Evidence map›Paper›PMID 41053535›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

An Aptamer-Based EXACT Anticoagulant as a Sustainable, Animal-Free Alternative to Unfractionated Heparin.

Haixiang Yu, George Pitoc, Manqi Zhang, Jeffrey Clancy, James Frederiksen, Amy Yan, Samuel Francis, Rebecca Sullenger, Rachel Rempel, Susannah Gammell and 2 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

12 authors.

Haixiang YuDepartment of Surgery, Duke University, Durham, NC, 27710, USA.
George PitocDepartment of Surgery, Duke University, Durham, NC, 27710, USA.
Manqi ZhangDepartment of Medicine, Duke University, Durham, NC, 27710, USA.
Jeffrey ClancyDepartment of Surgery, Duke University, Durham, NC, 27710, USA.
James FrederiksenDepartment of Surgery, Duke University, Durham, NC, 27710, USA.
Amy YanDepartment of Surgery, Duke University, Durham, NC, 27710, USA.
Samuel FrancisDepartment of Emergency Medicine, Duke University Hospital, Durham, NC, 27710, USA.
Rebecca SullengerSchool of Medicine, Duke University, Durham, NC, 27710, USA.
Rachel RempelDepartment of Surgery, Duke University, Durham, NC, 27710, USA.
Susannah GammellDepartment of Surgery, Duke University, Durham, NC, 27710, USA.
Jillian CaiazziDepartment of Surgery, Duke University, Durham, NC, 27710, USA.
Bruce A SullengerDepartment of Surgery, Duke University, Durham, NC, 27710, USA.ORCID https://orcid.org/0000-0002-5113-5541

Funding

Translating Mechanistic Insights into Intrinsic Xase FunctionP01HL139420 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI Sriram Krishnaswamy · 2018 to 2026
$22.4M
Genetics and Genomics Training GrantT32GM136627 · NIGMS · DUKE UNIVERSITY · PI ALLISON E ASHLEY-KOCH · 2020 to 2026
$3.1M
American Heart Association 23POST1018721NHLBI NIH HHS P01 HL139420NHLBI NIH HHS P01-HL139420NIGMS NIH HHS T32 GM136627
6 · The paper itself

Abstract

Unfractionated heparin (UFH), designated as an essential medicine by the World Health Organization (WHO), is indispensable in cardiac surgery and various clinical applications. However, its production depends on the farming of over a billion large animals annually, posing sustainability challenges, especially amidst increasing efforts to mitigate greenhouse gas (GHG) emissions by reducing animal farming. The rising demand for UFH has outpaced its supply, and previous attempts to develop synthetic alternatives have fallen short because of their limited potency and reversibility. Here, HD1-12dmA-DAB is presented, a novel synthetic anticoagulant developed through chemical conjugation of a thrombin exosite-binding aptamer (HD1) with a thrombin active-site inhibitor (dabigatran). By optimizing dual-site synergistic binding, HD1-12dmA-DAB achieves an enhancement of over three orders of magnitude in thrombin-binding affinity and specificity compared to HD1 alone. It also demonstrates superior plasma stability and anticoagulant efficacy comparable to UFH, as validated in in vitro, in vivo, and ex vivo clotting models. This breakthrough highlights a promising step toward a sustainable, animal-free alternative to UFH, addressing the growing clinical demand and advancing environmental sustainability objectives.

Indexed as

AnticoagulantsAptamers, NucleotideHeparinAnimalsBlood CoagulationDabigatranHumansThrombinAnticoagulantsAptamers, NucleotideDabigatranHeparinThrombinanticoagulationaptamerscooperative effectsdrug designsustainability

Identifiers

PMID41053535
PMCPMC12822440

What Socratic 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 Socratic graph.