A microfluidic toolbox for cell fusion

Cellular fusion is a key process in many fields ranging from historical gene mapping studies and monoclonal antibody production, through to cell reprogramming. Traditional methodologies for cell fusion rely on the random pairing of different cell types and generally result in low and variable fusion efficiencies. These approaches become particularly limiting where substantial numbers of bespoke one‐to‐one fusions are required, for example, for in‐depth studies of nuclear reprogramming mechanisms. In recent years, microfluidic technologies have proven valuable in creating platforms where the manipulation of single cells is highly efficient, rapid and controllable. These technologies also allow the integration of different experimental steps and characterisation processes into a single platform. Although the application of microfluidic methodologies to cell fusion studies is promising, current technologies that rely on static trapping are limited both in terms of the overall number of fused cells produced and their experimental accessibility. Here we review some of the most exciting breakthroughs in core microfluidic technologies that will allow the creation of integrated platforms for controlled cell fusion at high throughput. © 2015 Society of Chemical Industry     

Effects of Some Metals and Chelating Agents on Patulin Degradation by Ozone

The efficiency of ozone treatment for degradation of the mycotoxin patulin in the presence of various metal ions was evaluated in model systems. An initial patulin concentration of 250 μg/L was ozonated and residual ozone concentration was about 0.17±0.01 mg/L at the end of the experiment. Patulin showed a weak resistance to ozone, because up to 98% of this toxin was oxidized in only one minute. Degradation rates in the presence of calcium, aluminum, copper and zinc were almost the same in the absence of these metals. However, degradation of patulin was reduced from 98 to 37% when the concentration of manganese increased from 0 to 3 mg/L. Patulin was almost completely degraded in the absence of iron, while the degradation was only 8.5% in the presence of 0.5 mg/L of iron. These results have revealed that manganese and iron significantly reduce the detoxification of patulin by ozone. Agents such as ethylenediaminetetraacetic acid and sodium polyphosphate effectively chelated iron and increased the degradation rate of patulin. None of the tested agents were able to chelate manganese and to enhance patulin degradation by ozone.     

Preconcentration and matrix elimination for the determination of Pb(II), Cd(II), Ni(II), and Co(II)by 8‐hydroxyquinoline anchored poly(styrene‐divinylbenzene) microbeads

Poly(styrene-divinylbenzene), PS-DVB, microbeads were modified with 8-hydroxyquinoline (8-HQ) following nitration, reduction of  NO₂ to NH₂, and conversion of NH₂ to diazonium salt. Characterization of pristine,  NO₂,  NH₂,  NN⁺Cl⁻, and 8-QH functional groups modified microbeads was made by Fourier transform-infrared spectrometry (FTIR) and porosimetry. Total reflectron-X-ray florescence spectrometer (TXRF) was used to test the affinity of the 8-HQ modified microbeads to toxic metal ions. 8-HQ-modified microbeads were used to examine the adsorption capacity, recovery, preconcentration, and the matrix elimination efficiency for Pb(II), Cd(II), Ni(II), and Co(II) ions as a function of changing pH, initial metal-ion concentrations, and also equilibrium adsorption time of the studied metal ions. Preconcentration factors for the studied toxic metal ions were found to be more than 500-fold and recovery between 93.8% and 100.6%. Ultratrace toxic metal-ion concentrations in sea water were determined easily by using modified microbeads. Reference sea-water sample was used for the validation of the method, and it was found that recovery, preconcentration, and the matrix elimination were performed perfectly. For the desorption of the toxic metal ions, 3M of HNO₃ was used and desorption ratio shown to be more than 96%. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Non-destructive determination of residual stress state in steel weldments by Magnetic Barkhausen Noise technique

The purpose of this study is non-destructive determination of residual stresses in the welded steel plates by Magnetic Barkhausen Noise (MBN) technique. A MBN-stress calibration set-up and a residual stress measurement system with scanning ability were developed. To control the accuracy and the effectiveness of the developed system and procedure, various MBN measurements were carried out. The MBN results were verified by the hole-drilling method. Microstructural investigation and hardness measurements were also conducted. It was concluded that if the calibration procedure including the effect of microstructure is appropriate then MBN is a very promising method for non-destructive, fast and accurate prediction of residual stresses in the welded plates.     

