Cytocompatibility of titanium metal injection molding with various anodic oxidation post-treatments

Metal injection molding (MIM) is a near net shape manufacturing method that allows for the production of components of small to moderate size and complex shape. MIM is a cost-effective and flexible manufacturing technique that provides a large innovative potential over existing methods for the industry of implantable devices. Commercially pure titanium (CP-Ti) samples were machined to the same shape as a composite feedstock with titanium and polyoxymethylene, and these metals were injected, debinded and sintered to assess comparative biological properties. Moreover, we treated MIM-Ti parts with BIOCOAT®, BIODIZE® and BIOCER®, three different anodic oxidation techniques that treat titanium using acid, alkaline and anion enriched electrolytes, respectively. Cytocompatibility as well as morphological and chemical features of surfaces was comparatively assessed on each sample, and the results revealed that MIM-Ti compared to CP-Ti demonstrated a specific surface topography with a higher roughness. MIM-Ti and BIOCER® samples significantly enhanced cell proliferation, cell adhesion and cell differentiation compared to CP-Ti. Interestingly, in the anodization post-treatment established in this study, we demonstrated the ability to improve osseointegration through anionic modification treatment. The excellent biological response we observed with MIM parts using the injection molding process represents a promising manufacturing method for the future implantable devices in direct contact with bones.     

Orientation Gradients at Boundaries in Micron‐Sized Bicrystals

In micron‐sized Ni bicrystals, after compression tests, orientation gradients are measured by electron back scattering diffraction (EBSD). The results clearly show that EBSD can be used to study dislocation pile‐ups at boundaries. Using bicrystals with single and multiple slip orientations our results show that with decreasing the size of the pillars the orientation changes due to cross‐slip decreases and the orientation changes at the boundary increases. This directly indicates a change in the hardening mechanism when the probability of dislocation–dislocation interaction decreases due to source‐limited plasticity in the bicrystals with diameters below approximately two microns.     

Model-based test case generation and prioritization: a systematic literature review

Software and Systems Modeling - Model-based test case generation (MB-TCG) and prioritization (MB-TCP) utilize models that represent the system under test (SUT) for test generation and...     

Electrospinning and Imaging

Polymer processing via electrospinning is a cost effective and scalable method for preparing nanofibers with industrial, electrical, and biomedical applications, particularly tissue engineering and drug delivery. Characterization methods for these fibers include microscopy techniques for vitro surface morphology information, spectroscopy methods to determine in vitro chemical composition, and medical imaging tools for in vivo assessment of morphology and efficacy of implanted material. The focus of this paper is be on recent applications for electrospun nanofibers, in vitro characterization methods, and medical imaging modalities that can be used for in vivo assessment of the fibers, as well as insights in how to adapt existing techniques toward the characterization of electrospun materials.     

Quantification of 1,8‐cineole and of its metabolites in humans using stable isotope dilution assays

The metabolism of 1,8‐cineole after ingestion of sage tea was studied. After application of the tea, the metabolites 2‐hydroxy‐1,8‐cineole, 3‐hydroxy‐1,8‐cineole, 9‐hydroxy‐1,8‐cineole and, for the first time in humans, 7‐hydroxy‐1,8‐cineole were identified in plasma and urine of one volunteer. For quantitation of these metabolites and the parent compound, stable isotope dilution assays were developed after synthesis of [²H₃]‐1,8‐cineole, [9/10‐²H₃]‐2‐hydroxy‐1,8‐cineole and [¹³C,²H₂]‐9‐hydroxy‐1,8‐cineole as internal standards. Using these standards, we quantified 1,8‐cineole by solid phase microextraction GC‐MS and the hydroxyl‐1,8‐cineoles by LC‐MS/MS after deconjugation in blood and urine of the volunteer. After consumption of 1.02 mg 1,8‐cineole (19 μg/kg bw), the hydroxycineoles along with their parent compound were detectable in the blood plasma of the volunteer under study after liberation from their glucuronides with 2‐hydroxycineole being the predominant metabolite at a maximum plasma concentration of 86 nmol/L followed by the 9‐hydroxy isomer at a maximum plasma concentration of 33 nmol/L. The parent compound 1,8‐cineole showed a low maximum plasma concentration of 19 nmol/L. In urine, 2‐hydroxycineole also showed highest contents followed by its 9‐isomer. Summing up the urinary excretion over 10 h, 2‐hydroxycineole, the 9‐isomer, the 3‐isomer and the 7‐isomer accounted for 20.9, 17.2, 10.6 and 3.8% of the cineole dose, respectively.     

Review: tailoring the properties of macroporous carbon foams

Carbon foams are non-toxic, highly porous, light materials which demonstrate a wide range of properties. That fact allows carbon foams to be applied in many areas of life, ranging from electronics industry, through machinery, car and construction industry, to environmental protection. The properties of carbon foams are closely connected with their density, and its value is especially influenced by their internal structure, i.e. mainly size and number of pores, pore wall thickness and structural order of solid matrix. That is why it is possible to design the properties of carbon foams by controlling their growth. The main control factors are selecting the suitable raw material, the process parameters (temperature and pressure) and the suitable production method. Additionally, the properties of carbon foams may be modified by doping them with carbon or mineral fillers. The second method is the enrichment of carbon matrix with heteroatoms, mainly of boron and nitrogen. This paper presents the review of the possibilities of tailoring the structure and properties of carbon foams, based on the current level of knowledge available in the literature.     

A process for the production of a diacylglycerol‐based milk fat analogue

We propose a novel process for the production of a DAG‐rich acylglycerol mixture derived from milk fat. This product has potentially interesting nutritional properties, derived from both its high content of DAG and of short‐chain fatty acids (FAs). The proposed process consists of three steps: lipase‐catalysed partial ethanolysis of milk fat, extraction of the by‐product fatty acid ethyl esters (FAEEs) using supercritical carbon dioxide (SC‐CO₂) and isomerization of DAG to increase the proportion of 1,3‐DAG. The experimental investigation of the process steps was done using milk fat and trilaurin. Several lipases were tested for maximizing the percentage of DAG in the acylglycerol mixture produced by ethanolysis. The selectivity of the chosen lipase was such that the produced AG mixture was enriched in short‐chain FAs in relation to the original milk fat. FAEEs were completely extracted from the ethanolysis mixture by SC‐CO₂. In the final process step, we explored the reaction conditions for facilitating acyl migration in the DAG mixture, so that the equilibrium proportion of 1,3‐DAG (～64%) was attained. Our results set the basis for the development of a simple process for the production of a DAG‐rich milk fat analogue.     

Optically detected magnetic resonance of thiol-capped CdTe nanocrystals

The optical properties of thiol-stabilized CdTe nanocrystals have been examined. The thiol groups -SR generate a CdS shell at the interface, leading to a CdTe/CdS core—shell structure. The present paper describes our efforts to identify the influence of the CdTe–SR interface on the optical properties of the nanocrystals, utilizing photoluminescence and optically detected magnetic resonance (ODMR) spectroscopy. The photoluminescence spectrum consists of an excitonic peak, overlapped by a broad band at lower energies. The ODMR spectrum, in the spectral regime of the broad band, showed two resonance signals. They are associated with a trapped hole at an anisotropic site of a cadmium vacancy at the Cd–SR interface and an electron in the conduction band.