Evidence map›Paper›PMID 35832077›Full record

ArticleTheranostics2022

Selective brain entry of lipid nanoparticles in haemorrhagic stroke is linked to biphasic blood-brain barrier disruption.

Zahraa S Al-Ahmady, Ben R Dickie, Isabelle Aldred, Dhifaf A Jasim, Jack Barrington, Michael Haley, Eloise Lemarchand, Graham Coutts, Satinderdeep Kaur, Jessica Bates and 6 more

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. caADAMTS13 reduces neutrophil-mediated vascular inflammation without exacerbating bleeding in experimental intracerebral haemorrhage.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2026
    Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Transforming stroke treatment through nanotherapies.Nanomedicine (London, England) · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. The blood-brain barrier: structure, regulation, and drug delivery.Signal transduction and targeted therapy · 2023
    Review
  14. Review
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

16 authors at 3 institutions in 1 country.

Zahraa S Al-AhmadyPharmacology Department, School of Science and Technology, Nottingham Trent University, Nottingham, NG11 8NS, United Kingdom.
Ben R DickieDivision of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, United Kingdom.
Isabelle AldredNanomedicine Lab, Division of Pharmacy and Optometry, Faculty of Biology, Medicine and Health, AV Hill Building, The University of Manchester, Manchester M13 9PT, United Kingdom.
Dhifaf A JasimNanomedicine Lab, Division of Pharmacy and Optometry, Faculty of Biology, Medicine and Health, AV Hill Building, The University of Manchester, Manchester M13 9PT, United Kingdom.
Jack BarringtonDivision of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, United Kingdom.
Michael HaleyDivision of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, United Kingdom.
Eloise LemarchandDivision of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, United Kingdom.
Graham CouttsDivision of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, United Kingdom.
Satinderdeep KaurPharmacology Department, School of Science and Technology, Nottingham Trent University, Nottingham, NG11 8NS, United Kingdom.
Jessica BatesPharmacology Department, School of Science and Technology, Nottingham Trent University, Nottingham, NG11 8NS, United Kingdom.
Sarah CurranPharmacology Department, School of Science and Technology, Nottingham Trent University, Nottingham, NG11 8NS, United Kingdom.
Ruth GoddardPharmacology Department, School of Science and Technology, Nottingham Trent University, Nottingham, NG11 8NS, United Kingdom.
Megan WalkerPharmacology Department, School of Science and Technology, Nottingham Trent University, Nottingham, NG11 8NS, United Kingdom.
Adrian Parry-JonesDivision of Cardiovascular Sciences, Lydia Becker Institute of Immunology and Inflammation, School of Medical Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, United Kingdom.
Kostas KostarelosNanomedicine Lab, Division of Pharmacy and Optometry, Faculty of Biology, Medicine and Health, AV Hill Building, The University of Manchester, Manchester M13 9PT, United Kingdom.
Stuart M AllanDivision of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, United Kingdom.
Nottingham Trent University · GBUniversity of Manchester · GBManchester Academic Health Science Centre · GB

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council MR/N003586/1
6 · The paper itself

Abstract

Haemorrhagic stroke represents a significant public health burden, yet our knowledge and ability to treat this type of stroke are lacking. Previously we showed that we can target ischaemic-stroke lesions by selective translocation of lipid nanoparticles through the site of blood-brain barrier (BBB) disruption. The data we presented in this study provide compelling evidence that haemorrhagic stroke in mice induces BBB injury that mimics key features of the human pathology and, more importantly, provides a gate for entry of lipid nanoparticles-based therapeutics selectively to the bleeding site.

Indexed as

Hemorrhagic StrokeStrokeAnimalsBlood-Brain BarrierBrainHumansLiposomesMagnetic Resonance ImagingMiceNanoparticlesLipid NanoparticlesLiposomesblood-brain barrierdrug deliveryhaemorrhagic strokelipid nanoparticlesLiposomes

Identifiers

PMID35832077
PMCPMC9254235
OpenAlexW4285267575

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.