CONSIDERAÇÕES SOBRE O PERFIL LONGITUDINAL E ÍNDICE RDE DO RIBEIRÃO ARAQUÁ, MUNICÍPIO DE SÃO PEDRO E CHARQUEADA-SP

O objetivo deste trabalho é apresentar parte das pesquisas referentes às formações superficiais da bacia do Ribeirão Araquá, municípios de São Pedro e Charqueada-SP, inserida no contato entre a Depressão Periférica Paulista e o relevo de cuestas. Os resultados da análise do índice RDE e do Perfil Longitudinal indicaram setores com significativos knick-points que podem estar correlacionadas a controles litológicos e estruturais regionais e locais, além de processos de origem climática

Detection of Toxoplasma gondii soluble antigen, SAG-1 (p30), antibody and immune complex in the cerebrospinal fluid of HIV positive or negative individuals

Active infection by T. gondii was evaluated by immunoassay for soluble SAG-1 (p30), the major surface antigen from T. gondii, specific antibodies and immune complexes in human cerebrospinal fluid (CSF) samples. A total of 263 samples of CSF were collected from hospitalized patients presenting neurological disorders and analyzed for antibodies to HIV. Patients were divided into two groups: HIV positive (n = 96) or HIV negative (n = 167). The results of the assays showed that 45% of all samples were positive for soluble SAG-1. Toxoplasma Ag/Ab immune complexes were detected in 19% of the CSF samples and 62% were positive for T. gondii- specific IgG. A combination of these assays in the presence of clinical findings consistent with active Toxoplasma infection may predict the presence of toxoplasmic encephalitis. Moreover, detection of soluble SAG-1 in the CSF of these individuals appears consistent with active infection

Comparative characterization of three Tetraselmis chui (Chlorophyta) strains as sources of nutraceuticals

Species of the genus Tetraselmis have traditionally been used as a valuable nutritional source in aquaculture for their high fatty acid content (5-10% dry weight). Their use in nutraceutical production for humans is growing worldwide. Among them, Tetraselmis chui is generally reported in the literature as rich in polyunsaturated fatty acids (PUFAs), especially eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). We evaluated the potential of three T. chui strains for the production of these nutraceuticals: the model strain CCAP 8/6, which is broadly used in the aquaculture industry due to its high PUFA content, and two strains (TCBG-1 and TCBG-2) isolated from Guanabara Bay (Rio de 28 Janeiro, Brazil). The two Brazilian strains grew faster than CCAP 8/6 with higher percentage of PUFAs (up to 70% of total FA at the exponential growth phase). They also produced unique fatty acids in significant quantities: TCBG-1 produced arachidonic acid (ARA) and EPA during the exponential phase (> 20% of total FA), while TCBG-2 produced these PUFAs in addition to DHA (>18% of total FA) at the late exponential phase. A two-stage growth system using co-cultures of the two Brazilian strains is proposed as an optimal model for PUFA production, based on their simultaneous scaling cultivation in photobioreactors. Furthermore, both strains are suitable candidates for upscaling in open systems in tropical regions since they are adapted to the environmental conditions in Guanabara Bay, where they form massive blooms by outcompeting other microalga

Antimycobacterial And Cytotoxicity Activities Of Free And Liposome-encapsulated 3-(4'-bromo[1,1'-biphenyl-4-yl)-3-(4-bromo-phenyl)-n,n- Dimethyl-2-propen-1-amine

The antimycobacterial activity of 3-(4'-bromo[1,1'-biphenyl-4-yl)-3-(4- bromo-phenyl)-N,N-dimethyl-2-propen-1-amine (BBAP), free or incorporated in preformed liposomes, on extracellular M. tuberculosis H37Rv was 8 and 25 μM (MIC), respectively. Extracellular antimycobacterial activity was not significantly improved by entrapment of BBAP in liposomes, but there was a 6.1-fold reduction of BBAP cytotoxicity on J774 macrophages. Liposomal BBAP or its free form showed IC50 values of 165 and 27 μM, resulting in a selectivity index (SI=IC50/MIC) of 3.4 and 6.6, respectively. Free BBAP in concentrations from 10 to 80 μM were quite effective in eliminating intracellular M. tuberculosis while liposomal formulation was less effective at these concentrations.334871874Corbett, E.L., Watt, C.J., Walker, N., Mayer, D.B.M., Willians, B.G., Raviglione, M.C., Dye, C., (2003) Arch. Intern. Med., 163, p. 1009Vynnycky, E., Fine, P.E., (1997) Epidemiol. Infec., 119, p. 183Pandey, R., Khuller, G.K., (2005) J. Antimicrob. Chemother., 55, p. 430De Souza, A.O., Aily D., C.G., Sato, D.N., Durán, N., (1998) J. Antimicrob. Chemother., 42, p. 407De Souza, A.O., Junior, R.R.S., Ferreira-Julio, J.F., Rodriguez, J.A., Melo, P.S., Haun, M., Sato, D.N., Durán, N., (2001) Eur. J. Med. Chem., 36, p. 843De Souza, A.O., Pereira, D.G., Durán, N., (2002) Ann. Rev. Biomed. Sci., 4, p. 53De Souza, A.O., Hemerly, F.P., Busollo, A.C., Melo, P.S., Machado, G.M.C., Miranda, C.C., Santa-Rita, R.M., Durán, N., (2002) J. Antimicrob. Chemother., 50, p. 629De Souza, A.O., Santos, R.R., Sato, D.N., De Azevedo, M.M.M., Ferreira, D.A., Melo, P.S., Haun, M., Durán, N., (2004) J. Braz. Chem. Soc., 15, p. 682De Souza, A.O., Alderete, J.B., Faljoni-Alario, A., Silva, C.L., Durán, N., (2005) J. Chil. Chem. Soc., 50, p. 591De Conti, R., Gimenez, S.M.M., Haun, M., Pilli, R.A., De Castro, S.L., Durán, N., (1996) Eur. J. Med. Chem., 31, p. 915Bangham, A.D., Standish, M.M., Watkins, J.C., (1965) J. Mol. Biol., 13, p. 238Chen, P.S., Toribara, T.Y., Warner, H., (1956) Anal. Chem., 28, p. 1756Oh, Y.K., Nix, D.E., Straubinger, R.M., (1995) Antimicrob. Agents Chemother., 39, p. 2104Collins, L.A., Franzblau, S.G., (1997) Antimicrob. Agents Chemother., 41, p. 1004Denizot, F., Lang, R., (1986) J. Immun. Methods, 89, p. 27

