Evidence map›Paper›PMID 41716478›Full record

ArticleFrontiers in medical technology2025

Drug-loaded nanoparticles reduced platelet aggregation and blood coagulation.

Sarah Majin, Afrida Malik, Pratima Poudel, E Vincent S Faustino, Nubia Zuverza-Mena, John Hwa, Seyedtaghi Takyar, Susan Shea, Kagya A Amoako

Abstract read
In one paragraph

Article in Frontiers in medical technology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Sarah MajinDepartment of Chemistry and Chemical & Biomedical Engineering, University of New Haven, West Haven, CT, United States.
Afrida MalikDepartment of Chemistry and Chemical & Biomedical Engineering, University of New Haven, West Haven, CT, United States.
Pratima PoudelDepartment of Chemistry and Chemical & Biomedical Engineering, University of New Haven, West Haven, CT, United States.
E Vincent S FaustinoDepartment of Pediatrics, Yale University, New Haven, CT, United States.
Nubia Zuverza-MenaAnalytical Chemistry, Connecticut Agricultural Experiment Station, New Haven, CT, United States.
John HwaYale Cardiovascular Research Center and Yale Cooperative Center of Excellence in Hematology, Yale School of Medicine, New Haven, CT, United States.
Seyedtaghi TakyarCritical Care & Sleep Medicine, Yale University Pulmonary, New Haven, CT, United States.
Susan SheaDepartment of Surgery, University of Pittsburgh, Pittsburgh, PA, United States.
Kagya A AmoakoDepartment of Chemistry and Chemical & Biomedical Engineering, University of New Haven, West Haven, CT, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Surface-induced thrombosis remains a significant limitation of blood-contacting medical devices, driven primarily by platelet activation and rapid clot formation. Nitric oxide (NO), a potent endogenous antiplatelet agent, has therefore inspired the development of targeted NO-delivery strategies to mitigate device-associated thrombosis. In this study, nitric oxide-releasing antiplatelet lipid nanoparticles (anti-PLT LNPs) were formulated and characterized for their physicochemical properties and NO-release kinetics. Their platelet aggregation inhibition was evaluated in vitro, while mammalian cell biocompatibility and effects on whole-blood coagulation were evaluated using activated clotting time (ACT) measurements. Anti-PLT LNPs exhibited sustained and measurable NO release after 22 weeks of storage and demonstrated high mammalian cell biocompatibility. The nanoparticles inhibited platelet aggregation by up to 84.4% (

Indexed as

anti-coagulationblood-contacting medical devicesdrug deliveryliposomesnanoparticlesnitric oxideplateletsthrombosis

Identifiers

PMID41716478
PMCPMC12913426

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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.