Evidence map›Paper›PMID 39590035›Full record

ArticleGels (Basel, Switzerland)2024

Arginine-Biofunctionalized Ternary Hydrogel Scaffolds of Carboxymethyl Cellulose-Chitosan-Polyvinyl Alcohol to Deliver Cell Therapy for Wound Healing.

Alexandra A P Mansur, Sandhra M Carvalho, Ramayana M de M Brito, Nádia S V Capanema, Isabela de B Duval, Marcelo E Cardozo, José B R Rihs, Gabriela G M Lemos, Letícia C D Lima, Marina P Dos Reys and 8 more

Abstract read
In one paragraph

Article in Gels (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

18 authors.

Alexandra A P MansurCenter of Nanoscience, Nanotechnology, and Innovation-CeNano2I, Department of Metallurgical and Materials Engineering, Federal University of Minas Gerais, UFMG, Av. Presidente Antônio Carlos, 6627-Escola de Engenharia, Bloco 2-Sala 2233, Belo Horizonte 31270-901, MG, Brazil.
Sandhra M CarvalhoCenter of Nanoscience, Nanotechnology, and Innovation-CeNano2I, Department of Metallurgical and Materials Engineering, Federal University of Minas Gerais, UFMG, Av. Presidente Antônio Carlos, 6627-Escola de Engenharia, Bloco 2-Sala 2233, Belo Horizonte 31270-901, MG, Brazil.ORCID 0000-0001-6665-8647
Ramayana M de M BritoLaboratory of Immunobiology and Control of Parasites, Department of Parasitology, Institute of Biological Sciences, Federal University of Minas Gerais, UFMG, Belo Horizonte 31270-901, MG, Brazil.ORCID 0000-0003-0611-6859
Nádia S V CapanemaCenter of Nanoscience, Nanotechnology, and Innovation-CeNano2I, Department of Metallurgical and Materials Engineering, Federal University of Minas Gerais, UFMG, Av. Presidente Antônio Carlos, 6627-Escola de Engenharia, Bloco 2-Sala 2233, Belo Horizonte 31270-901, MG, Brazil.
Isabela de B DuvalLaboratory of Immunobiology and Control of Parasites, Department of Parasitology, Institute of Biological Sciences, Federal University of Minas Gerais, UFMG, Belo Horizonte 31270-901, MG, Brazil.
Marcelo E CardozoLaboratory of Immunobiology and Control of Parasites, Department of Parasitology, Institute of Biological Sciences, Federal University of Minas Gerais, UFMG, Belo Horizonte 31270-901, MG, Brazil.
José B R RihsLaboratory of Immunobiology and Control of Parasites, Department of Parasitology, Institute of Biological Sciences, Federal University of Minas Gerais, UFMG, Belo Horizonte 31270-901, MG, Brazil.
Gabriela G M LemosCenter of Nanoscience, Nanotechnology, and Innovation-CeNano2I, Department of Metallurgical and Materials Engineering, Federal University of Minas Gerais, UFMG, Av. Presidente Antônio Carlos, 6627-Escola de Engenharia, Bloco 2-Sala 2233, Belo Horizonte 31270-901, MG, Brazil.
Letícia C D LimaDepartment of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, UFMG, Belo Horizonte 31270-901, MG, Brazil.ORCID 0000-0001-7810-8511
Marina P Dos ReysLaboratory of Compared Pathology, Department of Pathology, Institute of Biological Sciences, Federal University of Minas Gerais, UFMG, Belo Horizonte 31270-901, MG, Brazil.ORCID 0000-0003-1642-6957
Ana P H RodriguesChemistry Department, Federal University of Minas Gerais, UFMG, Belo Horizonte 31270-901, MG, Brazil.
Luiz C A OliveiraChemistry Department, Federal University of Minas Gerais, UFMG, Belo Horizonte 31270-901, MG, Brazil.
Marcos Augusto de SáDepartment of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, UFMG, Belo Horizonte 31270-901, MG, Brazil.
Geovanni D CassaliLaboratory of Compared Pathology, Department of Pathology, Institute of Biological Sciences, Federal University of Minas Gerais, UFMG, Belo Horizonte 31270-901, MG, Brazil.ORCID 0000-0002-5650-6743
Lilian L BuenoLaboratory of Immunobiology and Control of Parasites, Department of Parasitology, Institute of Biological Sciences, Federal University of Minas Gerais, UFMG, Belo Horizonte 31270-901, MG, Brazil.
Ricardo T FujiwaraLaboratory of Immunobiology and Control of Parasites, Department of Parasitology, Institute of Biological Sciences, Federal University of Minas Gerais, UFMG, Belo Horizonte 31270-901, MG, Brazil.ORCID 0000-0002-4713-575X
Zelia I P LobatoDepartamento de Medicina Veterinária Preventiva, Federal University of Minas Gerais, UFMG, Belo Horizonte 31270-901, MG, Brazil.
Herman S MansurCenter of Nanoscience, Nanotechnology, and Innovation-CeNano2I, Department of Metallurgical and Materials Engineering, Federal University of Minas Gerais, UFMG, Av. Presidente Antônio Carlos, 6627-Escola de Engenharia, Bloco 2-Sala 2233, Belo Horizonte 31270-901, MG, Brazil.ORCID 0000-0002-3032-495X

