Evidence map›Paper›PMID 36335359›Full record

ArticleJournal of nanobiotechnology2022

Exosomes loaded with ultrasmall Pt nanoparticles: a novel low-toxicity alternative to cisplatin.

María Sancho-Albero, Ana Martín-Pardillos, Lluís Lujan, Víctor Sebastian, Jesús Santamaria, Pilar Martín-Duque

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2022. 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
1.6field-weighted citation impact, top 17% 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, 21 citations in OpenAlex.

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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

6 authors at 4 institutions in 1 country.

María Sancho-AlberoInstituto de Nanociencia y Materiales de Aragón (INMA), CSIC-Universidad de Zaragoza, Zaragoza, Spain.
Ana Martín-PardillosInstituto de Nanociencia y Materiales de Aragón (INMA), CSIC-Universidad de Zaragoza, Zaragoza, Spain.
Lluís LujanDepartment of Animal Pathology, University of Zaragoza, Zaragoza, Spain.
Víctor SebastianInstituto de Nanociencia y Materiales de Aragón (INMA), CSIC-Universidad de Zaragoza, Zaragoza, Spain. victorse@unizar.es.
Jesús SantamariaInstituto de Nanociencia y Materiales de Aragón (INMA), CSIC-Universidad de Zaragoza, Zaragoza, Spain. jesus.santamaria@unizar.es.
Pilar Martín-DuqueNetworking Research Center on Bioengineering Biomaterials and Nanomedicine (CIBER-BBN), Madrid, Spain.
Universidad de Zaragoza · ESBiomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine · ESFundacion Agencia Aragonesa para la Investigacion y el Desarrollo · ESInstituto de Nanociencia y Materiales de Aragón · ES

Funding

DGA DGA/Fondos FEDER LMP154_21ERC-Advanced Grant 742684Fundacion BBVA MicroVexOsFundación Ramón Areces ExoFluidTTInstituto de Salud Carlos III DTS21/00130Instituto de Salud Carlos III PI19/01007
6 · The paper itself

Abstract

backgroundPlatinum nanoparticles have been demonstrated to have excellent anticancer properties. However, because of the lack of specificity they must be delivered to the tumor in amounts sufficient to reach the desired therapeutic objectives. Interestingly, exosomes are considered as excellent natural selective delivery nanotools, but until know their targeting properties have not being combined with the anticancer properties of platinum nanoparticles.

resultsIn this work we combine the targeting capabilities of exosomes and the antitumoral properties of ultrasmall (< 2 nm) platinum nanoparticles as a novel, low toxicity alternative to the use of cisplatin. A mild methodology based on the room temperature CO-assisted in situ reduction of Pt

conclusionsIn this study, a nanoscale vector based on ultrasmall PtNPs and exosomes has been created exhibiting antitumoral properties comparable or higher to those of the FDA approved cisplatin. The preferential uptake of PtNPs mediated by exosomal transfer between certain cell types has been exploited to create a selective antitumoral novel bioartificial system. We have demonstrated their anticancer properties both in vitro and in vivo comparing the results obtained with the administration of equivalent amounts of cisplatin, and showing a spectacular reduction of toxicity.

Indexed as

ExosomesMetal NanoparticlesNanoparticlesNeoplasmsCell Line, TumorCisplatinHumansPlatinumCisplatinPlatinumCancerExosomesExtracellular vesiclesPlatinum nanoparticlesSelectivitySystemic toxicity

Identifiers

PMID36335359
PMCPMC9636640
OpenAlexW4308262761

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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.