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Presence of benznidazole conjugated metabolites in urine identified by β-glucuronidase treatment
Departamento de Ciencias BiológicasMarson, María Elena; Bournissen, Facundo García; Altcheh, Jaime; Moscatelli, Guillermo; Moroni, Samantha; Departamento de Ciencias BiológicasMastrantonio, Guido Enrique.
  • Departamento de Ciencias BiológicasMarson, María Elena; Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Departamento de Ciencias BiológicasMarson, María Elena. La Plata. AR
  • Bournissen, Facundo García; Hospital de Niños Ricardo Gutiérrez. Parasitología Chagas. Buenos Aires. AR
  • Altcheh, Jaime; Hospital de Niños Ricardo Gutiérrez. Parasitología Chagas. Buenos Aires. AR
  • Moscatelli, Guillermo; Hospital de Niños Ricardo Gutiérrez. Parasitología Chagas. Buenos Aires. AR
  • Moroni, Samantha; Hospital de Niños Ricardo Gutiérrez. Parasitología Chagas. Buenos Aires. AR
  • Departamento de Ciencias BiológicasMastrantonio, Guido Enrique; Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Departamento de Ciencias BiológicasMastrantonio, Guido Enrique. La Plata. AR
Braz. J. Pharm. Sci. (Online) ; 56: e18034, 2020. tab, graf
Article in English | LILACS-Express | LILACS | ID: biblio-1089207
ABSTRACT
Chagas disease is a serious public health problem in Latin America and, due to migration, in other non-endemic regions. Benznidazole (BNZ) is first choice drug in pediatric therapeutics. However, little is known regarding its metabolism in humans. The aim of the study was to isolate and identify products of human BZN metabolism in urine samples obtained from a pediatric Chagas patient and a healthy adult volunteer both treated with BZN. Urine samples were collected after dose of BNZ. Urine was treated with β-glucuronidase followed by an extraction procedure under two different pH conditions and a HPLC/UV and MS/MS identification of BZN and its metabolites. BZN (m/z 260.09847) was identified in all urine extracts. Peaks from each extracted chromatograms were selected for MS and MS/MS identification. Three compounds structurally related to BZN were identified BZN-Na+ (m/z 283.08009), N-amine-BZN (m/z 230.12307) and N-hydroxi-amine-BZN (m/z 246.11702). BNZ-Na+ was identified in all extracts, but N-amine-BZN and N-hydroxi-amine-BZN were only observed in those extracts treated with β-glucuronidase. This is the first experimental report showing elimination of BZN N-reduced metabolites in urine. As they were released after treatment with β-glucuronidase it can be suggested that glucuronization plays a role in BNZ metabolism and renal elimination.


Full text: Available Index: LILACS (Americas) Language: English Journal: Braz. J. Pharm. Sci. (Online) Journal subject: Farmacologia / Terapˆutica / Toxicologia Year: 2020 Type: Article Affiliation country: Argentina Institution/Affiliation country: Hospital de Niños Ricardo Gutiérrez/AR / Universidad Nacional de La Plata/AR

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Full text: Available Index: LILACS (Americas) Language: English Journal: Braz. J. Pharm. Sci. (Online) Journal subject: Farmacologia / Terapˆutica / Toxicologia Year: 2020 Type: Article Affiliation country: Argentina Institution/Affiliation country: Hospital de Niños Ricardo Gutiérrez/AR / Universidad Nacional de La Plata/AR