1,441 research outputs found
O efeito da adição de 40% de cinzas volantes sobre o ingresso de cloretos no betão face à ação combinada entre a carbonatação e os iões cloreto
Além de imprimir um caráter sustentável ao betão, as cinzas volantes (CV) têm sido bastante
utilizadas para tornar a matriz cimentícia mais resistente à penetração de
Cl-uma vez
que tornam a estrutura porosa mais densa e ajudam a fixar Cl-. Por outro lado, sabe-se que
o Ca(OH)2 existente na matriz é parcialmente consumido pelas reações pozolânicas,
facilitando o avanço da carbonatação
e, consequentemente, aumentando a quantidade de Cl-livres.
Considerando a ação conjunta destes agentes, especula-se sobre o
papel das CV na penetração de Cl-. Foram moldados provetes com 0% e
40% de CV. Após 90 dias de cura os provetes foram submetidos a
12 ciclos de imersão em solução com NaCl
e secagem
em câmara de carbonatação , num total de 168 dias.
Observou-se que os provetes contendo CV, e submetidos à ação combinada, apresentaram perfis de
Cl-com teores superiores quando comparados à ação exclusiva dos
Cl
Ruin and dividend measures in the renewal dual risk model
In this manuscript we consider the dual risk model with financial application, where the random gains occur under a renewal process. We particularly work the Erlang(n) case for common distribution of the inter-arrival times, from there it is easy to understand that our method or procedures can be generalised to other cases under the matrix-exponential family case. We work several and different problems involving future dividends and ruin. We also show that our results are valid even if the usual income condition is not satisfied. In most known works under the dual model, the main target under study have been the calculation of expected discounted future dividends and optimal strategies, where the dividend calculation have been done on aggregate. We can find works, at first using the classical compound Poisson model, then some examples of other renewal Erlang models. Knowing that ruin is ultimately achieved, we find important that dividends should be evaluated on an individual basis, where the early dividend contribution for the aggregate are of utmost importance. From our calculations we can really see how much important is the contribution of the first dividend. Afonso et al. (Insur Math Econ, 53(3), 906–918, 2013) had worked similar problems for the classical compound Poisson dual model. Besides that we find explicit formulae for both the probability of getting a dividend and the distribution of the amount of a single dividend. We still work the probability distribution of the number of gains to reach a given upper target (like a constant dividend barrier) as well as for the number of gains down to ruin. We complete the study working some illustrative numerical examples that show final numbers for the several problems under study.info:eu-repo/semantics/publishedVersio
Secreted extracellular vesicle molecular cargo as a novel liquid biopsy diagnostics of central nervous system diseases
Secreted extracellular vesicles (EVs) are heterogeneous cell-derived membranous granules which carry a large diversity of molecules and participate in intercellular communication by transferring these molecules to target cells by endocytosis. In the last decade, EVs role in several pathological conditions, from etiology to disease progression or therapy evasion, has been consolidated, including in central nervous system (CNS)-related disorders. For this review, we performed a systematic search of original works published, reporting the presence of molecular components expressed in the CNS via EVs, which have been purified from plasma, serum or cerebrospinal fluid. Our aim is to provide a list of molecular EV components that have been identified from both nonpathological conditions and the most common CNS-related disorders. We discuss the methods used to isolate and enrich EVs from specific CNS-cells and the relevance of its components in each disease context.This research was funded by the MindGaP-H2020-FETOPEN-2018-2020, Grant agreement
ID: 829040. S.M.-R., C.C.-M., and J.P. hold a fellowship from MindGaP.info:eu-repo/semantics/publishedVersio
Extraction and characterization of collagen from Antarctic and Sub-Antarctic squid and its potential application in hybrid scaffolds for tissue engineering
