Evidence map›Paper›PMID 42557699›Full record

ArticleMacromolecular bioscience2026

Development and Characterization of a Structurally Supportive of Hybrid PLGA Decellularized ECM Biomembrane for Ocular Progenitor Cell Anchorage and Epithelial Repair.

Ana Karulline Garcia Ungaratti, Aliny Pereira de Lima, Jordana Andrade Santos, Paula Leticia de Melo, Daniel Graziani, Artur Christian G da Silva, Luis Antônio Dantas Silva, Marize Campos Valadares

Abstract read
In one paragraph

Article in Macromolecular bioscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Ana Karulline Garcia UngarattiLaboratory of Education and Research in In Vitro Toxicology (Tox In), Faculty of Pharmacy, Federal University of Goiás, Goiânia, Goiás, Brazil.
Aliny Pereira de LimaLaboratory of Education and Research in In Vitro Toxicology (Tox In), Faculty of Pharmacy, Federal University of Goiás, Goiânia, Goiás, Brazil.
Jordana Andrade SantosLaboratory of Education and Research in In Vitro Toxicology (Tox In), Faculty of Pharmacy, Federal University of Goiás, Goiânia, Goiás, Brazil.
Paula Leticia de MeloLaboratory of Education and Research in In Vitro Toxicology (Tox In), Faculty of Pharmacy, Federal University of Goiás, Goiânia, Goiás, Brazil.
Daniel GrazianiMultiuser Laboratory for the Evaluation of Molecules, Cells, and Tissues, School of Veterinary Medicine and Animal Science, Federal University of Goiás, Goiânia, Goiás, Brazil.
Artur Christian G da SilvaLaboratory of Education and Research in In Vitro Toxicology (Tox In), Faculty of Pharmacy, Federal University of Goiás, Goiânia, Goiás, Brazil.ORCID https://orcid.org/0000-0001-7790-9771
Luis Antônio Dantas SilvaCenter For Research, Technological Development, and Innovation in Drugs, Medicines, and Cosmetics, Federal University of Goiás, Goiânia, Goiás, Brazil.
Marize Campos ValadaresLaboratory of Education and Research in In Vitro Toxicology (Tox In), Faculty of Pharmacy, Federal University of Goiás, Goiânia, Goiás, Brazil.ORCID https://orcid.org/0000-0002-0379-1325

Funding

Conselho Nacional de Desenvolvimento Científico e TecnológicoCoordenação de Aperfeiçoamento de Pessoal de Nível SuperiorFinanciadora de Estudos e Projetos
6 · The paper itself

Abstract

Degenerative ocular diseases are among the leading causes of visual impairment worldwide and require innovative therapeutic approaches capable of promoting tissue regeneration. In this context, biomaterial-based cell therapies have emerged as promising alternatives, although challenges remain regarding the maintenance of a supportive microenvironment after transplantation. This study developed and characterized a hybrid biomembrane composed of poly(lactic-co-glycolic acid) (PLGA) and decellularized corneal extracellular matrix (dCECM) to provide structural and biochemical support for ocular progenitor cells. PLGA membranes were fabricated and coated with dCECM layers. Their morphological, physicochemical, mechanical, and biocompatibility properties were evaluated. Biocompatibility was assessed using stem cells from the apical papilla (SCAP), periodontal ligament (PDLC), and corneal stroma (CSSC). The capacity of the membranes to preserve ocular progenitor markers (PAX6 and RX) and to exert cytoprotective effects on oxidatively damaged retinal pigment epithelial (RPE) cells was also investigated. Hybrid PLGA-dCECM membranes exhibited suitable thickness, increased hydrophilicity, improved tensile strength, and enhanced cell adhesion without evidence of chemical incompatibility. SCAP and CSSC maintained high expression of ocular progenitor markers, while co-culture with injured RPE cells reduced LDH release and cell death. The PLGA-dCECM biomembrane showed both structural support and bioactive cues, supporting its potential application in ocular regenerative therapies.

Indexed as

Decellularized Extracellular MatrixExtracellular MatrixPolylactic Acid-Polyglycolic Acid CopolymerRetinal Pigment EpitheliumStem CellsAnimalsBiocompatible MaterialsCell AdhesionEpithelial CellsHumansPAX6 Transcription FactorTissue ScaffoldsBiocompatible MaterialsDecellularized Extracellular MatrixPAX6 protein, humanPAX6 Transcription FactorPolylactic Acid-Polyglycolic Acid Copolymerbiocompatibilitybiomaterialcell adhesioncell biologydecellularizationextracellular matrixplgaprogenitor cellstem celltransplantation

Identifiers

PMID42557699
PMCPMC13443275

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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.