Advanced diagnostics and innovative solutions for leather defects: the problem of yellowing

Content: Providing peculiar enhanced features to leather items is a factor of primary importance for the marketing of high-end articles; although the tanning production is oriented to satisfy a wide market range, it is mainly in the 'high end' and 'premium luxury' categories that the quality properties of the material are more expressed, indeed, and where the main current challenges have been focalized, in terms of technological innovation, sustainability and product quality. The light-coloured leathers belongs to the category of materials designed especially for the luxury market. For this type of articles, the uniformity of the colour and the agreeableness of the overall surface appearance are crucial requirements for the most of international fashion and luxury brands. One of the most common and undesirable defects of this type of article is the alteration of the color, with particular reference to the effects of yellowing of the surface of the material. There are several causes able to contribute to this type of defects, due to the complexity of the matrix and to the variability of traditional or innovative production processes used: from the fragility, photosensitivity and thermo-sensitivity of the finishing polymers, to the chemical instability of some finishing pigments, further than the presence of photosensitive additives, the migration of skin components or assembly components of the articles (fats, fillers, plasticizers, glues, etc.), up to the indirect contribution of environmental and thermo-climatic factors able to affect negatively the performance of the material. SSIP, which has always been involved in research and consulting activities for the leather industry with regards to defect monitoring, through this work, would offer an overview of all the main tools for advanced diagnostics (with particular reference to Scanning Electronic Microscopy and to chromatographic and spectroscopic methods) aimed to the identification of the causes of yellowing, beside to explore innovative solutions for the development of strategies for the resolution and / or minimization of the problem of yellowing. The technical solutions will include innovative tanning processes, innovative finishing methods, and leather surface treatments carried out in order to provide a sensible attenuation of surface absorption of IR (infrared) and UV (ultraviolet)-visible radiation. Take-Away: Advanced Diagnostics and innovative solutions for leather yellowin

Transthyretin binding heterogeneity and antiamyloidogenic activity of natural polyphenols and their metabolites

Transthyretin (TTR) is an amyloidogenic protein, the amyloidogenic potential of which is enhanced by a number of specific point mutations. The ability to inhibit TTR fibrillogenesis is known for several classes of compounds, including natural polyphenols, which protect the native state of TTR by specifically interacting with its thyroxine binding sites. Comparative analyses of the interaction and of the ability to protect the TTR native state for polyphenols, both stilbenoids and flavonoids, and some of their main metabolites have been carried out. A main finding of this investigation was the highly preferential binding of resveratrol and thyroxine, both characterized by negative binding cooperativity, to distinct sites in TTR, consistent with the data of x-ray analysis of TTR in complex with both ligands. Although revealing the ability of the two thyroxine binding sites of TTR to discriminate between different ligands, this feature has allowed us to evaluate the interactions of polyphenols with both resveratrol and thyroxine preferential binding sites, by using resveratrol and radiolabeled T4 as probes. Among flavonoids, genistein and apigenin were able to effectively displace resveratrol from its preferential binding site, whereas genistein also showed the ability to interact, albeit weakly, with the preferential thyroxine binding site. Several glucuronidated polyphenol metabolites did not exhibit significant competition for resveratrol and thyroxine preferential binding sites and lacked the ability to stabilize TTR. However, resveratrol-3-O-sulfate was able to significantly protect the protein native state. A rationale for the in vitro properties found for polyphenol metabolites was provided by x-ray analysis of their complexes with TTR

Characterization of Volatile Organic Compounds (VOC) in wet-white and metal-free leathers

Content: As it is known in the tanning sector, in recent times, the so-called wet-white and/or metal-free concepts have had a certain increase. For example, in the automotive sector, the wet-white tanning system, carried out with glutaraldehyde and tannins, has been widely diffused. In fact, car manufacturers offer, for interior furnishings, leather not only for high-end cars but increasingly also in the lower segments. The components on which the leather upholstery is applied are mainly steering wheel, seats, dashboard and panels. Therefore, the use of leather also in this context must be able to meet both the aesthetic/performance criteria and the environmental ones; environmental criteria should also consider the air quality of the interior of a motor vehicle. In practice, the interior furniture consisting of finished leather must be able to release a few volatile substances and, at the same time, provide a typical smell of leather. Considering, therefore, the diffusion of alternative chrome tanning systems for the different uses, in this work, wet-white (glutaraldehyde and tannins) will be investigated, both from the point of view of the performance characteristics and from the ecotoxicological ones. and leathers deriving from the latest generation of metal-free tanning. For the characterization of Volatile Organic Compounds (VOC) the GC-MS will be used coupled with the 'Purge and Trap' technique with the aim of obtaining information on the new substances used in the wetwhite / metal free production process and then avoiding undesired effects during use (eg bad smell, SVHC substances, etc.) Take-Away: metal-free automotive VO

