290 resultados para TEORIA DA ARTE


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The determination of veterinary drug residues in foods of animal origin is an important issue because of the risk these compounds pose to human health in addition to their persistence and tendency to bioaccumulate. In recent years, significant progress has been made in the area and this review presents the state of the art in sample preparation procedures associated with chromatographic techniques coupled to mass spectrometry for multiresidue determination of veterinary drugs in food of animal origin at concentration levels suitable for the control of residues and contaminants in food.

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The year 2013 marks the centennial of that wondrous year in which Niels Bohr proposed a novel theory about the constitution of atoms and small molecules after which the way we regard atoms and their behaviour began to be drastically altered. Bohr drew on several sources for his original description of the atoms, most importantly on spectroscopy and Balmer's equation thereof, the new quantum hypothesis advanced a few years earlier by Planck, and the planetary atom proposed by Rutherford. Although Bohr's ideas were to be eventually overtaken by the advent of quantum mechanics, his theory was the basis of a new thinking about atoms and molecules which constitutes an invaluable asset in the development of science ever since.

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This paper reports the use of alternative materials for teaching experimental chemistry. In this context, nimesulide and propranolol tablets were used to teach chemical concepts about acid-base reactions according to Brönsted-Lowry protonic Theory. Important topics of Organic, Analytical and Pharmaceutical Chemistry were discussed, such as purification by acid-base extraction, solubility of organic compounds in aqueous solutions, buffers, the dissociation constant (pKa), potentiometric titration and ionization of drugs in biological fluids. The purification of propranolol and nimesulide from tablets produced yields of 75% and 90%, respectively. The experimental values of pKa for both drugs were in agreement with those from the literature.

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Brazilian biodiversity is a colossal source of secondary metabolites with remarkable structural features, which are valuable in further biodiscovery studies. In order to fully understand the relations and interactions of a living system with its surroundings, efforts in natural product chemistry are directed toward the challenge of detecting and identifying all the molecular components present in complex samples. It is plausible that this endeavor was born out of recent technological sophistication in secondary metabolite identification with sensitive spectroscopic instruments (MS and NMR) and higher resolving power of chromatographic systems, which allow a decrease in the amount of required sample and time to acquire data. Nevertheless, the escalation of data acquired in these analyses must be sorted with statistical and multi-way tools in order to select key information. Chromatography is also of paramount importance, more so when selected compounds need to be isolated for further investigation. However, in the course of pursuing a "greener" environment, new policies, with an aim to decrease the use of energy and solvents, are being developed and incorporated into analytical methods. Metabolomics could be an effective tool to answer questions on how living organisms in our huge biodiversity work and interact with their surroundings while also being strategic to the development of high value bio-derived products, such as phytotherapeutics and nutraceuticals. The incorporation of proper phytotherapeutics in the so-called Brazilian Unified Health System is considered an important factor for the urgent improvement and expansion of the Brazilian national health system. Furthermore, this approach could have a positive impact on the international interest toward scientific research developed in Brazil as well as the development of high value bio-derived products, which appear as an interesting economic opportunity in national and global markets. Thus, this study attempts to highlight the recent advances in analytical tools used in detection of secondary metabolites, which can be useful as bioproducts. It also emphasizes the potential avenues to be explored in Brazilian biodiversity, known for its rich chemical diversity.

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We report a didactic experience in teaching Pearson's theory (HSAB) to graduate students in organic chemistry. This approach was based on teaching students how to use computer programs to calculate frontier orbitals (HOMO-LUMO). The suggested level of calculation was a semi-empiric PM3, proving to be efficient for obtaining robust and fast numerical results that can be performed easily in the classroom. We described a practical computational exercise and asked students to compare these numerical data with qualitative analysis using valence bond theory. A comprehensive solution of this exercise is presented, aiming to support teachers in their lessons.

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The constant evolution of science and the growing demand for new technologies have led to new techniques in instrumentation that can improve detection, separation, resolution, and peak capacity. Comprehensive two-dimensional liquid chromatography (LC×LC) is presented as a powerful tool in complex sample analyses. During an analysis, a sample is subjected to two independent separation mechanisms that are combined, resulting in increased resolving power. For appropriate application of LC×LC, understanding the influence of parameters that require optimization is necessary. The main purpose of optimization is to predict the combination of stationary phases, separation conditions, and instrumental requirements to obtain the best separation performance. This review discusses theoretical, intrumental, and chemometric aspects of LC×LC and focuses on its applications in foods. It aims to provide a clear understanding of the aspects that can be used as strategies in the optimization of this analytical method.

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Along the historical background of science, the hydrogen bond became widely known as the universal interaction, thus playing a key role in many molecular processes. Through the available theoretical approaches, many of these processes can be unveiled on the basis of the molecular parameters of the subject intermolecular system, such as the variation of bond length and mainly the frequency shift observed in the proton donor. Supported by the natural bond analysis (NBO) with the quantification of the hybridization contributions, the structural deformations and vibrational effects cited above are also attributed to the outcome of the intermolecular interaction strength, which consequently can be estimated by means of the quantum theory of atoms in molecules (QTAIM) as well as evaluated by the symmetry-adapted perturbation theory (SAPT). Moreover, to identify the preferential interaction sites for proton donors and acceptors, the molecular electrostatic potential (MEP) is useful in this regard.

