Evidence map›Paper›PMID 39728145›Full record

ArticleMarine drugs2024

Chondroitin Sulfate Nanovectorized by LC-PUFAs Nanocarriers Extracted from Salmon (

Louis Pruvost, Maureen Gerlei, Cédric Paris, Émilie Velot, Cyril J-F Kahn, Arnaud Bianchi, Michel Linder

Abstract read
In one paragraph

Article in Marine drugs, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Louis PruvostLIBio, Université de Lorraine, F-54000 Nancy, France.ORCID 0009-0000-2041-8066
Maureen GerleiLIBio, Université de Lorraine, F-54000 Nancy, France.ORCID 0009-0009-2485-811X
Cédric ParisLIBio, Université de Lorraine, F-54000 Nancy, France.ORCID 0000-0001-8673-3130
Émilie VelotCNRS, IMoPA, Université de Lorraine, F-54000 Nancy, France.ORCID 0000-0001-8620-5696
Cyril J-F KahnLIBio, Université de Lorraine, F-54000 Nancy, France.ORCID 0000-0001-5282-6558
Arnaud BianchiCNRS, IMoPA, Université de Lorraine, F-54000 Nancy, France.ORCID 0000-0003-4925-5269
Michel LinderLIBio, Université de Lorraine, F-54000 Nancy, France.ORCID 0000-0002-8658-6828

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chondroitin sulfate (CS), a glycosaminoglycan, supports health through various physiological functions, including tissue protection, bone growth, and skin aging prevention. It also contributes to anticoagulant or anti-inflammatory processes, with its primary clinical use being osteoarthritis treatment. This study presents the results of the valorization of lipids and CS, both extracted from salmon co-products through enzymatic processes. The polar lipids, naturally rich in long-chain fatty acids (docosahexaenoic acid DHA C22:6 n-3 and eicosapentaenoic acid EPA C20:5 n-3), and the CS, primarily located in the nasal cartilage, were separated and concentrated before being characterized using various techniques to determine functional and lipid composition. These compounds were then used to formulate liposomes of 63 to 95 nm in size composed of 19.38% of DHA and 7.44% of EPA and encapsulating CS extract with a Δdi-4S/Δdi-6S ratio of 0.53 at 2 weight masses (10-30 kDa and >30 kDa) or CS standard all at two different concentrations. Liposomes were tested on human chondrocytes in inflamed conditions. Thus, compatibility tests, the expression of various inflammation markers at transcriptional and molecular levels, nitrites, and the amount of collagenase produced were analyzed. The results showed that CS, in synergy with the liposomes, played a positive role in combating chondrocyte inflammation even at a low concentration.

Indexed as

ChondrocytesChondroitin SulfatesInterleukin-1betaLiposomesAnimalsAnti-Inflammatory AgentsBiomarkersCells, CulturedDocosahexaenoic AcidsDrug CarriersEicosapentaenoic AcidHumansNanoparticlesSalmo salarAnti-Inflammatory AgentsBiomarkersChondroitin SulfatesDocosahexaenoic AcidsDrug CarriersEicosapentaenoic AcidInterleukin-1betaLiposomesanti-inflammatorychondroitin sulfateencapsulationenzymatic hydrolysisliposomephospholipidSalmo salar

Identifiers

PMID39728145
PMCPMC11676681

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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.