Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 8 de 8
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
Environ Sci Pollut Res Int ; 24(30): 24029-24037, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-28879624

RESUMO

Brazil has been the largest world consumer of pesticides since 2008, followed by the USA. The herbicides trifluralin and tebuthiuron have been widely applied in agriculture. These herbicides are selective for some plant species, and their use brings various benefits. However, the genotoxic and mutagenic effects of tebuthiuron on non-target organisms are poorly known, and in addition, the effects of trifluralin must be better investigated. Therefore, this study employed genetic tests including the comet assay and micronucleus test to evaluate the genotoxic effects of trifluralin and tebuthiuron on HepG2 cells. In addition, we have used the Ames test to assess the mutagenic effects of the herbicides on the TA97a, TA98, TA100, and TA1535 strains of Salmonella typhimurium. On the basis of the comet assay and the micronucleus test, trifluralin did not cause genetic damage to HepG2 cells. In addition, trifluralin did not impact the tested S. typhimurium strains. Regarding tebuthiuron, literature has shown that this herbicide damaged DNA in Oreochromis niloticus. Nevertheless, we have found that tebuthiuron was not genotoxic to either HepG2 cells or the S. typhimurium strains. Therefore, neither trifluralin nor tebuthiuron exerted genotoxic or mutagenic potential at the tested conditions.


Assuntos
Ciclídeos/genética , Compostos de Metilureia/química , Mutagênicos/farmacologia , Praguicidas/química , Salmonella typhimurium/genética , Trifluralina/química , Animais , Brasil , Ensaio Cometa , Dano ao DNA , Testes Genéticos , Células Hep G2 , Herbicidas/farmacologia , Humanos , Testes para Micronúcleos , Mutagênese , Testes de Mutagenicidade , Praguicidas/farmacologia , Salmonella typhimurium/química
2.
Exp Parasitol ; 135(1): 153-65, 2013 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-23845259

RESUMO

Parasitic protozoa of the Leishmania genus cause leishmaniasis, an important complex of tropical diseases that affect about 12 million people around the world. The drugs used to treat leishmaniasis are pentavalent antimonials, miltefosine, amphotericin B and pentamidine. In the present study, we evaluated the effect of a novel alkyl phosphocholine-dinitroaniline hybrid molecule, TC95, against Leishmania amazonensis promastigotes and intracellular amastigotes. Antiproliferative assays indicated that TC95 is a potent inhibitor of promastigotes and intracellular amastigotes with IC50 values of 2.6 and 1.2 µM, respectively. Fluorescence microscopy with anti-α-tubulin antibody revealed changes in the cytoskeleton, whilst scanning electron microscopy showed alterations in the shape, plasma membrane, length of the flagellum, and cell cycle. Flow cytometry confirmed the cell cycle arrest mainly in G1 phase, however a significant population appeared in sub G0/G1 and super-G2. The alterations in the plasma membrane integrity were confirmed by fluorometric analysis using Sytox Blue. Transmission electron microscopy also revealed an accumulation of lipid bodies, confirmed by fluorescence microscopy and fluorometric analysis using Nile Red. Important lesions were also observed in organelles such as mitochondrion, endoplasmic reticulum and Golgi complex. In summary, our study suggests that TC95, an alkyl phosphocholine-trifluralin hybrid molecule, is a promising novel compound against L. amazonensis.


Assuntos
Compostos de Anilina/farmacologia , Antiprotozoários/farmacologia , Leishmania mexicana/efeitos dos fármacos , Fosforilcolina/análogos & derivados , Fosforilcolina/farmacologia , Trifluralina/análogos & derivados , Trifluralina/farmacologia , Compostos de Anilina/química , Compostos de Anilina/toxicidade , Animais , Antiprotozoários/química , Antiprotozoários/toxicidade , Pontos de Checagem do Ciclo Celular/efeitos dos fármacos , Membrana Celular/efeitos dos fármacos , Citoesqueleto/efeitos dos fármacos , Citometria de Fluxo , Histocitoquímica , Humanos , Corpos de Inclusão/efeitos dos fármacos , Concentração Inibidora 50 , Leishmania mexicana/citologia , Leishmania mexicana/ultraestrutura , Leishmaniose Tegumentar Difusa/parasitologia , Macrófagos Peritoneais/efeitos dos fármacos , Camundongos , Microscopia Eletrônica de Varredura , Microscopia Eletrônica de Transmissão , Microscopia de Fluorescência , Microscopia de Interferência , Fosforilcolina/química , Fosforilcolina/toxicidade , Trifluralina/química , Trifluralina/toxicidade
3.
Chemotherapy ; 55(5): 327-34, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19641315

