Academic literature on the topic '(Biol.)'
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Journal articles on the topic "(Biol.)"
Cotrina Cabello, Guillermo Gomer, Lorgio Noel Masgo Sanchez, Yosely Yomayra Tumbay Ambrocio, Italo Wile Alejos Patiño, Pedro Córdova Mendoza, and Alberto Rivelino Patiño Rivera. "Efectos del biol y súper biol en la producción agroecológica de la lechuga (lactuca sativa) variedad seda en el centro poblado de Chinchopampa –Chaglla – Pachitea – Huánuco." Julio-Diciembre 2020, no. 3 (July 6, 2020): 17–31. http://dx.doi.org/10.47058/joa3.2.
Full textMallén Rivera, Carlos. "BIOL. JUANA HUERTA CRESPO 1929 - 2011." Revista Mexicana de Ciencias Forestales 2, no. 5 (May 28, 2019): 3–4. http://dx.doi.org/10.29298/rmcf.v2i5.579.
Full textDay, P. L., W. C. Langston, and W. J. Darby. "Proc. SOc. Exp. Biol. and Med." Nutrition Reviews 37, no. 4 (April 27, 2009): 114–15. http://dx.doi.org/10.1111/j.1753-4887.1979.tb02227.x.
Full textPloegh, Hidde. "A European slant on mol biol." Nature 413, no. 6857 (October 2001): 679–80. http://dx.doi.org/10.1038/35099630.
Full textNot Available, Not Available. "Corrigendum: Mar. Biol. 132: 21-28." Marine Biology 136, no. 2 (March 28, 2000): 378. http://dx.doi.org/10.1007/s002270050696.
Full textGutierrez Arce, Felipe, Sandy Diaz Plasencia, Zulema Rojas Vásquez, Luis Asunción Vallejos Fernández, and Walter Gutierrez Arce. "Elaboración de abono orgánico (biol) para su utilización en la producción de alfalfa (Medicago sativa v. vicus) en Cajamarca." REVISTA PERSPECTIVA 20, no. 4 (February 7, 2020): 441–47. http://dx.doi.org/10.33198/rp.v20i2.00057.
Full textVogel, K., T. Opfermann, S. Wiegand, J. Biermann, M. Busch, T. Winkens, and M. Freesmeyer. "Relationship between estimated glomerular filtration rate and biological half-life of 131I." Nuklearmedizin 52, no. 05 (2013): 164–69. http://dx.doi.org/10.1055/s-0038-1625739.
Full textDÍAZ, Percy, Cheryl TELLO, and Luis ARÉVALO-LÓPEZ. "EFECTO DEL USO DE TUTORES Y APLICACIÓN DE BIOFERTILIZANTES EN EL CRECIMIENTO Y DESARROLLO DE Plukenetia volubilis L. “SACHA INCHI”." Folia Amazónica 23, no. 2 (December 12, 2014): 119. http://dx.doi.org/10.24841/fa.v23i2.17.
Full textLinares Gabriel, Ariadna, Catalino Jorge López-Collado, Mario Alejandro Hernández-Chontal, Joel Velasco-Velasco, and Gustavo López-Romero. "Application of soil amendments and their effect in the growth of heliconia." Ornamental Horticulture 24, no. 3 (September 28, 2018): 248–54. http://dx.doi.org/10.14295/oh.v24i3.1252.
Full textLan, Weijie, and Don W. Cleveland. "A chemical tool box defines mitotic and interphase roles for Mps1 kinase." Journal of Cell Biology 190, no. 1 (July 12, 2010): 21–24. http://dx.doi.org/10.1083/jcb.201006080.
Full textDissertations / Theses on the topic "(Biol.)"
Quintero, Emmeris Ivan Quintero. "Insumos e indicadores Biol?gicos em Agrossistemas com Bananeiras." Universidade Federal Rural do Rio de Janeiro, 2010. https://tede.ufrrj.br/jspui/handle/jspui/1165.
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Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior - CAPES
Studies were performed in the experimental area of Embrapa Agrobiologia, region - RJ, in order to evaluate the association of arbuscular mycorrhizal fungi (AMF) with a variety of banana ?Grand nine ", and the potential antagonist in AMF biocontrol nematodes. We also tested biological indicators and products as alternatives to monitoring and restoration of ecosystems with bananas. The first study evaluated the microbial activity in soil samples from two management systems with bananas in the municipality of Casimiro de Abreu, RJ. In the second study, was evaluated the AGAS organic product for the control of nematodes in banana. In the third, was evaluated the potential antagonist in AMF biocontrol nematode Radophulus similis and their contribution in the development of banana plants in the greenhouse. In the fourth study was estimated the effect of using two management systems with bananas in the community of soil fauna in Casimiro de Abreu, RJ. The indices of diversity, richness and density of macrofauna groups was calculate in each system. The results indicated no significant differences between management systems in relation to carbon and nitrogen levels of microbial biomass and soil organic carbon ratio vs. carbon microbial biomass in each season, while the variables soil basal respiration and metabolic quotient indicated that the organic farming system was greater efficiency of microbial biomass and the use of substrate by soil microorganisms than the system with conventional tillage. The organic product AGAS showed significant difference in population of the nematode Meloidogyne spp. and Radophulus similis both in samples of roots after 60 days of treated. In the field was control to phytoparasitic R. similis with the AGAS treatment showing a decrease in soil at 120 days. In the laboratory tests were performed with R. similis and the results demonstrated that the effects of exposure of nematodes to organic product showed a high percentage of control, especially in higher dosages with a 100% with respect to the nematicide effect in Radophulus. Regarding the development of plants in treatments with species of arbuscular mycorrhizal fungi inoculated in banana no significant difference. The foliar phosphorus analyzed varied significantly in the treatment with the fungus Scutellospora calospora, and foliar calcium and magnesium for the treatments with fungi: S. calospora, Entrhopospora colombiana and S. calospora + Glomus clarum. AMF reduced the population of the nematode R. similis in roots of banana plants in a greenhouse, and S. calospora and G. clarum were the most efficient. In soil macrofauna results indicated a reduction in the banana organic system, with lower density and lower richness of taxonomic groups when compared with the conventional system. The group of decomposers and predators showed better soil quality in organic farming system especially in the summer due to its greater diversity and density at this season of year.
Os trabalhos foram realizados com o objetivo de avaliar a associa??o de fungos micorr?zicos arbusculares (FMAs) com a variedade de banana ?Grand nine?, e o potencial antagonista dos FMAs no biocontrole dos nemat?ides. Tamb?m foram testados indicadores e insumos biol?gicos como alternativas para recupera??o e monitoramento de ecossistemas pertubados com bananeiras. O primeiro estudo avaliou a atividade microbiana do solo em amostras de dois sistemas de manejo com bananeiras no municipio de Casimiro de Abreu, RJ. No segundo estudo avaliou-se o insumo org?nico com ?cido glut?mico e saponinas (AGAS) para o controle de nemat?ides em bananeiras na Pesagro, Serop?dica, RJ. O terceiro avaliou o potencial antagonista dos FMAs no biocontrole do nemat?ide Radophulus similis e seu aporte no desenvolvimento de plantas de bananeira em casa de vegeta??o da Embrapa Agrobiologia. No quarto estudo se estimou o efeito do uso de dois sistemas de manejo com bananeiras na comunidade da macrofauna ed?fica em Casimiro de Abreu, RJ. Foram calculados os ?ndices de biodiversidade, riqueza e densidade dos grupos de macrofauna em cada sistema. Os resultados indicaram que n?o houve diferen?a significativa entre sistemas de manejo com rela??o a valores de carbono e nitrog?nio da biomassa microbiana, e rela??o carbono org?nico vs carbono da biomassa microbiana nas ?pocas de ver?o e inverno, enquanto que as vari?veis respira??o basal do solo e quociente metab?lico indicaram que no sistema com cultivo org?nico houve uma maior efici?ncia da biomassa microbiana e do uso do substrato pelos microorganismos do solo do que o sistema com cultivo convencional. O produto org?nico AGAS proporcionou uma redu??o nos ?ndices populacionais de Meloidogyne spp nas doses de 1,51 e 2,02 ml.cm?? e de Radophulus similis na dose de 2,02 ml.cm?? ambos nas amostras de ra?zes ap?s 60 dias das plantas serem tratadas. No campo houve redu??o da popul??o de R. similis no solo aos 120 dias ap?s o tratamento com AGAS nas doses de 0,5 e 1,0 ml.cm??. No laborat?rio, quando diferentes estadios de R. similis foram expostos ao produto AGAS nas doses 1,0; 1,5 e 2,0 ml.m?? observou-se uma alta taxa de mortalidade chegando a 100% nas doses mais altas demonstrando efeito nematicida ?in vitro?. Com rela??o ao desenvolvimento das plantas, nos tratamentos com esp?cies de fungos micorr?zicos arbusculares inoculadas em plantas de bananeiras n?o houve diferen?a significativa. Por?m o teor de f?sforo foliar analisado aumentou significativamente no tratamento com o fungo Scutellospora calospora, e nos teores foliares de c?lcio e magn?sio para os tratamentos com os fungos: S. calospora, Entrhopospora colombiana e S. calospora+Glomus clarum. Os FMAs reduziram a popula??o do nemat?ide R. similis nas ra?zes das plantas de bananeira em casa de vegeta??o, sendo que S. calospora e G. clarum foram as mais eficientes. Na macrofauna do solo os resultados indicaram uma redu??o no sistema org?nico com bananeira, apresentando menor densidade e menor riqueza de grupos taxon?micos quando comparado com o sistema convencional. Os grupos decompositores e predadores apresentaram no ver?o a maior diversidade e densidade indicando uma melhor qualidade do solo no sistema com cultivo org?nico.
Silveira, Raniere Fagundes de Melo. "Atividades biol?gicas de xilana de sabugo de milho." Universidade Federal do Rio Grande do Norte, 2010. http://repositorio.ufrn.br:8080/jspui/handle/123456789/12555.
Full textConselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico
The corn cob is an agricultural by-product still little used, this in part due to the low knowledge of the biotechnological potential of their molecules. Xylan from corn cobs (XSM) is a polysaccharide present in greater quantity in the structure of plant and its biotechnology potential is little known. This study aimed to the extraction, chemical characterization and evaluation of biological activities of xylan from corn cobs. To this end, corncobs were cleaned, cut, dried and crushed, resulting in flour. This was subjected to a methodology that combines the use of alkaline conditions with waves of ultrasound. After methanol precipitation, centrifugation and drying was obtained a yield of 40% (g/g flour). Chemical analysis indicated a high percentage of polysaccharides in the sample (60%) and low contamination by protein (0.4%) and phenolic compounds (> 0.01%). Analysis of monosaccharide composition indicated the presence of xylose:glucose:arabinose:galactose:mannose:glucuronic acid in a molar ratio 50:20:15:10:2.5:2.5. The presence of xylan in the sample was confirmed by nuclear magnetic resonance (?H and ??C) and infrared spectroscopy (IR). Tests were conducted to evaluate the antioxidant potential of XSM. This showed a total antioxidant capacity of 48.45 EAA/g sample. However, did not show scavenging activity of superoxide and hydroxyl radical and also reducing power. But, showing a high capacity chelating iron ions with 70% with about 2 mg/mL. The ability to XSM to influence cell proliferation in culture was also evaluated. This polymer did not influence the proliferation of normal fibroblast cells (3T3), however, decreased the rate of proliferation of tumor cells (HeLa) in a dose-dependent, reaching an inhibition of about 50% with a concentration around 2 mg/mL. Analyzing proteins related to cell death, by immunoblotting, XSM increases the amount of Bax, Bcl-2 decrease, increase cytochrome c and AIF, and reduce pro-caspase-3, indicating the induction of cell death induced apoptosis dependent and independent of caspase. XSM did not show anticoagulant activity in the PT test. However, the test of activated partial thromboplastin time (aPTT), XSM increased clotting time at about 5 times with 600 ?g of sample compared with the negative control. The presence of sulfate on the XSM was discarded by agarose gel electrophoresis and IR. After carboxyl-reduction of XSM the anticoagulant activity decreased dramatically. The data of this study demonstrate that XSM has potential as antioxidant, antiproliferative and anticoagulant compound. Future studies to characterize these activities of XSM will help to increase knowledge about this molecule extracted from corn and allow their use in functional foods, pharmaceuticals and chemical industries.
O sabugo de milho ? um subproduto agr?cola ainda pouco utilizado, isto se deve em parte ao baixo conhecimento do potencial biotecnol?gico de suas biomol?culas. Xilana de sabugo de milho (XSM) ? um polissacar?deo presente em maior quantidade na estrutura do vegetal e seu potencial biotecnol?gico ? pouco conhecido. Este trabalho teve como objetivo a extra??o, caracteriza??o qu?mica e avalia??o de atividades biol?gicas de XSM. Sabugos de milho foram limpos, cortados, desidratados e triturados, dando origem a uma farinha. Esta foi submetida a uma metodologia que combina o uso de meio alcalino com ondas de ultra-som. Ap?s precipita??o metan?lica, centrifuga??o e secagem obteve-se um rendimento de 40% (g/g de farinha). An?lises qu?micas indicaram um alto percentual de polissacar?deos na amostra (60%) e baixa contamina??o por prote?nas (0.4%) e compostos fen?licos (>0.01%). An?lises da composi??o monossacar?dica por cromatografia em papel e por cromatografia l?quida de alta performance (CLAE) indicaram a presen?a de xilose:glicose:arabinose:galactose:manose:?cido glucur?nico em uma propor??o molar de 50:20:15:10:2,5:2,5. A presen?a de xilana na amostra foi confirmada por resson?ncia magn?tica nuclear (13C e 1H) e por espectroscopia de infravermelho (IR). Testes foram realizados para avalia??o do potencial antioxidante de XSM. Esta mostrou uma capacidade antioxidante total de 48.45 EAA/g de amostra. Contudo, a mesma n?o mostrou atividade sequestradora de super?xido, radical hidroxila bem como poder redutor. Em contra partida, apresentou 70% de atividade quelante de ?ons de ferro na concentra??o de 2 mg/mL. A capacidade de XSM em influenciar a prolifera??o celular em cultura tamb?m foi avaliada. Este polissacar?deo n?o influenciou a prolifera??o de c?lulas fibrobl?sticas normais (3T3), entretanto, diminuiu a taxa de prolifera??o de c?lulas tumorais (HeLa) de maneira dose-dependente, chegando a uma inibi??o de aproximadamente 50% com concentra??o em torno de 2 mg/mL. Analisando prote?nas relacionadas ? morte celular, atrav?s de immunoblotting, XSM aumenta a quantidade de Bax, citocromo c e AIF e diminui Bcl-2 e procaspase- 3, indicando a indu??o de morte celular por apoptose dependente e independente de caspase. XSM n?o apresentou atividade anticoagulante pelo teste de PT. Todavia, no teste de tempo de tromboplastina parcial ativada (aPTT), XSM aumentou o tempo de coagula??o em cerca de 5 vezes utilizando 600 ?g de amostra, quando comparadas com o controle negativo. A presen?a de sulfato ligado a XSM foi descartada por eletroforese em gel de agarose e por IR. Ap?s carboxirredu??o de XSM a atividade anticoagulante diminuiu drasticamente. Os dados deste trabalho demonstram que XSM apresenta potencial como composto antioxidante, antiproliferativo e anticoagulante. Estudos futuros de caracteriza??o dessas atividades do XSM contribuir?o para aumentar o conhecimento sobre esta mol?cula extra?da de milho e permitir?o a sua utiliza??o em alimentos funcionais, produtos farmac?uticos e ind?strias qu?micas.
