Evidence map›Paper›PMID 38353746›Full record

ArticleJournal of materials science. Materials in medicine2024

Cannabidiol-loaded microparticles embedded in a porous hydrogel matrix for biomedical applications.

Carla David, Jaqueline F de Souza, Adriana F Silva, Guillermo Grazioli, Andressa S Barboza, Rafael G Lund, André R Fajardo, Rafael R Moraes

Abstract read
In one paragraph

Article in Journal of materials science. Materials in medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
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  11. Antimicrobial, Probiotic, and Immunomodulatory Potential ofAntibiotics (Basel, Switzerland) · 2024
    Article
  12. 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

8 authors.

Carla DavidBiopathological Research Group, Faculty of Dentistry (GIBFO), University of the Andes, Mérida, Venezuela. cldp58@gmail.com.ORCID http://orcid.org/0000-0001-7970-1093
Jaqueline F de SouzaLaboratory of Technology and Development of Composites and Polymeric Materials-LaCoPol, Universidade Federal de Pelotas, Pelotas, Brazil.
Adriana F SilvaGraduate Program in Dentistry, Universidade Federal de Pelotas, Pelotas, Brazil.
Guillermo GrazioliDepartment of Dental Materials, Universidad de la República, Montevideo, Uruguay.
Andressa S BarbozaGraduate Program in Dentistry, Universidade Federal de Pelotas, Pelotas, Brazil.
Rafael G LundGraduate Program in Dentistry, Universidade Federal de Pelotas, Pelotas, Brazil.
André R FajardoLaboratory of Technology and Development of Composites and Polymeric Materials-LaCoPol, Universidade Federal de Pelotas, Pelotas, Brazil.
Rafael R MoraesGraduate Program in Dentistry, Universidade Federal de Pelotas, Pelotas, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, poly (lactic-co-glycolic acid) (PLGA) microparticles loaded with cannabidiol (CBD) were synthesized (PLGA@CBD microparticles) and embedded up to 10 wt% in a chondroitin sulfate/polyvinyl alcohol hydrogel matrix. In vitro chemical, physical, and biological assays were carried out to validate the potential use of the modified hydrogels as biomaterials. The microparticles had spherical morphology and a narrow range of size distribution. CBD encapsulation efficiency was around 52%, loading was approximately 50%. Microparticle addition to the hydrogels caused minor changes in their morphology, FTIR and thermal analyses confirmed these changes. Swelling degree and total porosity were reduced in the presence of microparticles, but similar hydrophilic and degradation in phosphate buffer solution behaviors were observed by all hydrogels. Rupture force and maximum strain at rupture were higher in the modified hydrogels, whereas modulus of elasticity was similar across all materials. Viability of primary human dental pulp cells up to 21 days was generally not influenced by the addition of PLGA@CBD microparticles. The control hydrogel showed no antimicrobial activity against Staphylococcus aureus, whereas hydrogels with 5% and 10% PLGA@CBD microparticles showed inhibition zones. In conclusion, the PLGA@CBD microparticles were fabricated and successfully embedded in a hydrogel matrix. Despite the hydrophobic nature of CBD, the physicochemical and morphological properties were generally similar for the hydrogels with and without the CBD-loaded microparticles. The data reported in this study suggested that this original biomaterial loaded with CBD oil has characteristics that could enable it to be used as a scaffold for tissue/cellular regeneration.

Indexed as

CannabidiolBiocompatible MaterialsBiological AssayHumansHydrogelsPorosityBiocompatible MaterialsCannabidiolHydrogelsBiomaterialsChondroitin sulfateComposite materialsPhytocannabinoidsPolyvinyl alcoholScaffolds

Identifiers

PMID38353746
PMCPMC10866797

What OpenQuestion holds

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LicenceCC BY
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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.