Comparative analysis of viscosity of complex liquids and cytoplasm of mammalian cells at the nanoscale

We present a scaling formula for size-dependent viscosity coefficients for proteins, polymers, and fluorescent dyes diffusing in complex liquids. The formula was used to analyze the mobilities of probes of different sizes in HeLa and Swiss 3T3 mammalian cells. This analysis unveils in the cytoplasm two length scales: (i) the correlation length ξ (approximately 5 nm in HeLa and 7 nm in Swiss 3T3 cells) and (ii) the limiting length scale that marks the crossover between nano- and macroscale viscosity (approximately 86 nm in HeLa and 30 nm in Swiss 3T3 cells). During motion, probes smaller than ξ experienced matrix viscosity: η(matrix) ≈ 2.0 mPa·s for HeLa and 0.88 mPa·s for Swiss 3T3 cells. Probes much larger than the limiting length scale experienced macroscopic viscosity, η(macro) ≈ 4.4 × 10(-2) and 2.4 × 10(-2) Pa·s for HeLa and Swiss 3T3 cells, respectively. Our results are persistent for the lengths scales from 0.14 nm to a few hundred nanometers.     

Resonant localization, enhancement, and polarization of optical fields in nano-scale interface regions for photo-catalytic applications

We report results of theoretical simulations of optical field enhancement in a system consisting of spherical and hemispherical noble metal nanoparticles on a smooth titania surface, which is a model system relevant to applications in photo-catalysis and solar energy harvesting. Simulations conducted using Finite-Difference Time-Domain (FDTD) technique reveal presence of resonant optical extinction bands at visible wavelengths, whose optical scattering is weak, but the associated localization and intensity enhancement of optical near-field are significant. For hemispheres, the field is strongly localized at the metal-substrate interface, where intensity enhancement of up to 10(4) times is reached. Moreover, the field is predominantly polarized along the normal to the substrate. These findings indicate potential of the hemisphere-substrate system for applications relying on optically promoted charge transport through the metal-substrate interface, such as photochemical reactions and light-to-current conversion. The results of theoretical analysis are compared with reported experimental data on photo-catalytic reactions.     

Synthesis of polylactide/clay composites using structurally different kaolinites and kaolinite nanotubes

Polymer/clay nanocomposites receive much attention due to their interesting mechanical and thermal properties. Currently, the vast majority of plastics are made from petroleum-based synthetic polymers that do not degrade in a natural environment and their disposal poses a serious problem. An environmentally-conscious alternative is to design polymer nanocomposites that are biodegradable.In the present work the synthesis and properties of novel polymer/clay nanocomposites based on biodegradable polymer-polylactide (PLA) were investigated. Kaolinite nanotubes obtained by an intercalation/deintercalation method as well as platey kaolinites of different structural orders were used as fillers. Mechanical properties of composites (tensile strength (S_U) and Young's modulus (E)) were measured. The surface of the formed polymer derivatives was examined by AFM (Atomic Force Microscopy). The structural characterization was carried out using infrared spectroscopy (IR). Composites surface wettability was studied by measuring the water contact angle.The mechanical tests revealed that both S_U and E values increased significantly after addition of the nano-filler in comparison to the pure PLA. Regardless of the filler content the increase of S_U and E values was higher in the case of the nanotubular kaolinite. In particular, a threefold increase of the E value was noticed. For the most homogeneous kaolinite nanotubes/PLA nanocomposite S_U increased from ~ 29 MPa (pure PLA) to ~ 43 MPa, while E increased from ~ 0.7 GPa (pure PLA) to ~ 2.3 GPa. These mechanical parameters were comparable with the ones measured for polypropylene (S_U = 40 MPa; E = 1.5–2.0 GPa) and polystyrene (S_U = 40 MPa; E = 3.0–3.5 GPa). Differential IR spectra of the nanocomposites indicated an interaction of kaolinites inner surface hydroxyls with PLA which was confirmed by an intensity decrease of a band at ~ 3690 cm^? 1. The presence of highly dispersed nanotubular kaolinite particles in the polymer matrix which contributed to the improvement of PLA mechanical properties was observed using AFM. The contact angle measurements showed that the addition of kaolinites led to changes of wettability, yet the synthesized materials still possessed hydrophilic surfaces.     

