Robust mean absolute deviation problems on networks with linear vertex weights

This article deals with incorporating the mean absolute deviation objective function in several robust single facility location models on networks with dynamic evolution of node weights, which are modeled by means of linear functions of a parameter. Specifically, we have considered two robustness criteria applied to the mean absolute deviation problem: the MinMax criterion, and the MinMax regret criterion. For solving the corresponding optimization problems, exact algorithms have been proposed and their complexities have been also analyzed.Ministerio de Ciencia e Innovación MTM2007-67433-C02-(01,02)Ministerio de Ciencia e Innovación MTM2009-14243Ministerio de Ciencia e Innovación MTM2010-19576-C02-(01,02)Ministerio de Ciencia e Innovación DE2009-0057Junta de Andalucía P09-TEP-5022Junta de Andalucía FQM-584

In Vitro Mutagenic and Genotoxic Assessment of a Mixture of the Cyanotoxins Microcystin-LR and Cylindrospermopsin

The co-occurrence of various cyanobacterial toxins can potentially induce toxic effects different than those observed for single cyanotoxins, as interaction phenomena cannot be discarded. Moreover, mixtures are a more probable exposure scenario. However, toxicological information on the topic is still scarce. Taking into account the important role of mutagenicity and genotoxicity in the risk evaluation framework, the objective of this study was to assess the mutagenic and genotoxic potential of mixtures of two of the most relevant cyanotoxins, Microcystin-LR (MC-LR) and Cylindrospermopsin (CYN), using the battery of in vitro tests recommended by the European Food Safety Authority (EFSA) for food contaminants. Mixtures of 1:10 CYN/MC-LR (CYN concentration in the range 0.04-2.5 µg/mL) were used to perform the bacterial reverse-mutation assay (Ames test) in Salmonella typhimurium, the mammalian cell micronucleus (MN) test and the mouse lymphoma thymidine-kinase assay (MLA) on L5178YTk± cells, while Caco-2 cells were used for the standard and enzyme-modified comet assays. The exposure periods ranged between 4 and 72 h depending on the assay. The genotoxicity of the mixture was observed only in the MN test with S9 metabolic fraction, similar to the results previously reported for CYN individually. These results indicate that cyanobacterial mixtures require a specific (geno)toxicity evaluation as their effects cannot be extrapolated from those of the individual cyanotoxins.España Ministerio de Economía y Competitividad AGL2015-64558-

In Vitro Safety Assessment of Reduced Graphene Oxide in Human Monocytes and T Cells.

Considering the increase in the use of graphene derivatives in different fields, the environmental and human exposure to these materials is likely, and the potential consequences are not fully elucidated. This study is focused on the human immune system, as this plays a key role in the organism's homeostasis. In this sense, the cytotoxicity response of reduced graphene oxide (rGO) was investigated in monocytes (THP-1) and human T cells (Jurkat). A mean effective concentration (EC50-24 h) of 121.45 ± 11.39 μg/mL and 207.51 ± 21.67 μg/mL for cytotoxicity was obtained in THP-1 and Jurkat cells, respectively. rGO decreased THP-1 monocytes differentiation at the highest concentration after 48 h of exposure. Regarding the inflammatory response at genetic level, rGO upregulated IL-6 in THP-1 and all cytokines tested in Jurkat cells after 4 h of exposure. At 24 h, IL-6 upregulation was maintained, and a significant decrease of TNF-α gene expression was observed in THP-1 cells. Moreover, TNF-α, and INF-γ upregulation were maintained in Jurkat cells. With respect to the apoptosis/necrosis, gene expression was not altered in THP-1 cells, but a down regulation of BAX and BCL-2 was observed in Jurkat cells after 4 h of exposure. These genes showed values closer to negative control after 24 h. Finally, rGO did not trigger a significant release of any cytokine at any exposure time assayed. In conclusion, our data contributes to the risk assessment of this material and suggest that rGO has an impact on the immune system whose final consequences should be further investigated.Fondo Europeo de Desarrollo Regional US-1259106Junta de Andalucía P18-RT-199

In Vitro Toxicity Assessment of Stilbene Extract for Its Potential Use as Antioxidant in the Wine Industry