Collagen is the most abundant protein found in mammals and it exhibits a low immunogenicity, high biocompatibility and biodegradability when compared with others natural polymers. For this reason, it has been explored for the development of biologically instructive biomaterials with applications for tissue substitution and regeneration. Marine origin collagen has been pursued as an alternative to the more common bovine and porcine origins. This study focused on squid (Teuthoidea: Cephalopoda), particularly the Antarctic squid Kondakovia longimana and the Sub-Antarctic squid Illex argentinus as potential collagen sources. In this study, collagen has been isolated fromthe skins of the squids using acid-based and pepsin-based protocols, with the higher yield being obtained from I. argentinus in the presence of pepsin. The produced collagen has been characterized in terms of physicochemical properties, evidencing an amino acid profile similar to the one of calf collagen, but exhibiting a less preserved structure, with hydrolyzed portions and a lower melting temperature. Pepsin-soluble collagen isolated fromI. argentinus was selected for further evaluation of biomedical potential, exploring its incorporation on poly-ε-caprolactone (PCL) 3D printed scaffolds for the development of hybrid scaffolds for tissue engineering, exhibiting hierarchical features.This work was partially funded by ERDF through POCTEP Project
0687_NOVOMAR_1_P and by the European Union Seventh Framework
Programme for research, technological development and demonstration
under grant agreement on ERC-2012-ADG 20120216-321266
(ComplexiTE). The Portuguese Foundation for Science and Technology (FCT) is also acknowledged for post-doctoral fellowships of JMS (SFRH/BPD/70230/2010) and RPP (SFRH/BPD/101886/2014), financed by
POPH/FSE, and FCT Investigator grant of JX (IF/00616/2013). The authors
also want to thank Dr. Julio Maroto (Fundación CETMAR, Spain)
for the kind offer of the samples of skins of I. argentinus, to Dr. Dario
Fassini for the assistance in SDS-PAGE and to Raphael Canadas for assistance
in micro-CT data processing.info:eu-repo/semantics/publishedVersio
A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile
Objectives/Hypothesis: To develop and characterize a new model of laryngeal inflammation by analyzing the presence of neurogenic peptides and expression of cyclooxygenases (COX) and cytokines in the mucosa.Study Design: Laryngitis induced by nasogastric intubation (NGI) was evaluated by histopathologic changes of the mucosa, alterations in calcitonin gene related peptide (CGRP) and substance P (SP) neuropeptides in sensory fibers, and COX-1,2, and cytokine (interleukin [IL]-1, IL-6, IL-10, tumor necrosis factor [TNF]-alpha) expression in the laryngeal mucosa.Methods: Rats submitted to NGI for 1 to 5 weeks were compared with controls. Laryngeal sections were immunostained for stereologic analysis of SP and CGRP fiber density and number of mucosal cells expressing COX-2. Alterations in inflammatory mediators were evaluated by quantitative reverse-transcriptase polymerase chain reaction.Results: NGI induced metaplasia of the epithelium and narrowing of the laryngeal lumen because of hypertrophy of laryngeal glandules and edema. An initial decrease in CGRP- and SP-immunoreactive fibers in the laryngeal mucosa (1-3 wk) was reverted with time (5 wk). COX-2 expression in mucosal cells increased progressively, reaching a maximum level at 5 weeks, and was observed in mononuclear immune cells, which is indicative of a chronic inflammatory process. In regard to mRNA expression levels of inflammatory mediators, TNF-alpha was increased during the 5 week NGI, and IL-10 decreased during the 5 weeks,whereas IL-beta, IL-6, and COX-2 increased in the first 1 to 2 weeks and returned to baseline at 5 weeks.Conclusions: This NGI model results in laryngeal chronic inflammation without direct mechanical aggression of the mucosa and may contribute to the study of future therapeutic approaches to this pathology.FEDERFundação para a Ciência e Tecnologia
(FCT) - POCTI/NSE/46399/2002Fundação Calouste Gulbenkian - projecto nº 7455
KO-Homology and Type I String Theory
We study the classification of D-branes and Ramond-Ramond fields in Type I
string theory by developing a geometric description of KO-homology. We define
an analytic version of KO-homology using KK-theory of real C*-algebras, and
construct explicitly the isomorphism between geometric and analytic
KO-homology. The construction involves recasting the Cl(n)-index theorem and a
certain geometric invariant into a homological framework which is used, along
with a definition of the real Chern character in KO-homology, to derive
cohomological index formulas. We show that this invariant also naturally
