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Benznidazole Extended-Release Tablets for Improved Treatment of Chagas Disease: Preclinical Pharmacokinetic Study

Authors :
Elias Carvalho Padilha
Pedro José Rolim-Neto
Rosângela Gonçalves Peccinini
Larissa Araújo Rolim
Marcelo Gomes Davanço
Talita Atanazio Rosa
Alejandro Henao Alzate
Michel Leandro Campos
Universidade Estadual Paulista (Unesp)
Universidade Federal de Pernambuco (UFPE)
Universidade Federal do Vale do São Francisco (UNIVASF)
Source :
Scopus, Repositório Institucional da UNESP, Universidade Estadual Paulista (UNESP), instacron:UNESP
Publication Year :
2016
Publisher :
American Society for Microbiology, 2016.

Abstract

Made available in DSpace on 2018-12-11T17:02:19Z (GMT). No. of bitstreams: 0 Previous issue date: 2016-04-01 Benznidazole (BNZ) is the first-line drug for the treatment of Chagas disease. The drug is available in the form of immediaterelease tablets for 100-mg (adult) and 12.5-mg (pediatric) doses. The drug is administered two or three times daily for 60 days. The high frequency of daily administrations and the long period of treatment are factors that significantly contribute to the abandonment of therapy, affecting therapeutic success. Accordingly, this study aimed to evaluate the preclinical pharmacokinetics of BNZ administered as extended-release tablets (200-mg dose) formulated with different types of polymers (hydroxypropyl methylcellulose K4M and K100M), compared to the tablets currently available. The studies were conducted with rabbits, and BNZ quantification was performed in plasma and urine by ultraperformance liquid chromatography methods previously validated. The bioavailability of BNZ was adequate in the administration of extended-release tablets; however, with the administration of the pediatric tablet, the bioavailability was lower than with other tablets, which showed that the clinical use of this formulation should be monitored. The pharmacokinetic parameters demonstrated that the extended-release tablets prolonged drug release from the pharmaceutical matrix and provided an increase in the maintenance of the drug concentration in vivo, which would allow the frequency of administration to be reduced. Thus, a relative bioavailability study in humans will be planned for implementation of a new product for the treatment of Chagas disease. Departamento de Princípios Ativos Naturais E Toxicologia Universidade Estadual Paulista (UNESP), Campus Araraquara Departamento de Ciências Farmacêuticas Laboratório de Tecnologia Dos Medicamentos (LTM) Universidade Federal de Pernambuco (UFPE) Colegiado de Ciências Farmacêuticas Universidade Federal do Vale do São Francisco (UNIVASF) Departamento de Princípios Ativos Naturais E Toxicologia Universidade Estadual Paulista (UNESP), Campus Araraquara

Details

ISSN :
10986596 and 00664804
Volume :
60
Database :
OpenAIRE
Journal :
Antimicrobial Agents and Chemotherapy
Accession number :
edsair.doi.dedup.....17a3ac60fa9770de7b5e406796ce44ca
Full Text :
https://doi.org/10.1128/aac.02506-15