The reduction of sulfur dioxide in wine is a consumer’s demand, considering the allergic effects that may occur in people who are sensitive to it. Stilbenes are candidates of great interest for this purpose because of their antioxidant/antimicrobial activities and health properties, and also because they are naturally found in the grapevine. In the present study, the in vitro toxicity of an extract from grapevine shoots (with a stilbene richness of 45.4%) was assessed in two human cell lines. Significant damage was observed from 30 μg/mL after 24 h, and 40 µg/mL after 48 h of exposure. Similarly, the ultrastructural study revealed a significant impairment of cell growing. The extract was able to protect cells against an induced oxidative stress at all concentrations studied. In view of the promising results, a more exhaustive toxicological assessment of the extract is needed to confirm the safety of its further use as additive in wine.España,Ministerio de Economía, Industria y Competitividad and INIA for the financial support for this project (RTA2015-00005-C02-02

Immunomodulatory Effects of Cylindrospermopsin in Human T Cells and Monocytes

Cylindrospermopsin (CYN) is a cyanotoxin with an increasing occurrence, and therefore it is important to elucidate its toxicity profile. CYN has been classified as a cytotoxin, although the scientific literature has already revealed that it affects a wide range of organs and systems. However, research on its potential immunotoxicity is still limited. Thus, this study aimed to evaluate the impact of CYN on two human cell lines representative of the immune system: THP-1 (monocytes) and Jurkat (lymphocytes). CYN reduced cell viability, leading to mean effective concentrations (EC50 24 h) of 6.00 ± 1.04 µM and 5.20 ± 1.20 µM for THP-1 and Jurkat cells, respectively, and induced cell death mainly by apoptosis in both experimental models. Moreover, CYN decreased the differentiation of monocytes to macrophages after 48 h of exposure. In addition, an up-regulation of the mRNA expression of different cytokines, such as interleukin (IL) 2, IL-8, tumor necrosis factor-alpha (TNF-α) and interferon-gamma (INF-γ), was also observed mainly after 24 h exposure in both cell lines. However, only an increase in TNF-α in THP-1 supernatants was observed by ELISA. Overall, these results suggest the immunomodulatory activity of CYN in vitro. Therefore, further research is required to evaluate the impact of CYN on the human immune system.Ministerio de Ciencia e Innovación PID 2019-104890RB-I0, PRE 2020-094412Acciones Marie Sklodowska-Curie 823860Universidad de Sevilla CITIUS–VIIPPIT-2023-I.

Intestinal transport of Cylindrospermopsin using the Caco-2 cell line

Cylindrospermopsin (CYN) is a cyanotoxin produced by various cyanobacterial species. It is a water soluble zwitterion, stable at extreme temperatures and pH. Despite the main route of exposure to CYN is through drinking water and food, there is a lack of data concerning its intestinal absorption and the mechanisms implicated. The aim of this study was to characterize the mechanisms involved in the intestinal absorption of CYN, using Caco-2 human cell line as a model of the intestinal epithelium. The results obtained in the present work increases the limited knowledge regarding CYN transport across the intestinal epithelium and identifies the paracellular route as an important pathway in CYN absorption. A minor carrier-mediated transcellular transport has been evidenced. This transport is not affected by low temperatures, suggesting that an active mechanism is not involved. Moreover, the transport through the intestinal monolayer is H+ and GSH dependent and Na + independent. The transport characteristics elucidated in this study prepare the ground for future studies directed at identifying transporters involved in the intestinal absorption of this toxin.Ministerio de Economía y Competitividad AGL2015-64558R (MINECO/FEDER, UE) y AGL2012-3346

Commissioning and validation of a method for the determination of gluten in different foods and ready meals

