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

Autor(es)

Davanco, Marcelo Gomes ^[1] ; Campos, Michel Leandro ^[1] ; Rosa, Talita Atanazio ^[2] ; Padilha, Elias Carvalho ^[1] ; Alzate, Alejandro Henao ^[1] ; Rolim, Larissa Araujo ^[3] ; Rolim-Neto, Pedro Jose ^[2] ; Peccininia, Rosangela Goncalves ^[1]

Afiliação do(s) autor(es)

^[1] Univ Estadual Paulista UNESP, Fac Ciencias Farmaceut, Dept Principios Ativos Nat & Toxicol, Campus Araraquara, Sao Paulo - Brazil

^[2] Univ Fed Pernambuco UFPE, Dept Ciencias Farmaceut, Lab Tecnol Medicamentos LTM, Recife, PE - Brazil

^[3] Univ Fed Vale Sao Francisco UNIVASF, Colegiado Ciencias Farmaceut, Petrolina, PE - Brazil

• Tipo de documento: Artigo Científico
• Fonte: Antimicrobial Agents and Chemotherapy; v. 60, n. 4, p. 2492-2498, APR 2016.
• Citações Web of Science: 5

Resumo

Benznidazole (BNZ) is the first-line drug for the treatment of Chagas disease. The drug is available in the form of immediate-release 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. (AU)

• Processo FAPESP: 13/25882-6 - Farmacocinética pré-clínica de novas formulações de benznidazol para o tratamento da Doença de Chagas
• Beneficiário: Marcelo Gomes Davanço
• Modalidade de apoio: Bolsas no Brasil - Mestrado
• Processo FAPESP: 14/13192-8 - Avaliação da farmacocinética do benznidazol administrado na forma de comprimidos de liberação prolongada e comprimidos pediátricos em coelhos albinos
• Beneficiário: Rosangela Gonçalves Peccinini
• Modalidade de apoio: Auxílio à Pesquisa - Regular