RESUMO

BACKGROUND: Trifluralin displays anti-Trypanosoma cruzi activity and a potential therapeutic effect for the treatment of Chagas disease. We assessed peroral and intramuscular trifluralin pharmacokinetics in mouse blood and heart tissue. METHODS: A parallel experimental design was used. Healthy adult male CF1 albino mice (n = 108, 25-35 g bw) received a single peroral or intramuscular trifluralin dose (50 mg/kg in peanut oil). Blood and heart tissue samples were taken at set times after intramuscular and peroral trifluralin administration. Feces and tissue samples were taken 12 h after intramuscular trifluralin administration. Trifluralin concentrations in whole blood, feces and tissues were determined by HPLC. RESULTS: After intramuscular and peroral administration, maximum whole blood concentration (C(max)) was attained at 30 min and 2.0 h (t(max)) (28.2 +/- 0.7 and 7.8 +/- 0.033 microg/ml; p < 0.05). C(max) in heart tissue was attained at 1.0 and 2.0 h (0.6 +/- 0.004 and 0.2 +/- 0.002 microg/g; p < 0.05). Liver, perirenal and subcutaneous fat concentrations were 55.1, 66.3 and 59.7 ng/mg tissue protein. Peroral and intramuscular penetration ratios determined by comparing heart tissue areas under the curve were 6.3 and 4.0%, respectively. CONCLUSION: Intramuscular trifluralin could be a new alternative for the treatment of Chagas disease.


Assuntos
Miocárdio/metabolismo , Trifluralina/farmacocinética , Tripanossomicidas/farmacocinética , Tecido Adiposo/metabolismo , Animais , Cardiomiopatia Chagásica/tratamento farmacológico , Doença de Chagas/tratamento farmacológico , Fezes/química , Humanos , Fígado/metabolismo , Masculino , Camundongos , Trifluralina/sangue , Trifluralina/química , Tripanossomicidas/sangue
4.
J Environ Sci Health B ; 41(3): 245-52, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16484085

RESUMO

The treatment of an effluent from the production of trifluraline was studied using a 1-L, semi-batch, tank-stirred glass reactor for performing three different advanced oxidation processes (photoperoxidation, Fenton, photo-Fenton). A commercial, medium-pressure mercury lamp was used for sample irradiation. The degradation was monitored by measurements of absorptiometric color reduction, UV-visible absorption spectra, and chemical oxygen demand (COD). The obtained results showed that the photo-Fenton process was the most effective treatment for the trifluraline effluent.


Assuntos
Herbicidas/química , Trifluralina/química , Purificação da Água/métodos , Reatores Biológicos , Peróxido de Hidrogênio/química , Ferro , Oxirredução , Fotoquímica , Poluição Química da Água
5.
Photochem Photobiol Sci ; 4(11): 869-75, 2005 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16252042

RESUMO

The herbicide trifluralin (I)(N,N-di-n-propyl-2,6-dinitro-4-trifluoromethylaniline) decomposes, by the action of UV-Vis light (lambda > 300 nm), to several products, the most important (because they give subsequent photochemical reactions) being N-n-propyl-2,6-dinitro-4-trifluoromethylaniline (VI), 2-ethyl-7-nitro-5-trifluoromethyl-1H-benzimidazole 3-oxide (VII) and 2,6-dinitro-4-trifluoromethylaniline (XII). The time evolution of degradation of trifluralin (I) and the aforementioned three main photoproducts was studied in water and acetonitrile as solvents. The pseudo-first order rate constants allow one to calculate the branching ratios for some of the reactions involved. The preference for either N-dealkylation or cyclization depends on the solvent employed. Dissolved oxygen accelerates the photodegradation, especially the dealkylation.


Assuntos
Resíduos de Praguicidas/química , Trifluralina/química , Acetonitrilas/química , Fotoquímica , Solubilidade , Fatores de Tempo , Água/química
6.
J Agric Food Chem ; 50(16): 4619-27, 2002 Jul 31.
Artigo em Inglês | MEDLINE | ID: mdl-12137486

