4,464 research outputs found

    DNA Typing Compatibility with a One Step Saliva Screening Test

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    Screening a substrate for bodily fluids is an extremely important step for locating areas that may contain DNA. Several different methods have been developed for saliva (1). The Phadebas® Forensic Press (PFP) test is a presumptive saliva test that utilizes a preloaded paper that will react with the enzyme amylase, a component of saliva (2-5). Because of its ability to screen for amylase while simultaneously locating stains, the PFP may prove to be an effective, rapid method for screening. However it is important to assess whether the PFP introduces any inhibitors (7) to downstream processing such as PCR amplification. Based on previous studies, we hypothesize that the PFP will provide a rapid and sensitive method for locating multiple saliva stains simultaneously, without introducing inhibitors to DNA profiling. To test the limitations of PFP as well as evaluated its effects on DNA profiling we first created a dilution series of saliva ranging from neat to 1:5000. After this we preformed sensitivity tests on an indirect method, UV degraded samples and washed samples as well as with bodily fluid mixtures. Once all sensitivity tests were done, cuttings were taken from the substrate and PFP paper and analyzed for DNA. Tests found that the sensitivity ranges of the PFP were between 1:10 and 1:1000, indirect tests were less sensitive than direct, all bodily fluid mixtures were detected, and UV degraded samples took more time to react. In addition our DNA results confirmed our hypothesis that PFP does not inhibit DNA and is a useful method for locating stains. This project was funded by NSFREU Grant DBI 1262832

    The dynamics of speciale fficiency of sportsmen, who specialize in middle distance running

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    In sports training man tries to broaden the boundaries of his own capacities and the physical efϐiciency is an informative index, which deϐines a set of properties of the organism and, in the ϐirst place, the efϐiciency of blood ϐlow and breathing mechanisms. In the article the impact of training load on the bodies of athletes, who specialize in middle distance running is analyzed and the dynamics of special efϐiciency, physiological mechanisms, responsible for the quality of athletes’endurance, is determined.The dynamics of female athletes’ special efϐiciency manifestation has cyclical character and depends on the hormonal status change inϐluence on the athletes’ body during the biological cycle. Special efϐiciency of male athletes has tendency of gradual results growth, which is explained by the functional possibilities change, resulted by the effective inϐluence of training loads on their body. The highest efϐiciency has been found in the second and fourth phases, the lowest one - in the third and especially in the ϐirst and ϐifth phases of MC. This is due to the increased functionality of the cardiovascular system and the effectiveness of powerensuring in the second and fourth phases and its decrease in the ϐirst and ϐifth phases of MC, leading to stress of adaptation processes of women’s bodies during these phases. As for men, their dynamics of special efϐiciency tended to gradual increase of the results, that, we think, can be explained by the growth of functional capabilities of the cardiovascular system and the ffectiveness of power-ensuring on account of effective inϐluence of training loads upon their organism

    Influence of specific Loadings on physical Preparedness of Students.

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    У статті висвітлено характеристику навантажень, які застосовуються в спортивному тренуванні та докладно розглянуто специфіку впливу специфічних навантажень на організм студенток, які спецілізуються з бігу на 400 м. Description of loadings, which are used in the sporting training and the specific of influencing of the specific loadings, is thoroughly considered on the organism of students which are specialized from at run on 400м

    Liposomes characterization for market approval as pharmaceutical products: Analytical methods, guidelines and standardized protocols

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    Liposomes are nano-sized lipid-based vesicles widely studied for their drug delivery capabilities. Compared to standard carries they exhibit better properties such as improved site-targeting and drug release, protection of drugs from degradation and clearance, and lower toxic side effects. At present, scientific literature is rich of studies regarding liposomes-based systems, while 14 types of liposomal products have been authorized to the market by EMA and FDA and many others have been approved by national agencies. Although the interest in nanodevices and nanomedicine has steadily increased in the last two decades the development of documentation regulating and standardizing all the phases of their development and quality control still suffers from major inadequacy due to the intrinsic complexity of nano-systems characterization. Many generic documents (Type 1) discussing guidelines for the study of nano-systems (lipidic and not) have been proposed while there is a lack of robust and standardized methods (Type 2 documents). As a result, a widespread of different techniques, approaches and methodologies are being used, generating results of variable quality and hard to compare with each other. Additionally, such documents are often subject to updates and rewriting further complicating the topic. Within this context the aim of this work is focused on bridging the gap in liposome characterization: the most recent standardized methodologies suitable for liposomes characterization are here reported (with the corresponding Type 2 documents) and revised in a short and pragmatical way focused on providing the reader with a practical background of the state of the art. In particular, this paper will put the accent on the methodologies developed to evaluate the main critical quality attributes (CQAs) necessary for liposomes market approval

    Garnet as Indicator of Pegmatite Evolution: The Case Study of Pegmatites from the Oxford Pegmatite Field (Maine, USA)

