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Basil-based semi-finished products, which are mainly used as an intermediate to produce the typical pesto sauce, are prepared and exported all over the world. Color is a fundamental organoleptic requirement for the acceptability of these semi-finished products by the manufacturers of the pesto sauce. Some alternative formulations, which adjust the typical industrial recipe by both changing the preservative agent (ascorbic acid, citric acid, or a mixture of both) and introducing a preliminary thermic treatment (blast chilling), were evaluated. In this work, a fast and non-destructive spectrophotometric analysis, to monitor the color variations in these food products during their shelf-life, was proposed. The raw diffuse reflectance spectra (380-900 nm) obtained by a UV-visible spectrophotometer, endowed with an integrating sphere, together with the CIELab parameters (L*, a*, b*) automatically obtained from these, were considered, and elaborated using multivariate statistical analysis (principal component analysis). From this preliminary study, blast chilling, together with the use of ascorbic acid, proved to be the best solution to better preserve the color of these products during their shelf-life.
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Ocimum basilicum , Antioxidantes , Ácido Ascórbico , CorRESUMO
Despite unifloral honeys from Sardinia, Italy, being appreciated worldwide for their peculiar organoleptic features, their elemental signature has only partly been investigated. Hence, the principal aim of this study was to measure the concentration of trace and toxic elements (i.e., Ag, As, Ba, Be, Bi, Cd, Co, Cr, Cu, Fe, Hg, Li, Mn, Mo, Ni, Pb, Sb, Sn, Sr, Te, Tl, V, and Zn) in four unifloral honeys produced in Sardinia. For this purpose, an original ICP-MS method was developed, fully validated, and applied on unifloral honeys from asphodel, eucalyptus, strawberry tree, and thistle. Particular attention was paid to the method's development: factorial design was applied for the optimization of the acid microwave digestion, whereas the instrumental parameters were tuned to minimize the polyatomic interferences. Most of the analytes' concentration ranged between the relevant LoDs and few mg kg-1, while toxic elements were present in negligible amounts. The elemental signatures of asphodel and thistle honeys were measured for the first time, whereas those of eucalyptus and strawberry tree honeys suggested a geographical differentiation if compared with the literature. Chemometric analysis allowed for the botanical discrimination of honeys through their elemental signature, whereas linear discriminant analysis provided an accuracy level of 87.1%.
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Mel , Geografia , Mel/análise , Micro-Ondas , Projetos de Pesquisa , Análise EspectralRESUMO
Pollution caused by plastics and, in particular, microplastics has become a source of environmental concern for Society. Their ubiquity, with millions of tons of plastic debris spilled in both land and sea, requires efficient technological improvements in the ways residues are collected, handled, characterized and recycled. For reliable decision-making, dependable chemical information is essential to assess both the nature of the plastics found in the environment and their fate. In this work an efficient method to identify the polymeric composition of microplastic fragments is proposed. It combines infrared reflectance spectra and chemometric methods. A breakthrough result is that the models include polymers weathered under both dry (shoreline) and submerged (in sea water) conditions and, hence, they are very promising as a starting point for eventual practical applications. In addition, no spectral processing is required after the initial measurement. SYNOPSIS: This approach to identify microplastics in aquatic environments combines infrared measurements and multivariate data analysis to fight against (micro)plastic pollution.
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Plásticos , Poluentes Químicos da Água , Plásticos/análise , Microplásticos , Poluentes Químicos da Água/análise , Monitoramento Ambiental/métodos , AlgoritmosRESUMO
In this work, a detailed study of Monte Arci obsidian sub-sources using the increasingly accessible technique of pXRF is presented based upon a large dataset of 68 geological samples, for the development of X-ray fluorescence-based analytical standardless procedure. In addition, a non-conventional (for obsidian provenance study) direct application of multivariate analysis on XRF spectra (continuous variables), rather than absolute concentrations or intensity ratios (discrete variables) is proposed. Results from different softwares and data analysis approaches (bi-/trivariate versus multivariate) were compared. In a blind test, the bi-/trivariate approach led to the correct assignment for the main SA, SB, and SC sub-sources, taking into account averaged values of intensity ratios with their standard deviation obtained from three independent measurements. A high intra-source variability for the SB subgroups was detected (almost 13% of error in the assignment, 9 samples out of 68). A non-conventional application of multivariate analysis was carried out directly on the XRF spectra and correct assignments were obtained for SA, SB1, SC groups, while 71% of the SB2 samples were correctly identified. The non-destructive analysis on 14 archaeological samples from Su Carroppu (Carbonia, southwestern Sardinia) rockshelter and from the Middle Neolithic (MN) 422 structure of the open-air dwelling site at Cuccuru is Arrius (Cabras, central-western Sardinia) permitted to test the method and hypothesise their provenance. The comparison with visual characterization or previous analyses by Particle Induced X-Ray Emission (PIXE) permitted to verify the correct provenance assignment of all artifacts for the bi-/trivariate method, and for 12/14 samples in the case of the multivariate one. The standardless analytical approach proposed in this work can represent a more general method exploitable for other obsidian sources, other glassy materials, besides other materials of archaeological interest.