Preparation of stable Pd nanoparticles with tunable size for multiple immunolabeling in biomedicine

Stable Pd nanoparticles (PdNP) with a tunable size (3-15 nm) were synthesized by controlled chemical reduction of PdCl₂ with sodium citrate in water. The morphology of PdNP was characterized by transmission electron microscopy, while their stability in solution was verified by quasi-elastic light scattering and small-angle X-ray scattering. Intensive stirring of reacting mixture played a vital role in achieving reproducible particle sizes. Controlled changes of pH and initial concentrations were employed in fine-tuning particle size distributions. Finally, 10 nm PdNP were conjugated with goat anti-mouse IgG antibody as proved by electrophoresis (SDS-PAGE) and used for ultrastructural immunolabeling, which confirmed suitability of PdNP for multiple immunolabeling in biomedicine.     

The perfluoroalkyl substances (PFASs) contamination of fruits and vegetables

Fruit and vegetables play a major role in human nutrition due to richness of nutrients, dietary fibre, and phytochemicals. As dietary intake is identified as one of the dominant exposure pathways to perfluoroalkyl substances (PFASs), a cross-sectional study involving determination of their levels in food of plant origin has been conducted. Locally-grown and imported fruit and vegetable samples, collected in 2016 were inspected for 10 perfluoroalkyl acids (PFAAs) using QuEChERS as sample pre-treatment procedure followed by micro-HPLC-MS/MS. Three of 10 target analytes, perfluorobutanoic acid (PFBA), perfluorooctanoic acid (PFOA), and perfluorooctane sulfonate (PFOS) were quantitatively determined. The detection frequency for PFASs across the 55 samples analysed was less than 10%. The major contributor of the total PFASs concentration in the investigated group was PFBA for which the concentration, reported only for banana, apple and orange samples, was 50.740 ng g^?1 ww. The most often detected compound was PFOA. The origin and growing region are possible factors with the potential to influence PFASs distribution profile and their levels in food.     

Polylactide composites with waste cotton fibers: Thermal and mechanical properties

Recently, agricultural by‐products, for instance, corn husks, oat husks, or cocoa shells, have gained attention as a source of cellulose fibers and fillers because they can save the land and other natural resources required to grow fiber crops. It has to be noted, however, that textile processing, for example, shearing, is also a source of waste fibers. Our study focuses on utilization of waste cotton fibers, amassed during shearing of textiles, as a filler for polylactide (PLA). PLA composites with 10–30 wt% of waste cotton fibers were prepared and their thermal and mechanical properties were studied. The composite with 30 wt% of fibers exhibited markedly higher storage and loss moduli as compared with neat PLA; at 25°C the storage moduli increased by 53% whereas the loss modulus increased by 76%. In addition, the yield strength was slightly improved, by 11% at 25°C. Although the composites were thermally less stable than neat PLA, their 5% weight loss temperature remained high, about 300°C. POLYM. COMPOS., 35:747–751, 2014. © 2013 Society of Plastics Engineers     

Optimization of the QuEChERS Method for Determination of Pesticide Residues in Chicken Liver Samples by Gas Chromatography-Mass Spectrometry

The goal of this research was to evaluate the application of Quick, Easy, Cheap, Effective, Rugged, and Safe (QuEChERS) method for the determination of organochlorine, organophosphate, and carbamate pesticides in fatty animal matrices such as liver of chicken obtained from National Research Institute of Animal Production in Balice (Poland). Pesticides extraction effectiveness was evaluated at two different spiking levels (0.010 and 0.020 mg kg^?1) and efficiency of the dispersive solid-phase extraction (d-SPE) clean-up step was evaluated by comparison adding different d-SPE sorbent combinations (PSA?+?GCB, PSA?+?C₁₈, PSA?+?SAX, and PSA?+?NH₂). The analysis of pesticide residues was performed by gas chromatography ion trap mass spectrometry (GC/IT-MS). The linear relation was observed from 0 to 400 ng mL^?1 and the determination coefficient R ²?>?0.997 in all instances for all target analytes. Better recoveries were obtained in samples at 0.020 mg kg^?1 spiking level. The recoveries were in the range 70–120 %, with relative standard deviation (RSD) values lower than 15 % at 0.020 mg kg^?1 spiking level for most pesticides. Similar recovery ratios were obtained with the four different combinations of sorbents tested in the clean-up step, with better precision when the (PSA?+?SAX) combination was tested. Limits of detection (LODs) ranged from 0.001 to 0.005 mg kg^?1 and limits of quantification (LOQs) ranged from 0.003 to 0.015 mg kg^?1. The proposed method was successfully applied analyzing pesticide residues in real chicken liver samples; detectable pesticide residues were observed, but in all of the cases, the contamination level was lower than the default maximum residue levels (MRLs) set by European Union (EU), Regulation (EC) N 396/2005.