Modeling nonspecific toxicity of organic compounds to the fathead minnow fish by means of chromatographic systems

The performance of chromatographic systems to mimic aquatic toxicity to the fathead minnow fish is evaluated taking into account the factors that contribute to the variance of biological-chromatographic correlations. These factors are the precision to measure the fathead minnow toxicity, the precision of the surrogate chromatographic system, and the error from the dissimilarity between the fathead minnow and chromatographic systems. The precisions are estimated through the characterization of the systems by the solvation parameter model. Several chromatographic systems as well as the common reference octanol-water partition system have been selected to test their ability to model the nonspecific toxicity to the fathead minnow by means of the proposed approach. Predictions and experimental tests show that the micellar electrokinetic chromatography system of sodium taurocholate and chromatographic measurements using an immobilized artificial membrane column provide the most precise estimations of this biopartitioning property. The octanol-water partition system, the conventional C18 high-performance liquid chromatography systems, and the micellar electrokinetic chromatography system of sodium dodecylsulfate show worse performances.     

Screening and selective quantification of illicit drugs in wastewater by mixed-mode solid-phase extraction and quadrupole-time-of-flight liquid chromatography-mass spectrometry

For the first time, a mixed-mode solid-phase extraction with fractionation of basic analytes from neutral and acidic species during cartridge elution and liquid chromatography-quadrupole-time-of-flight mass spectrometry (LC-QTOF-MS) was combined for the quantitative determination of 24 illicit drugs and metabolites in urban sewage samples. The effects of several sample preparation and instrumental parameters in the sensitivity and selectivity of the quantitative method are thoroughly discussed. Under final working conditions, recoveries above 63% and 82% were attained for all species in raw and treated sewage, respectively; whereas, the limits of quantification of the method, defined for a signal-to-noise of 10 (S/N = 10), ranged from 2 to 50 ng L(-1). Sequential elution of mixed-mode cartridges allowed a significant reduction of matrix effects observed during electrospray ionization of basic drugs versus those measured for hydrophilic balance reversed-phase sorbents and the same mixed-mode polymer without fractionated elution. Analysis of raw wastewater samples confirmed the ubiquity of cocaine (COC), benzoylecgonine (BE), and 11-nor-9-carboxy-Δ(9)-tetrahydrocannabinol (THCCOOH) in this matrix. The capability of the above methodology to identify new illicit drugs and/or metabolites in sewage samples is also discussed. With this aim, a two step strategy is proposed. First, high-resolution MS chromatograms, acquired throughout each chromatographic run, are automatically searched against an in-house built database, a reduced list of candidate drugs is generated, and the corresponding extracted ion chromatograms are obtained. In a further LC run, the tandem mass spectrometry (MS/MS) spectra of unknown peaks are acquired using different collision energies and compared with those existing in public libraries, or interpreted, to assign the unknown peak to one of the previously selected candidates.     

Back-focal-plane position detection with extended linear range for photonic force microscopy

In photonic force microscopes, the position detection with high temporal and spatial resolution is usually implemented by a quadrant position detector placed in the back focal plane of a condenser. An objective with high numerical aperture (NA) for the optical trap has also been used to focus a detection beam. In that case the displacement of the probe at a fixed position of the detector produces a unique and linear response only in a restricted region of the probe displacement, usually several hundred nanometers. There are specific experiments where the absolute position of the probe is a relevant measure together with the probe position relative the optical trap focus. In our scheme we introduce the detection beam into the condenser with low NA through a pinhole with tunable size. This combination permits us to create a wide detection spot and to achieve the linear range of several micrometers by the probe position detection without reducing the trapping force.     

Force mapping of an optical trap using an acousto-optical deflector in a time-sharing regime

We suggest and study experimentally a time-sharing protocol for acousto-optical deflectors (AODs) that permits one to map the radial optical trapping force of optical tweezers without using a controllable flux control or an additional beam. Variations of the trapping potential due to modifications of the optical system are easily detected in terms of the force map. The protocol can be used in optical tweezers that already include an AOD without adding new elements in the existing optical system.     

Characterization of a SrF2 Scintillating Bolometer

We present the analysis of the data obtained with a 53?g SrF₂ scintillating bolometer operated at 20?mK. We have analyzed its heat and light response (time constants, linearity and energy resolution) and measured its scintillation relative efficiency factor for different particles (alpha, beta/gamma and neutrons). We have studied the spatial uniformity of the light output profiting from its internal contamination. The light amplitude of alphas from the delayed coincidence ²²⁴Ra→²²⁰Rn→²¹⁶Po (emitted from the same crystal position) shows a positive correlation, evidence of a non-uniformity that worsens the light signal energy resolution by more than?50%.     