Funding

Coordenação de Aperfeicoamento de Pessoal de Nível Superior PROINFRA-2010-2014; PROEX-2018-2024; PNPD-2018-2024Financiadora de Estudos e Projetos CTIN-FRA/PROINFRA 2008/2010/2011/2018; SOS/Equipamentos/2018-01.19.0032.00Fundação de Amparo à Pesquisa do Estado de Minas Gerais UNIVERSAL-APQ-00291-18; APQ-01838-22; PROBIC-2018-2024National Council for Scientific and Technological Development Plataformas Inovadoras em Terapias Avançadas - 442737/2020-3; PQ1A-303893/2018-4; PQ1A-307720/2023-3; UNIVERSAL-421312/2018-1; UNIVERSAL-407686/2023-1; PDS-102412/2024-3; PIBIC-2017-2024Universidade Federal de Minas Gerais PRPQ/PRPG-2023-2024
6 · The paper itself

Abstract

Wound healing is important for skin after deep injuries or burns, which can lead to hospitalization, long-term morbidity, and mortality. In this field, tissue-engineered skin substitutes have therapy potential to assist in the treatment of acute and chronic skin wounds, where many requirements are still unmet. Hence, in this study, a novel type of biocompatible ternary polymer hybrid hydrogel scaffold was designed and produced through an entirely eco-friendly aqueous process composed of carboxymethyl cellulose, chitosan, and polyvinyl alcohol and chemically cross-linked by citric acid, forming three-dimensional (3D) matrices, which were biofunctionalized with L-arginine (L-Arg) to enhance cellular adhesion. They were applied as bilayer skin biomimetic substitutes based on human-derived cell cultures of fibroblasts and keratinocytes were seeded and grown into their 3D porous structures, producing cell-based bio-responsive hybrid hydrogel scaffolds to assist the wound healing process. The results demonstrated that hydrophilic hybrid cross-linked networks were formed via esterification reactions with the 3D porous microarchitecture promoted by foam templating and freeze-drying. These hybrids presented chemical stability, physicochemical properties, high moisture adsorption capacity, surface properties, and a highly interconnected 3D porous structure well suited for use as a skin substitute in wound healing. Additionally, the surface biofunctionalization of these 3D hydrogel scaffolds with L-arginine through amide bonds had significantly enhanced cellular attachment and proliferation of fibroblast and keratinocyte cultures. Hence, the in vivo results using

Indexed as

biopolymerscell therapyliving biomaterialsskin substituteswound healing

Identifiers

PMID39590035
PMCPMC11594054

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.