Evidence map›Paper›PMID 38836363›Full record

ArticleACS nano2024

Clot-Targeted Nanogels for Dual-Delivery of AntithrombinIII and Tissue Plasminogen Activator to Mitigate Disseminated Intravascular Coagulation Complications.

Anastasia Sheridan, Kimberly Nellenbach, Sanika Pandit, Elizabeth Byrnes, Grace Hardy, Halle Lutz, Nina Moiseiwitsch, Grant Scull, Emily Mihalko, Jerrold H Levy and 1 more

Abstract read
In one paragraph

Article in ACS nano, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Transfusion biomaterials for hemostasis.Journal of thrombosis and haemostasis : JTH · 2025
    Review
  5. Article
  6. Review
  7. 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

11 authors.

Anastasia SheridanJoint Department of Biomedical Engineering of University of North Carolina, Chapel Hill and North Carolina State University, Raleigh, North Carolina 27695, United States.ORCID 0000-0003-0255-6929
Kimberly NellenbachJoint Department of Biomedical Engineering of University of North Carolina, Chapel Hill and North Carolina State University, Raleigh, North Carolina 27695, United States.
Sanika PanditJoint Department of Biomedical Engineering of University of North Carolina, Chapel Hill and North Carolina State University, Raleigh, North Carolina 27695, United States.
Elizabeth ByrnesJoint Department of Biomedical Engineering of University of North Carolina, Chapel Hill and North Carolina State University, Raleigh, North Carolina 27695, United States.
Grace HardyJoint Department of Biomedical Engineering of University of North Carolina, Chapel Hill and North Carolina State University, Raleigh, North Carolina 27695, United States.
Halle LutzComparative Medicine Institute, North Carolina State University, Raleigh, North Carolina 27606, United States.
Nina MoiseiwitschJoint Department of Biomedical Engineering of University of North Carolina, Chapel Hill and North Carolina State University, Raleigh, North Carolina 27695, United States.
Grant ScullJoint Department of Biomedical Engineering of University of North Carolina, Chapel Hill and North Carolina State University, Raleigh, North Carolina 27695, United States.
Emily MihalkoJoint Department of Biomedical Engineering of University of North Carolina, Chapel Hill and North Carolina State University, Raleigh, North Carolina 27695, United States.
Jerrold H LevyDepartments of Anesthesiology, Critical Care, and Surgery, Duke University School of Medicine, Durham, North Carolina 27710, United States.
Ashley C BrownJoint Department of Biomedical Engineering of University of North Carolina, Chapel Hill and North Carolina State University, Raleigh, North Carolina 27695, United States.ORCID 0000-0001-6995-1785

Funding

NC STATE MOLECULAR BIOTECHNOLOGY TRAINING PROGRAM (MBTP)T32GM133366 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Jason M. Haugh, Robert M Kelly · 2020 to 2026
$3.3M
Targeted treatment of thrombotic occlusions using a dual-delivery microgel therapeuticR01HL146701 · NHLBI · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI BROWN, ASHLEY CARSON · 2019 to 2023
$2.0M
Training Grant in Comparative Molecular MedicineT32GM133393 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Matthew B Fisher, Caroline Laplante · 2021 to 2026
$1.7M
U-TEAM: Undergraduate Interdisciplinary Training in Comparative Biomedical ResearchT34GM131947 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI PIEDRAHITA, JORGE A · 2019 to 2023
$1.3M
Interdisciplinary Biomedical Research Training ProgramT35OD011070 · OD · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Ronald Hak Long Li · 2012 to 2026
$1.1M
Fibrin-Based Nanoparticles as a Novel Sealant for Vascular AnastomosisF30HL163869 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MOISEIWITSCH, NINA ALEXANDRA · 2022 to 2025
$187k
NHLBI NIH HHS F30 HL163869NHLBI NIH HHS R01 HL146701NIGMS NIH HHS T32 GM133366NIGMS NIH HHS T32 GM133393NIGMS NIH HHS T34 GM131947NIH HHS T35 OD011070
6 · The paper itself

Abstract

Disseminated intravascular coagulation (DIC) is a pathologic state that follows systemic injury and other diseases. Often a complication of sepsis or trauma, DIC causes coagulopathy associated with paradoxical thrombosis and hemorrhage. DIC upregulates the thrombotic pathways while simultaneously downregulating the fibrinolytic pathways that cause excessive fibrin deposition, microcirculatory thrombosis, multiorgan dysfunction, and consumptive coagulopathy with excessive bleeding. Given these opposing disease phenotypes, DIC management is challenging and includes treating the underlying disease and managing the coagulopathy. Currently, no therapies are approved for DIC. We have developed clot-targeted therapeutics that inhibit clot polymerization and activate clot fibrinolysis to manage DIC. We hypothesize that delivering both an anticoagulant and a fibrinolytic agent directly to clots will inhibit active clot polymerization while also breaking up pre-existing clots; therefore, reversing consumptive coagulopathy and restoring hemostatic balance. To test this hypothesis, we single- and dual-loaded fibrin-specific nanogels (FSNs) with antithrombinIII (ATIII) and/or tissue plasminogen activator (tPA) and evaluated their clot preventing and clot lysing abilities

Indexed as

Disseminated Intravascular CoagulationDrug Delivery SystemsNanogelsTissue Plasminogen ActivatorAnimalsAntithrombinsBlood CoagulationFibrinFibrinolytic AgentsHumansMaleRatsThrombosisAntithrombinsFibrinFibrinolytic AgentsNanogelsTissue Plasminogen Activatoranticoagulantfibrinfibrinolytichemorrhagenanogelthrombosis

Identifiers

PMID38836363
PMCPMC11607481

What OpenQuestion holds

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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.