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    Almandine-spessartine garnets, from the Oxford County pegmatites and the Palermo No. 1 pegmatite, record significant compositional variations according to the degree of evolution of their hosting rock. Garnets from the most fractionated pegmatites (Mt. Mica, Berry-Havey, and Emmons) show the highest Mn, Nb, Ta, Zr, and Hf values, followed by those from the intermediate grade pegmatites (Palermo No. 1) and, finally, garnets from the barren pegmatites show the lowest values (Perham and Stop-35). Iron, Ca, and Mg contents follow an inverse order, with the highest contents in the latter pegmatites. Major element zoning shows increasing Mn values from core to rim in most garnet samples, while trace element zoning is not systematic except for some crystals which show a core to rim depletion for most of these elements. Chondrite normalized HREE (Heavy Rare Earth Elements) spectra show positive slopes for garnets from barren pegmatites, both positive and negative slopes for those associated with the intermediate pegmatite, and negative or flat slopes in garnets from the highly fractionated pegmatites. Ion exchange mechanisms, including Fe2+−1Mn2+1, (Fe2+, Mn2+)−1Si−1Li1P1; and, (Y, Ho3+)2(vac)1(Fe2+, Mn2+)−3, could explain most of the compositional variations observed in these garnets. These compositional variations are the reflection of the composition of the pegmatitic magma (barren pegmatites originate from a more ferromagnesian magma than fractionated pegmatites); and of the coexisting mineral phases competing with garnets to host certain chemical elements, such as biotite, schorl, plagioclase, apatite, Fe-Mn phosphates, Nb-Ta oxides, zircon, xenotime, and monazite.This research was funded by the Spanish Ministry of Economy, Industry and Competitiveness (project no. RTI2018‐094097‐B‐100, with ERDF funds), the University of the Basque Country UPV/EHU (grant no. GIU18/084) and the European Union’s Horizon 2020 Innovation Programme (grant agreement no. 869274, project GREENPEG: New Exploration Tools for European Pegmatite Green‐Tech Resources). Maine Mineral and Gem Museum (USA) also contributed economically

    Garnet as Indicator of Pegmatite Evolution: The Case Study of Pegmatites from the Oxford Pegmatite Field (Maine, USA)

    Get PDF
    Almandine-spessartine garnets, from the Oxford County pegmatites and the Palermo No. 1 pegmatite, record significant compositional variations according to the degree of evolution of their hosting rock. Garnets from the most fractionated pegmatites (Mt. Mica, Berry-Havey, and Emmons) show the highest Mn, Nb, Ta, Zr, and Hf values, followed by those from the intermediate grade pegmatites (Palermo No. 1) and, finally, garnets from the barren pegmatites show the lowest values (Perham and Stop-35). Iron, Ca, and Mg contents follow an inverse order, with the highest contents in the latter pegmatites. Major element zoning shows increasing Mn values from core to rim in most garnet samples, while trace element zoning is not systematic except for some crystals which show a core to rim depletion for most of these elements. Chondrite normalized HREE (Heavy Rare Earth Elements) spectra show positive slopes for garnets from barren pegmatites, both positive and negative slopes for those associated with the intermediate pegmatite, and negative or flat slopes in garnets from the highly fractionated pegmatites. Ion exchange mechanisms, including Fe2+−1Mn2+1, (Fe2+, Mn2+)−1Si−1Li1P1; and, (Y, Ho3+)2(vac)1(Fe2+, Mn2+)−3, could explain most of the compositional variations observed in these garnets. These compositional variations are the reflection of the composition of the pegmatitic magma (barren pegmatites originate from a more ferromagnesian magma than fractionated pegmatites); and of the coexisting mineral phases competing with garnets to host certain chemical elements, such as biotite, schorl, plagioclase, apatite, Fe-Mn phosphates, Nb-Ta oxides, zircon, xenotime, and monazite.This research was funded by the Spanish Ministry of Economy, Industry and Competitiveness (project no. RTI2018-094097-B-100, with ERDF funds), the University of the Basque Country UPV/EHU (grant no. GIU18/084) and the European Union’s Horizon 2020 Innovation Programme (grant agreement no. 869274, project GREENPEG: New Exploration Tools for European Pegmatite Green-Tech Resources). Maine Mineral and Gem Museum (USA) also contributed economically

    Microfluidic tools for enhanced characterization of therapeutic stem cells and prediction of their potential antimicrobial secretome

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    Antibiotic resistance is creating enormous attention on the development of new antibiotic-free therapy strategies for bacterial diseases. Mesenchymal stromal stem cells (MSCs) are the most promising candidates in current clinical trials and included in several cell-therapy protocols. Together with the well-known immunomodulatory and regenerative potential of the MSC secretome, these cells have shown direct and indirect anti-bacterial effects. However, the low reproducibility and standardization of MSCs from different sources are the current limitations prior to the purification of cell-free secreted antimicrobial peptides and exosomes. In order to improve MSC characterization, novel label-free functional tests, evaluating the biophysical properties of the cells, will be advan-tageous for their cell profiling, population sorting, and quality control. We discuss the potential of emerging microfluidic technologies providing new insights into density, shape, and size of live cells, starting from heterogeneous or 3D cultured samples. The prospective application of these technologies to studying MSC populations may contribute to developing new biopharmaceutical strategies with a view to naturally overcoming bacterial defense mechanisms

