Evidence map›Paper›PMID 31711496›Full record

ArticleJournal of nanobiotechnology2019

The synergistic effect of chlorotoxin-mApoE in boosting drug-loaded liposomes across the BBB.

Beatrice Formicola, Roberta Dal Magro, Carlos V Montefusco-Pereira, Claus-Michael Lehr, Marcus Koch, Laura Russo, Gianvito Grasso, Marco A Deriu, Andrea Danani, Sandrine Bourdoulous and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

15 citing papers in PubMed, 31 citations in OpenAlex.

  1. Peptide-functionalized nanoparticles for brain-targeted therapeutics.Drug delivery and translational research · 2026
    Review
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  4. Biomacromolecules · 2024
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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

11 authors at 7 institutions in 4 countries.

Beatrice FormicolaSchool of Medicine and Surgery, University of Milano-Bicocca, Via Raoul Follereau 3, 20854, Vedano al Lambro, MB, Italy. b.formicola@campus.unimib.it.
Roberta Dal MagroSchool of Medicine and Surgery, University of Milano-Bicocca, Via Raoul Follereau 3, 20854, Vedano al Lambro, MB, Italy.
Carlos V Montefusco-PereiraDepartment of Drug Delivery, Helmholtz Institute for Pharmaceutical Research Saarland, Saarland University, 66123, Saarbrücken, Germany.
Claus-Michael LehrDepartment of Drug Delivery, Helmholtz Institute for Pharmaceutical Research Saarland, Saarland University, 66123, Saarbrücken, Germany.
Marcus KochLeibniz Institute for New Materials, Campus D2 2, 66123, Saarbrücken, Germany.
Laura RussoBio Organic Chemistry Laboratory, Department of Biotechnology and Biosciences, University of Milano-Bicocca, Via Raoul Follereau 3, 20854, Vedano al Lambro, MB, Italy.
Gianvito GrassoIstituto Dalle Molle di Studi Sull'Intelligenza Artificiale (IDSIA), Scuola Universitaria Professionale Della Svizzera Italiana (SUPSI), Università Della Svizzera Italiana (USI), Manno, Switzerland.
Marco A DeriuDepartment of Mechanical and Aerospace Engineering (DIMEAS), Politecnico di Torino, Corso Duca degli Abruzzi 24, 10128, Turin, Italy.
Andrea DananiIstituto Dalle Molle di Studi Sull'Intelligenza Artificiale (IDSIA), Scuola Universitaria Professionale Della Svizzera Italiana (SUPSI), Università Della Svizzera Italiana (USI), Manno, Switzerland.
Sandrine BourdoulousU1016, Institut Cochin, Inserm, Paris, France.
Francesca ReSchool of Medicine and Surgery, University of Milano-Bicocca, Via Raoul Follereau 3, 20854, Vedano al Lambro, MB, Italy.
University of Milano-Bicocca · ITDalle Molle Institute for Artificial Intelligence Research · CHHelmholtz Institute for Pharmaceutical Research Saarland · DEInserm · FRLeibniz-Institute for New Materials · DEPolytechnic University of Turin · ITSaarland University · DE

Funding

H2020-MSCA-ITN-2014 642028JPND JPND-COFUND_FP-829-031 (2016-2019)
6 · The paper itself

Abstract

We designed liposomes dually functionalized with ApoE-derived peptide (mApoE) and chlorotoxin (ClTx) to improve their blood-brain barrier (BBB) crossing. Our results demonstrated the synergistic activity of ClTx-mApoE in boosting doxorubicin-loaded liposomes across the BBB, keeping the anti-tumour activity of the drug loaded: mApoE acts promoting cellular uptake, while ClTx promotes exocytosis of liposomes.

Indexed as

AnimalsAntibiotics, AntineoplasticApolipoproteins EBlood-Brain BarrierBrain NeoplasmsCell Line, TumorDoxorubicinHumansLiposomesModels, MolecularPeptidesPolyethylene GlycolsScorpionsScorpion VenomsAntibiotics, AntineoplasticApolipoproteins EChlorotoxinDoxorubicinliposomal doxorubicinLiposomesPeptidesPolyethylene GlycolsScorpion VenomsBlood–brain barrierBrainChlorotoxinDoxorubicinDrug deliveryGlioblastomaLiposomesNanoparticles

Identifiers

PMID31711496
PMCPMC6844026
OpenAlexW2984250052

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.