Quantificação do carbono das substâncias húmicas em diferentes sistemas de uso do solo e épocas de avaliação.

A quantificação do carbono nas diferentes frações da matéria orgânica do solo (MOS) torna-se necessária devido ao interesse de se conhecer o potencial de captura e armazenamento do carbono nos diferentes sistemas de uso do solo. O objetivo deste trabalho foi quantificar o carbono das substâncias húmicas em diferentes sistemas de uso do solo e épocas de avaliação e correlacioná-lo com algumas propriedades químicas e físicas do solo. Os sistemas selecionados foram: preparo convencional (PC-milho/feijão), plantio direto (PD-berinjela/milho), consórcio maracujá/Desmodium sp, cultivo com figo e sistema agroflorestal. As amostras de solo foram coletadas em duas profundidades (0-5 e 5-10 cm) e épocas (17/11/2005–verão e 23/6/2006-inverno). Foi determinado o carbono orgânico total (COT) e realizado o fracionamento químico da MOS, quantificando-se o carbono da fração humina (C-HUM), fração ácido húmico (C-FAH) e fração ácido fúlvico (C-FAF). O C-HUM constituiu a maior parte do COT, havendo correlação significativa com o COT em todos os sistemas avaliados e estações. Analisando o C-FAH foi possível identificar alterações no solo relacionadas aos sistemas de uso, na profundidade de 0-5 cm e no verão, destacando-se o PD com os maiores teores. Com o C-FAF ocorreu este mesmo comportamento, mas na profundidade de 5-10 cm e no inverno, destacando-se o PC com maiores valores. Foram verificadas correlações significativas entre Valor S, Valor T e DMP em todos os sistemas, com exceção da área de PC. O PD aumenta os teores de C-FAH, nas duas profundidades e nas duas estações, quando comparado ao PC do solo

Free 2-propen-1-amine Derivative And Inclusion Complexes With β-cyclodextrin: Scanning Electron Microscopy, Dissolution, Cytotoxicity And Antimycobacterial Activity