Soil bacterial community response to differences in agricultural management along with seasonal changes in a Mediterranean region

Land-use change is considered likely to be one of main drivers of biodiversity changes in grassland ecosystems. To gain insight into the impact of land use on the underlying soil bacterial communities, we aimed at determining the effects of agricultural management, along with seasonal variations, on soil bacterial community in a Mediterranean ecosystem where different land-use and plant cover types led to the creation of a soil and vegetation gradient. A set of soils subjected to different anthropogenic impact in a typical Mediterranean landscape, dominated by Quercus suber L., was examined in spring and autumn: a natural cork-oak forest, a pasture, a managed meadow, and two vineyards (ploughed and grass covered). Land uses affected the chemical and structural composition of the most stabilised fractions of soil organic matter and reduced soil C stocks and labile organic matter at both sampling season. A significant effect of land uses on bacterial community structure as well as an interaction effect between land uses and season was revealed by the EP index. Cluster analysis of culture-dependent DGGE patterns showed a different seasonal distribution of soil bacterial populations with subgroups associated to different land uses, in agreement with culture-independent T-RFLP results. Soils subjected to low human inputs (cork-oak forest and pasture) showed a more stable bacterial community than those with high human input (vineyards and managed meadow). Phylogenetic analysis revealed the predominance of Proteobacteria, Actinobacteria, Bacteroidetes, and Firmicutes phyla with differences in class composition across the site, suggesting that the microbial composition changes in response to land uses. Taken altogether, our data suggest that soil bacterial communities were seasonally distinct and exhibited compositional shifts that tracked with changes in land use and soil management. These findings may contribute to future searches for bacterial bio-indicators of soil health and sustainable productivity. X Maite Sampedro Pellicer, Affiliation: ENEA (Italian National Agency for New Technologies, Energy and Sustainable Economic Development) Casaccia Research Center, Technical Unit for Sustainable Development and Innovation of Agro-Industrial System, Rome, Italy X Maria Cristiana Papaleo, Affiliation: Laboratory of Microbial and Molecular Evolution, Department of Biology, University of Florence, Florence, Italy X Alessio Mengoni, Affiliation: Laboratory of Microbial and Molecular Evolution, Department of Biology, University of Florence, Florence, Italy X Luigi Ledda, Affiliation: Dipartimento di Agraria, University of Sassari, Sassari, Italy X Renato Fani, Affiliation: Laboratory of Microbial and Molecular Evolution, Department of Biology, University of Florence, Florence, Italy X Anna Benedetti, Affiliation: Consiglio per la Ricerca e la Sperimentazione in Agricoltura - Research Centre for the Soil-Plant System, Rome, Italy X Claudia Dalmastr

In vitro study of uptake and synthesis of creatine and its precursors by cerebellar granule cells and astrocytes suggests some hypotheses on the physiopathology of the inherited disorders of creatine metabolism

