Determination of Glyphosate and Its Metabolite AMPA (Aminomethylphosphonic Acid) in Cereals After Derivatization by Isotope Dilution and UPLC-MS/MS”

A straightforward analytical method has been developed for the determination of glyphosate and aminomethylphosphonic acid (AMPA), its major metabolite in cereals. This method entails a rapid extraction and derivatization with 9-fluorenylmethyl chloroformate followed by separation with a conventional reversed-phase rapid chromatography used in daily routine analysis and detection by electrospray ionization tandem mass spectrometry. To overcome matrix effects and compensate for any analyte losses during sample treatment, an isotopic dilution approach was used. Since 2010, the monitoring of cereals for the widely used herbicide glyphosate is obligatory to all European Union (EU)-member states, laid down in Commission Regulation (EC) No. 1213/2008. Hence, there is definitively a need for a reliable and easy-to-handle analytical method for monitoring of this compound. The proposed method can be run without having to make time-consuming changes on the equipment used for daily routine analysis. The analytical performance of the method was evaluated according to SANCO/10684/2009 criteria and demonstrated that this method is rugged and cost-effective, therefore suitable for monitoring purposes as well as legislative enforcements within the EU. The apparent recoveries of both analytes were between 97% and 113% with relative standard deviations less than 20%. The limits of quantification of glyphosate and AMPA were 0.02 mg/kg in cereal matrices. Finally, the accuracy of the method was assessed by analyzing a proficiency test material which was available from a previous round (EUPT-C4).     

Cultured beef: from small biopsy to substantial quantity

Cultured meat is an emerging technology with the potential to solve huge challenges related to the environmental, ethical, and health implications of conventional meat production. Establishing the basic science of cultured meat has been the primary focus of the last decade but it is now feasible that cultured meat products will enter the market within the next 3 to 4 years. This proximity to market introduction demands an evaluation of aspects of the cultured meat production process that have not yet been outlined or discussed in significant detail. For example, one technological approach for the production of cultured meat uses adult muscle stem cells, the limited proliferative capacity of which necessitates repeated collection of tissue samples via biopsies of living donor animals. The selection of donor animals and the details of biopsy processes must be optimized, as this is a key bottleneck in the cultured meat production process. The number of stem cells harvested from a biopsy, together with their proliferative capacity, determines a ‘multiplicity factor’ achieved by a cultured meat production process, thus dictating the reduction in number of animals required to produce a given quantity of meat. This article considers potential scenarios for these critical upstream steps, focusing on the production of cultured beef as an example. Considerations related to donor selection and details of the biopsy process are discussed in detail. The practicalities of various scenarios for cultured beef production, the health of donor animals, and regulatory issues associated with the safety of cultured meat for consumers are also considered. © 2020 The Authors. Journal of The Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.     

Metabolic profile biomarkers of metal contamination in a sentinel terrestrial species are applicable across multiple sites

In this study, we addressed the question of whether an omic approach could genuinely be useful for biomarker profile analysis across different field sites with different physicochemical characteristics. We collected earthworms (Lumbricus rubellus) from seven sites with very different levels of metal contamination and prevailing soil type and analyzed tissue extracts by 1H nuclear magnetic resonance spectroscopy. Pattern recognition analysis of the data showed that both site- and contaminant-specific effects on the metabolic profiles could be discerned. Zinc was identified as the probable major contaminant causing a metabolic change in the earthworms. Individual sites could be resolved on the basis of NMR spectral profiles by principal component analysis; these site differences may also have been caused by additional abiotic factors such as soil pH. Despite an inevitable degree of confounding between site and contaminant concentrations, it was possible to identify metabolites which were correlated with zinc across all different sites. This study therefore acts as a proof of principle for the use of NMR-based metabolic profiling as a diagnostic tool for ecotoxicological research in polluted field soils.     

Surface Modification of Sisal (Agavae sisalana) Fiber by Photocuring: Effect of Additives

The sisal fiber (Agavae sisalana) was grafted with methacrylonitrile (MAN) under UV radiation in order to modify its mechanical and degradable properties. A number of MAN solutions of different concentrations in methanol (MeOH) along with photoinitiator Darocur-2959 were prepared. The soaking time, radiation dose and monomer concentration were optimized. Sisal fiber soaked for 60 min in 50% MAN and irradiated at 8th UV pass achieved highest values of tensile properties like tensile strength (TS = 140.2 MPa), and elongation at break factor (Ef = 8) with 8% polymer loading (PL). To further improve the properties of sisal fiber, a number of additives (1%) such as urea (U), polyvinylpyrrolidone (PNVP), tripropelene glycol diacrylate (TPGDA), hexanediol diacrylate (HDDA), trimethyl propane triacrylate (TMPTA), ethylene glycol dimethacrylate (EGDMA) were used in the 50% MAN formulation to graft at the optimized condition. Among the additives used, urea has significantly influenced the PL (9%), TS (190 MPa), and Ef (9) values of the treated sisal fiber. Water uptake and accelerated weathering test were also performed.     