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Background: Malignant melanoma is the most lethal form of skin cancer which shows BRAF mutation in 50% of patients. In this context, the identification of BRAFV600E mutation led to the development of specific inhibitors like PLX4032. Nevertheless, although its initial success, its clinical efficacy is reduced after six-months of therapy leading to cancer relapse due to the onset of drug resistance. Therefore, investigating the mechanisms underlying PLX4032 resistance is fundamental to improve therapy efficacy. In this context, several models of PLX4032 resistance have been developed, but the discrepancy between in vitro and in vivo results often limits their clinical translation. Methods: The herein reported model has been realized by treating with PLX4032, for six months, patient-derived BRAF-mutated melanoma cells in order to obtain a reliable model of acquired PLX4032 resistance that could be predictive of patient's treatment responses. Metabolic analyses were performed by evaluating glucose consumption, ATP synthesis, oxygen consumption rate, P/O ratio, ATP/AMP ratio, lactate release, lactate dehydrogenase activity, NAD+/NADH ratio and pyruvate dehydrogenase activity in parental and drug resistant melanoma cells. The intracellular oxidative state was analyzed in terms of reactive oxygen species production, glutathione levels and NADPH/NADP+ ratio. In addition, a principal component analysis was conducted in order to identify the variables responsible for the acquisition of targeted therapy resistance. Results: Collectively, our results demonstrate, for the first time in patient-derived melanoma cells, that the rewiring of oxidative phosphorylation and the maintenance of pyruvate dehydrogenase activity and of high glutathione levels contribute to trigger the onset of PLX4032 resistance. Conclusion: Therefore, it is possible to hypothesize that inhibitors of glutathione biosynthesis and/or pyruvate dehydrogenase activity could be used in combination with PLX4032 to overcome drug resistance of BRAF-mutated melanoma patients. However, the identification of new adjuvant targets related to drug-induced metabolic reprogramming could be crucial to counteract the failure of targeted therapy in metastatic melanoma.
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BACKGROUND: Tennis is an open-skill sport in which the athletes have a short period of time to elaborate all the information coming from the surrounding environment and produce a motor answer based on them. The aim of this study was divided in two hypotheses: 1) to assess if belonging to a certain category, athlete, or non-athlete, older or younger, can affect the development of reaction time on children; and 2) if a protocol based on visual training (VT) of 6 weeks could improve the motor performance on the field in young tennis players using FitLight Trainer (Medical Graphics, Milan, Italy). METHODS: In this evidence a group of young children (N.=40) have been tested on light board through reaction test then some young tennis players (N.=15, age: 7-12 years old) were taken as reference for the second hypothesis. They were divided in two groups: 7 of them were in the group Under-10 (U10) while 8 in a second group (U12). They performed a VT protocol once a week for at least 40 minutes for 6 weeks. They were tested at baseline (T0) and follow-up (T6) to evaluate the reaction time, time in specific lateral shift and precision about forehand and backhand. RESULTS: The development of reaction time of the athletes is principally caused by their growth (P<0.05). Principal components analysis (PCA) showed significant improvements in the Under-10 category in all the tests while in the Under-12 category not every individual showed a significant result in terms of performance. CONCLUSIONS: The developing of reaction time and coordination eye-hand is mainly due to the growth of young athletes. Also, performing a 6-week VT using FitLight Trainer is possible improve the reaction time and the motor performance on the field especially in young tennis players under 10 years old.
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Desempenho Atlético , Tênis , Atletas , Criança , Pré-Escolar , Mãos , Humanos , Tempo de ReaçãoRESUMO
Cancer stem cells (CSCs) are a limited cell population inside a tumor bulk characterized by high levels of glutathione (GSH), the most important antioxidant thiol of which cysteine is the limiting amino acid for GSH biosynthesis. In fact, CSCs over-express xCT, a cystine transporter stabilized on cell membrane through interaction with CD44, a stemness marker whose expression is modulated by protein kinase Cα (PKCα). Since many chemotherapeutic drugs, such as Etoposide, exert their cytotoxic action by increasing reactive oxygen species (ROS) production, the presence of high antioxidant defenses confers to CSCs a crucial role in chemoresistance. In this study, Etoposide-sensitive and -resistant neuroblastoma CSCs were chronically treated with Etoposide, given alone or in combination with Sulfasalazine (SSZ) or with an inhibitor of PKCα (C2-4), which target xCT directly or indirectly, respectively. Both combined approaches are able to sensitize CSCs to Etoposide by decreasing intracellular GSH levels, inducing a metabolic switch from OXPHOS to aerobic glycolysis, down-regulating glutathione-peroxidase-4 activity and stimulating lipid peroxidation, thus leading to ferroptosis. Our results suggest, for the first time, that PKCα inhibition inducing ferroptosis might be a useful strategy with which to fight CSC chemoresistance.
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Neuroblastoma (NB) accounts for about 8-10% of pediatric cancers, and the main causes of death are the presence of metastases and the acquisition of chemoresistance. Metastatic NB is characterized by MYCN amplification that correlates with changes in the expression of miRNAs, which are small non-coding RNA sequences, playing a crucial role in NB development and chemoresistance. In the present study, miRNA expression was analyzed in two human MYCN-amplified NB cell lines, one sensitive (HTLA-230) and one resistant to Etoposide (ER-HTLA), by microarray and RT-qPCR techniques. These analyses showed that miRNA-15a, -16-1, -19b, -218, and -338 were down-regulated in ER-HTLA cells. In order to validate the presence of this down-regulation in vivo, the expression of these miRNAs was analyzed in primary tumors, metastases, and bone marrow of therapy responder and non-responder pediatric patients. Principal component analysis data showed that the expression of miRNA-19b, -218, and -338 influenced metastases, and that the expression levels of all miRNAs analyzed were higher in therapy responders in respect to non-responders. Collectively, these findings suggest that these miRNAs might be involved in the regulation of the drug response, and could be employed for therapeutic purposes.