Evidence map›Paper›PMID 41941047›Full record

ArticleApplied biochemistry and biotechnology2026

Analysis of the Anti-inflammatory Effects of a Delivery System Based on Alginate Hydrogels Enriched with Bioactive Compounds from Marine Sponge Dysidea robusta.

Homero Garcia-Motta, Cintia Cristina Santi Martignago, Mirian Bonifacio, Dalete Christine da Silva Souza, Lais Caroline Souza-Silva, Beatriz Soares-Silva, Anabella Patricia Rosso, Isabelly Bertochi Veroneze, Marcelo Assis, Fernando Carlos Giacomelli and 6 more

Abstract read
In one paragraph

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

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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

16 authors.

Homero Garcia-MottaDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Silva Jardim Street, 136, Santos, SP, 11015020, Brazil. homero.gmotta@outlook.com.ORCID http://orcid.org/0000-0001-9797-6891
Cintia Cristina Santi MartignagoDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Silva Jardim Street, 136, Santos, SP, 11015020, Brazil.
Mirian BonifacioDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Silva Jardim Street, 136, Santos, SP, 11015020, Brazil.
Dalete Christine da Silva SouzaCenter for Natural and Human Sciences, Federal University of ABC (UFABC), Av. dos Estados, 5001 - Bangú, Santo André, SP, 09280-560, Brazil.
Lais Caroline Souza-SilvaDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Silva Jardim Street, 136, Santos, SP, 11015020, Brazil.
Beatriz Soares-SilvaDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Silva Jardim Street, 136, Santos, SP, 11015020, Brazil.
Anabella Patricia RossoCenter for Natural and Human Sciences, Federal University of ABC (UFABC), Av. dos Estados, 5001 - Bangú, Santo André, SP, 09280-560, Brazil.
Isabelly Bertochi VeronezeChemistry Department, Federal University of São Carlos (UFSCar), Rod. Washington Luís, s/n - Monjolinho, São Carlos, SP, 13565-905, Brazil.
Marcelo AssisDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Silva Jardim Street, 136, Santos, SP, 11015020, Brazil.
Fernando Carlos GiacomelliCenter for Natural and Human Sciences, Federal University of ABC (UFABC), Av. dos Estados, 5001 - Bangú, Santo André, SP, 09280-560, Brazil.
Sandra Andrea CruzChemistry Department, Federal University of São Carlos (UFSCar), Rod. Washington Luís, s/n - Monjolinho, São Carlos, SP, 13565-905, Brazil.
João Henrique Ghilardi LagoCenter for Natural and Human Sciences, Federal University of ABC (UFABC), Av. dos Estados, 5001 - Bangú, Santo André, SP, 09280-560, Brazil.
Renata GranitoDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Silva Jardim Street, 136, Santos, SP, 11015020, Brazil.
Lívia AssisScientific Institute and Technological Department - University Brazil, Itaquera, São Paulo, SP, 08230-030, Brazil.
Alessandra Mussi RibeiroDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Silva Jardim Street, 136, Santos, SP, 11015020, Brazil.
Ana Claudia Muniz RennóDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Silva Jardim Street, 136, Santos, SP, 11015020, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Articular inflammatory processes are common in rheumatoid arthritis, osteoarthritis, and psoriatic arthritis. Standard therapy relies on oral anti-inflammatory drugs, which can cause systemic side effects with prolonged use. This has driven the search for natural alternatives and safer drug delivery systems. Intra-articular hydrogels enriched with bioactive compounds represent a promising approach, providing localized release of therapeutic molecules and reducing adverse effects. This study developed and characterized alginate (ALG)-based hydrogels enriched with bioactive compounds from the marine sponge Dysidea robusta and evaluated their anti-inflammatory potential in vitro. Hydrogels were prepared by dissolving ALG (1.5% and 3% w/v) and cross-linking with CaCO₃. Characterization included mass stability, scanning electron microscopy (SEM), and oscillatory rheology. Biological assays on fibroblasts and chondrocytes measured cytokine expression (IL-6 and TNF-α) by enzyme-linked immunosorbent assay (ELISA). The hydrogels showed initial mass gain followed by controlled degradation and a lamellar porous structure. Rheological analysis revealed tunable gelation and elasticity, while in vitro assays confirmed biocompatibility and a significant reduction of inflammatory markers. These findings indicate that ALG-based hydrogels containing D. robusta bioactives combine desirable physicochemical properties with anti-inflammatory activity, making them promising candidates for targeted drug delivery and tissue engineering.

Indexed as

AlginatesAnti-Inflammatory AgentsDrug Delivery SystemsHydrogelsPoriferaAnimalsChondrocytesFibroblastsGlucuronic AcidHexuronic AcidsHumansRheologyTumor Necrosis Factor-alphaAlginatesAnti-Inflammatory AgentsGlucuronic AcidHexuronic AcidsHydrogelsTumor Necrosis Factor-alphaAlginate hydrogelsAnti-inflammatory activityControlled releaseDysidea robustaMarine bioactive compounds

Identifiers

PMID41941047
PMCPMC13287294

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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.