The impact of single and combined amendment of elemental sulphur and graphene oxide on soil microbiome and nutrient transformation activities.

Background: Sulphur (S) deficiency has emerged in recent years in European soils due to the decreased occurrence of acid rains. Elemental sulphur (S0) is highly beneficial as a source of S in agriculture, but it must be oxidized to a plant-accessible form. Micro- or nano-formulated S0 may undergo accelerated transformation, as the oxidation rate of S0 indirectly depends on particle size. Graphene oxide (GO) is a 2D-carbon-based nanomaterial with benefits as soil amendment, which could modulate the processes of S0 oxidation. Micro-and nano-sized composites, comprised of S0 and GO, were tested as soil amendments in a pot experiment with unplanted soil to assess their effects on soil microbial biomass, activity, and transformation to sulphates. Fourteen different variants were tested, based on solely added GO, solely added micro- or nano-sized S0 (each in three different doses) and on a combination of all S0 doses with GO. Results: Compared to unamended soil, nano-S0 and nano-S0+GO increased soil pH(CaCl2). Micro-S0 (at a dose 4 g kg-1) increased soil pH(CaCl2), whereas micro-S0+GO (at a dose 4 g kg-1) decreased soil pH(CaCl2). The total bacterial and ammonium oxidizer microbial abundance decreased due to micro-S0 and nano-S0 amendment, with an indirect dependence on the amended dose. This trend was alleviated by the co-application of GO. Urease activity showed a distinct response to micro-S0+GO (decreased value) and nano-S0+GO amendment (increased value). Arylsulfatase was enhanced by micro-S0+GO, while sulphur reducing bacteria (dsr) increased proliferation due to high micro-S0 and nano-S0, and co-amendment of both with GO. In comparison to nano-S0, the amendment of micro-S0+GO more increased soluble sulphur content more significantly. Conclusions: Under the conditions of this soil experiment, graphene oxide exhibited a significant effect on the process of sulphur oxidation.

Rapid determination of uracil in biological fluids at mercury thin film electrode for early detection of potential 5-fluorouracil toxicity due to dihydropyrimidine dehydrogenase deficiency.

Determination of plasma uracil was reported as a method for evaluation of Dihydropyrimidine dehydrogenase (DPD) activity that is highly demanded to ensure the safe administration of 5-fluorouracil (5-FU)-based therapies to cancer patients. This work reports the development of a simple electroanalytical method based on adsorptive stripping square wave voltammetry (AdSWV) at mercury film-coated glassy carbon electrode (MF/GCE) for the highly sensitive determination of uracil in biological fluids that can be used for diagnosis of decreased DPD activity. Due to the formation of the HgII-Uracil complex at the electrode surface, the accuracy of the measurement was not affected by the complicated matrices in biological fluids including human serum, plasma, and urine. The high sensitivity of the developed method results in a low limit of detection (≈1.3 nM) in human plasma samples, falling below the practical cut-off level of 15 ng mL-1 (≈0.14 µM). This threshold concentration is crucial for predicting 5-FU toxicity, as reported in buffer, and ≤1.15% in biological samples), and accuracy (recovery percentage close to 100%).

New insight into the biocompatibility/toxicity of graphene oxides and their reduced forms on Chlamydomonas reinhardtii.

Graphene oxides (GOs) and their reduced forms are often discussed both positively and negatively due to the lack of information about their chemistry and structure. This study utilized GOs with two sheet sizes that were further reduced by two reducing agents (sodium borohydride and hydrazine) to obtain two different degrees of reduction. The synthesized nanomaterials were characterized using scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), elemental analysis (EA), Fourier transform infrared (FTIR) spectroscopy, and Raman spectroscopy (RA) to understand their chemistry and structure. The second focus of our investigation included in vitro testing of the biocompatibility/toxicity of these materials on a model organism, the freshwater microalga Chlamydomonas reinhardtii. The effects were studied on the basis of biological endpoints complemented by biomass investigation (FTIR spectroscopy, EA, and atomic absorption spectrometry (AAS)). The results showed that the biocompatibility/toxicity of GOs is dependent on their chemistry and structure and that it is impossible to generalize the toxicity of graphene-based nanomaterials.

Modifications of Parylene by Microstructures and Selenium Nanoparticles: Evaluation of Bacterial and Mesenchymal Stem Cell Viability.

Parylene-based implants or coatings introduce surfaces suffering from bacteria colonization. Here, we synthesized polyvinylpyrrolidone-stabilized selenium nanoparticles (SeNPs) as the antibacterial agent, and various approaches are studied for their reproducible adsorption, and thus the modification of parylene-C-coated glass substrate. The nanoparticle deposition process is optimized in the nanoparticle concentration to obtain evenly distributed NPs on the flat parylene-C surface. Moreover, the array of parylene-C micropillars is fabricated by the plasma etching of parylene-C on a silicon wafer, and the surface is modified with SeNPs. All designed surfaces are tested against two bacterial pathogens, Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive). The results show no antibacterial effect toward S. aureus, while some bacteriostatic effect is observed for E. coli on the flat and microstructured parylene. However, SeNPs did not enhance the antibacterial effect against both bacteria. Additionally, all designed surfaces show cytotoxic effects toward mesenchymal stem cells at high SeNP deposition. These results provide valuable information about the potential antibacterial treatment of widely used parylene-C in biomedicine.