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Hydrophilic interaction liquid chromatography (HILIC) has been gaining increased attention for its effective separation of highly polar compounds, which include carbohydrates, amino acids, pharmaceutical compounds, proteins, glycoproteins, nucleosides, etc. Polar compounds are usually poorly retained on reverse-phase liquid chromatography (RP-HPLC) columns or have poor solubility in the apolar mobile phase of normal-phase high performance liquid chromatography (NP-HPLC). Since HILIC uses organic solvents such as ACN or MeOH ( > 70%), also used in RP-HPLC and polar stationary phases similar to NP-HPLC (bare silica, diol, amino, amide, saccharide, zwitterionic stationary phases, etc.), it represents a hybrid of the two separation modes. The high organic content in the MP leads to good compatibility with mass spectrometry (MS), increasing the detectivity. This review describes the fundamentals of HILIC and highlights some interesting applications.

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Dinâmica Molecular (DM) é uma ferramenta computacional poderosa usada em Química Medicinal para o planejamento racional de fármacos. DM é uma extensão da Mecânica Molecular, onde o comportamento dinâmico de um sistema molecular é simulado através da integração numérica das equações de movimento. Esta técnica tem sido usada extensivamente para auxiliar e complementar o planejamento de novos ligantes de um alvo terapêutico, bem como estimar a sua potência. Este artigo enfoca a teoria básica da DM clássica e suas importantes aplicações no planejamento racional de potenciais compostos bioativos, particularmente compostos com atividade anti-HIV.

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Em vista da eficiência comprovada da biorremediação na degradação de compostos tóxicos ao ser humano, como o benzeno, tolueno, etilbenzeno e xilenos (BTEX), diversas empresas, principalmente as relacionadas com consultorias e remediação ambiental, têm despertado grandes interesses pela implantação da biorremediação como opção para a reabilitação de áreas contaminadas. Em países desenvolvidos, como os Estados Unidos, Canadá e vários países da Europa, a técnica bioquímica de remediação vem sendo amplamente utilizada em trabalhos que se baseiam, por exemplo, no tratamento de solos contaminados por hidrocarbonetos de petróleo. Porém, ao contrário do que se tem notado nesses países, no Brasil, os projetos de biorremediação ainda estão no campo da teoria, com poucos casos práticos, embora exista uma probabilidade real de expansão. A esse despeito, uma das maiores pertinências dessa revisão é elucidar as vantagens que essa técnica pode oferecer quando é utilizada para a degradação de compostos, como os BTEX, em solos tipicamente brasileiros, cujas características físico-químicas contribuem, em muito, para a degradação desses contaminantes. Nessa conjuntura, pesquisas revelam que os fatores ambientais (como teores de umidade e oxigênio) e a disponibilidade de nutrientes nos solos, além das condições climáticas do Brasil, são bastante adequadas para o emprego dessa técnica. Isso pode trazer como vantagens, ótima relação custo-benefício e maior eficiência na degradação de compostos tóxicos e recalcitrantes frente à maioria das técnicas convencionais de remediação. Em síntese, a presente revisão busca enfocar o estado da arte das técnicas de biorremediação de contaminantes em solos, apresentando as mais atuais e recentes aplicações e inovações, tanto no âmbito nacional quanto no internacional.

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O artigo examina o que está envolvido no processo de conhecer e julgar outras pessoas, questão central para a compreensão do projeto autobiográfico de Rousseau. Isso é feito sobretudo a partir da análise de algumas figuras de "observadores" que encontramos na obra de Rousseau: o "Rousseau" dos Dialogues, Émile, Saint-Preux e Wolmar.

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Este artigo analisa e compara a reflexão de Hegel e de W. Benjamin sobre a crise da arte na época moderna, a partir de semelhanças e diferenças entre a tese do fim da arte, defendida pelo primeiro, e a concepção da perda da aura na arte, afirmada pelo segundo. Ao contrário de W Benjamin, que se detém na mudança do conceito de arte promovida pelos meios técnicos, Hegel pensa a transformação da arte a partir de um ponto de vista histórico amplo, que envolve toda a história da arte, desde os tempos antigos até a época moderna.

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Este artigo pretende oferecer uma re-interpretação da suposta tese hegeliana sobre o fim da arte. A especulação estética de Hegel não envolve uma constatação do fim da arte enquanto fenômeno histórico, mas apenas da sua transformação gradual a partir do predomínio da reflexão sobre intuição na idade moderna.

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O objetivo deste texto é apontar os pontos de proximidade e de diferença entre as reflexões de Nietzsche e de Platão sobre o papel da arte para o autogoverno do indivíduo e a autonomia e soberania da cultura.

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