Frizzo, Matias Nunes. "Avalia??o das bases biol?gicas e sociais do temperamento." Pontif?cia Universidade Cat?lica do Rio Grande do Sul, 2013. http://tede2.pucrs.br/tede2/handle/tede/5463.
Full textTemperament can be regarded as the basis of mood, behavior and personality. It has a strong biological basis, manifested early in the development of the individual, guiding the formation of habits and is relatively stable over time. Although it is known that there are environmental influences, the relationship of temperament with biological markers and social environment is not well defined. Evidence suggests that the temperament and personality traits predict psychiatric disorders and that most of them are recurrent and chronic. Thus, this study aims to investigate the biological and social basis of behavior and in animal models of traits to assess the relationship of temperament with hyperucemia and with self-report of having been bullied in humans. To study the neurobiological basis of this trait, we selected mice with high and low exploration of a central object in an open field. Out of one hundred mice tested, the ten mice with higher (HE) and lower exploratory (LE) activity were evaluated with gene expression (Genechip Mouse Gene 1.0 ST Array Affymetrix) in the striatum and frontal cortex. The results showed 118 and 86 differentially expressed genes (DEGs) in the striatum and frontal cortex, respectively. Through analysis of DEGs biological processes were significantly more enriched in nervous system were development and function and cell-to-cell signaling, particularly in the striatum. These results suggest the involvement of translational and post-translational processes as well as striatal synaptic elements in the trait differences of exploratory behavior. Human studies were conducted with the data collected in a large web-survey on psychological and psychiatric measures (BRAINSTEP). In the study of biological basis of behavior we analyzed temperament in 7.155 males (5.1% hyperuricemic) and 25.225 women (1.8% hyperuricemic). Hyperuricemic subjects scored higher in anger and lower in inhibition and control, but hyperuricemic women also showed a higher emotional sensitivity and a lower degree of volition and coping. Subjects with hyperuricemia present more more externalizing and unstable emotional traits and affective temperaments In the study of the social bases of temperament assessed bullying during childhood and adolescence, through a question on time of exposure to bullying (none, <1 year, 1-3 years and> 3 years). Emotional traits and affective temperaments were evaluated with The Affective and Emotional Composite Temperament Scale (AFECTS). About half of the sample reported exposure to bullying and 10% reported being victimized by peers for longer than 3 years. Longer exposure to bullying was associated with lower Volition, Coping and Control. Bullying victimization was also associated with a much lower proportion of euthymic and hyperthymic types in both genders, which was compensated by an increase mainly in the proportion of depressive, cyclothymic and volatile types. Being bullied was associated with a broad and profound impact on emotional and cognitive domains in all dimensions of emotional traits, and with internalized and unstable affective temperaments. These results, taken together, show the importance of social factors and serum markers, as well as genetic markers of temperament.
O temperamento pode ser considerado como a base do humor, do comportamento e da personalidade, tem uma base biol?gica forte, manifesta-se cedo no desenvolvimento do indiv?duo, norteia a forma??o dos h?bitos sendo relativamente est?vel no decorrer do tempo. Apesar de se saber que h? influ?ncias do meio, n?o est? bem definida a rela??o entre temperamento e o meio social. Evid?ncias sugerem que o temperamento e os tra?os de personalidade predisp?em aos transtornos psiqui?tricos e que a maioria deles ? recorrente e cr?nico. Dessa forma, o presente estudo tem como objetivo investigar as bases biol?gicas e sociais do temperamento em modelos animais de temperamento e avaliar a rela??o do temperamento com hiperuricemia (eleva??o dos n?veis s?ricos de ?cido ?rico) e com o autorrelato de ter sido v?tima de bullying em humanos. Na avalia??o das bases neurobiol?gicas do temperamento foram usados modelos animais, no qual foram selecionados camundongos com alta e baixa explora??o em um teste campo aberto. Foram testados cem camundongos, e posteriormente selecionados os dez camundongos mais exploradores (HE) e os dez menos exploradores (LE), cujo mRNA de c?rtex frontal e estriado foi coletado para posteriormente ser avaliado atrav?s de chips para avalia??o da express?o g?nica (Genechip Mouse Gene 1.0 ST Array - Affymetrix). Os resultados mostraram 86 e 118 genes expressos diferencialmente (DEGS) no estriado e no c?rtex frontal, respectivamente. Atrav?s da an?lise dos DEGs os processos biol?gicos mais significativamente enriquecidos foram o do desenvolvimento do sistema nervoso e da fun??o e sinaliza??o celular, especialmente no estriado, numa compara??o entre animas HE com LE. Estes resultados sugerem o envolvimento de processos de transla??o e p?s-tradu??o, assim como os elementos sin?pticos do estriado nas diferen?as de caracter?sticas de comportamento explorat?rio. Nos estudos em humanos, os dados foram coletados em um grande levantamento via Web atrav?s do Brazilian Internet Study on Temperament and Psychopathology (BRAINSTEP). No estudo de bases biol?gicas do temperamento em humanos, analisamos o temperamento em 7.155 homens (5,1% hiperuric?micos) e 22.225 mulheres (1,8% hiperuric?micas). Indiv?duos hiperuric?micos apresentaram escores mais elevados em raiva e inferiores na inibi??o e controle, j? as mulheres hiperuric?micas tamb?m mostram uma maior sensibilidade emocional e um menor grau de vontade e de enfrentamento. Os resultados demonstraram que indiv?duos com hiperuricemia t?m mais tra?os emocionais e temperamentos afetivos externalizados e inst?veis. No estudo sobre as bases sociais do temperamento avaliamos o bullying durante a inf?ncia e adolesc?ncia, atrav?s de uma pergunta sobre tempo de exposi??o ao bullying (nenhum, <1 ano, 1 a 3 anos e > 3 anos). Tra?os emocionais e temperamentos afetivos foram avaliados com a Escala de Temperamento Afetivo e Emocional (AFECTS). Cerca de metade da amostra relatou exposi??o ao bullying e 10% relataram ter sido v?timas por mais de 3 anos. Vitimas de bullying tamb?m apresentam uma propor??o muito menor de temperamentos eut?micos e hipert?micos em ambos os sexos, o que foi compensado por um aumento, principalmente, na propor??o de tra?os depressivos, ciclot?micos e vol?til. Sofrer bullying foi associado com um impacto amplo e profundo sobre os dom?nios cognitivos e emocionais em todas as dimens?es de tra?os emocionais, e com temperamento afetivo internalizado e inst?vel. Esses resultados, em conjunto, mostram a import?ncia de poss?veis marcadores s?ricos (?cido ?rico) e fatores gen?ticos e sociais sobre os tra?os de temperamento.
Melo, Luciana Fentanes Moura de. "Extratos de Coccoloba alnifolia Casar e suas atividades biol?gicas." PROGRAMA DE P?S-GRADUA??O EM BIOQU?MICA, 2018. https://repositorio.ufrn.br/jspui/handle/123456789/24994.
