Evidence map›Paper›PMID 39635869›Full record

ArticleJournal of materials chemistry. B2025

PEGylation of indium phosphide quantum dots prevents quantum dot mediated platelet activation.

Leigh Naylor-Adamson, Thomas W Price, Zoe Booth, Sophie V L Leonard, Juan Gallo, Le Duc Tung, Stanley Harvell-Smith, Nguyen Thi Kim Thanh, Zabeada Aslam, David Allsup and 7 more

Abstract read
In one paragraph

Article in Journal of materials chemistry. B, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. 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

17 authors.

Leigh Naylor-AdamsonBiomedical Institute for Multimorbidity, Hull York Medical School, University of Hull, Hull, HU6 7RX, UK. simon.calaminus@hyms.ac.uk.ORCID 0000-0001-5936-9281
Thomas W PriceDepartment of Imaging Chemistry and Biology, School of Biomedical Engineering and Imaging Sciences, King's College London, London, SE1 7EH, UK. graeme.stasiuk@kcl.ac.uk.
Zoe BoothBiomedical Institute for Multimorbidity, Hull York Medical School, University of Hull, Hull, HU6 7RX, UK. simon.calaminus@hyms.ac.uk.
Sophie V L LeonardBiomedical Institute for Multimorbidity, Hull York Medical School, University of Hull, Hull, HU6 7RX, UK. simon.calaminus@hyms.ac.uk.
Juan GalloAdvanced Magnetic Theranostic Nanostructures Lab, International Iberian Nanotechnology Laboratory, Av. Mestre José Veiga, Braga 4715-330, Portugal.ORCID 0000-0002-2028-3234
Le Duc TungUCL Healthcare Biomagnetics and Nanomaterials Laboratories, 21 Albemarle Street, London, W1S 4BS, UK.
Stanley Harvell-SmithUCL Healthcare Biomagnetics and Nanomaterials Laboratories, 21 Albemarle Street, London, W1S 4BS, UK.ORCID 0000-0001-9663-7564
Nguyen Thi Kim ThanhUCL Healthcare Biomagnetics and Nanomaterials Laboratories, 21 Albemarle Street, London, W1S 4BS, UK.ORCID 0000-0002-4131-5952
Zabeada AslamLeeds Electron Microscopy and Spectroscopy Centre, LEMAS, The Bragg Centre for Materials Research, Faculty of Engineering and Physical Sciences, University of Leeds, LS2 9JT, UK.
David AllsupBiomedical Institute for Multimorbidity, Hull York Medical School, University of Hull, Hull, HU6 7RX, UK. simon.calaminus@hyms.ac.uk.
Nicole HondowLeeds Electron Microscopy and Spectroscopy Centre, LEMAS, The Bragg Centre for Materials Research, Faculty of Engineering and Physical Sciences, University of Leeds, LS2 9JT, UK.
Thomas ChamberlainInstitute of Process Research and Development, School of Chemistry, University of Leeds, Leeds, LS2 9JT, UK.ORCID 0000-0001-8100-6452
Jürgen E SchneiderSchool of Medicine, University of Leeds, Leeds, LS2 9JT, UK.ORCID 0000-0003-0999-5684
Khalid NaseemLeeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, LS2 9JT, UK.
Jean-Sebastien G BouillardDepartment of Physics and Mathematics, Nano3 Research grouping - Nanophotonics group, G. W. Gray Centre for Advanced Materials, University of Hull, Cottingham Road, Hull, HU6 7RX, UK.ORCID 0000-0002-6942-1749
Graeme J StasiukDepartment of Imaging Chemistry and Biology, School of Biomedical Engineering and Imaging Sciences, King's College London, London, SE1 7EH, UK. graeme.stasiuk@kcl.ac.uk.ORCID 0000-0002-0076-2246
Simon D J CalaminusBiomedical Institute for Multimorbidity, Hull York Medical School, University of Hull, Hull, HU6 7RX, UK. simon.calaminus@hyms.ac.uk.ORCID 0000-0002-1124-7848

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantum dots (QDs) are semiconducting inorganic nanocrystals, that have garnered interest in biological and medical spheres due, to their potential benefits in biomedical imaging and drug-delivery systems. Indium phosphide QDs shelled with zinc sulphide (InP/ZnS) are viewed as more biocompatible than previous heavy metal based QDs. However, little is known about how InP/ZnS QDs affect a key blood cell, the platelet. Understanding how platelets interact with QDs is critical as unwanted activation can lead to pathological thrombus formation. Herein, we demonstrate PEGylation of InP/ZnS QDs coated with lipoic acid (QD-LA) or coated with penicillamine (QD-Pen) surface ligands induced markedly less platelet aggregation, platelet-QD interactions, integrin activation, alpha granule secretion and restored platelet spreading in washed platelets in comparison to their non-PEGylated counterparts. Furthermore, in whole blood, PEGylation of QDs reduced the number of QDs in the thrombus, thereby helping to minimise the chance of dysfunctional thrombus formation. Overall, we show that QD PEGylation is important to help prevent QD mediated platelet activation. In combination with the most biocompatible coating, PEGylation markedly reduced platelet activation, widening the concentrations at which QDs were viable for development as potential drug delivery or imaging agents.

Indexed as

IndiumPhosphinesPlatelet ActivationPolyethylene GlycolsQuantum DotsBlood PlateletsHumansParticle SizePlatelet AggregationSulfidesSurface PropertiesZinc CompoundsIndiumindium phosphidePhosphinesPolyethylene GlycolsSulfidesZinc Compoundszinc sulfide

Identifiers

PMID39635869
PMCPMC11619005

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.