Evidence mapPaperPMID 39683333Full record

ArticleNanomaterials (Basel, Switzerland)2024

A Graphene-Based Bioactive Product with a Non-Immunological Impact on Mononuclear Cell Populations from Healthy Volunteers.

María Del Prado Lavín-López, Mónica Torres-Torresano, Eva María García-Cuesta, Blanca Soler-Palacios, Mercedes Griera, Martín Martínez-Rovira, José Antonio Martínez-Rovira, Diego Rodríguez-Puyol, Sergio de Frutos

Abstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 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

9 authors.

María Del Prado Lavín-LópezGraphenano S.L., 30510 Yecla, Spain.
Mónica Torres-TorresanoDepartment of Immunology and Oncology, National Center for Biotechnology, Consejo Superior de Investigaciones Científicas (CSIC), 28049 Madrid, Spain.ORCID 0000-0002-1411-3458
Eva María García-CuestaDepartment of Immunology and Oncology, National Center for Biotechnology, Consejo Superior de Investigaciones Científicas (CSIC), 28049 Madrid, Spain.ORCID 0000-0003-2311-4353
Blanca Soler-PalaciosDepartment of Immunology and Oncology, National Center for Biotechnology, Consejo Superior de Investigaciones Científicas (CSIC), 28049 Madrid, Spain.ORCID 0000-0001-6031-1896
Mercedes GrieraGraphenano S.L., 30510 Yecla, Spain.
Martín Martínez-RoviraGraphenano S.L., 30510 Yecla, Spain.
José Antonio Martínez-RoviraGraphenano S.L., 30510 Yecla, Spain.
Diego Rodríguez-PuyolDepartment of Medicine, Universidad de Alcalá, Nephrology Service at Hospital Príncipe de Asturias, Instituto Ramon y Cajal de Investigación Sanitaria, Fundación Renal Iñigo Álvarez de Toledo, 28871 Alcalá de Henares, Spain.
Sergio de FrutosDepartment of Systems Biology, Universidad de Alcalá, Instituto Ramon y Cajal de Investigación Sanitaria, Fundación Renal Iñigo Álvarez de Toledo, 28871 Alcalá de Henares, Spain.ORCID 0000-0002-1225-5911

Funding

ANALYSIS OF THC IN URINE USING A SIMPLIFIED IMMUNOASSAYR43DA003751 · GENESIS LABS, INC. · 1985 to 1985
Comunidad de Madrid B2017/BMD3751Comunidad de Madrid P2022/BMD7221Instituto de Salud Carlos III PI17/00625Instituto de Salud Carlos III PI17/01513Instituto de Salud Carlos III PI20/00634Instituto de Salud Carlos III RD16/0009/0018Instituto de Salud Carlos III RD21/0005/0023Universidad de Alcalá art.60 LOSU 2022/024
6 · The paper itself

Abstract

We previously described GMC, a graphene-based nanomaterial obtained from carbon nanofibers (CNFs), to be biologically compatible and functional for therapeutic purposes. GMC can reduce triglycerides' content in vitro and in vivo and has other potential bio-functional effects on systemic cells and the potential utility to be used in living systems. Here, immunoreactivity was evaluated by adding GMC in suspension at the biologically functional concentrations, ranging from 10 to 60 µg/mL, for one or several days, to cultured lymphocytes (T, B, NK), either in basal or under stimulating conditions, and monocytes that were derived under culture conditions to pro-inflammatory (GM-MØ) or anti-inflammatory (M-MØ) macrophages. All stirpes were obtained from human peripheral mononuclear cells (PBMCs) from anonymized healthy donors. The viability (necrosis, apoptosis) and immunological activity of each progeny was analyzed using either flow cytometry and/or other analytical determinations. A concentration of 10 to 60 µg/mL GMC did not affect lymphocytes' viability, either in basal or active conditions, during one or more days of treatment. The viability and expression of the inflammatory interleukin IL-1β in the monocyte cell line THP-1 were not affected. Treatments with 10 or 20 µg/mL GMC on GM-MØ or M-MØ during or after their differentiation process promoted phagocytosis, but their viability and the release of the inflammatory marker activin A by GM-MØ were not affected. A concentration of 60 µg/mL GMC slightly increased macrophages' death and activity in some culture conditions. The present work demonstrates that GMC is safe or has minimal immunological activity when used in suspension at low concentrations for pre-clinical or clinical settings. Its biocompatibility will depend on the dose, formulation or way of administration and opens up the possibility to consider GMC or other CNF-based biomaterials for innovative therapeutic strategies.

Indexed as

activin Acarbon nanofibergrapheneleucocyteslymphocytesmacrophagesmonocytesnatural killersphagocytosistoxicity

Identifiers

PMID39683333
PMCPMC11643509

What Socratic holds

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LicenceCC BY
Read underepoch 390

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 Socratic graph.