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Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior (CAPES)
O uso de plantas medicinais ? uma pr?tica comum da humanidade desde a antiguidade. Tal conhecimento baseado na experi?ncia tem sido repassado por muitas comunidades e grupos ?tnicos, e serve como ponto de partida para estudos bioqu?micos e farmacol?gicos dos princ?pios ativos presentes nas plantas. Para isto, neste trabalho foram avaliados o potencial antioxidante e tamb?m biol?gico, utilizando sistemas in vitro e in vivo dos diferentes extratos obtidos de folhas da planta Coccoloba alnifolia. Foram obtidos inicialmente seis extratos: hexano (EH), clorof?rmio (EC), etan?lico (EE), metan?lico (EM), ?gua final (EAF) e aquoso (EA) a partir das folhas frescas da planta. Posteriormente, foram avaliados o teor de a??car, prote?nas e compostos fen?licos. Os resultados obtidos na triagem fitoqu?mica sugerem a presen?a de fen?is, flavonoides, saponinas, n?cleo triterp?nicos e esteroidais e n?cleo esteroidal insaturado, j? com a metodologia de cromatografia em camada delgada (CCD), foi observado uma abund?ncia de flavonoides. Foram realizados quatro ensaios: Teste do Poder Redutor, Quela??o de ?ons Metais, Quela??o de Cobre e Atividade Sequestradora de Radical Hidroxila. Estes ensaios permitiram verificar que os extratos apresentaram atividade antioxidante nas concentra??es avaliadas de 100, 250 e 500 ?g/mL. Foi verificado principalmente para os extratos EE, EM e EA as atividades antioxidante nos ensaios poder redutor e sequestro do radical hidroxila. A correla??o de Pearson mostrou que estes dados est?o associados aos compostos fen?licos e a??cares. E com o modelo das linhagens celulares foi observado que a maioria dos extratos avaliados neste trabalho n?o mostrou-se citot?xico para as linhagens celulares. Os extratos tamb?m n?o inibiram o crescimento da levedura Candida parapsilosis. Os extratos obtidos da folha de C. alnifolia apresenta um potencial antioxidante interessante, e os resultados obtidos tanto nos modelos in vitro, como as linhagens celulares, refor?am que s?o necess?rios mais estudos para compreender o potencial destes extratos in vivo e identificar quais s?o as biomol?culas associadas com estas atividades e seus respectivos potenciais biotecnol?gicos.
The use of medicinal plants has been a common practice in folk medicine. This knowledge has been based on the experience that it has been passed though many generations. However, many times this knowledge do not have any scientific base. The molecules responsive for these activities are the secondary metabolic produce as a response to environmental conditions (biotic or abiotic stress). The Mata atl?ntica biome has a rich flora, which needs to be studied for its biological activities, and its potential to identify new biomolecules. In order to do this, six extracts (HE, CE, EE, ME, WEE e WE) were obtained from Coccoloba alnifolia leaves and then it was evaluated the antioxidant and the biological potential using different in vitro and in vivo systems. First, it was measured the sugar content, proteins and phenolic compounds. Based on these results, qualitative experiments were carried out to determine the secondary metabolites present in these extracts. It was detected the presence of phenols, flavonoids, saponins, triterpenic, and steroidal nuclei and unsaturated steroidal nuclei. After that, it was evaluated the antioxidant potential by four in vitro assay: Redution Power test, Metal Ion Chelation, Copper Chelation and Hydroxyl Radical Scavenging Activity. These assays allowed us verify that the extracts presented antioxidant activity at extract concentrations: 100, 250 and 500 ?g/mL. It was observed the ethanolic, methanolic and aqueous extracts had activity in reducing power and scavenging of the hydroxyl radical. The Pearson?s correlation showed that these results may be associated to the presence of phenolic compounds and sugars. The third in vitro model used in this work was cell culture. When it was used the 3T3 lineage it was observed that these extracts were not cytotoxic. However, it was not observed any antiproliferative activity in tumor cell lineages. In sumary, the data obtained here showed that using in vitro assays that these extracts in special ethanolic and aqueous had an interesting antioxidant potential and it will be important to go further in this research.
Alves, Jovelina Samara Ferreira. "Estudo qu?mico e biol?gico de Genipa americana L. (Jenipapo)." PROGRAMA DE P?S-GRADUA??O EM CI?NCIAS FARMAC?UTICAS, 2014. https://repositorio.ufrn.br/jspui/handle/123456789/22388.
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Genipa americana Linnaeus (Rubiaceae), ocorre amplamente na regi?oNordeste e em outras regi?es do Brasil, como tamb?m em outros pa?ses. Sob oponto de vista medicinal, a esp?cie ? usada pela popula??o para diferentes finscomo: cat?rtico, antidiarr?ico, antigonorr?ico, antiulceroso, analg?sico, emcasos de s?filis, anemia, icter?cia, asma, dentre outros. Devido ao reconhecidouso popular e a escassez de estudos qu?micos e farmacol?gicos, o principalobjetivo deste estudo foi caracterizar os marcadores e/ou compostos ativos eavaliar atividades farmacol?gicas da esp?cie. O estudo iniciou-se com a coletade folhas, frutos maduros e verdes nas media??es da Praia de Barreta (N?siaFloresta-RN), dos quais as folhas foram submetidas ? secagem e moagem.Posteriormente, foram preparados os extratos hidroetan?licos (EH) das folhas,pericarpo e endocarpo dos frutos e fracionados com solventes org?nicos comordem de polaridade crescente (?ter de petr?leo, diclorometano, acetato deetila, e n-butanol). Para an?lise qualitativa do extrato das folhas e frutos foramutilizadas as t?cnicas de Cromatografia em Camada Delgada (CCD) eCromatografia L?quida de Alta Efici?ncia (CLAE). Diversos procedimentoscromatogr?ficos (Cromatografia L?quida a V?cuo, Cromatografia em ColunaCl?ssica e Cromatografia L?quida de Alta Efici?ncia Semi-preparativa) foramutilizados para o isolamento de compostos qu?micos. Adicionalmente,realizaram-se ensaios de atividade anti-inflamat?ria do extrato das folhas, nomodelo de peritonite aguda em camundongos e o ensaio de atividadeantimicrobiana, pelo m?todo de difus?o em disco, com extrato do endocarpo edas folhas de G. americana. Foi observado por CCD e CLAE a presen?a deflavonoides e iridoides no extrato das folhas e iridoides nos extratos dos dopericarpo e endocarpo dos frutos. A partir do extrato da folha foram isolados ecaracterizados dois iridoides, denominados tetrahidro-7-(hidroximetil)1-metoxiciclo-pentapiran-4-carbalde?do, in?dito para a esp?cie e o GF2,provavelmente in?dito na literatura, os carboidratos manitol e GF7 e cincoflavonoides GF4, GF5, GF6, GF8 e GF9. Os seis ?ltimos compostos est?o emfase de elucida??o estrutural. A partir do extrato do endocarpo foram isoladosos compostos GE1, GE2, GE3, GE4 e GE5, os quais est?o em fase deelucida??o estrutural. O extrato das folhas e do endocarpo de G. americanan?o apresentaram atividade antimicrobiana promissora. O extrato das folhasapresentou atividade anti-inflamat?ria nas doses 50, 100, 200 e 300 mg/Kg,observada por meio da inibi??o da migra??o de leuc?citos para o local dainflama??o. T?cnicas de elucida??o estrutural est?o sendo realizadas paraelucida??o de todos os compostos isolados de G. americana. O estudofitoqu?mico e de atividades farmacol?igicas desenvolvidos com as folhas daesp?cie s?o resultados inovadores, pois at? o momento era registrada apresen?a de irirdoides, monoterpenos, ?cidos carbox?licos apenas nos frutos daG. americana. Para as folhas da esp?cie n?o h? relatos na literatura sobre apresen?a de irid?ides e flavonoides.
