Physico-chemical characterization of inclusion complex between hydroxymethylnitrofurazone and hydroxypropyl-beta-cyclodextrin

Hydroxymethylnitrofurazone (NFOH) is a prodrug that is active against Trypanosoma cruzi. It however presents low solubility and high toxicity. Hydroxypropyl-beta-cyclodextrin (HP-beta-CD) can be used as a drug-delivery system for NFOH modifying its physico-chemical properties. The aim of this work is to characterize the inclusion complex between NFOH and HP-beta-CD. The rate of NFOH release decreases after complexation and thermodynamic parameters from the solubility isotherm studies revealed that a stable complex is formed (deltaGº= 1.7 kJ/mol). This study focuses on the physico-chemical characterization of a drug-delivery formulation that comes out as a potentially new therapeutic option for Chagas disease treatment.FAPESPCoordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES

Transcriptome analysis of Loxosceles laeta (Araneae, Sicariidae) spider venomous gland using expressed sequence tags

<p>Abstract</p> <p>Background</p> <p>The bite of spiders belonging to the genus <it>Loxosceles </it>can induce a variety of clinical symptoms, including dermonecrosis, thrombosis, vascular leakage, haemolysis, and persistent inflammation. In order to examine the transcripts expressed in venom gland of <it>Loxosceles laeta </it>spider and to unveil the potential of its products on cellular structure and functional aspects, we generated 3,008 expressed sequence tags (ESTs) from a cDNA library.</p> <p>Results</p> <p>All ESTs were clustered into 1,357 clusters, of which 16.4% of the total ESTs belong to recognized toxin-coding sequences, being the Sphingomyelinases D the most abundant transcript; 14.5% include "possible toxins", whose transcripts correspond to metalloproteinases, serinoproteinases, hyaluronidases, lipases, C-lectins, cystein peptidases and inhibitors. Thirty three percent of the ESTs are similar to cellular transcripts, being the major part represented by molecules involved in gene and protein expression, reflecting the specialization of this tissue for protein synthesis. In addition, a considerable number of sequences, 25%, has no significant similarity to any known sequence.</p> <p>Conclusion</p> <p>This study provides a first global view of the gene expression scenario of the venom gland of <it>L. laeta </it>described so far, indicating the molecular bases of its venom composition.</p

Capítulo 4: Financiamento da infraestrutura de transportes no Brasil

A indicação de autoria do capítulo 4 está sinalizada na página 34Bibliografia: p. 131 - 132Disponível online em : http://www.ipea.gov.br/portal/index.php?option=com_content&view=article&id=14050É permitida a reprodução deste texto e dos dados nele contidos, desde que citada a fonte. Reproduções para fins comerciais são proibida

Physico-chemical characterization of inclusion complex between hydroxymethylnitrofurazone and hydroxypropyl-b-cyclodextrin

Hydroxymethylnitrofurazone (NFOH) is a prodrug that is active against Trypanosoma cruzi. It however presents low solubility and high toxicity. Hydroxypropyl-b-cyclodextrin (HP-b-CD) can be used as a drug-delivery system for NFOH modifying its physico-chemical properties. The aim of this work is to characterize the inclusion complex between NFOH and HP-b-CD. The rate of NFOH release decreases after complexation and thermodynamic parameters from the solubility isotherm studies revealed that a stable complex is formed (DGº= 1.7 kJ/mol). This study focuses on the physico-chemical characterization of a drug-delivery formulation that comes out as a potentially new therapeutic option for Chagas disease treatment312290295COORDENAÇÃO DE APERFEIÇOAMENTO DE PESSOAL DE NÍVEL SUPERIOR - CAPESFUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO - FAPESP00019-08-0305/03045-9; 04/02091-4; 06/00787-

An optimized nanoparticle delivery system based on chitosan and chondroitin sulfate molecules reduces the toxicity of amphotericin B and is effective in treating tegumentary leishmaniasis

Amphotericin B (AmpB) is active against leishmaniasis, but its use is hampered due to its high toxicity observed in patients. In this study, a nanoparticles-delivery system for AmpB (NQC-AmpB), containing chitosan and chondroitin sulfate molecules, was evaluated in BALB/c mice against Leishmania amazonensis. An in vivo biodistribution study, including biochemical and toxicological evaluations, was performed to evaluate the toxicity of AmpB. Nanoparticles were radiolabeled with technetium-99m and injected in mice. The products presented a similar biodistribution in the liver, spleen, and kidneys of the animals. Free AmpB induced alterations in the body weight of the mice, which, in the biochemical analysis, indicated hepatic and renal injury, as well as morphological damage to the kidneys of the animals. In general, no significant organic alteration was observed in the animals treated with NQC-AmpB. Mice were infected with L. amazonensis and treated with the nanoparticles or free AmpB; then, parasitological and immunological analyses were performed. The NQC-AmpB group, as compared to the control groups, presented significant reductions in the lesion size and in the parasite burden in all evaluated organs. These animals presented significantly higher levels of IFN-γ and IL-12, and low levels of IL-4 and IL-10, when compared to the control groups. The NQC-AmpB system was effective in reducing the infection in the animals, and proved to be effective in diminishing the toxicity evoked by AmpB, which was observed when it was administered alone. In conclusion, NQC-AmpB could be considered a viable possibility for future studies in the treatment of leishmaniasisThis work was supported by grants from Pró-Reitoria de Pesquisa from UFMG (Edital 01/2014), Instituto Nacional de Ciência e Tecnologia em Nano-biofarmacêutica (INCT-Nanobiofar), FAPEMIG (CBB-APQ-00496-11 and CBB-APQ-00819-12), and CNPq (APQ-472090/2011-9 and APQ-482976/2012-8). MACF is a grant recipient of FAPEMIG/CAPES. EAFC, VNC, and AAGF are grant recipients of CNPq. Eduardo AF Coelho and André AG Faraco are co-senior authors of this stud