Superplastic behavior of Zn–Al eutectoid alloy with 2?% Cu

The effects of deformation temperature and strain rate on the superplastic behavior of the Zn–21Al–2Cu alloy (Zinalco alloy) were investigated by uniaxial tensile tests. Results were compared with those of the Zn–22Al eutectoid alloy without Cu. It was observed that additions of 2 % Cu leads to a decrease of the maximum strain attainable from 2600 % to 1000 %. The maximum strain in Zinalco alloy is obtained at lower strain rates. The presence of Cu increases the values of flow stress up to 600 % compared with those reported in the Zn-22Al alloy. Grain size sensitivity (p), true activation energy (Q _t ), and constant A of the constitutive equation were not affected by presence of Cu unlike the stress exponent (n) which increased from 2.5 to 3.9. The main effect of Cu was to decrease the plastic flow stability of the Zn–22Al alloy. The results indicate that presence of Cu in the Zinalco alloy causes a hardening effect at low strain rates leading to a decrease in the strain rate sensitivity which promotes the formation and growth of sharp necks. Microstructural characterization suggests that the large deformations at necking could possibly be due to the substantial elongation capability of the Zn-rich phase (η).     

Compressive Viscoplastic Response of 6082‐T6 and 7075‐T6 Aluminium Alloys Under Wide Range of Strain Rate at Room Temperature: Experiments and Modelling

Abstract: In this work, the viscoplastic behaviour of 6082‐T6 and 7075‐T6 aluminium alloys is examined over a wide range of strain rates. Three different testing techniques were applied to this investigation: low‐rate experiments were performed using a regular servo‐hydraulic testing machine, high‐rate tests were conducted using a split Hopkinson bar apparatus and very‐high‐rate experiments were carried out using a miniaturised direct impact test arrangement. The latter testing set‐up allowed for the characterisation of material flow at strain rates up to . These experimental results showed a sharp increase in the rate sensitivity of the materials once a threshold loading rate of is exceeded. This behaviour may be attributed to the presence of viscous drag on high‐velocity dislocation motion. In addition, the thermo‐viscoplastic behaviour of the 6082‐T6 and 7075‐T6 aluminium alloys was analytically described using the extended Rusinek–Klepaczko model of viscous drag effects. Satisfactory correlation was observed between the experiments and the constitutive model results over the entire range of strain rates studied,      

Tracking mesenchymal stem cells with iron oxide nanoparticle loaded poly(lactide-co-glycolide) microparticles

Monitoring the location, distribution and long-term engraftment of administered cells is critical for demonstrating the success of a cell therapy. Among available imaging-based cell tracking tools, magnetic resonance imaging (MRI) is advantageous due to its noninvasiveness, deep penetration, and high spatial resolution. While tracking cells in preclinical models via internalized MRI contrast agents (iron oxide nanoparticles, IO-NPs) is a widely used method, IO-NPs suffer from low iron content per particle, low uptake in nonphagocytotic cell types (e.g., mesenchymal stem cells, MSCs), weak negative contrast, and decreased MRI signal due to cell proliferation and cellular exocytosis. Herein, we demonstrate that internalization of IO-NP (10 nm) loaded biodegradable poly(lactide-co-glycolide) microparticles (IO/PLGA-MPs, 0.4-3 μm) in MSCs enhances MR parameters such as the r(2) relaxivity (5-fold), residence time inside the cells (3-fold) and R(2) signal (2-fold) compared to IO-NPs alone. Intriguingly, in vitro and in vivo experiments demonstrate that internalization of IO/PLGA-MPs in MSCs does not compromise inherent cell properties such as viability, proliferation, migration and their ability to home to sites of inflammation.     

Structuration and integration of magnetic nanoparticles on surfaces and devices

Different experimental approaches used for structuration of magnetic nanoparticles on surfaces are reviewed. Nanoparticles tend to organize on surfaces through self-assembly mechanisms controlled by non-covalent interactions which are modulated by their shape, size and morphology as well as by other external parameters such as the nature of the solvent or the capping layer. Further control on the structuration can be achieved by the use of external magnetic fields or other structuring techniques, mainly lithographic or atomic force microscopy (AFM)-based techniques. Moreover, results can be improved by chemical functionalization or the use of biological templates. Chemical functionalization of the nanoparticles and/or the surface ensures a proper stability as well as control of the formation of a (sub)monolayer. On the other hand, the use of biological templates facilitates the structuration of several families of nanoparticles, which otherwise may be difficult to form, simply by establishing the experimental conditions required for the structuration of the organic capsule. All these experimental efforts are directed ultimately to the integration of magnetic nanoparticles in sensors which constitute the future generation of hybrid magnetic devices.