Inclusion complexes and physical mixtures of isomeric mixture of E/Z (50:50) of 3-(4′-bromo-[1,1′-biphenyl]-4-yl)-3-(4-bromophenyl)-N,N- dimethyl-2-propen-1-amine (BBAP) and β-cyclodextrin (β-CD) in the molar proportion of 1:1 and 1:2 were analyzed by scanning electron microscopy. The dissolution behavior of BBAP and of the inclusion complexes were also evaluated for six hours. By scanning electron microscopy (SEM), it was possible to observe an inclusion complex formed between BBAP and β-CD by co-evaporation, either in the molar proportion of 1:1 or 1:2. In the physical mixtures, no complex was observed as previously detected by physicochemical analysis. The dissolution studies showed that the inclusion complexes BBAP/β-CD 1:1 and 1:2 released respectively 49.07 ± 1.48 and 40.26 ± 3.90% of BBAP during six hours. Free BBAP was less soluble than the inclusion complex and reached 9.00 ± 0.75% of dissolution. Biological assays, such as cytotoxicity to J774 macrophages and to a permanent lung fibroblast cell line (V79), indicated that the BBAP does not exhibit any additional toxic effect with the β-CD complexes. However, the complexes were less cytotoxic to V79 cells than the free form. The BBAP/β-CD inclusion complexes were more effective (MIC) than the free compound on several mycobacteria strains. Similar behavior was observed for BBAP/β-CD complexes and rifampicin, a front-line antitubercular drug, on M. tuberculosis H37Rv growing inside J774 macrophages.155682689Bibby, D.C., Davies, N.M., Tucker, I.G., (2000) Int. J. Pharm., 197, p. 1De Souza, A.O., Sato, D.N., Aily, D.C.G., Durán, N., (1998) J. Antimicrob. Chemother., 42, p. 407Pereira, D.G., De Castro, S.L., Durán, N., (1998) Acta Tropica, 69, p. 205De Souza, A.O., Santos Júnior, R.R., Ferreira-Júlio, J.F., Rodrigues, J.A., Melo, P.S., Haun, M., Sato, D.N., Durán, N., (2001) Eur. J. Med. Chem., 36, p. 843De Souza, A.O., Hemerly, F.P., Busollo, A.C., Melo, P.S., Machado, G.M.C., Miranda, C.C., Santa-Rita, R.M., Durán, N., (2002) J. Antimicrob. Chemother., 50, p. 629De Conti, R., Gimenez, S.M.N., Haun, M., Pilli, R.A., De Castro, S.L., Durán, N., (1996) Eur. J. Med. Chem., 31, p. 915De Souza, A.O., Santos Jr., R.R., Sato, D.N., Lima, H.O.S., Andrade-Santana, M.H., Alderete, J.B., Faljoni-Alario, A., Durán, N., (2000) Abstracts of the 29 a Reunião Anual Da Sociedade Brasileira de Bioquímica, , Caxambu, BrazilHiguchi, T., Connors, K.A., (1965) Adv. Anal. Chem. Instrum., 4, p. 117Collins, L.A., Franzblau, S.G., (1997) Antimicrob. Agents Chemother., 41, p. 1004Oh, Y.K., Nix, D.E., Straubinger, R.M., (1995) Antimicrob Agents Chemother., 39, p. 2104Cingi, M.R., De Angelis, I., Fortunati, E., Reggiani, D., Bianchi, V., Tiozzo, R., Zucco, F., (1991) Toxicol. In Vitro, 5, p. 119Denizot, F., Lang, R., (1986) J. Immun. Methods, 89, p. 271Borenfreund, E., Puerner, J.A., (1984) J. Tiss. Cult. Meth., 9, p. 7Melo, P.S., Maria, S.S., Vidal, B.C., Haun, M., Durán, N., (2000) In Vitro Cell Rev. Biol. Animal, 36, p. 539Melo, P.S., Durán, N., Haun, M., (2001) Toxicology, 159, p. 135Shrivastava, R., John, G.W., Rispat, G., Chevalier, A., Massingham, R., (1991) ATLA - Alt. Lab. Anim., 19, p. 39

Erratum To: Quality Of Sweat Test (st) Based On The Proportion Of Sweat Sodium (na) And Sweat Chloride (cl) As Diagnostic Parameter Of Cystic Fibrosis: Are We On The Right Way?

During production of the original article [1] the Methods section included an incorrect sentence. The following sentence "For the analysis of variables with numerical distribution, Fisher's exact test and one-way analysis of variance were used" should be corrected as "For the analysis of variables with numerical distribution, Student's t-test and one-way analysis of variance were used". © The Author(s).12

SU(1,1) Coherent States For Position-Dependent Mass Singular Oscillators

The Schroedinger equation for position-dependent mass singular oscillators is solved by means of the factorization method and point transformations. These systems share their spectrum with the conventional singular oscillator. Ladder operators are constructed to close the su(1,1) Lie algebra and the involved point transformations are shown to preserve the structure of the Barut-Girardello and Perelomov coherent states.Comment: 11 pages, 5 figures. This shortened version (includes new references) has been adapted for its publication in International Journal of Theoretical Physic

Variation and genetic structure of Melipona quadrifasciata Lepeletier (Hymenoptera, Apidae) populations based on ISSR pattern

For a study of diversity and genetic structuring in Melipona quadrifasciata, 61 colonies were collected in eight locations in the state of Minas Gerais, Brazil. By means of PCR analysis, 119 ISSR bands were obtained, 80 (68%) being polymorphic. He and H B were 0.20 and 0.16, respectively. Two large groups were obtained by the UPGMA method, one formed by individuals from Januária, Urucuia, Rio Vermelho and Caeté and the other by individuals from São João Del Rei, Barbacena, Ressaquinha and Cristiano Otoni. The Φst and θB values were 0.65 and 0.58, respectively, thereby indicating high population structuring. UPGMA grouping did not reveal genetic structuring of M. quadrifasciata in function of the tergite stripe pattern. The significant correlation between dissimilarity values and geographic distances (r = 0.3998; p < 0.05) implies possible geographic isolation. The genetic differentiation in population grouping was probably the result of an interruption in gene flow, brought about by geographic barriers between mutually close geographical locations. Our results also demonstrate the potential of ISSR markers in the study of Melipona quadrifasciata population structuring, possibly applicable to the studies of other bee species