Gluten is the main storage protein of grains from Triticum genus (wheat, rye, barley and oat). Thus, it is present in diary diet, being 5-20g/d the average intake of this protein in east population. However, it has been demonstrated that gluten can provoke allergies (0,4 per cent of the world population), celiac disease (1-3 per cent of east population) and non-celiac gluten sensitivity. The way to solve gluten intolerance is to avoid gluten intake or not to exceed their tolerable intake, in case of people who are able to tolerate a small amount of gluten. Thus, it is important to know the quantity of gluten present in food and show this information on food labels (1). Commission Regulation (EC) No. 41/2009 of 20th January 2009 states the composition and labeling of food products appropriate for gluten-intolerant people and the maximum limit allowed based on the food (2).There are several methods for the detection of gluten in food, such as ELISA assays, PCR techniques, Western Blot, mass spectrometry, chromatography, immunochromatographic strips, biosensors and lab on a chip. In this work, the implementation of the sandwich ELISA technique is carried out, since this technique has received the recognition of the Codex Alimentarius as the most reliable technique (Type I). This method is simple, fast, and economical and it has a high sensitivity (3) that is based on selective and specific antibody-antigen recognition (4). As for the development of the technique, a calibration line was constructed with standards and a flour-ethanol solution was used as the reference material with which the samples were fortified to a desired concentration of gluten. After the calibration, the technique was validated in different food matrices (pre-cooked products, liquids, meats, fishes, cereals, flours and dairy products) with Prolamin Working Group (PWG) as the standard reference material. Regarding the validation, parameters such as accuracy, recovery, correction, repeatability and reproducibility were studied. Finally, the uncertainty was calculated, and a hypothesis test was performed

Ionic liquids for low-tension oil recovery processes: Phase behavior tests

This is the accepted manuscript of the following article: Rodriguez-Escontrela, I., Puerto, M., Miller, C., & Soto, A. (2017). Ionic liquids for low-tension oil recovery processes: Phase behavior tests. Journal Of Colloid And Interface Science, 504, 404-416. doi: 10.1016/j.jcis.2017.05.102Chemical flooding with surfactants for reducing oil-brine interfacial tensions (IFTs) to mobilize residual oil trapped by capillary forces has a great potential for Enhanced Oil Recovery (EOR). Surface-active ionic liquids (SAILs) constitute a class of surfactants that has recently been proposed for this application. For the first time, SAILs or their blends with an anionic surfactant are studied by determining equilibrium phase behavior for systems of about unit water-oil ratio at various temperatures. The test fluids were model alkane and aromatic oils, NaCl brine, and synthetic hard seawater (SW). Patterns of microemulsions observed are those of classical phase behavior (Winsor I-III-II transition) known to correlate with low IFTs. The two anionic room-temperature SAILs tested were made from common anionic surfactants by substituting imidazolium or phosphonium cations for sodium. These two anionic and two cationic SAILs were found to have little potential for EOR when tested individually. Thus, also tested were blends of an anionic internal olefin sulfonate (IOS) surfactant with one of the anionic SAILs and both cationic SAILs. Most promising for EOR was the anionic/cationic surfactant blend of IOS with [C12mim]Br in SW. A low equilibrium IFT of 2 10 3 mN/m was measured between n-octane and an aqueous solution having the optimal blend ratio for this system at 25 CA. Soto acknowledges the Ministry of Economy and Competitiveness (Spain) for financial support throughout project CTQ2015-68496-P (including European Regional Development Fund advanced funding)S

Stability and Thermal Properties Study of Metal Chalcogenide-Based Nanofluids for Concentrating Solar Power

Nanofluids are colloidal suspensions of nanomaterials in a fluid which exhibit enhanced thermophysical properties compared to conventional fluids. The addition of nanomaterials to a fluid can increase the thermal conductivity, isobaric-specific heat, diffusivity, and the convective heat transfer coefficient of the original fluid. For this reason, nanofluids have been studied over the last decades in many fields such as biomedicine, industrial cooling, nuclear reactors, and also in solar thermal applications. In this paper, we report the preparation and characterization of nanofluids based on one-dimensional MoS2 and WS2 nanosheets to improve the thermal properties of the heat transfer fluid currently used in concentrating solar plants (CSP). A comparative study of both types of nanofluids was performed for explaining the influence of nanostructure morphologies on nanofluid stability and thermal properties. The nanofluids prepared in this work present a high stability over time and thermal conductivity enhancements of up to 46% for MoS2-based nanofluid and up to 35% for WS2-based nanofluid. These results led to an increase in the efficiency of the solar collectors of 21.3% and 16.8% when the nanofluids based on MoS2 nanowires or WS2 nanosheets were used instead of the typical thermal oil