RESUMO

The dissipation rate of seven currently used soybean and corn pesticides in two tropical soils (Ustox and Psamments) of Brazil was studied in a laboratory incubation experiment. Dissipation half-lives of pesticides ranged between 2 (monocrotofos) and 90 days (endosulfan-beta). The contrasting clay contents of the studied tropical soils (130 versus 470 g of clay kg(-1) of soil) did not influence the dissipation dynamics of pesticides substantially. Mineralization to CO(2) was high [up to 78% of the applied radioactivity (AR)] for the studied organophosphorus compounds and deltamethrin, which also formed considerable amounts of bound residues (>20% of AR) during the 80 days of incubation. The highest portion of nonextractable residues was found for alachlor and simazine (55-60% of AR). In contrast, the nonpolar trifluralin and endosulfan formed only small amounts of bound residues (mostly <20% of AR) but showed the highest dissipation half-lives (>14 days) in the studied soils, also due to a low mineralization rate. When endosulfan-sulfate, as the main metabolite of endosulfan, was considered, the half-life time of endosulfan compounds (sum of -alpha, -beta, and -sulfate) was enhanced to >160 days in both soils. In comparison with the laboratory experiments, dissipation half-life times of chlorpyrifos, endosulfan-alpha, and trifluralin were shortened by a factor of 10-30 in field trials with the same soils, which was related to the volatilization potential of pesticides from soils.


Assuntos
Glycine max , Resíduos de Praguicidas/análise , Praguicidas/química , Solo/análise , Zea mays , Acetamidas/química , Brasil , Radioisótopos de Carbono , Clorpirifos/química , Endossulfano/química , Meia-Vida , Herbicidas/química , Inseticidas/química , Marcação por Isótopo , Monocrotofós/química , Nitrilas , Piretrinas/química , Simazina/química , Trifluralina/química , Clima Tropical
7.
Trends Parasitol ; 17(3): 136-41, 2001 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-11286798

RESUMO

The drugs presently in use against Chagas disease are very toxic, inducing a great number of side effects. Alternative treatments are necessary, not only for Chagas disease but also for other diseases caused by protozoan parasites where current drugs pose toxicity problems. The plant microtubule inhibitor trifluralin has previously been tested with success against Leishmania, Trypanosoma brucei and several other protozoan parasites. Trypanosoma cruzi, the causative agent of Chagas disease, is also sensitive to the drug. This sensitivity has been correlated with the deduced amino acid sequences of alpha- and beta-tubulin of T. cruzi as compared with plant, mammal and other parasite sequences.


Assuntos
Herbicidas/farmacologia , Trifluralina/farmacologia , Trypanosoma cruzi/efeitos dos fármacos , Sequência de Aminoácidos , Compostos de Anilina , Animais , Doença de Chagas/parasitologia , Herbicidas/química , Humanos , Dados de Sequência Molecular , Trifluralina/química , Trypanosoma cruzi/crescimento & desenvolvimento , Tubulina (Proteína)/química , Tubulina (Proteína)/efeitos dos fármacos , Tubulina (Proteína)/genética
8.
Chemosphere ; 41(9): 1441-9, 2000 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11057581

RESUMO

Pesticide pollution of ground and surface water is of growing concern in tropical countries. The objective of this pilot study was to evaluate the leaching potential of eight pesticides in a Brazilian Oxisol. In a field experiment near Cuiabá, Mato Grosso, atrazine, chlorpyrifos, lambda-cyhalothrin, endosulfane alpha, metolachlor, monocrotofos, simazine, and trifluraline were applied onto a Typic Haplustox. Dissipation in the topsoil, mobility within the soil profile and leaching of pesticides were studied for a period of 28 days after application. The dissipation half-life of pesticides in the topsoil ranged from 0.9 to 14 d for trifluraline and metolachlor, respectively. Dissipation curves were described by exponential functions for polar pesticides (atrazine, metolachlor, monocrotofos, simazine) and bi-exponential ones for apolar substances (chlorpyrifos, lambda-cyhalothrin, endosulfane alpha, trifluraline). Atrazine, simazine and metolachlor were moderately leached beyond 15 cm soil depth, whereas all other compounds remained within the top 15 cm of the soil. In lysimeter percolates (at 35 cm soil depth), 0.8-2.0% of the applied amounts of atrazine, simazine, and metolachlor were measured within 28 days after application. Of the other compounds less than 0.03% of the applied amounts was detected in the soil water percolates. The relative contamination potentials of pesticides, according to the lysimeter study, were ranked as follows: metolachlor > atrazine = simazine >> monocrotofos > endsulfane alpha > chlorpyrifos > trifluraline > lambda-cyhalothrin. This order of the pesticides was also achieved by ranking them according to their effective sorption coefficient Ke, which is the ratio of Koc to field-dissipation half-life.


Assuntos
Glycine max , Praguicidas/química , Solo/análise , Zea mays , Acetamidas/química , Atrazina/química , Biodegradação Ambiental , Brasil , Fenômenos Químicos , Físico-Química , Clorpirifos/química , Endossulfano/química , Meia-Vida , Monocrotofós/química , Nitrilas , Praguicidas/análise , Piretrinas/química , Simazina/química , Trifluralina/química , Clima Tropical , Poluição da Água
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA