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    Modulation Of The Catalytic Activity Of Porphyrins By Lipid- And Surfactant-containing Nanostructures

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    The structural factors modulating porphyrin activity encompass pyrrole and equatorial ligands, as well as the central metal and the number and structure of their axial ligands. Of equal importance is the microenvironment provided by apoproteins, solvents and membranes. Porphyrins are often used to construct supramolecular structures with different applications. The modulation of activity of the porphyrins has been frequently achieved by mimicking nature, i.e., by the provision of different microenvironments for these molecules. The association of porphyrins to surfactant- and lipid-containing nanostructures has changed the activity of these compounds to mimic different enzymes such as SOD, cytochrome P450, peroxidases and others. In determined conditions, the reactive forms of the porphyrins are high-valence states of oxo-metal-π cations and oxo-metal produced by the reaction with peroxides and peracids. The modulation of porphyrin activity by surfactant- and lipid-containing nanostructures has also been achieved for hemeproteins, as the lipid nanostructures affect the conformation of proteins. ©2011 Sociedade Brasileira de Química.22916211633Drain, C.M., Varotto, A., Radivojevic, I., (2009) Chem. Rev., 109, p. 1630Aida, T., Inoue, S., (2000) The Porphyrin Handbook, , Kadish, K., M. Smith, K., M. Guillard R., eds.Academic Press: San Diego ch. 42Ponka, P., (1999) Am. J. Med. Sci., 318, p. 241Da Silva, D.C., De Freitas-Silva, G., Do Nascimento, E., Rebouças, J.S., Barbeira, P.J., De Carvalho, M.E., Idemori, Y.M., (2008) J. Inorg. Biochem., 102, p. 1932Bochot, C., Bartoli, J.F., Frapart, Y., Dansette, P.M., Mansuy, D., Battioni, P., (2007) J. Mol. Catal. A.: Chem., 263, p. 200Alkordi, M.H., Liu, Y.L., Larsen, R.W., Eubank, J.F., Eddaoudi, M., (2008) J. Am. Chem. Soc., 130, p. 12639Suijkerbuijk, B., Schamhart, D.J., Kooijman, H., Spek, A.L., Van Koten, G., Gebbink, R., (2010) Dalton Trans., 39, p. 6198Groves, J.T., Nemo, T.E., (1983) J. Am. Chem. Soc., 10, p. 5786Drain, C.M., Smeureanu, G., Patel, S., Gong, X.C., Garno, J.A., (2006) New. J. Chem., 30, p. 1834Wang, Y.T., Jin, W.J., (2008) Spectrochim. Acta, Part A., 70, p. 871Komatsu, T., Moritake, W., Nakagawa, A., Tsuchida, E., (2002) Chem. - Eur. J., 8, p. 5469Nagami, H., Umakoshi, H., Shimanouchi, T., Kuboi, R., (2004) Biochem. Eng. J., 21, p. 221Szoka, F., Papahadjopoulos, D., (1980) Annu. Rev. Biophys. Bioeng., 9, p. 467Atkin, R., Craig, V.S.J., Wanless, E.J., Biggs, S., (2003) Adv. Colloid Interface Sci., 103, p. 219Grassert, I., Schinkowski, K., Vollhardt, D., Oehme, G., (1998) Chirality, 10, p. 754Hait, S.K., Moulik, S.P., (2001) J. Surfactants Deterg., 4, p. 303Glick, J., Santoyo, G., Casey, P.J., (1996) J. Biol. Chem., 271, p. 2949Maldotti, A., Andreotti, L., Molinari, A., Varani, G., Cerichelli, G., Chiarini, M., (2001) Green Chem., 3, p. 42Batrakova, E.V., Kabanov, A.V., (2008) J. Controlled Release, 130, p. 98Bangham, A.D., Standish, M.M., Watkins, J.C., (1965) J. Mol. Biol., 13, p. 238Johnson, S.M., Bangham, A.D., Hill, M.W., Korn, E.D., (1971) Biochim. Biophys. Acta. Biomembr., 233, p. 820Papahadj, D., Watkins, J.C., (1967) Biochim. Biophys. Acta, Biomembr., 135, p. 639Abramson, M.B., Katzman, R., Gregor, H.P., (1964) J. Biol. Chem., 239, p. 70Hauser, H.O., (1971) Biochem. Biophys. Res. Commun., 45, p. 1049Huang, C.H., (1969) Biochemistry, 8, p. 344Saunders, L., Gammack, D., Perrin, J., (1962) J. Pharm. Pharmacol., 14, p. 567Tien, H.T., (1974) Theory and Practice, , 1th ed.Bilayer Lipid Membranes (BLM): Marcel Dekker: New YorkRazin, S., (1972) Biochim. Biophys. Acta, Biomembr., 265, p. 241Korenbrot, J.I., (1977) Annu. Rev. Physiol., 39, p. 19Batzri, S., Korn, E.D., (1973) Biochim. Biophys. Acta, Biomembr., 298, p. 1015Deamer, D., Bangham, A.D., (1976) Biochim. Biophys. Acta, Biomembr., 443, p. 629Szoka, F., Papahadjopoulos, D., (1978) Proc. Natl. Acad. Sci. U. S. A., 75, p. 4194Mishra, P.P., Bhatnagar, J., Datta, A., (2005) J. Phys. Chem. B., 109, p. 24225Pessoto, F.S., Inada, N.M., Nepomuceno, M.D., Ruggiero, A.C., Nascimento, O.R., Vercesi, A.E., Nantes, I.L., (2009) Chem. Biol. Interact., 181, p. 400Steinbeck, C.A., Hedin, N., Chmelka, B.F., (2004) Langmuir, 20, p. 10399Vanesch, J.H., Feiters, M.C., Peters, A.M., Nolte, R.J.M., (1994) J. Phys. Chem., 98, p. 5541Barber, D.C., Freitagbeeston, R.A., Whitten, D.G., (1991) J. Phys. Chem., 95, p. 4074Maiti, N.C., Mazumdar, S., Periasamy, N.J., (1998) J. Porphyrins Phthalocyanines, 2, p. 369Schmehl, R.H., Whitten, D.G., (1981) J. Phys. Chem., 85, p. 3473Perrin, M.H., (1973) J. Chem. Phys., 59, p. 2090Zhou, X.T., Ji, H.B., (2010) Chem. Eng. J., 156, p. 411Monnereau, C., Ramos, P.H., Deutman, A.B.C., Elemans, J., Nolte, R.J.M., Rowan, A.E., (2010) J. Am. Chem. Soc., 132, p. 1529Merlau, M.L., Grande, W.J., Nguyen, S.T., Hupp, J.T., (2000) J. Mol. Catal. A: Chem., 156, p. 79Anzenbacher, P., Kral, V., Jursikova, K., Gunterova, J., Kasal, A., (1997) J. Mol. Catal. A: Chem., 118, p. 63Zhao, Y.C., Xiang, Y.Z., Pu, L., Yang, M., Yu, X.Q., (2006) Appl. Catal. A, 301, p. 176Zhou, X.T., Tang, Q.H., Ji, H.B., (2009) Tetrahedron Lett., 50, p. 6601Monfared, H.H., Aghapoor, V., Ghorbanloo, M., Mayer, P., (2010) Appl. Catal. A, 372, p. 209Heijnen, J.H.M., De Bruijn, V.G., Van Den Broeke, L.J.P., Keurentjes, J.T.F., (2003) Chem. Eng. Process., 42, p. 223Santos, A.C., Luz, R.A.S., Ferreira, L.G.F., Santos-Júnior, J.R., Silva, W.C., (2010) Quim. Nova, 33, p. 539Zhou, Y.B., Ryu, E.H., Zhao, Y., Woo, L.K., (2007) Organometallics, 26, p. 358Nantes, I.L., Crespilho, F.N., Mugnol, K.C.U., Chaves, J.C.A., Luz, R.A.S., Nascimento, O.R., Pinto, S.M.S., (2010) Circular Dichroism: Theory and Spectroscopy, , Rodgers D. S., ed.Nova Science Publishers: New York ch. 8Travascio, P., Sen, D., Bennet, A.J., (2006) Can. J. Chem., 84, p. 613Omodeo-Sale, F., Monti, D., Olliaro, P., Taramelli, D.P., (2001) Biochem. Pharmacol., 61, p. 999Ishigure, S., Mitsui, T., Ito, S., Kondo, Y., Kawabe, S., Kondo Dewa M, T., Mino, H., Nango, M., (2010) Langmuir, 26, p. 7774Umakoshi, H., Morimoto, K., Ohama, Y., Nagami, H., Shimanouchi, T., Kuboi, R., (2008) Langmuir, 24, p. 4451Prieto, T., Marcon, R.O., Prado, F.M., Caires, A.C.F., Di Mascio, P., Brochsztain, S., Nascimento, O.R., Nantes, I.L., (2006) J. Phys.Chem., 8, p. 1963Mugnol, K.C.U., Ando, R.A., Nagayasu, R.Y., Faljoni-Alario, A., Brochsztain, S., Santos, P.S., Nascimento, R.O., Nantes, I.L., (2008) Biophys. J., 94, p. 4066Nagatomo, H., Matsushita, Y., Sugamoto, K., Matsui, T., (2003) Tetrahedron: Asymmetry, 14, p. 2339Cantonetti, V., Monti, D., Venanzi, M., Bombelli, C., Ceccacci, F., Mancini, G., (2004) Tetrahedron: Asymmetry, 15, p. 1969Hiraka, K., Kanehisa, M., Tamai, M., Asayama, S., Nagaoka, S., Oyaizu, K., Yuasa, M., Kawakami, H., (2008) Colloids Surf. B, 67, p. 54Yuasa, M., Oyaizu, K., Horiuchi, A., Ogata, A., Hatsugai, T., Yamaguchi, A., Kawakami, H., (2004) Mol. Pharm., 1, p. 387Aron, J., Baldwin, D.A., Marques, H.M., Pratt, J.M., Adams, P.A., (1986) J. Inorg. Biochem., 27, p. 227Wang, J.S., Vanwart, H.E., (1989) J. Phys. Chem., 93, p. 7925Munro, O.Q., Marques, H.M., (1996) Inorg. Chem., 35, p. 3752Prieto, T., Nascimento, O.R., Tersariol, I.L.S., Faljoni-Alario, A., Nantes, I.L., (2004) J. Phys. Chem. B, 108, p. 11124Prieto, T., Nantes, I.L., Nascimento, O.R., (2004) Prog. Colloid Polym. Sci., 128, p. 1Makarska, M., Radzki, S., Legendziewicz, J., (2002) J. Alloys Compd., 341, p. 233Riposati, A., Prieto, T., Shida, C.S., Nantes, I.L., Nascimento, O.R., (2006) J. Inorg. Biochem., 100, p. 226Claiborne, A., Fridovich, I., (1979) J. Biol. Chem., 254, p. 4245Hiner, A.N.P., Ruiz, J.H., Lopez, J.N.R., Canovas, F.G., Brisset, N.C., Smith, A.T., Arnao, M.B., Acosta, M., (2002) J. Biol. Chem., 277, p. 26879Primus, J.L., Grunenwald, S., Hagedoorn, P.L., Albrecht-Gary, A.M., Mandon, D., Veeger, C.T., (2002) J. Am. Chem. Soc., 124, p. 1214Demontellano, P.R.O., (1992) Annu. Rev. Pharmacol. Toxicol., 32, p. 89Savenkova, M.I., Kuo, J.M., De Montellano, P.R.O., (1998) Biochemistry, 37, p. 10828Smith, A.T., Veitch, N.C., (1998) Curr. Opin. Chem. Biol., 2, p. 269Prieto, T., Mugnol, K.C.U., Araujo, J.C., Sousa, F.L., Soares, V.A., Cilento, G., Nantes, I.L., (2007) Catalysis and Photochemistry in Heterogeneous Media, , Nantes I. L.Brochesztain, S. eds.Research Signpost: Kerala ch. 1Zucchi, M.R., Nascimento, O.R., Faljoni-Alario, A., Prieto, T., Nantes, I.L., (2003) Biochem. J., 370, p. 671Kinnunen, P.K.J., (1992) Chem. Phys. Lipids, 63, p. 251Kawai, C., Prado, F.M., Nunes, G.L.C., Di Mascio, P., Carmona-Ribeiro, A.M., Nantes, I.L., (2005) J. Biol. Chem., 280, p. 34709Araujo, J.C., Prieto, T., Prado, F.M., Trindade, F.J., Nunes, G.L.C., Dos Santos, J.G., Di Masco, P., Nantes, I.L., (2007) J. Nanosci. Nanotechnol., 7, p. 3643Estevam, M.L., Nascimento, O.R., Baptista, M.S., Di Mascio, P., Prado, F.M., Faljoni-Alario, A., Zucchi, M.D., Nantes, I.L., (2004) J. Biol. Chem., 279, p. 39214Kawai, C., Nantes, I.L., Baptista, M.D.S., (2010) FEBS J., 277, p. 224Nantes, I.L., Faljoni-Alario, A., Vercesi, A.E., Santos, K.E., Bechara, E.J.H., (1998) Free Radic. Biol. Med., 25, p. 54

    Compostos bioativos e atividade antioxidante do café (Coffea arabica L.) Coffee (Coffea arabica L.) bioactive compounds and antioxidant activity

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    Conduziu-se este trabalho, com a proposta de avaliar o potencial antioxidante de dois padrões da bebida do café (rio e mole), verdes e torrados, utilizando modelos in vitro. Foram determinados o teor de fenólicos totais, ácido clorogênico (ácido 5-cafeoilquínico) e cafeína das bebidas. A avaliação in vitro do potencial antioxidante foi investigada pelos métodos de captação do radical DPPH e pelo poder redutor de metais. Os dois padrões de bebida do café analisados não apresentaram diferenças quanto aos parâmetros cor, ácido clorogênico e cafeína. Observou-se que houve redução nos valores de ácido clorogênico à medida que os grãos foram torrados. O café verde bebida rio apresentou maior teor de fenólicos totais que o café bebida mole. Nos grãos torrados não foi observada diferença. A bebida do café independente da qualidade sensorial apresentou alto poder redutor e importante atividade sequestrante de radicais livres. A atividade sequestrante de radicais livres foi significativamente superior nas amostras obtidas a partir dos grãos torrados, quando comparados aos extratos dos grãos verdes. A torração, porém, reduziu o poder redutor das bebidas do café. Os dados obtidos permitem sugerir que, independente da classificação sensorial da bebida, o café apresenta expressiva capacidade sequestrante de radicais livres e poder redutor de metais.<br>The present work intended to evaluate the antioxidant potential of two coffee sorts (soft and river), green and roasted, in vitro. Phenolic compounds content, chlorogenic acid (5-cafeoyolquinic) and caffeine of the beverages were evaluated. In vitro evaluation of the antioxidant potential was investigated by DPPH radical scavenging assay and by reducing the power of metals. Both sorts of coffee did not present statistical differences for color, chlorogenic acid and caffeine. After roasting, 5-cafeoyolquinic acid levels decreased. River coffee beverage presented greater content of phenolics than the soft coffee beverage. In the roasted coffees no significant difference was observed. All sorts of coffee beverages presented high reducing ability and important scavenging activity of free radicals. The scavenging activity was higher in the roasted samples. The roast process decreased the reducing ability of the coffee beverage. Results allow suggesting that independent of the sort, coffee presents expressive antioxidant activity and reducing ability

    Computational analysis of nanofluids: A review

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    Heterogeneous contributions of change in population distribution of body mass index to change in obesity and underweight

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    From 1985 to 2016, the prevalence of underweight decreased, and that of obesity and severe obesity increased, in most regions, with significant variation in the magnitude of these changes across regions. We investigated how much change in mean body mass index (BMI) explains changes in the prevalence of underweight, obesity, and severe obesity in different regions using data from 2896 population-based studies with 187 million participants. Changes in the prevalence of underweight and total obesity, and to a lesser extent severe obesity, are largely driven by shifts in the distribution of BMI, with smaller contributions from changes in the shape of the distribution. In East and Southeast Asia and sub-Saharan Africa, the underweight tail of the BMI distribution was left behind as the distribution shifted. There is a need for policies that address all forms of malnutrition by making healthy foods accessible and affordable, while restricting unhealthy foods through fiscal and regulatory restrictions. © Copyright
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