    Pt(IV)Ac-POA: new platinum compound Induced caspase independent apoptosis In B50 neuroblastoma stem cells

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    Neuroblastoma is a tumour that affects adults and children, characterized by a stem cells component. To date, cisplatin is the main antitumor agent used in the clinical treatment of this tumour; however, it induces side effects such as neurotoxicity in healthy cells and induces chemo resistance to therapy in cancer cells. New platinum-based compounds, platinum (II) have recently been synthesized, and due to their chemical characteristics, they are able to identify new cellular targets. These complexes act as prodrugs and performing their cytotoxic effect as platinum (II) after a reduction reaction within the hypoxic tumour cells. Among these prodrugs, Pt(IV)Ac-POA appears to be very promising, thanks to the presence of ligand (2 propinyl)octanoic acid (POA), which acts as an inhibitor of histone deacetylase (HDACi) and leads to the increase of histone acetylation, decreasing the interactions between histone and DNA, so as to produce chemo-sensitization to DNA-damaging agents. The greater cytotoxic effect of Pt(IV)Ac-POA on tumour cells, would therefore be mainly due to the mechanism of inhibition of histone deacetylase, which would increase the accessibility of DNA to platination mechanisms that induce cell death. In this study the results show that Pt(IV)Ac-POA, used at a concentration ten times lower than cisplatin, can induce apoptosis in B50 cells in culture both through the intrinsic pathway and through the independent caspase pathway. The data, obtained by immunohistochemical techniques in fluorescence microscopy, show that treatment with Pt(IV)Ac-POA has a greater proapoptotic effect on stem cells compared to the cisplatin standard treatment

    Ursodeoxycholic acid and lithocholic acid exert anti-inflammatory actions in the colon

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    Inflammatory bowel diseases (IBD) comprise a group of common and debilitating chronic intestinal disorders for which currently available therapies are often unsatisfactory. The naturally occurring secondary bile acid, ursodeoxycholic acid (UDCA), has well-established anti-inflammatory and cytoprotective actions and may therefore be effective in treating IBD. We aimed to investigate regulation of colonic inflammatory responses by UDCA and to determine the potential impact of bacterial metabolism on its therapeutic actions. The anti-inflammatory efficacy of UDCA, a nonmetabolizable analog, 6 alpha-methyl-UDCA (6-MUDCA), and its primary colonic metabolite lithocholic acid (LCA) was assessed in the murine dextran sodium sulfate (DSS) model of mucosal injury. The effects of bile acids on cytokine (TNF-alpha, IL-6, Il-1 beta, and IFN-alpha) release from cultured colonic epithelial cells and mouse colonic tissue in vivo were investigated. Luminal bile acids were measured by gas chromatography-mass spectrometry. UDCA attenuated release of proinflammatory cytokines from colonic epithelial cells in vitro and was protective against the development of colonic inflammation in vivo. In contrast, although 6-MUDCA mimicked the effects of UDCA on epithelial cytokine release in vitro, it was ineffective in preventing inflammation in the DSS model. In UDCA-treated mice, LCA became the most common colonic bile acid. Finally, LCA treatment more potently inhibited epithelial cytokine release and protected against DSS-induced mucosal inflammation than did UDCA. These studies identify a new role for the primary metabolite of UDCA, LCA, in preventing colonic inflammation and suggest that microbial metabolism of UDCA is necessary for the full expression of its protective actions.NEW & NOTEWORTHY On the basis of its cytoprotective and anti-inflammatory actions, the secondary bile acid ursodeoxycholic acid (UDCA) has well-established uses in both traditional and Western medicine. We identify a new role for the primary metabolite of UDCA, lithocholic acid, as a potent inhibitor of intestinal inflammatory responses, and we present data to suggest that microbial metab-olism of UDCA is necessary for the full expression of its protective effects against colonic inflammation

    Conceptual Framework for a Data Model to Support Asset Management Decision-Making Process

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    Part 4: Product and Asset Life Cycle Management in Smart Factories of Industry 4.0International audienceInformation and data management is nowadays a central issue to support the Asset Management (AM) decision-making process. Manufacturing companies have to take different decisions along the asset lifecycle and at different organisational levels, and, to this end, they require proper information and data management. In the literature, besides the crucial role played by information and data, there is evidence of existing gaps, especially related to information management and integration, and transformation of data into useful information. Thus, a conceptual framework is proposed to guide the definition of a data model to fulfil the previously identified gap. Generally, the framework aims at contributing to the improvement of the integration of information along the AM decision-making process. Specifically, it is intended to be aligned with the AM theory and, in particular, its fundamentals defined in the scientific literature and the ISO 5500x body of standards. Overall, thanks to the improvement of the information management and integration along with the AM decision-making, the expectation is to be capable of achieving more value-oriented decisions for the asset lifecycle
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