Evidence map›Paper›PMID 38059035›Full record

ArticleNanoscale advances2023

Compartmentalized drug localization studies in extracellular vesicles for anticancer therapy.

Arunkumar Pitchaimani, Miguel Ferreira, Annalisa Palange, Martina Pannuzzo, Claudia De Mei, Raffaele Spano, Roberto Marotta, Beatriz Pelacho, Felipe Prosper, Paolo Decuzzi

Abstract read
In one paragraph

Article in Nanoscale advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

10 authors.

Arunkumar PitchaimaniNanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia (IIT) Genova GE Italy arunkumar.pitchaimani@vit.ac.in paolo.decuzzi@iit.it.ORCID https://orcid.org/0000-0003-2664-7913
Miguel FerreiraNanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia (IIT) Genova GE Italy arunkumar.pitchaimani@vit.ac.in paolo.decuzzi@iit.it.ORCID https://orcid.org/0000-0002-1560-3571
Annalisa PalangeNanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia (IIT) Genova GE Italy arunkumar.pitchaimani@vit.ac.in paolo.decuzzi@iit.it.
Martina PannuzzoNanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia (IIT) Genova GE Italy arunkumar.pitchaimani@vit.ac.in paolo.decuzzi@iit.it.ORCID https://orcid.org/0000-0001-8629-0173
Claudia De MeiNanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia (IIT) Genova GE Italy arunkumar.pitchaimani@vit.ac.in paolo.decuzzi@iit.it.
Raffaele SpanoNanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia (IIT) Genova GE Italy arunkumar.pitchaimani@vit.ac.in paolo.decuzzi@iit.it.
Roberto MarottaElectron Microscopy Facility, Fondazione Istituto Italiano di Tecnologia (IIT) Genova GE Italy.
Beatriz PelachoCentre for Applied Medical Research (CIMA), University of Navarra Navarra Spain.
Felipe ProsperCentre for Applied Medical Research (CIMA), University of Navarra Navarra Spain.
Paolo DecuzziNanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia (IIT) Genova GE Italy arunkumar.pitchaimani@vit.ac.in paolo.decuzzi@iit.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the development of therapeutic extracellular vesicles (EVs), drug encapsulation efficiencies are significantly lower when compared with synthetic nanomedicines. This is due to the hierarchical structure of the EV membrane and the physicochemical properties of the candidate drug (molecular weight, hydrophilicity, lipophilicity, and so on). As a proof of concept, here we demonstrated the importance of drug compartmentalization in EVs as an additional parameter affecting the therapeutic potential of drug-loaded EVs. In human adipose mesenchymal stem cell (hADSC) derived EVs, we performed a comparative drug loading analysis using two formulations of the same chemotherapeutic molecule - free doxorubicin (DOX) and 1,2-distearoyl-

Identifiers

PMID38059035
PMCPMC10696952

What OpenQuestion holds

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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.