Evidence map›Paper›PMID 39085675›Full record

ArticleAAPS PharmSciTech2024

Bioadhesive Polymeric Films Containing Rhamnolipids, An Innovative Antimicrobial Topical Formulation.

Jéssica B Carra, Kamila B B Wessel, Giovana N Pereira, Mariana C Oliveira, Pietra M T Pattini, Bianca L Masquetti, Ismael R Amador, Marcos L Bruschi, Rúbia Casagrande, Sandra R Georgetti and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in AAPS PharmSciTech, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Exploring Biosurfactants as Antimicrobial Approaches.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
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

15 authors.

Jéssica B CarraDepartamento de Química, Universidade Estadual de Londrina, Rodovia Celso Garcia Cid, PR-445, Km 380 - Campus Universitário, Londrina, Paraná, 86057-970, Brazil.
Kamila B B WesselDepartamento de Bioquímica E Biotecnologia, Universidade Estadual de Londrina, Rodovia Celso Garcia Cid, PR-445, Km 380 - Campus Universitário, Londrina, Paraná, 86057-970, Brazil.
Giovana N PereiraDepartamento de Microbiologia, Universidade Estadual de Londrina, Londrina, PR, Brazil.
Mariana C OliveiraDepartamento de Farmácia, Universidade Estadual de Maringá, Londrina, PR, Brazil.
Pietra M T PattiniDepartamento de Ciências Farmacêuticas, Universidade Estadual de Londrina, Londrina, PR, Brazil.
Bianca L MasquettiDepartamento de Ciências Farmacêuticas, Universidade Estadual de Londrina, Londrina, PR, Brazil.
Ismael R AmadorDepartamento de Bioquímica E Biotecnologia, Universidade Estadual de Londrina, Rodovia Celso Garcia Cid, PR-445, Km 380 - Campus Universitário, Londrina, Paraná, 86057-970, Brazil.
Marcos L BruschiDepartamento de Farmácia, Universidade Estadual de Maringá, Londrina, PR, Brazil.
Rúbia CasagrandeDepartamento de Ciências Farmacêuticas, Universidade Estadual de Londrina, Londrina, PR, Brazil.
Sandra R GeorgettiDepartamento de Ciências Farmacêuticas, Universidade Estadual de Londrina, Londrina, PR, Brazil.
Waldiceu A VerriDepartamento de Ciências Patológicas, Universidade Estadual de Londrina, Londrina, PR, Brazil.
Gerson NakazatoDepartamento de Microbiologia, Universidade Estadual de Londrina, Londrina, PR, Brazil.
Josiane A VignoliDepartamento de Bioquímica E Biotecnologia, Universidade Estadual de Londrina, Rodovia Celso Garcia Cid, PR-445, Km 380 - Campus Universitário, Londrina, Paraná, 86057-970, Brazil.
Doumit Camilios-NetoDepartamento de Bioquímica E Biotecnologia, Universidade Estadual de Londrina, Rodovia Celso Garcia Cid, PR-445, Km 380 - Campus Universitário, Londrina, Paraná, 86057-970, Brazil. camiliosneto@uel.br.
Marcela M BaracatDepartamento de Química, Universidade Estadual de Londrina, Rodovia Celso Garcia Cid, PR-445, Km 380 - Campus Universitário, Londrina, Paraná, 86057-970, Brazil. baracat@uel.br.ORCID http://orcid.org/0000-0003-0400-7413

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acne affects most of the world's population, causing an impact on the self-esteem of adolescents and young adults. One of the causes is the presence of the bacteria Cutibacterium acnes which are part of the natural microbiota of the skin. Topical treatments consist of anti-inflammatory and antibiotics, which could select resistant strains. Alternatives to the antibiotic are biocomposites that have antimicrobial activity like biosurfactants which are produced by bacteria. An innovative way of applying these compounds is bioadhesive polymeric films that adhere to the skin and release the active principle topically. Rhamnolipids have great potential to be used in the treatment of acne because they present antimicrobial activity against C. acnes in low and safe concentrations (MIC of 15.62 µg/mL, CBM of 31.25 µg/mL and CC50 of 181.93 µg/mL). Four films with different rhamnolipids concentrations (0.0; 0.1; 0.2; and 0.3%, w/w) were obtained as to visual appearance, mass variation, thickness, density, solubility, pH, water vapor transmission, mechanical properties (folding endurance, bioadhesion strength, tensile strength, elongation at break and Young's modulus), scanning electron microscopy and infrared. The results show that these formulations had a homogeneous appearance; elastic mechanical properties; pH similar to human skin and bioadhesive. The polymeric films containing rhamnolipids were effective against C. acnes, in the in vitro test, at the three concentrations tested, the film with the highest concentration (0.3%, w/w) being the most promising for presenting the highest antimicrobial activity. Thus, the polymeric film containing rhamnolipids has the potential to be used in the treatment of acne.

Indexed as

GlycolipidsMicrobial Sensitivity TestsPolymersAcne VulgarisAdministration, TopicalAnti-Bacterial AgentsAnti-Infective AgentsChemistry, PharmaceuticalHumansPropionibacterium acnesSkinSolubilityTensile StrengthAnti-Bacterial AgentsAnti-Infective AgentsGlycolipidsPolymersrhamnolipidbiosurfactantCutibacterium acnesmechanical propertiestopical formulation

Identifiers

PMID39085675

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.