OCT) is described. Calculations of microstructural features are performed on OCT data using a custom algorithm, demonstrating close correspondence with scanning electron microscopy (SEM). For example, OCT calculations of fiber diameter and scaffold thickness are within an average of 0.31 and 1.79 Όm, respectively, of corresponding SEM–derived calculations. Additionally, the 3D capabilities of OCT enable the nondestructive characterization of scaffolds with depth–varying microstructures, overcoming some main limitations of SEM. Finally, in situ characterization is achieved by integrating the OCT scanner within an MEW printer, enabling the scaffold microstructure to be evaluated and optimized during manufacture. This new capability represents an important step toward achieving an efficient fabrication–characterization cycle with the guaranteed scaffold quality and reproducibility required to validate the manufacturing process.<br/

    EDGE: Explorer of diffuse emission and gamma-ray burst explosions

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    International audienceHow structures of various scales formed and evolved from the early Universe up to present time is a fundamental question of astrophysical cosmology. EDGE (Piro et al., 2007) will trace the cosmic history of the baryons from the early generations of massive stars by Gamma-Ray Burst (GRB) explosions, through the period of galaxy cluster formation, down to the very low redshift Universe, when between a third and one half of the baryons are expected to reside in cosmic filaments undergoing gravitational collapse by dark matter (the so-called warm hot intragalactic medium). In addition EDGE, with its unprecedented capabilities, will provide key results in many important fields. These scientific goals are feasible with a medium class mission using existing technology combined with innovative instrumental and observational capabilities by: (a) observing with fast reaction Gamma-Ray Bursts with a high spectral resolution. This enables the study of their star-forming and host galaxy environments and the use of GRBs as back lights of large scale cosmological structures; (b) observing and surveying extended sources (galaxy clusters, WHIM) with high sensitivity using two wide field of view X-ray telescopes (one with a high angular resolution and the other with a high spectral resolution). The mission concept includes four main instruments: a Wide-field Spectrometer (0.1–2.2 eV) with excellent energy resolution (3 eV at 0.6 keV), a Wide-Field Imager (0.3–6 keV) with high angular resolution (HPD = 15”) constant over the full 1.4 degree field of view, and a Wide Field Monitor (8–200 keV) with a FOV of ÂŒ of the sky, which will trigger the fast repointing to the GRB. Extension of its energy response up to 1 MeV will be achieved with a GRB detector with no imaging capability. This mission is proposed to ESA as part of the Cosmic Vision call. We will outline the science drivers and describe in more detail the payload of this mission
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