Evidence map›Paper›PMID 29795592›Full record

ArticlePloS one2018

Dissolution and uniformity of content of tablets developed with extract of Ximenia americana L.

Cleildo P Santana, Francinalva D Medeiros, Lidiane P Correia, Paulo Henrique G D Diniz, Germano Véras, Ana Cláudia D Medeiros

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Evaluation of How Methacrylate Gelatin Hydrogel Loaded withJournal of functional biomaterials · 2023
    Article
  5. Tablet ofMolecules (Basel, Switzerland) · 2021
    Article
  6. Tablet ofPolymers · 2019
    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

6 authors.

Cleildo P SantanaLaboratório de Desenvolvimento e Ensaios de Medicamentos, Centro de Ciências Biológicas e da Saúde, Universidade Estadual da Paraíba, Campina Grande, Paraíba, Brasil.
Francinalva D MedeirosLaboratório de Desenvolvimento e Ensaios de Medicamentos, Centro de Ciências Biológicas e da Saúde, Universidade Estadual da Paraíba, Campina Grande, Paraíba, Brasil.
Lidiane P CorreiaDepartamento de Farmácia, Centro de Ciências Biológicas e da Saúde, Universidade Estadual da Paraíba, Campina Grande, Paraíba, Brasil.
Paulo Henrique G D DinizLaboratório de Química Analítica e Quimiometria, Universidade Estadual da Paraíba, Campina Grande, Paraíba, Brasil.ORCID 0000-0002-8652-5478
Germano VérasLaboratório de Química Analítica e Quimiometria, Universidade Estadual da Paraíba, Campina Grande, Paraíba, Brasil.
Ana Cláudia D MedeirosLaboratório de Desenvolvimento e Ensaios de Medicamentos, Centro de Ciências Biológicas e da Saúde, Universidade Estadual da Paraíba, Campina Grande, Paraíba, Brasil.ORCID 0000-0002-8682-0178

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herbal medicines currently represent an important part of the world pharmaceutical market, which shows growing interest in the use of herbal medicines. However, the production of such medicines involves a complex series of steps, which determine the production viability and the quality of the final product. Ximenia americana L. is a plant occurring in several regions of the world, with well-known and applied medicinal properties. Thus, the aim of this work was to develop and evaluate the physical and physical-chemical quality of tablets produced with X. americana L. extract. The extract was spray-dried from a hydroethanolic extractive solution and characterized as to its phytochemical composition. The chemical marker was determined and quantified using validated chromatographic methods. These methods indicated the presence of gallic acid at a concentration of 1.61 mg g(-1). Formulations were proposed and analyzed for their flow and compaction properties. The best formulation was used to obtain a batch of tablets, which was evaluated for its quality characteristics and showed to be within the pharmacopoeial specifications for average weight, hardness, friability, and disintegration time. The dissolution profile of the tablets produced was obtained, showing the release of about 70% of the vegetable extract content within 30 minutes. Results showed that it was possible to obtain herbal tablets containing a high content of vegetal extract by direct compression, developing a rapid process of formulation and production and guaranteeing the quality characteristics of the final product.

Indexed as

OlacaceaeDrug LiberationExcipientsHardnessPhytochemicalsPlant ExtractsPowdersSolubilityTabletsExcipientsPhytochemicalsPlant ExtractsPowdersTablets

Identifiers

PMID29795592
PMCPMC5993115

What OpenQuestion holds

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Registered trials

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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.