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Metodología UV para la determinación de los antichagásicos Nifurtimox y Benznidazol en sangre ABCL
Bulffer,Romina Fernanda; Castro,José Alberto; Fanelli,Silvia Laura.
El Mal de Chagas es una enfermedad parasitaria endémica en América del Sur y Central. Existen dos fármacos disponibles para el tratamiento médico de la enfermedad, el Nifurtimox (Nfx) y el Benznidazol (Bz). No existen protocolos estandarizados, validados y accesibles en laboratorios regionales para determinar niveles de los antichagásicos en sangre. En este trabajo se presenta un método espectrofotométrico para la determinación de Nfx y Bz en sangre. Los metabolitos en sangre se extraen con columnas Extrelut®. Los extractos se evaporan, se redisuelven en mezclas de metanol/agua y se analizan espectrofotométricamente a 400 nm y a 320 nm para Nfx y Bz, respectivamente. Se cuantifica comparando con soluciones estándar de Nfx o Bz en el solvente. La...
Tipo: Info:eu-repo/semantics/article Palavras-chave: Benznidazol; Nifurtimox; Sangre; Enfermedad de Chagas espectrofotometría.
Ano: 2011 URL: http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0325-29572011000300008
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Enfermedad de Chagas: Contribuciones del Centro de Investigaciones Toxicológicas ABCL
Castro,José Alberto; Montalto de Mecca,María; Díaz Gómez,María Isabel; Castro,Gerardo Daniel.
La quimioterapia de la enfermedad de Chagas cuenta en la actualidad con el empleo de dos fármacos solamente: Nifurtimox y Benznidazol. Nifurtimox es un nitrofurano y Benznidazol es un compuesto nitroimidazólico. El uso de estas drogas para tratar la fase aguda de la enfermedad se acepta ampliamente. Sin embargo, su utilización en el tratamiento de la fase crónica no está exenta de cuestionamientos serios. Los efectos colaterales de ambas son un inconveniente mayor en su uso, y frecuentemente fuerza a los médicos a detener el tratamiento. Los estudios de toxicidad experimentales con Nifurtimox evidenciaron neurotoxicidad, daño testicular, toxicidad ovárica y efectos deletéreos en corazón, tejido mamario, adrenales, colon y esófago. Para el Benznidazol, se...
Tipo: Info:eu-repo/semantics/article Palavras-chave: Benznidazol; Nifurtimox; Enfermedad de Chagas; Quimioterapia; Quimioprofilaxis; Violeta de Genciana; Tripanosomiasis americana.
Ano: 2015 URL: http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0325-29572015000100009
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Effects of buthionine sulfoximine nifurtimox and benznidazole upon trypanothione and metallothionein proteins in Trypanosoma cruzi. Biol. Res.
MAYA,JUAN DIEGO; RODRÍGUEZ,ANDRÉS; PINO,LAURA; PABÓN,ADRIANA; FERREIRA,JORGE; PAVANI,MARIO; REPETTO,YOLANDA; MORELLO,ANTONIO.
Proteins rich in sulfhydryl groups, such as metallothionein, are present in several strains of the parasite Trypanosoma cruzi, the etiological agent of Chagas' disease. Metallothionein-like protein concentrations ranged from 5.1 to 13.2 pmol/mg protein depending on the parasite strain and growth phase. Nifurtimox and benznidazole, used in the treatment of Chagas' disease, decreased metallothionein activity by approximately 70%. T. cruzi metallothionein was induced by ZnCl2. Metallothionein from T. cruzi was partially purified and its monobromobimane derivative showed a molecular weight of approximately 10,000 Da by SDS-PAGE analysis. The concentration of trypanothione, the major glutathione conjugate in T. cruzi, ranged from 3.8 to 10.8 nmol/mg protein,...
Tipo: Journal article Palavras-chave: Trypanosoma cruzi; Metallothionein; Glutathione; Trypanothione; Benznidazole; Nifurtimox; Buthionine sulfoximine.
Ano: 2004 URL: http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602004000100007
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Cytotoxicity and trypanocidal activity of nifurtimox encapsulated in ethylcyanoacrylate nanoparticles Biol. Res.
SÁNCHEZ,GITTITH; CUELLAR,DANIELA; ZULANTAY,INES; GAJARDO,MARTA; GONZÁLEZ-MARTIN,GUILLERMO.
The aim of the present study was to study the trypanocidal activity of nanoparticles loaded with nifurtimox in comparison with the free drug against Trypanosoma cruzi, responsible for Chagas' disease. Ethylcyanoacrylate nanoparticles acted as the delivery system into cells. As the obligate replicative intracellular form is amastigote, in vitro studies were performed on this form of parasite as well as on cell culture derived trypomastigotes. The fluorescence method used here was very useful as it allowed for the simultaneous study of trypanocide activity and cytotoxicity by determining living or dead parasites within living or dead host cells. According to these results, the greatest trypanocide activity on cell culture-derived trypomastigotes was recorded...
Tipo: Journal article Palavras-chave: Nifurtimox; Nanoparticles; Amastigotes; Trypomastigotes; Trypanosoma cruzi.
Ano: 2002 URL: http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602002000100007
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Chagas disease: Present status of pathogenic mechanisms and chemotherapy Biol. Res.
Maya,Juan Diego; Orellana,Myriam; Ferreira,Jorge; Kemmerling,Ulrike; López-Muñoz,Rodrigo; Morello,Antonio.
There are approximately 7.8 million people in Latin America, including Chile, who suffer from Chagas disease and another 28 million who are at risk of contracting it. Chagas is caused by the flagellate protozoan Trypanosoma cruzi. It is a chronic disease, where 20%-30% of infected individuals develop severe cardiopathy, with heart failure and potentially fatal arrhythmias. Currently, Chagas disease treatment is more effective in the acute phase, but does not always produce complete parasite eradication during indeterminate and chronic phases. At present, only nifurtimox or benznidazole have been proven to be superior to new drugs being tested. Therefore, it is necessary to find alternative approaches to treatment of chronic Chagas. The current treatment...
Tipo: Journal article Palavras-chave: Chagas disease; Chemotherapy; Nifurtimox; Trypanosoma cruzi; Prostaglandins.
Ano: 2010 URL: http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602010000300009
Registros recuperados: 5
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