Flowering, germination and rooting of cuttings of Lippia L. (Verbenaceae)

Lippia species from Cadeia do Espinhaço (MG, Brazil), were collected and established at the Botanical Experimental Station, Juiz de Fora, MG. The flowering of plants was evaluated in both natural and controlled conditions. Germination test was accomplished with seeds obtained from natural conditions. The rooting of cuttings was evaluated in plants cultivated in the Botanical Experimental Station. The majority of species blossomed either in the dry or in the rainy seasons. Only one species blooms in both seasons. At controlled conditions, the flowering period increased in species that flourish in the summer. Some species presented better germination with fresh collected seeds while others when the seeds were stored, evidencing both viability loss and seed dormancy. GA3 stimulates the germination in some species, while it inhibited or not influenced on others. Some species germinate better in the darkness, while others under white light. Some of them germinate in the light or in the darkness. Adventitious roots formation in cuttings of wild species was very low and did not vary in response to season variation and auxin concentration. On the other hand, rooting of cuttings of L. alba (Mill.) N.E. Br. varied in response both to season variation and to auxin types and concentration. This is the first report on physiological reproductive aspects of endemic Lippia species from the Cadeia do Espinhaço. The results indicate the possibility to use seeds in the propagation of wild Lippia species and, they also show that reproduction through conventional vegetative propagation techniques presents quite reduced efficiency.Plantas de dez espécies de Lippia foram coletadas na Cadeia do Espinhaço, MG, Brasil e cultivadas em canteiros em Juiz de Fora, MG. A época de florescimento das espécies de Lippia foi observada nos ambientes de origem e em canteiro. A germinação foi testada com sementes coletadas em ambiente natural. Os materiais estabelecidos ex situ foram avaliados quanto ao enraizamento de estacas. As análises das plantas em ambiente natural e das cultivadas em canteiro evidenciaram que a maioria das espécies estudadas apresenta floração no período seco (inverno), enquanto um menor número, no chuvoso (verão). Uma única espécie floresceu nessas duas estações. Em cultivo controlado, o período de floração das espécies com floração característica no verão foi aumentado. Algumas espécies germinaram melhor quando recém coletadas enquanto outras quando armazenadas, evidenciando a ocorrência de perda de viabilidade e de dormência. O GA3 estimulou a germinação em algumas espécies, enquanto inibiu ou não apresentou efeitos sobre outras. Sementes de algumas espécies germinaram melhor no escuro, enquanto de outras sob luz branca, existindo ainda espécies que germinaram tanto na luz quanto no escuro. O enraizamento das estacas das espécies não domesticadas de Lippia foi muito baixo, independente da estação do ano e da concentração da auxina. O enraizamento em estacas de L. alba (Mill.) N.E. Br. variou em resposta à época de coleta das estacas e quanto ao tipo e à concentração das auxinas utilizadas. Os resultados do presente trabalho constituem os primeiros relatos envolvendo a reprodução de espécies de Lippia endêmicas da Cadeia do Espinhaço. Eles indicam a possibilidade de utilização das sementes na propagação das plantas desse gênero e também evidenciam que a reprodução das plantas das espécies não domesticadas de Lippia através de técnicas convencionais de propagação assexuada apresenta eficiência bastante reduzida

Brazilian consensus on guidelines for diagnosis and treatment for restless legs syndrome

The Consensus on restless legs syndrome is an effort of neurologists from several Brazilian states, which tirelessly reviewed the literature of recent years in search of evidence, both in regard to diagnosis and treatment, according to the Oxford Centre for Evidence-based Medicine.Serv Neurol & Neurocirurgia, Passo Fundo, RS, BrazilUniv São Paulo, Fac Med Ribeirao Preto, BR-14049 Ribeirao Preto, SP, BrazilClin Carlos Bacelar, Rio de Janeiro, RJ, BrazilUniversidade Federal de São Paulo, Dept Psicobiol, São Paulo, BrazilHosp Moinhos Vento, BR-90560030 Porto Alegre, RS, BrazilUniversidade Federal de São Paulo, Dept Neurol, São Paulo, BrazilHosp Israelita Albert Einstein, São Paulo, BrazilUniv Fed Alagoas, Fac Med, Maceio, AL, BrazilUniv Fed Pernambuco, Recife, PE, BrazilClin Rio Sono, Rio de Janeiro, RJ, BrazilUniv São Paulo, Fac Med, Hosp Clin, São Paulo, BrazilPontificia Univ Catolica Rio Grande do Sul, Porto Alegre, RS, BrazilUniv Brasilia, Fac Med, Brasilia, DF, BrazilHosp Clin Porto Alegre, Porto Alegre, RS, BrazilProSSono Ctr Med Sono, Ribeirao Preto, BrazilUniversidade Federal de São Paulo, Dept Psicobiol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Neurol, São Paulo, BrazilWeb of Scienc