Performance of scientific cameras with different sensor types in measuring dynamic processes in fluorescence microscopy

The plethora of available scientific cameras of different types challenges the biologically oriented experimenter when picking the appropriate camera for his experiment. In this study, we chose to investigate camera performances in a typical nonsingle molecule situation in life sciences, that is, quantitative measurements of fluorescence intensity changes from video data with typically skewed intensity distributions. Here, intensity profile dynamics of pH‐sensors upon triggered changes of pH‐environments in living cells served as a model system. The following camera types were tested: sCMOS, CCD (scientific and nonscientific) and EM‐CCD (back‐ and front‐illuminated). We found that although the EM‐CCD cameras achieved the best absolute spatial SNR (signal‐to‐noise ratio) values, the sCMOS was at least of equal performance when the spatial SNR was related to the effective dynamic range, and it was superior in terms of temporal SNR. In the measurements of triggered intensity changes, the sCMOS camera had the advantage that it used the smallest fraction of its dynamic range when depicting intensity changes, and thus featured the best SNR at full usage of its dynamic range. Microsc. Res. Tech. 76:835–843, 2013. © 2013 Wiley Periodicals, Inc.     

The Antimicrobial Peptide Gad-1 Clears Pseudomonas aeruginosa Biofilms under Cystic Fibrosis Conditions

Bacterial infections in cystic fibrosis (CF) patients are an emerging health issue and lead to a premature death. CF is a hereditary disease that creates a thick mucus in the lungs that is prone to bacterial biofilm formation, specifically Pseudomonas aeruginosa biofilms. These biofilms are very difficult to treat because many of them have antibiotic resistance that is worsened by the presence of extracellular DNA (eDNA). eDNA helps to stabilize biofilms and can bind antimicrobial compounds to lessen their effects. The metallo-antimicrobial peptide Gaduscidin-1 (Gad-1) eradicates established P. aeruginosa biofilms through a combination of modes of action that includes nuclease activity that can cleave eDNA in biofilms. In addition, Gad-1 exhibits synergistic activity when used with the antibiotics kanamycin and ciprofloxacin, thus making Gad-1 a new lead compound for the potential treatment of bacterial biofilms in CF patients.     

Improved trapped field performance of single grain Y-Ba-Cu-O bulk superconductors containing artificial holes

The intrinsic mechanical properties of single-grain RE-Ba-Cu-O bulk high-temperature superconductors can be improved by employing a thin-wall geometry. This is where the samples are melt-processed with a predefined network of artificial holes to decrease the effective wall thickness. In this study, the tensile strengths of thin-wall YBCO disks were determined using the Brazilian test at room temperature. Compared with conventional single grain YBCO disks, the thin-wall YBCO disks displayed an average tensile strength that is 93% higher when the holes were filled with Stycast epoxy resin. This implies a thin-wall sample should, in theory, be able to sustain a trapped field that is 39% higher without exceeding the mechanical limit of the sample. High-field magnetization experiments were performed by applying magnetization fields of up to 11.5 T, specifically to break the samples in order to verify the effect of increased mechanical strength (and improved cooling) on the ability of bulk (RE)BCO to trap field successfully. The standard YBCO sample failed when it was magnetized with a field of 10 T at 35 K, suffering permanent damage. As a result, the standard sample could only trap a maximum surface field of 7.6 T without failure. On the other hand, the thin-wall YBCO sample survived all magnetization cycles, including a maximum magnetization field of 11.5 T at 35 K, demonstrating a greater intrinsic ability to withstand significantly higher electromagnetic stresses. By subsequently field-cooling the thin-wall sample with 11 T at 30 K, a surface field of 8.8 T was trapped successfully without requiring any external ring reinforcement.     

Production and manipulation of elevated temperatures in pig abdomen with a three-electrode capacitive heating device

The ability of a three-electrode capacitive heating device operating at 13.56 MHz to produce and effect spatial redistribution of hyperthermic temperatures is demonstrated through abdominal heating studies conducted with 80 kg female and 65 kg male pigs. Temperature-time profiles over the respective heating periods were obtained in anterior and posterior superficial tissue and in selected abdominal organs. At selected times during heating, spatial redistribution of elevated temperatures was effected through adjustment of power settings for one or more of the three electrodes, i.e. through manipulation of the specific absorption rate (SAR) in-vivo.