<p>Abstract</p> <p>Background</p> <p>The discovery of the inherited disorders of creatine (Cr) synthesis and transport in the last few years disclosed the importance of blood Cr supply for the normal functioning of the brain. These putatively rare diseases share a common pathogenetic mechanism (the depletion of brain Cr) and similar phenotypes characterized by mental retardation, language disturbances, seizures and movement disorders. In the effort to improve our knowledge on the mechanisms regulating Cr pool inside the nervous tissue, Cr transport and synthesis and related gene transcripts were explored in primary cultures of rat cerebellar granule cells and astrocytes.</p> <p>Methods</p> <p>Cr uptake and synthesis were explored in vitro by incubating monotypic primary cultures of rat type I astrocytes and cerebellar granule cells with: a) D₃-Creatine (D₃Cr) and D3Cr plus β-guanidinopropionate (GPA, an inhibitor of Cr transporter), and b) labelled precursors of Guanidinoacetate (GAA) and Cr (Arginine, Arg; Glycine, Gly). Intracellular D3Cr and labelled GAA and Cr were assessed by ESI-MS/MS. Creatine transporter (<it>CT1</it>), L-arginine:glycine amidinotransferase (<it>AGAT</it>), and S-adenosylmethionine:guanidinoacetate N-methyltransferase (<it>GAMT</it>) gene expression was assessed in the same cells by real time PCR.</p> <p>Results</p> <p>D3Cr signal was extremely high in cells incubated with this isotope (labelled/unlabelled Cr ratio reached about 10 and 122, respectively in cerebellar granule cells and astrocytes) and was reduced by GPA. Labelled Arg and Gly were taken up by the cells and incorporated in GAA, whose concentration paralleled that of these precursors both in the extracellular medium and inside the cells (astrocytes). In contrast, the increase of labelled Cr was relatively much more limited since labelled Cr after precursors' supplementation did not exceed 2,7% (cerebellar granule cells) and 21% (astrocytes) of unlabelled Cr. Finally, <it>AGAT, GAMT </it>and <it>SLC6A8 </it>were expressed in both kind of cells.</p> <p>Conclusions</p> <p>Our results confirm that both neurons and astrocytes have the capability to synthesize and uptake Cr, and suggest that at least in vitro intracellular Cr can increase to a much greater extent through uptake than through <it>de novo </it>synthesis. Our results are compatible with the clinical observations that when the Cr transporter is defective, intracellular Cr is absent despite the brain should be able to synthesize it. Further research is needed to fully understand to what extent our results reflect the in vivo situation.</p

Improving electrical conductivity of leather surface: a new technology versus industrial applications

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Monensin Controlled-release Capsules do not Change Performance and Metabolic Profile in Unchallenged Beef Cattle

ABSTRACT Background: Some additives are able to improve animal performance in growing and finishing periods. Monensin was first used to control coccidiosis in poultry and was extended to other animals, like ruminants, to act also as a growth promoter and improve cattle performance. In this species, monensin improves the synthesis of propionic acid in the rumen and decreases methane synthesis and protein degradation, resulting in better performance in protein and energy metabolism. The objective of this study was to evaluate the use of monensin controlled-release capsules on animals grazing Lolium multiflorum intercropped with Trifolium repens on metabolic profile and performance. Materials, Methods &amp; Results: Thirty Hereford cows were randomly distributed into two groups: control (CG) and monensin group (MG). Monensin was individually administered by controlled-release capsules placed in the rumen through oroesophageal pathway. All animals were identified through earring and kept under the same management condition, grazing on upland pasture mixture of Trifolium repens and Lolium multiflorum. Data from biochemical profile and performance were collected during 45 days. Blood samples started on the day of monensin controlled-release capsule placement (day 0) and continued in periods of 15, 30 and 45 days, after initial placement. Serum levels of albumin, glucose, urea, lactate dehydrogenase (LDH) and aspartate aminotransferase (AST) were evaluated using colorimetric diagnostic kits. In the rumen fluid, pH was measured and protozoa count was performed. All statistical analyses were made using software SAS. Albumin, AST, glucose, LDH and urea were analyzed through MIXED procedure and Tukey-Kramer test was applied for comparison of means. For average daily gain, the orthogonal polynomials test was applied. Treatments did not differ in BSC, body weight and average daily gain (ADG). None of these performance parameters were significantly affected by the addition of monensin. Blood biomarkers did not show statistical differences between treatments and markers of rumen activity did not suffer interference from monensin supplementation. There was only a tendency (P = 0.07) for the first time (0) to a higher pH value in CG. Discussion: Animals grazing in the finishing period, characterized by a continuous and linear weight gain, did not suffer any kind of stress situation. This condition did not provide a striking challenge that could reach the level of a metabolic change in animals. Facing feed shortages, or other stressful condition, supplementation with monensin and other additives, such as yeast, showed to be more effective, compared to animals in nutritional comfort. Weight gain increase is related to the expected changes in biochemical profile, as increased AST, glucose and LDH. The increase in AST levels on day 30 (P &lt; 0.0001) is explained by the greater weight gain of animals in the previous period (day 15, P &lt; 0.0001), where there was a higher hepatic activity to meet this anabolism and also by AST been an enzyme indicator of liver activity. This study did not show statistical treatment differences in relation to ruminal pH but, just a trend (P = 0.07) of higher pH in CG which is not caused by monensin supplementation that occurred since the first time (0), when animals were moved to pasture and receiving the monensin capsule. Since there was a low consumption of monensin capsules, the results were consistent with environment conditions and the phase in which the animals were. The results were also in agreement with finishing period, metabolic changes and animal performance at the same moment