Genipa americana Linnaeus (Rubiaceae), ocorre amplamente na regi?oNordeste e em outras regi?es do Brasil, como tamb?m em outros pa?ses. Sob oponto de vista medicinal, a esp?cie ? usada pela popula??o para diferentes finscomo: cat?rtico, antidiarr?ico, antigonorr?ico, antiulceroso, analg?sico, emcasos de s?filis, anemia, icter?cia, asma, dentre outros. Devido ao reconhecidouso popular e a escassez de estudos qu?micos e farmacol?gicos, o principalobjetivo deste estudo foi caracterizar os marcadores e/ou compostos ativos eavaliar atividades farmacol?gicas da esp?cie. O estudo iniciou-se com a coletade folhas, frutos maduros e verdes nas media??es da Praia de Barreta (N?siaFloresta-RN), dos quais as folhas foram submetidas ? secagem e moagem.Posteriormente, foram preparados os extratos hidroetan?licos (EH) das folhas,pericarpo e endocarpo dos frutos e fracionados com solventes org?nicos comordem de polaridade crescente (?ter de petr?leo, diclorometano, acetato deetila, e n-butanol). Para an?lise qualitativa do extrato das folhas e frutos foramutilizadas as t?cnicas de Cromatografia em Camada Delgada (CCD) eCromatografia L?quida de Alta Efici?ncia (CLAE). Diversos procedimentoscromatogr?ficos (Cromatografia L?quida a V?cuo, Cromatografia em ColunaCl?ssica e Cromatografia L?quida de Alta Efici?ncia Semi-preparativa) foramutilizados para o isolamento de compostos qu?micos. Adicionalmente,realizaram-se ensaios de atividade anti-inflamat?ria do extrato das folhas, nomodelo de peritonite aguda em camundongos e o ensaio de atividadeantimicrobiana, pelo m?todo de difus?o em disco, com extrato do endocarpo edas folhas de G. americana. Foi observado por CCD e CLAE a presen?a deflavonoides e iridoides no extrato das folhas e iridoides nos extratos dos dopericarpo e endocarpo dos frutos. A partir do extrato da folha foram isolados ecaracterizados dois iridoides, denominados tetrahidro-7-(hidroximetil)1-metoxiciclo-pentapiran-4-carbalde?do, in?dito para a esp?cie e o GF2,provavelmente in?dito na literatura, os carboidratos manitol e GF7 e cincoflavonoides GF4, GF5, GF6, GF8 e GF9. Os seis ?ltimos compostos est?o emfase de elucida??o estrutural. A partir do extrato do endocarpo foram isoladosos compostos GE1, GE2, GE3, GE4 e GE5, os quais est?o em fase deelucida??o estrutural. O extrato das folhas e do endocarpo de G. americanan?o apresentaram atividade antimicrobiana promissora. O extrato das folhasapresentou atividade anti-inflamat?ria nas doses 50, 100, 200 e 300 mg/Kg,observada por meio da inibi??o da migra??o de leuc?citos para o local dainflama??o. T?cnicas de elucida??o estrutural est?o sendo realizadas paraelucida??o de todos os compostos isolados de G. americana. O estudofitoqu?mico e de atividades farmacol?igicas desenvolvidos com as folhas daesp?cie s?o resultados inovadores, pois at? o momento era registrada apresen?a de irirdoides, monoterpenos, ?cidos carbox?licos apenas nos frutos daG. americana. Para as folhas da esp?cie n?o h? relatos na literatura sobre apresen?a de irid?ides e flavonoides.
Nogueira, Lilian Capanema. "Resist?ncia adesiva ? microtra??o de restaura??es biol?gicas posteriores." UFVJM, 2014. http://acervo.ufvjm.edu.br:8080/jspui/handle/1/299.
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Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior (CAPES)
Funda??o de Amparo ? Pesquisa do estado de Minas Gerais (FAPEMIG)
A ?Restaura??o Biol?gica? ? uma t?cnica que pode oferecer uma excelente biocompatibilidade, desgaste fisiol?gico e mant?m as caracter?sticas est?ticas e funcionais da estrutura do dente tais como brilho de superf?cie, textura, dureza, tamanho, forma, cor e resili?ncia. O objetivo do presente estudo foi comparar pelo ensaio de microtra??o a resist?ncia ? ades?o de restaura??es biol?gicas ap?s cimenta??o no substrato dentin?rio em compara??o as convencionais restaura??es est?ticas cer?micas e analisar suas ?reas de fratura. Foram selecionados vinte e quatro terceiros molares humanos h?gidos, rec?m-extra?dos, que tiveram suas por??es coron?rias seccionadas em dentina e aleatoriamente divididos em dois grupos (n=12), grupo controle (Restaura??es Cer?micas IPS e.max ZirPress) e grupo experimental (Restaura??es Biol?gicas). Para confec??o das restaura??es biol?gicas, discos de dentina foram seccionados com espessura de 2,0 mm cada. Pastilhas de cer?mica foram confeccionadas com as mesmas dimens?es dos discos de dentina. As restaura??es foram cimentadas com cimento resinoso Rely X ARC e ap?s 24 horas submetidos a 10.000 ciclos de termociclagem (5-55?C). Os dentes foram seccionados perpendicularmente ? interface de uni?o, gerando palitos de 1 mm2 e submetidos a ensaio de microtra??o com velocidade de 0,5 mm/min, utilizando uma c?lula de carga de 5Kg. Foi realizada an?lise do padr?o de fratura em lupa estereosc?pica com o aumento de 40x. Esp?cimes representativos foram caracterizados por MEV/EDS para an?lise da morfologia geral e composi??o qu?mica elementar quantitativa dos materiais. Esp?cimes representativos de cada grupo foram submetidas ao protocolo de nanoinfiltra??o com AgNO3 e analisados em MEV. Os dados foram analisados pelo teste t de Student para esp?cimes independentes (p ? 0.05) e do qui-quadrado. N?o foi observada diferen?a estat?stica significativa em rela??o ? resist?ncia ? ades?o. Houve diferen?a significativa (p=0,015) quanto ao tipo de fratura, com 75% de fraturas adesivas para o grupo experimental. As restaura??es biol?gicas apresentaram comportamento semelhante em termos de resist?ncia ? ades?o, quando comparadas ?s restaura??es cer?micas, podendo vir a ser consideradas alternativas para o restabelecimento est?tico-funcional de dentes posteriores.
Disserta??o (Mestrado) ? Programa de P?s-Gradua??o em Odontologia, Universidade Federal dos Vales do Jequitinhonha e Mucuri, 2014.
ABSTRACT ?Biological restoration? offers excellent biocompatibility and maintains the esthetic and functional characteristics of the tooth, such as physiological wear, surface shine, texture, hardness, size, shape, color and resilience. The aim of the present study was to evaluate the bond strength of biological restorations on dentin in comparison to conventional porcelain restorations through a microtraction test and characterize areas of fracture. The crowns of 24 recently extracted sound human third molars were planed to the dentin and randomly divided into a control group (n = 12; porcelain restorations ? IPS e.max ZirPress) and experimental group (n = 12, biological restorations). Biological restorations were made from fragments of the teeth cut to a thickness of 2.0 mm. Porcelain crowns were made with the same dimensions as the biological fragments. All restorations were cemented with Rely X ARC resin and, after 24 hours, submitted to 10,000 thermal cycles (5 to 55 ?C). The teeth were sectioned perpendicularly to the interface of the union for the obtainment of samples measuring 1 mm2, which were submitted to microtraction using the EZ Test - L universal testing machine operating at 0.5 mm/min with a 5 Kg cell load. Standard fracture analysis was performed with a stereomicroscopic magnifying glass (magnification: 40 x). Representative samples were characterized by scanning electron microscopy (SEM) for the analysis of general morphology and the quantitative element composition of the materials. Additional representative samples from each group were submitted to nano-injection with AgNO3 and analyzed using SEM. Data analysis involved the Student?s t-test for independent samples and the chi-squared test (p ? 0.05). No significant difference in bond strength was found, but a significant difference was found regarding the type of fracture (p = 0.015), with an adhesive fracture rate of 75% in the experimental group. Biological restorations demonstrate similar behavior to that found in porcelain restorations with regard to bond strength and constitute a viable option for the reestablishment of function and esthetics on posterior teeth.
Barroso, Poliana Ribeiro. "Fitoqu?mica e atividades biol?gicas de Miconia ferruginata DC. (Melastomataceae)." UFVJM, 2015. http://acervo.ufvjm.edu.br:8080/jspui/handle/1/759.
