Evidence map›Paper›PMID 26883698›Full record

ArticleAntimicrobial agents and chemotherapy2016

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

Marcelo Gomes Davanço, Michel Leandro Campos, Talita Atanazio Rosa, Elias Carvalho Padilha, Alejandro Henao Alzate, Larissa Araújo Rolim, Pedro José Rolim-Neto, Rosângela Gonçalves Peccinini

Abstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Review
  2. Effects of Free and Nanoencapsulated Benznidazole in AcutePharmaceuticals (Basel, Switzerland) · 2024
    Article
  3. Article
  4. Review
  5. Review
  6. Observational
  7. Review
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Marcelo Gomes DavançoFaculdade de Ciências Farmacêuticas, Universidade Estadual Paulista (UNESP), Campus Araraquara, Departamento de Princípios Ativos Naturais e Toxicologia, Araraquara, São Paulo, Brazil davanco.marcelo@gmail.com peccinin@fcfar.unesp.br.
Michel Leandro CamposFaculdade de Ciências Farmacêuticas, Universidade Estadual Paulista (UNESP), Campus Araraquara, Departamento de Princípios Ativos Naturais e Toxicologia, Araraquara, São Paulo, Brazil.
Talita Atanazio RosaLaboratório de Tecnologia dos Medicamentos (LTM), Departamento de Ciências Farmacêuticas, Universidade Federal de Pernambuco (UFPE), Recife, Pernambuco, Brazil.
Elias Carvalho PadilhaFaculdade de Ciências Farmacêuticas, Universidade Estadual Paulista (UNESP), Campus Araraquara, Departamento de Princípios Ativos Naturais e Toxicologia, Araraquara, São Paulo, Brazil.
Alejandro Henao AlzateFaculdade de Ciências Farmacêuticas, Universidade Estadual Paulista (UNESP), Campus Araraquara, Departamento de Princípios Ativos Naturais e Toxicologia, Araraquara, São Paulo, Brazil.
Larissa Araújo RolimColegiado de Ciências Farmacêuticas, Universidade Federal do Vale do São Francisco (UNIVASF), Petrolina, Pernambuco, Brazil.
Pedro José Rolim-NetoLaboratório de Tecnologia dos Medicamentos (LTM), Departamento de Ciências Farmacêuticas, Universidade Federal de Pernambuco (UFPE), Recife, Pernambuco, Brazil.
Rosângela Gonçalves PeccininiFaculdade de Ciências Farmacêuticas, Universidade Estadual Paulista (UNESP), Campus Araraquara, Departamento de Princípios Ativos Naturais e Toxicologia, Araraquara, São Paulo, Brazil davanco.marcelo@gmail.com peccinin@fcfar.unesp.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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 concentrationin 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.

Indexed as

AdultAnimalsAntiprotozoal AgentsBiological AvailabilityChagas DiseaseChildDelayed-Action PreparationsHumansMaleNitroimidazolesRabbitsSolubilityTabletsTrypanosoma cruziAntiprotozoal AgentsbenzonidazoleDelayed-Action PreparationsNitroimidazolesTablets

Identifiers

PMID26883698
PMCPMC4808161

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.