Evidence map›Paper›PMID 36240025›Full record

ArticleACS biomaterials science & engineering2022

Design of Mesoporous Silica Nanoparticles for the Treatment of Amyotrophic Lateral Sclerosis (ALS) with a Therapeutic Cocktail Based on Leptin and Pioglitazone.

Diana Díaz-García, Águeda Ferrer-Donato, José M Méndez-Arriaga, Marta Cabrera-Pinto, Miguel Díaz-Sánchez, Sanjiv Prashar, Carmen M Fernandez-Martos, Santiago Gómez-Ruiz

Open access · hybridAbstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

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  3. Pleiotrophin/Midkine Pathway Is Dysregulated in a TDP-43Neuropathology : official journal of the Japanese Society of Neuropathology · 2026
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  19. The blood-brain barrier: structure, regulation, and drug delivery.Signal transduction and targeted therapy · 2023
    Review
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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

8 authors at 3 institutions in 2 countries.

Diana Díaz-GarcíaCOMET-NANO Group, Departamento de Biología y Geología, Física y Química Inorgánica, E.S.C.E.T., Universidad Rey Juan Carlos, Calle Tulipán s/n, E-28933 Móstoles, Madrid, Spain.
Águeda Ferrer-DonatoNeurometabolism Group, Research Unit of the National Hospital of Paraplegics (UDI-HNP), Finca La Peraleda s/n, 45071 Toledo, Spain.
José M Méndez-ArriagaCOMET-NANO Group, Departamento de Biología y Geología, Física y Química Inorgánica, E.S.C.E.T., Universidad Rey Juan Carlos, Calle Tulipán s/n, E-28933 Móstoles, Madrid, Spain.
Marta Cabrera-PintoNeurometabolism Group, Research Unit of the National Hospital of Paraplegics (UDI-HNP), Finca La Peraleda s/n, 45071 Toledo, Spain.
Miguel Díaz-SánchezCOMET-NANO Group, Departamento de Biología y Geología, Física y Química Inorgánica, E.S.C.E.T., Universidad Rey Juan Carlos, Calle Tulipán s/n, E-28933 Móstoles, Madrid, Spain.
Sanjiv PrasharCOMET-NANO Group, Departamento de Biología y Geología, Física y Química Inorgánica, E.S.C.E.T., Universidad Rey Juan Carlos, Calle Tulipán s/n, E-28933 Móstoles, Madrid, Spain.
Carmen M Fernandez-MartosNeurometabolism Group, Research Unit of the National Hospital of Paraplegics (UDI-HNP), Finca La Peraleda s/n, 45071 Toledo, Spain.
Santiago Gómez-RuizCOMET-NANO Group, Departamento de Biología y Geología, Física y Química Inorgánica, E.S.C.E.T., Universidad Rey Juan Carlos, Calle Tulipán s/n, E-28933 Móstoles, Madrid, Spain.ORCID 0000-0001-9538-8359
Universidad Rey Juan Carlos · ESHospital Nacional de Parapléjicos · ESUniversity of Tasmania · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is a devasting neurodegenerative disease with no cure to date. Therapeutic agents used to treat ALS are very limited, although combined therapies may offer a more effective treatment strategy. Herein, we have studied the potential of nanomedicine to prepare a single platform based on mesoporous silica nanoparticles (MSNs) for the treatment of an ALS animal model with a cocktail of agents such as leptin (neuroprotective) and pioglitazone (anti-inflammatory), which have already demonstrated promising therapeutic ability in other neurodegenerative diseases. Our goal is to study the potential of functionalized mesoporous materials as therapeutic agents against ALS using MSNs as nanocarriers for the proposed drug cocktail leptin/pioglitazone (

Indexed as

Amyotrophic Lateral SclerosisNanoparticlesNeurodegenerative DiseasesAnimalsDNA-Binding ProteinsLeptinMiceMice, TransgenicPioglitazoneSilicon DioxideDNA-Binding ProteinsLeptinPioglitazoneSilicon Dioxideamyotrophic lateral sclerosisdrug deliveryleptinmesoporous silica nanoparticlespioglitazone

Identifiers

PMID36240025
PMCPMC9667463
OpenAlexW4306179552

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.