Evidence map›Paper›PMID 38559983›Full record

ArticleACS omega2024

Multifunctionalized Carbon Dots as an Active Nanocarrier for Drug Delivery to the Glioblastoma Cell Line.

Manuel Algarra, Juan Soto, Maria Soledad Pino-González, Elena Gonzalez-Munoz, Tanja Dučić

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.9field-weighted citation impact, top 5% of its field
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

9 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
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  5. Review
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  9. Carbon dots-based drug delivery for bone regeneration.Frontiers in bioengineering and biotechnology · 2025
    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

5 authors at 4 institutions in 1 country.

Manuel AlgarraINAMAT-Institute for Advanced Materials and Mathematics, Dept. Science, Public University of Navarra, Campus Arrosadía, 31006 Pamplona, Spain.ORCID https://orcid.org/0000-0003-2410-8430
Juan SotoDept. Physical Chemistry, Faculty of Science, University of Málaga, Avda. Cervantes, 2, 29071 Málaga, Spain.ORCID https://orcid.org/0000-0001-6702-2878
Maria Soledad Pino-GonzálezDept. Organic Chemistry, Faculty of Science, University of Málaga, Avda. Cervantes, 2, 29071 Málaga, Spain.ORCID https://orcid.org/0000-0001-7711-6771
Elena Gonzalez-MunozInstituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina-IBIMA Plataforma BIONAND., C/Severo Ochoa, 35, 29590 Málaga, Spain.ORCID https://orcid.org/0000-0001-8291-1518
Tanja DučićALBA-CELLS Synchrotron Light Source, Consorcio para la Construccion Equipamiento y Explotacion del Laboratorio de Luz Sincrotron, C. de la Llum 2-26, 08290 Cerdanyola del Vallès, Barcelona, Spain.ORCID https://orcid.org/0000-0003-2389-3887
Universidad de Málaga · ESALBA Synchrotron (Spain) · ESInstituto de Investigación Biomédica de Málaga · ESUniversidad Publica de Navarra · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanoparticle-based nanocarriers represent a viable alternative to conventional direct administration in cancer cells. This advanced approach employs the use of nanotechnology to transport therapeutic agents directly to cancer cells, thereby reducing the risk of damage to healthy cells and enhancing the efficacy of treatment. By approving nanoparticle-based nanocarriers, the potential for targeted, effective treatment is greatly increased. The so-called carbon-based nanoparticles, or carbon dots, have been hydrothermally prepared and initiated by a polymerization process. We synthesized and characterized nanoparticles of 2-acrylamido-2-methylpropanesulfonic acid, which showed biocompatibility with glioblastoma cells, and further, we tested them as a carrier for the drug riluzole. The obtained nanoparticles have been extensively characterized by techniques to obtain the exact composition of their surface by using Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), and nuclear magnetic resonance (NMR) spectroscopy, as well as cryo-transmission electron microscopy. We found that the surface of the synthesized nanoparticles (NPs) is covered mainly by sulfonated, carboxylic, and substituted amide groups. These functional groups make them suitable as carriers for drug delivery in cancer cells. Specifically, we have successfully utilized the NPs as a delivery system for the drug riluzole, which has shown efficacy in treating glioblastoma cancer cells. The effect of nanoparticles as carriers for the riluzole system on glioblastoma cells was studied using live-cell synchrotron-based FTIR microspectroscopy to monitor

Identifiers

PMID38559983
PMCPMC10976390
OpenAlexW4392747200

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.