Modifying of Cotton Fabric Surface with Nano-ZnO Multilayer Films by Layer-by-Layer Deposition Method

ZnO nanoparticle–based multilayer nanocomposite films were fabricated on cationized woven cotton fabrics via layer-by-layer molecular self-assembly technique. For cationic surface charge, cotton fabrics were pretreated with 2,3-epoxypropyltrimethylammonium chloride (EP3MAC) by pad-batch method. XPS and SEM were used to examine the deposited nano-ZnO multilayer films on the cotton fabrics. The nano-ZnO films deposited on cotton fabrics exhibited excellent antimicrobial activity against Staphylococcus aureus bacteria. The results also showed that the coated fabrics with nano-ZnO multilayer films enhanced the protection of cotton fabrics from UV radiation. Physical tests (tensile strength of weft and warp yarns, air permeability and whiteness values) were performed on the fabrics before and after the treatment with ZnO nanoparticles to evaluate the effect of layer-by-layer (LbL) process on cotton fabrics properties.     

Effect of tempering temperature and microstructure on the corrosion behavior of a tempered steel

In this study, a tempered martensitic matrix was obtained in a low carbon steel, by applying austenization, quenching and tempering heat treatments. After austenization at 1000°C for 30 minutes, steel samples were quenched in water and then tempered at 200, 540 and 600°C for 30 minutes. Hardness measurements were done and then immersion tests were carried out in a 3.5 wt % NaCl solution for periods ranging between 1–7 days. Weight losses of the samples were determined after each immersion period and microstructural studies were performed on the corroded surfaces. Corrosion rates were calculated using weight loss data and verified by potentiodynamic tests. Results revealed that corrosion behavior of the experimental steels was directly affected by tempering temperature, hardness and microstructure.     

Design of Lu2O3-reinforced Cf/SiC-ZrB2-ZrC ultra-high temperature ceramic matrix composites: Wetting and interfacial reactivity by ZrSi2 based alloys

The wettability and infiltration of molten ZrSi₂ and ZrSi₂-Lu₂O₃ alloys into C_f/SiC and B₄C-infiltrated C_f/SiC composites were investigated to understand the interfacial interactions that occur during the development of C_f/SiC-ZrC and C_f/SiC-ZrB₂-ZrC-Lu₂O₃ materials. A significant evaporation of Si from the liquid affected the wetting behaviour of the alloy when tested in a vacuum at 1670 °C. The better wetting and spreading of the alloy over the surface was observed for the composites with lower overall porosity (12 %). On the other hand, the formation of an outer dense layer, followed up by the uniform infiltrated region up to ～ 1 mm was observed for the C_f/SiC with higher porosity (21 %). The infiltrated alloy reacted with SiC matrix to form ZrC or with B₄C-infiltrated SiC matrix to form ZrB₂-ZrC-SiC. The Lu₂O₃ particles were not wetted by the melt, and were pushed away of the reaction zone by the solidification front.     

Conjugate natural convection in air filled tube inserted a square cavity

Numerical analyses of fluid flow and heat transfer due to buoyancy forces in a tube inserted square cavity filled with fluid were carried out by using control volume method in this study. The cavity was heated from the left wall and cooled from the right isothermally and horizontal walls were adiabatic. A circular tube filled with air was inserted into the square cavity. The case that the inside and outside of the tube were filled with the same fluid (air) was examined. Varied solid materials were chosen as the tube wall. Results were obtained for different Rayleigh numbers (Ra = 10⁴, 10⁵ and 10⁶), thermal conductivity ratio of the fluid to the tube wall (k = 0.1, 1 and 10) and different location centers of the tube (c (0.25 ≤ x ≤ 0.75, 0.25 ≤ y ≤ 0.75)). Comparison with benchmark solutions of the natural convection in a cavity was performed and numerical results gave an acceptable agreement. It was found that varied location of the tube center can lead to different flow fields and heat transfer intensities which are also affected by the value of Rayleigh number.