Evidence map›Paper›PMID 19839809›Full record

ArticleNanomedicine (London, England)2009

Biologic nanoparticles and platelet reactivity.

Virginia M Miller, Larry W Hunter, Kevin Chu, Vivasvat Kaul, Phillip D Squillace, John C Lieske, Muthuvel Jayachandran

Open access · greenAbstract read
In one paragraph

Article in Nanomedicine (London, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 34 citations in OpenAlex.

  1. Differential effects of hormone therapy on serotonin, vascular function and mood in the KEEPS.Climacteric : the journal of the International Menopause Society · 2016
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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

7 authors at 1 institution in 1 country.

Virginia M MillerDepartment of Surgery, College of Medicine, Mayo Clinic, Rochester, MN 55905, USA. miller.virginia@mayo.edu
Larry W Hunter
Kevin Chu
Vivasvat Kaul
Phillip D Squillace
John C Lieske
Muthuvel Jayachandran
Mayo Clinic in Arizona · US

Funding

Nanoparticles and Arterial DiseaseR21HL088988 · NHLBI · MAYO CLINIC ROCHESTER · PI MILLER, VIRGINIA M · 2008 to 2009
$416k
NHLBI NIH HHS HL88988NHLBI NIH HHS R21 HL088988
6 · The paper itself

Abstract

aimNanosized particles (NPs) enriched in hydroxyapatite and protein isolated from calcified human tissue accelerate occlusion of endothelium-denuded arteries when injected intravenously into rabbits. Since platelet aggregation and secretory processes participate in normal hemostasis, thrombosis and vascular remodeling, experiments were designed to determine if these biologic NPs alter specific platelet functions in vitro.

methodsPlatelet-rich plasma was prepared from citrate anticoagulated human blood. Platelet aggregation and ATP secretion were monitored in response to thrombin receptor agonists peptide (10 microM) or convulxin (50 microg/ml) prior to and following 15 min incubation with either control solution, human-derived NPs, bovine-derived NPs or crystals of hydroxyapatite at concentrations of 50 and 150 nephelometric turbidity units.

resultsIncubation of platelets for 15 min with either human- or bovine-derived NPs reduced aggregation induced by thrombin receptor activator peptide and convulxin in a concentration-dependent manner. Hydroxyapatite caused a greater inhibition than either of the biologically derived NPs. Human-derived NPs increased ATP secretion by unstimulated platelets during the 15 min incubation period.

conclusionEffects of bovine-derived and hydroxyapatite NPs on basal release of ATP were both time and concentration dependent. These results suggest that biologic NPs modulate both platelet aggregation and secretion. Biologically derived NPs could modify platelet responses within the vasculature, thereby reducing blood coagulability and the vascular response to injury.

Indexed as

Adenosine TriphosphateAdultAgedAnimalsBiocompatible MaterialsCattleDurapatiteFemaleHumansMaleMicroscopy, ConfocalMicroscopy, FluorescenceMicroscopy, Scanning TunnelingMiddle AgedNanomedicineNanoparticlesAdenosine TriphosphateBiocompatible MaterialsDurapatite

Identifiers

PMID19839809
PMCPMC2785539
OpenAlexW2142346880

What OpenQuestion holds

Textmetadata
LicenceTDM
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.