A expansão urbana da cidade do Salvador e os seus mananciais: estabelecendo paralelos

O sítio escolhido para implantação da cidade de Salvador se caracteriza por ser um reservatório natural de águas, sempre renovadas pelo clima úmido e pelo elevado índice pluviométrico. A população de Salvador que no inicio do século XX não chegava a 300 mil habitantes, no final ultrapassava dois milhões. Por outro lado, ao tempo em que a área urbana se amplia, a cidade segue em busca de atender às demandas de água da sua população, porém deixando para trás problemas ambientais de grande monta. Utilizando-se de fontes secundarias, este estudo descreve, a partir de recortes temporais, como ocorreu o abastecimento d’água nesta cidade. Sua expansão física e populacional deu-se associada ao desenvolvimento econômico, entretanto, as políticas de abastecimento hídrico não corresponderam às necessidades da sua população ao longo dos séculos, impactando assim de forma negativa na sua qualidade ambiental, confirmando um processo de urbanização perverso, marcado pela exclusão social.The site chosen for the implantation of the city of Salvador characterizes for being a natural water reservoir, always renewed by the humid climate and the elevated pluviometer index. Salvador’s population that, in the beginning of 20th century didn’t reach 300 thousand habitants, in the end would pass 2 millions. On the other hand, while the urban area grows, the city seeks to supply the water demands of its population, although leaving behind large scale environmental problems. Utilizing second sources this study describes, from time periods, how the water supply occurred in this city. The physical and population expansion were given to economic development, however the water supply politics didn’t correspond the needs of its population out the centuries impacting in a negative way on its environment quality, and witch means we satiate a perverse process of urbanization, marked by social exclusion

Polymer composites reinforced with natural fibers and nanocellulose in the automotive industry: a short review

Environmental concerns and cost reduction have encouraged the use of natural fillers as reinforcement in polymer composites. Currently, a wide variety of reinforcement, such as natural fibers and nanocellulose, are used for this purpose. Composite materials with natural fillers have not only met the environmental appeal, but also contribute to developing low-density materials with improved properties. The production of natural fillers is unlimited around the world, and many species are still to be discovered. Their processing is considered beneficial since the natural fillers do not cause corrosion or great wear of the equipment. For these reasons, polymer reinforced with natural fillers has been considered a good alternative for obtaining ecofriendly materials for several applications, including the automotive industry. This review explores the use of natural fillers (natural fibers, cellulose nanocrystals, and nanofibrillated cellulose) as reinforcement in polymer composites for the automotive industry323172016/09588-9; 2016/09588-9; 2016/09588-9CAPES - Coordenação de Aperfeiçoamento de Pessoal e Nível SuperiorCNPQ - Conselho Nacional de Desenvolvimento Científico e TecnológicoFAPESP – Fundação de Amparo à Pesquisa Do Estado De São Paul

Preparation of novel trifluoroacetylketene O,N-acetals and trifluoromethyl-containing S,S-sulfoximido N-substituted heterocycles

Two new trifluoroacetylketene O,N-acetals [CF3C(O)CH=C(OEt)(NS(O)R2), where R = CH3, Ph] derived from the reaction of 4,4-diethoxy-1,1,1-trifluorobut-3-en-2-one [CF3C(O)CH=C(OEt)2] with S,S-dimethyl- and S-methyl-S-phenyl-sulfoximide [HN=S(O)R2], in the presence of triethylamine, have been obtained, in 60-72% yields, and applied in the synthesis of S,S-dimethylsulfoximido-substituted pyrazoles, isoxazoles and pyrimidines, in 55-89% yields, from the reactions of 4-ethoxy-4-(S,S-dimethylsulfoximido)-1,1,1-trifluorobut-3-en-2-one with hydrazines, hydroxylamine hydrochloride and acetylguanidine

Aurora kinase A drives the evolution of resistance to third-generation EGFR inhibitors in lung cancer.

Although targeted therapies often elicit profound initial patient responses, these effects are transient due to residual disease leading to acquired resistance. How tumors transition between drug responsiveness, tolerance and resistance, especially in the absence of preexisting subclones, remains unclear. In epidermal growth factor receptor (EGFR)-mutant lung adenocarcinoma cells, we demonstrate that residual disease and acquired resistance in response to EGFR inhibitors requires Aurora kinase A (AURKA) activity. Nongenetic resistance through the activation of AURKA by its coactivator TPX2 emerges in response to chronic EGFR inhibition where it mitigates drug-induced apoptosis. Aurora kinase inhibitors suppress this adaptive survival program, increasing the magnitude and duration of EGFR inhibitor response in preclinical models. Treatment-induced activation of AURKA is associated with resistance to EGFR inhibitors in vitro, in vivo and in most individuals with EGFR-mutant lung adenocarcinoma. These findings delineate a molecular path whereby drug resistance emerges from drug-tolerant cells and unveils a synthetic lethal strategy for enhancing responses to EGFR inhibitors by suppressing AURKA-driven residual disease and acquired resistance

Nanocellulose/bioactive glass cryogels as scaffolds for bone regeneration

A major challenge exists in the preparation of scaffolds for bone regeneration, namely, achieving simultaneously bioactivity, biocompatibility, mechanical performance and simple manufacturing. Here, cellulose nanofibrils (CNF) are introduced for the preparation of scaffolds taking advantage of their biocompatibility and ability to form strong 3D porous networks from aqueous suspensions. CNF are made bioactive for bone formation through a simple and scalable strategy that achieves highly interconnected 3D networks. The resultant materials optimally combine morphological and mechanical features and facilitate hydroxyapatite formation while releasing essential ions for in vivo bone repair. The porosity and roughness of the scaffolds favor several cell functions while the ions act in the expression of genes associated with cell differentiation. Ion release is found critical to enhance the production of the bone morphogenetic protein 2 (BMP-2) from cells within the fractured area, thus accelerating the in vivo bone repair. Systemic biocompatibility indicates no negative effects on vital organs such as the liver and kidneys. The results pave the way towards a facile preparation of advanced, high performance CNF-based scaffolds for bone tissue engineering

RA-MAP, molecular immunological landscapes in early rheumatoid arthritis and healthy vaccine recipients

Rheumatoid arthritis (RA) is a chronic inflammatory disorder with poorly defined aetiology characterised by synovial inflammation with variable disease severity and drug responsiveness. To investigate the peripheral blood immune cell landscape of early, drug naive RA, we performed comprehensive clinical and molecular profiling of 267 RA patients and 52 healthy vaccine recipients for up to 18 months to establish a high quality sample biobank including plasma, serum, peripheral blood cells, urine, genomic DNA, RNA from whole blood, lymphocyte and monocyte subsets. We have performed extensive multi-omic immune phenotyping, including genomic, metabolomic, proteomic, transcriptomic and autoantibody profiling. We anticipate that these detailed clinical and molecular data will serve as a fundamental resource offering insights into immune-mediated disease pathogenesis, progression and therapeutic response, ultimately contributing to the development and application of targeted therapies for RA.</p