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Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior (Capes)
Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico (CNPq)
Funda??o de Amparo ? Pesquisa do estado de Minas Gerais (FAPEMIG)
As plantas medicinais s?o fontes promissoras de novas drogas, em que a regi?o do Cerrado se destaca pela sua vasta biodiversidade. Dentre as plantas medicinais utilizadas nesta regi?o se encontra a esp?cie Miconia ferruginata DC. que ? conhecida como pixirica-do-campo ou babaten?o. Esta esp?cie ? utilizada no tratamento de doen?as de pele, e outras de origens inflamat?rias, parasit?rias e infecciosas, por?m os estudos qu?micos s?o escassos. Assim, os objetivos deste trabalho foram avaliar o perfil qu?mico e o potencial biol?gico da M. ferruginata (Melastomataceae). A esp?cie foi coletada no munic?pio de Diamantina, MG do qual foram preparados os extratos aquosos e etan?licos das folhas/flores e do caule. Por meio da triagem fitoqu?mica e das an?lises de CLAE-DAD-EM obteve-se um perfil qu?mico rico em compostos fen?licos. Foi poss?vel a identifica??o da presen?a de taninos, ?cidos fen?licos, flavonoides, e derivados glicosilados da quercetina. Pela an?lise dos constituintes vol?teis por CG-EM foi poss?vel identificar a presen?a de quatorze compostos, sendo eles pertencentes as classes dos sesquiterpenos, hidrocarbonetos, monoterpenos, fenilpropanoides e alco?is. No qual os sesquiterpenos ?-cariofileno e ?-humuleno foram os compostos majorit?rios, os quais s?o associados na literatura a diversas atividades biol?gicas, em especial a a??es anti-inflamat?rias, antif?ngicas e antitumorais. A an?lise das fra??es por CG-EM e CLAE-DAD foi poss?vel identificar catequinas, ?cido g?lico e flavon?is nos extratos aquosos e ?steres graxos e as subclasses das flavonas e flavon?is nos extratos etan?licos. Nas avalia??es biol?gicas os extratos etan?licos e aquosos apresentaram baixa toxicidade em c?lulas de mam?feros, em que a concentra??o selecionada para a avalia??o das demais atividades biol?gicas foi de at? 500 ?g/mL. Para a atividade antitumoral, os extratos apresentaram um grande potencial concentra??o dependente, com valores de IC50 variando de 56,44 a 180,4 ?g/mL. Bem como o tempo de exposi??o aumentou a pot?ncia de todos os extratos. Tamb?m foi observado que os extratos aquosos promoveram a inibi??o da prolifera??o de linf?citos estimulados por mit?genos, apresentando uma efic?cia em rela??o ? dexametasona, de 39,94% para o extrato das folhas a 45 ?g/mL, e de 57,3%, 137,4% e 251,8% para os extratos do caule a 15, 20 e 30 ?g/mL, respectivamente. Este efeito proliferativo pode estar relacionado ao potencial anti-inflamat?rio da M. ferruginata, relatada na medicina popular. Possivelmente, as atividades biol?gicas est?o relacionadas ao rico perfil qu?mico desta esp?cie, principalmente em compostos fen?licos. Para as atividades antimicrobianas, tripanocida 9 e leishmanicida n?o foram observadas a inibi??o do crescimento ou toxicidade frentes as cepas avaliadas. Desta forma este trabalho contribuiu para o conhecimento qu?mico e biol?gico da M. ferruginata. Por?m ensaios futuros utilizando as fra??es e subst?ncias isoladas, se fazem necess?rios para fortalecer os dados aqui apresentados e para demonstrar quais os mecanismos moleculares envolvidos nas atividades biol?gicas investigadas.
Disserta??o (Mestrado) ? Programa de P?s-gradua??o em Ci?ncias Farmac?uticas, Universidade Federal dos Vales do Jequitinhonha e Mucuri, 2015.
ABSTRACT Medicinal plants are reassuring sources of new drugs, in which the Cerrado region stands out for its broad biodiversity. Among the medicinal plants used in this same region is the species Miconia ferruginata DC. which is also known as pixirica-docampo or babaten?o. This species is used in the treatment of skin diseases, and other inflammatory, infectious and parasitic sources, despite the chemical studies about it are lacking. Therefore, the objectives of this study were to evaluate the chemical profile and biological potential of the M. ferruginata (Melastomataceae).The species was collected in Diamantina, MG, in which it was prepared for water and ethanol extraction of the leaves/flowers and stem. Through phytochemical screening and analysis of HPLC-MSDAD, we obtained a rich chemical profile in phenolic compounds. The identification of tannins, phenolic acids, flavonoids, glycosides of quercetin and derivativeshas been detected. For the analysis of volatile constituents by GC-MS, it was possible to identify the presence of fourteen compounds, namely belonging classes of sesquiterpenes, hydrocarbons, monoterpenes, phenylpropanoids and alcohols. For that,? and?- caryophyllene, humulenesesquiterpenes were the main components, which are associated in the literature several biological activities, especially anti-inflammatory, antifungal and antitumor activities.In the analysis of the fractions by GC-MS and HPLC-DAD, we identified catechins, gallic acid and flavonols in aqueous extracts,including fatty esters and subclass of flavones and flavonols in ethanol extracts. Within the biological evaluations, aqueous and ethanolic extracts showed low toxicity to mammalian cells, wherein the concentration selected for analysis of other biological activities was up to 500 ?g/mL. For antitumor activity, the extracts showed a great potential concentration-dependent, with IC50 values ranging from 56.44 to 180.4 ?g/mL. Just as the exposure time increased the potency of all extracts, it was also observed that aqueous extracts promoted inhibition of the proliferation of mitogen-stimulated lymphocytes, showing a efficacy when compared to dexamethasone, 39.94% for the extract from the leaves of 45 ?g/mL, and 57.3%, 137.4% and 251.8% for the extracts of stem of 15.20 and 30 ?g/mL, respectively. This proliferative effect may be related to the anti-inflammatory potential of M. ferruginata, reported in folk medicine. Possibly, the biological activities are related to the rich chemical profile of this species, mainly in phenolic compounds. For the antimicrobial, trypanocidal and leishmanicidal activities, we have not observed growth inhibition or toxicity fronts of the evaluated strains. Thus 11 this work contributed to the chemical and biological knowledge of M. ferruginata. Nevertheless, future trials using isolated fractions and substances are needed to strengthen the data presented here and to demonstrate the molecular mechanisms involved in the biological activities investigated. It is likely that the biological activities are related to the rich chemical profile of this species, mainly regarding phenolic compounds. For antimicrobial activity, trypanocidal and leishmanicidal, it was not observed growth inhibition or toxicity regarding the evaluated strains. Thus, this work contributed to the chemical and biological knowledge of the M. ferruginata. However, future trials using isolated fractions and substances are needed to strengthen the data presented here and to demonstrate the molecular mechanisms involved in the biological activities hereby investigated.
Wakamatsu, Yuko. "Preface to Volume 11, the last volume of Fish Biol. J. MEDAKA." Laboratory of Freshwater Fish Stocks Bioscience and Biotechnology Center Nagoya University, 2007. http://hdl.handle.net/2237/13828.
Full textZampirolli, Leticia Silotti. "Dialquilfosforilidrazonas derivadas de isatinas N - substitu?das com potencial atividade biol?gica." Universidade Federal Rural do Rio de Janeiro, 2009. https://tede.ufrrj.br/jspui/handle/jspui/2077.
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Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior, CAPES, Brasil.