Plan estratégico de una empresa de teléfonos inteligentes - ZenMobile

ZenMobile se creó sobre la base de la ideología Zen, que busca promover una cultura de la personalidad, consciente del presente, que permita liberar la ansiedad, el estrés, la frustración y otras emociones. A partir de esta idea, se ha relanzado la marca de dispositivos fundada en el 2012 como una organización enfocada en China, con el objetivo de vender dispositivos 5G con un enfoque especial en el segmento gaming que, a través de nuestros productos, llevará la experiencia de los usuarios a un siguiente nivel. Se tomó la decisión de hacer el relanzamiento en China por dos principales motivos: el posicionamiento que tenía la organización durante los 10 primeros años, como marca número 1 en el mercado de dispositivos móviles; y por el potencial de crecimiento que tiene el país, con proyecciones mayores a 40% en la adquisición de dispositivos gaming

Effect of RNS60 in amyotrophic lateral sclerosis: a phase II multicentre, randomized, double-blind, placebo-controlled trial

Background and purpose Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with limited treatment options. RNS60 is an immunomodulatory and neuroprotective investigational product that has shown efficacy in animal models of ALS and other neurodegenerative diseases. Its administration has been safe and well tolerated in ALS subjects in previous early phase trials. Methods This was a phase II, multicentre, randomized, double-blind, placebo-controlled, parallel-group trial. Participants diagnosed with definite, probable or probable laboratory-supported ALS were assigned to receive RNS60 or placebo administered for 24 weeks intravenously (375 ml) once a week and via nebulization (4 ml/day) on non-infusion days, followed by an additional 24 weeks off-treatment. The primary objective was to measure the effects of RNS60 treatment on selected biomarkers of inflammation and neurodegeneration in peripheral blood. Secondary objectives were to measure the effect of RNS60 on functional impairment (ALS Functional Rating Scale-Revised), a measure of self-sufficiency, respiratory function (forced vital capacity, FVC), quality of life (ALS Assessment Questionnaire-40, ALSAQ-40) and survival. Tolerability and safety were assessed. Results Seventy-four participants were assigned to RNS60 and 73 to placebo. Assessed biomarkers did not differ between arms. The mean rate of decline in FVC and the eating and drinking domain of ALSAQ-40 was slower in the RNS60 arm (FVC, difference 0.41 per week, standard error 0.16, p = 0.0101; ALSAQ-40, difference -0.19 per week, standard error 0.10, p = 0.0319). Adverse events were similar in the two arms. In a post hoc analysis, neurofilament light chain increased over time in bulbar onset placebo participants whilst remaining stable in those treated with RNS60. Conclusions The positive effects of RNS60 on selected measures of respiratory and bulbar function warrant further investigation

Characterisation of age and polarity at onset in bipolar disorder

Background Studying phenotypic and genetic characteristics of age at onset (AAO) and polarity at onset (PAO) in bipolar disorder can provide new insights into disease pathology and facilitate the development of screening tools. Aims To examine the genetic architecture of AAO and PAO and their association with bipolar disorder disease characteristics. Method Genome-wide association studies (GWASs) and polygenic score (PGS) analyses of AAO (n = 12 977) and PAO (n = 6773) were conducted in patients with bipolar disorder from 34 cohorts and a replication sample (n = 2237). The association of onset with disease characteristics was investigated in two of these cohorts. Results Earlier AAO was associated with a higher probability of psychotic symptoms, suicidality, lower educational attainment, not living together and fewer episodes. Depressive onset correlated with suicidality and manic onset correlated with delusions and manic episodes. Systematic differences in AAO between cohorts and continents of origin were observed. This was also reflected in single-nucleotide variant-based heritability estimates, with higher heritabilities for stricter onset definitions. Increased PGS for autism spectrum disorder (β = −0.34 years, s.e. = 0.08), major depression (β = −0.34 years, s.e. = 0.08), schizophrenia (β = −0.39 years, s.e. = 0.08), and educational attainment (β = −0.31 years, s.e. = 0.08) were associated with an earlier AAO. The AAO GWAS identified one significant locus, but this finding did not replicate. Neither GWAS nor PGS analyses yielded significant associations with PAO. Conclusions AAO and PAO are associated with indicators of bipolar disorder severity. Individuals with an earlier onset show an increased polygenic liability for a broad spectrum of psychiatric traits. Systematic differences in AAO across cohorts, continents and phenotype definitions introduce significant heterogeneity, affecting analyses