Evidence map›Paper›PMID 41211195›Full record

ArticleNanotheranostics2025

Impact of the production method on the properties of erythrocyte-derived extracellular particles: a quantitative and qualitative evaluation.

Maria Chiara Ciferri, Nicole Grinovero, Maria Cristina Gagliani, Katia Cortese, Chiara Romiti, Alessia Brossa, Cristina Grange, Benedetta Bussolati, Gianluca Ubezio, Vanessa Agostini and 5 more

Abstract read
In one paragraph

Article in Nanotheranostics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Maria Chiara CiferriDepartment of Experimental Medicine (DIMES), University of Genova, Genova, Italy.
Nicole GrinoveroCore Facility for Omics Science, IRCCS Istituto G. Gaslini, Genova, Italy.
Maria Cristina GaglianiDepartment of Experimental Medicine (DIMES), University of Genova, Genova, Italy.
Katia CorteseDepartment of Experimental Medicine (DIMES), University of Genova, Genova, Italy.
Chiara RomitiDepartment of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.
Alessia BrossaDepartment of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.
Cristina GrangeDepartment of Medical Sciences, University of Turin, Turin, Italy.
Benedetta BussolatiDepartment of Medical Sciences, University of Turin, Turin, Italy.
Gianluca UbezioIRCCS Ospedale Policlinico San Martino, Genova, Italy.
Vanessa AgostiniIRCCS Ospedale Policlinico San Martino, Genova, Italy.
Andrea PetrettoCore Facility for Omics Science, IRCCS Istituto G. Gaslini, Genova, Italy.
Rodolfo QuartoDepartment of Experimental Medicine (DIMES), University of Genova, Genova, Italy.
Ulla ImpolaResearch and Development, Finnish Red Cross Blood Service, Vantaa, Finland.
Saara LaitinenResearch and Development, Finnish Red Cross Blood Service, Vantaa, Finland.
Roberta TassoDepartment of Experimental Medicine (DIMES), University of Genova, Genova, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Red blood cell-derived extracellular particles (RBCEPs) possess many benefits in healthcare applications representing a simple and powerful platform for drug delivery. Nowadays, whether the different methods proposed to produce them could influence their properties remains poorly investigated. We compared three main types of RBCEPs: (i) naturally released during the blood bag storage (EryErythrosomes, EryEs), (ii) produced artificially through RBC sonication (NanoErythrosomes, NanoEs), and (iii) released after RBC chemical stimulation (Vesiculation-Induced EryEs, VI-EryEs). Concentration, protein amount, size distribution, and morphology (TEM) were preliminary evaluated. Then the expression of EV- and erythrocyte-associated markers was assessed by flow cytometry and western blot while proteomic analyses estimated the differences in total protein content. The efficiency of membrane functionalization was assessed by copper-free click chemistry. All three subpopulations were able to be produced on a large scale, with NanoEs being the ones with the highest concentration, polydispersity, and largest dimension. The traditional EV-associated rounded shape was found to coexist with a tubular shape. Tetraspanin expression was absent while all three formulations expressed Alix, Flotillin-1, and Tsg101. On the other hand, Glycophorin A was the only RBC marker expressed ubiquitously. The analyzed subpopulations showed three distinct proteomic signatures which defined distinct enrichment profiles of molecular functions. Finally, NanoEs turned out to be the most efficient in surface functionalization adopting a copper-free click chemistry strategy. This work provides a pioneering contribution to the study and application of RBCEPs, indicating that the isolation method can significantly impact both the quantitative and qualitative properties of these natural nanoparticles.

Indexed as

Cell-Derived MicroparticlesErythrocytesHumansProteomicsErythrocytes-derived extracellular particlesextracellular particles isolationNatural nanoparticlesproteomic signaturetargeted drug delivery

Identifiers

PMID41211195
PMCPMC12595265

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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.