A series of new dialkylphosphorylhydrazones (phosphorohydrazidic acid, N?-[1,2-dihydro-2- oxo-(R1)-3H-indole-3-iliden]- dialkyl esters was synthesized and characterized by IR, 1H, 13C and 31P NMR and mass spectroscopy. These dialkylphosphorylhydrazones were synthesized in three steps. The first step involved the synthesis of different dialkylphosphites which are obtained by the reaction of PCl3 with three mols of the corresponding alcohols. The second step consisted of the reaction between the dialkylphosphites and hydrazine in a two phase system, leading to the formation of the dialkylphosphorylhydrazines. Finally, the last step was the condensation of these dialkylphosphorylhydrazines with different N-substituted isatins. The analysis of the 1H, 13C and 31P NMR spectra showed the existence of the two possible diastereoisomers E and Z for compounds 1, 2, 6, 10 and 12, while for the remaining compounds only the Z isomer is present. Ten of these compounds were preliminarily tested for their inhibition potential against two protozoa (Trypanosoma cruzi and Leishmania amazonensis). All compounds tested showed cell proliferation inhibition of 98% at 50 ?M for Leishmania amazonensis, whereas for T. cruzi, inhibition of epimastigote cell proliferation was found to be higher than 75% for all compounds tested except 6, which showed a 59% inhibition. These ten compounds were also evaluated against Plasmodium falciparum, affording inhibitions higher than 90% for a 1mM concentration. These compounds were also investigated for their fungicidal activity against phytopatogenic Rhizoctonia solani and Fusarium oxysporum. Compounds 9 and 11 showed a miscelial growth inhibition of 58% for Rhizoctonia solani while compound 12 afforde a 72% inhibition. Compounds 1, 2, 11 and 12 gave Fusarium oxysporum inhibition higher than 52%. Finally, the compounds synthesized were also evaluated for their inhibitory potential against lettuce seed germination and it was observed that the same compounds which showed fungicidal activity were not able to inhibit seed germination.
Uma s?rie de 16 dialquilfosforilidrazonas (?cido fosforoidraz?dico, N? -[1,2-diidro-2-oxo-(R1)- 3H- indol-3-ilideno] -, ?ster de dialquila), sendo todas in?ditas, foram sintetizadas e caracterizadas pelas t?cnicas de espectrometria de IV, RMN de 1H, RMN de 13C, RMN de 31P e massas. As novas dialquilfosforilidrazonas foram sintetizadas em tr?s etapas de rea??o. A primeira etapa consistiu na s?ntese de diferentes fosfitos de dialquila que foram obtidos atrav?s da rea??o do tricloreto de f?sforo (PCl3) com tr?s mols do ?lcool correspondente. Na segunda etapa, a rea??o dos fosfitos de dialquila com a hidrazina, em um sistema bif?sico, levou ? forma??o das dialquilfosforilidrazinas. A ?ltima etapa foi a condensa??o destas dialquilfosforilidrazinas com diferentes isatinas substitu?das. A an?lise dos espectros de RMN de 1H, RMN de 13C, RMN de 31P das dialquilfosforilidrazonas mostraram a coexist?ncia dos dois poss?veis diastereois?meros E e Z, para os compostos 1, 2, 6, 10 e 12, enquanto que para os compostos restantes observou-se apenas o diastereois?mero Z. Dos compostos sintetizados, dez foram avaliados preliminarmente quanto ao potencial inibit?rio de prolifera??o de dois protozo?rios (Trypanosoma cruzi e Leishmania amazonensis). Para Leishmania amazonensis todos os compostos testados apresentaram inibi??o da prolifera??o celular de 98 % a 50 ?M. Enquanto que para T.cruzi verificou-se inibi??o da prolifera??o celular de epimastigotas superior a 75% para todos compostos testados, a exce??o do composto (6) cuja inibi??o foi de 59 %. Esses dez compostos tamb?m foram avaliados frente ao protozo?rio Plasmodium falciparum apresentando inibi??o superior a 90 % para todos os compostos testados, a uma concentra??o de 1mM. Essas dialquilfosforilidrazonas tamb?m tiveram a a??o fungicida avaliada frente aos fungos fitopatog?nicos (Rhizoctonia solani e Fusarium oxysporum). Em Rhizoctonia solani os compostos (9) e (11) apresentaram inibi??o do crescimento miscelial de 58 %, j? o composto (12) apresentou inibi??o de 72%. Para o Fusarium oxysporum destacaram-se os compostos (1, 2, 11 e 12) com inibi??o superior a 52 %. Esses compostos tamb?m foram avaliados quanto ao potencial inibit?rio de germina??o em sementes de alface e verificouse que os mesmos compostos que apresentaram efeitos fungist?ticos, n?o inibiram a germina??o de sementes de alface.
Mac?do, Marina de Oliveira Cardoso. "Modifica??o de membranas de quitosana por plasma para uso biol?gico." Universidade Federal do Rio Grande do Norte, 2009. http://repositorio.ufrn.br:8080/jspui/handle/123456789/12681.
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Chitosan membranes have been modified by plasma, utilizing the following gases: nitrogen (N2), methane (CH4), argon (Ar), oxygen (O2) and hydrogen. The modified membranes by plasma were compared to the unmodified ones. The membranes were characterized by absorption assay, contact angle, atomic force microscopy (AFM). Also, permeability assay of sodium sulfamerazine from such membranes were carried out. Through the absorption assay and contact angle it was possible to obtain information of the wettability of the membranes and what changes the plasma treatment can promote in relation to it. The plasma treatment using oxygen promoted increase of the wetability and swelling while the samples treated with methane decrease of the wetability and swelling. Through the Optical Emission Spectroscopy (OES) it was possible to identify which species were present in the plasma during the treatment. And through the AFM analysis it was possible to observe the changes nanotopography occurred on the surface of the samples. Permeability assay were archived for all treated membranes and compared to no treated ones. Due to that assay it was possible verify which the plasma treatment increased the permeability spectrum of the membranes which has varied from 1,4548 *10-5cm2.min-1 to 2,7713*10-5cm2.min-1. Chitosan membranes with permeability varied are importance in systems drug delivery, to liberate a wide variety of drugs
Membranas de quitosana foram modificadas por plasma, utilizando os seguintes gases: nitrog?nio (N2), metano (CH4), arg?nio (Ar), oxig?nio (O2) e hidrog?nio (H2). Membranas n?o tratadas foram utilizadas para compara??o com as tratadas. As amostras foram caracterizadas por ensaio de ganho de massa (capacidade de absor??o de ?gua), ?ngulo de contato, microscopia de for?a at?mica (MFA) e quanto ? sua permeabilidade em rela??o ao f?rmaco sulfamerazina de s?dio. Atrav?s dos ensaios de absor??o e ?ngulo de contato foi poss?vel obter informa??es sobre a molhabilidade das membranas e quais mudan?as o tratamento a plasma pode promover em rela??o ? molhabilidade. O tratamento por plasma utilizando o oxig?nio promoveu um aumento da hidrofilicidade e do ganho de massa enquanto as amostras tratadas com metano tiveram uma diminui??o da hidrofilicidade e do ganho de massa. Atrav?s da Espectroscopia de Emiss?o ?tica (EEO) identificaram-se quais esp?cies estavam presentes no plasma durante o tratamento, pois estas influenciam o grau de molhabilidade das amostras, tornando-as mais hidrof?licas ou hidrof?bicas atrav?s da inser??o de grupos funcionais. Nos resultados da MFA foi poss?vel observar as modifica??es nanotopogr?ficas ocorridas na superf?cie das amostras, como o aumento da rugosidade em amostras tratadas com hidrog?nio e a diminui??o dessa rugosidade nas amostras tratadas com arg?nio. Ensaios de permea??o foram realizados para todas as membranas tratadas e comparados com as membranas n?o tratadas. Atrav?s desse ensaio foi poss?vel verificar que os tratamentos a plasma ampliaram o espectro de permeabilidade das membranas que variou de 1,4548 *10-5cm2.min-1 a 2,7713*10-5cm2.min-1. As amostras tratadas com oxig?nio apresentaram a menor permeabilidade enquanto que a amostras tratada com arg?nio apresentaram a maior permeabilidade. A obten??o de membranas de quitosana com permeabilidade variada ? de grande import?ncia na tecnologia de libera??o de f?rmacos, pois as mesmas podem ser utilizadas nos mais diversos sistemas carreadores de f?rmacos. Liberando uma ampla variedade de f?rmacos e/ou agente bioativos
Books on the topic "(Biol.)"