assigns torsion charges to non-BPS states in Type I string theory, in the
construction of classes of D-branes in terms of topological KO-cycles. The
formalism naturally captures the coupling of Ramond-Ramond fields to background
D-branes which cancel global anomalies in the string theory path integral. We
show that this is related to a physical interpretation of bivariant KK-theory
in terms of decay processes on spacetime-filling branes. We also provide a
construction of the holonomies of Ramond-Ramond fields in Type II string theory
in terms of topological K-chains.Comment: 40 pages; v4: Clarifying comments added, more detailed proof of main
isomorphism theorem given; Final version to be published in Reviews in
Mathematical Physic
Development of Inhalable Superparamagnetic Iron Oxide Nanoparticles (SPIONs) in microparticulate system for antituberculosis drug delivery
Tuberculosis (TB) is an infectious disease which affects millions of people worldwide. Inhalable polymeric dry powders are promising alternatives as anti-TB drug carriers to the alveoli milieu and infected macrophages, with potential to significantly improve the therapeutics efficiency. Here, the development of a magnetically responsive microparticulate system for pulmonary delivery of an anti-TB drug candidate (P3) is reported. Microparticles (MPs) are developed based on a cast method using calcium carbonate sacrificial templates and incorporate superparamagnetic iron oxide nanoparticles to concentrate MPs in alveoli and enable drug on demand release upon actuation of an external alternate magnetic field (AMF). The MPs are shown to be suitable for P3 delivery to the lower airways and for alveolar macrophage phagocytosis. The developed MPs reveal unique and promising features to be used as an inhalable dry powder allowing the AMF control over dosage and frequency of drug delivery anticipating improved TB treatments.The authors wish to acknowledge the financial support from the
Portuguese Foundation for Science and Technology (FCT) for the postdoctoral grant of M.S.M. (SFRH/BPD/110868/2015) and R.M.A.D
(SFRH/BPD/112459/2015), FCT grant of E.T. (IF/01390/2014) and
Recognize project (UTAP-ICDT/CTM-BIO/0023/2014). This article
is also a result of the project “Accelerating tissue engineering and
personalized medicine discoveries by the integration of key enabling
nanotechnologies, marine-derived biomaterials and stem cells,”
supported by Norte Portugal Regional Operational Programme
(NORTE 2020), under the PORTUGAL 2020 Partnership Agreement,
through the European Regional Development Fund (ERDF). The authors
acknowledge the financial support from the European Union Framework
Programme for Research and Innovation HORIZON 2020, under the
TEAMING Grant Agreement No. 739572 – The Discoveries CTR.info:eu-repo/semantics/publishedVersio
Coronarin D induces apoptotic cell death and cell cycle arrest in human glioblastoma cell line
Glioblastoma (GBM) is the most frequent and highest–grade brain tumor in adults. The prognosis is still poor despite the use of combined therapy involving maximal surgical resection, radiotherapy, and chemotherapy. The development of more efficient drugs without noticeable side effects is urgent. Coronarin D is a diterpene obtained from the rhizome extract of Hedychium coronarium, classified as a labdane with several biological activities, principally anticancer potential. The aim of the present study was to determine the anti–cancer properties of Coronarin D in the glioblastoma cell line and further elucidate the underlying molecular mechanisms. Coronarin D potently suppressed cell viability in glioblastoma U–251 cell line, and also induced G1 arrest by reducing p21 protein and histone H2AX phosphorylation, leading to DNA damage and apoptosis. Further studies showed that Coronarin D increased the production of reactive oxygen species, lead to mitochondrial membrane potential depolarization, and subsequently activated caspases and ERK phosphorylation, major mechanisms involved in apoptosis. To our knowledge, this is the first analysis referring to this compound on the glioma cell line. These findings highlight the antiproliferative activity of Coronarin D against glioblastoma cell line U–251 and provide a basis for further investigation on its antineoplastic activity on brain cancer.This research was funded by grants from the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP 2014/06636–7 and 2016/06137–6), financiadora de Estudos e Projetos FINEP (MCTI/FINEP/MS/SCTIE/DECIT–01/2013–FPXII–BIOPLAT)
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