Evidence map›Paper›PMID 40304423›Full record

ArticleACS applied bio materials2025

Tackling Microbial Contamination in Polydioxanone-Based Membranes for Regenerative Therapy: Bioengineering an Antibiotic-Loaded Platform.

Victoria L Abdo, Jamil A Shibli, Raphael C Costa, Maria H Rossy Borges, Ademar Wong, Maria D P T Sotomayor, Martinna Bertolini, Luciene C Figueiredo, Valentim A R Barão, Elidiane C Rangel and 1 more

Abstract read
In one paragraph

Article in ACS applied bio materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Victoria L AbdoDental Research Division, Universidade Universus Veritas Guarulhos, Guarulhos 07023-070, Brazil.
Jamil A ShibliDental Research Division, Universidade Universus Veritas Guarulhos, Guarulhos 07023-070, Brazil.
Raphael C CostaSchool of Dentistry, Alfenas Federal University (UNIFAL-MG), Alfenas 37130-001, Brazil.
Maria H Rossy BorgesDepartamento of Prosthodontics and Periodontology, Piracicaba Dental School, Universidade Estadual de Campinas (UNICAMP), Piracicaba 13414-903, Brazil.
Ademar WongInstitute of Chemistry, São Paulo State University, Araraquara 14801-970, Brazil.
Maria D P T SotomayorInstitute of Chemistry, São Paulo State University, Araraquara 14801-970, Brazil.ORCID 0000-0002-6173-7888
Martinna BertoliniDepartment of Periodontics and Preventive Dentistry, University of Pittsburgh School of Dental Medicine, Pittsburgh, Pennsylvania 15213, United States.
Luciene C FigueiredoDental Research Division, Universidade Universus Veritas Guarulhos, Guarulhos 07023-070, Brazil.
Valentim A R BarãoDepartamento of Prosthodontics and Periodontology, Piracicaba Dental School, Universidade Estadual de Campinas (UNICAMP), Piracicaba 13414-903, Brazil.ORCID 0000-0002-6391-9917
Elidiane C RangelLaboratory of Technological Plasmas, Institute of Science and Technology, São Paulo State University (UNESP), Sorocaba 18087-180, Brazil.ORCID 0000-0001-7909-190X
Joao Gabriel S SouzaDental Research Division, Universidade Universus Veritas Guarulhos, Guarulhos 07023-070, Brazil.ORCID 0000-0001-5944-6953

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Barrier membranes are essential components of tissue regenerative therapies, acting as physical barriers to protect the healing site. Although collagen-based membranes are widely used, they degrade enzymatically, often triggering inflammation and cytotoxicity arising from residual cross-linking agents. Synthetic polymer-based membranes, such as polydioxanone (PDO), present customizable properties, predictable degradation rates, and induce bone formation more effectively. However, both materials are at risk of exposure to the microbial contamination. To address this, antibiotics have been loaded onto membranes as drug-delivery systems, a strategy that has not yet been explored for PDO membranes. In this study, the oral polymicrobial contamination of PDO-based membranes was evaluated and compared with collagen membranes and aimed to develop an amoxicillin-loaded PDO (AMX-PDO) membrane. For this purpose, PDO membranes with different pore sizes (0.25, 0.50, and 1.00 mm) and two commercially available collagen membranes were evaluated, using in vitro and in situ models, in terms of polymicrobial accumulation. Next, AMX-PDO membranes were developed by glow discharge plasma using Ar and O

Indexed as

AmoxicillinAnti-Bacterial AgentsBiocompatible MaterialsMembranes, ArtificialPolydioxanoneHumansMaterials TestingMicrobial Sensitivity TestsParticle SizeRegenerative MedicineSurface PropertiesAmoxicillinAnti-Bacterial AgentsBiocompatible MaterialsMembranes, ArtificialPolydioxanoneamoxicillinantimicrobial propertiesbacteriabiofilmsguided bone regenerationmembranes

Identifiers

PMID40304423
PMCPMC12093370

What OpenQuestion holds

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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.