Zittlau, Jörg. Warum Robben kein Blau sehen und Elche ins Altersheim gehen: Pleiten und Pannen im Bauplan der Natur. Berlin: Ullstein, 2008.
Find full textHsü, Kenneth J. Die letzten Jahre der Dinosaurier: Meteoriteneinschlag, Massensterben und die Folgen für die Evolutionstheorie. Basel: Birkhäuser, 1990.
Find full textŽeiviniece, Anna. Dr. habil. biol. Alfons Piterāns: Bibliogrāfiskais rādītājs. Rīga: LU Akadēmiskais apgāds, 2005.
Find full textTrainor, F. R. Biol ogical aspects of Scenedesmus (Chlorophyceae) - phenotypic plasticity. Berlin: J. Cramer, 1998.
Find full textNA. Biol Concepts& Connectns& Get Ready for Biol. Addison Wesley Publishing Company, 2006.
Find full textNA. Biology& Biol Study GD Unbnd& Get Rdy Biol. Addison Wesley Publishing Company, 2007.
Find full textBook chapters on the topic "(Biol.)"
Villarreal, Alisson Patricia Bolaños, Diana Elizabeth García Tumipamba, and Freddy Vicente Cuarán Sarzosa. "Vermicomposting: Production of Humus and Biol." In Communication, Smart Technologies and Innovation for Society, 591–600. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-4126-8_53.
Full textSubklewe, Marion, and Reuben Benjamin. "Management of Myelotoxicity (Aplasia) and Infectious Complications." In The EBMT/EHA CAR-T Cell Handbook, 151–55. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-94353-0_29.
Full textSchilbach, Leonhard, and Juha M. Lahnakoski. "Clinical Neuroscience Meets Second-Person Neuropsychiatry." In Social and Affective Neuroscience of Everyday Human Interaction, 177–91. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-08651-9_11.
Full text"11 (biol) Biologie Biology." In 2019, 664. De Gruyter, 2019. http://dx.doi.org/10.1515/9783110616576-035.
Full text"11. (biol) Biologie/ Biology." In 2018, 645. De Gruyter, 2018. http://dx.doi.org/10.1515/9783110608144-038.
Full text"11 (biol) Biologie Biology." In IJBF (2016). Berlin, Boston: De Gruyter, 2016. http://dx.doi.org/10.1515/9783110419863-035.
Full text"11 (biol) Biologie / Biology." In 2021, 682. De Gruyter, 2021. http://dx.doi.org/10.1515/9783110723922-038.
Full text"11 (biol) Biologie / Biology." In 2022, 688. De Gruyter, 2022. http://dx.doi.org/10.1515/9783110769593-036.
Full text"Comparative Genomics of Brucella melitensis, B. suis, and B. abortus." In Brucella:Molecular & Cell Biol, 99–116. Taylor & Francis, 2005. http://dx.doi.org/10.1201/9780203017456-11.
Full text"Erythritol Metabolism and Virulence in Brucella." In Brucella:Molecular & Cell Biol, 245–56. Taylor & Francis, 2005. http://dx.doi.org/10.1201/9780203017456-17.
Full textConference papers on the topic "(Biol.)"
Lin, Fang-Tsyr, Victor T. G. Lin, Vivian Y. Lin, Yun-Ju Lai, Chen-Shan Chen, Kang Liu, and Weei-Chin Lin. "Abstract POSTER-BIOL-1333: TRIP6 regulates p27KIP1to promote ovarian tumorigenesis." In Abstracts: 10th Biennial Ovarian Cancer Research Symposium; September 8-9, 2014; Seattle, WA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1557-3265.ovcasymp14-poster-biol-1333.
Full textMeza-Perez, Selene, Maria de la Luz Garcia-Hernandez, Aaron Silva-Sanchez, Javier Rangel-Moreno, Uma Mudunuru, Edith M. Lord, and Troy D. Randall. "Abstract POSTER-BIOL-1337: Omentum promotes suppression against peritoneal tumors." In Abstracts: 10th Biennial Ovarian Cancer Research Symposium; September 8-9, 2014; Seattle, WA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1557-3265.ovcasymp14-poster-biol-1337.
Full textChhina, J., S. Dar, M. Deshpande, S. Giri, A. Munkarah, and R. Rattan. "Abstract POSTER-BIOL-1307: Bioenergetic adaptations in chemoresistant ovarian cancer cells." In Abstracts: 10th Biennial Ovarian Cancer Research Symposium; September 8-9, 2014; Seattle, WA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1557-3265.ovcasymp14-poster-biol-1307.
Full textMatthews, Dylan P., Sherine Taylor, and Neveen A. Said. "Abstract POSTER-BIOL-1344: Epigenetic regulation of SPARC in ovarian cancer." In Abstracts: 10th Biennial Ovarian Cancer Research Symposium; September 8-9, 2014; Seattle, WA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1557-3265.ovcasymp14-poster-biol-1344.
Full textBrown, Caitlin W., Alexander S. Brodsky, and Richard N. Freiman. "Abstract POSTER-BIOL-1352: Notch3 promotes anoikis resistance in ovarian cancer." In Abstracts: 10th Biennial Ovarian Cancer Research Symposium; September 8-9, 2014; Seattle, WA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1557-3265.ovcasymp14-poster-biol-1352.
Full textHansen, Karyn J., and Bennett Van Houten. "Abstract POSTER-BIOL-1314: Investigating fatty acid beta-oxidation in ovarian cancer cells." In Abstracts: 10th Biennial Ovarian Cancer Research Symposium; September 8-9, 2014; Seattle, WA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1557-3265.ovcasymp14-poster-biol-1314.
Full textHudson, LG, SR Kenney, Y. Guo, S. Adams, T. Rutledge, CY Muller, and A. Wandinger-Ness. "Abstract POSTER-BIOL-1320: Rho-family GTPases as therapeutic targets in ovarian cancer." In Abstracts: 10th Biennial Ovarian Cancer Research Symposium; September 8-9, 2014; Seattle, WA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1557-3265.ovcasymp14-poster-biol-1320.
Full textWalsh, Christine, Hoorig Nassanian, Hasmik Agadjanian, Carl Miller, Sandra Orsulic, and Beth Karlan. "Abstract POSTER-BIOL-1348: No association between PARK2 and BRCA1-associated gynecologic cancers." In Abstracts: 10th Biennial Ovarian Cancer Research Symposium; September 8-9, 2014; Seattle, WA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1557-3265.ovcasymp14-poster-biol-1348.
Full textReeve, E. B. "MODEL STUDIES OF NEUTRALIZATION OF THROMBIN." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643277.
Full textPejovic, Tanja, Yukie Bean, Jaeyeon Kim, Martin M. Matzuk, and Seth B. Coffelt. "Abstract POSTER-BIOL-1308: Macrophage infiltration in high-grade serous carcinomas of humans and mice." In Abstracts: 10th Biennial Ovarian Cancer Research Symposium; September 8-9, 2014; Seattle, WA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1557-3265.ovcasymp14-poster-biol-1308.
Full textReports on the topic "(Biol.)"
Nelson, Nathan, and Charles F. Yocum. Structure, Function and Utilization of Plant Photosynthetic Reaction Centers. United States Department of Agriculture, September 2012. http://dx.doi.org/10.32747/2012.7699846.bard.
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