Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Nature Communications
  • View all journals
  • Search
  • My Account Login
  • Content Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • RSS feed
  1. nature
  2. nature communications
  3. articles
  4. article
Hemostatic Tough Adhesives seal tissue and control hemorrhage
Download PDF
Download PDF
  • Article
  • Open access
  • Published: 08 April 2026

Hemostatic Tough Adhesives seal tissue and control hemorrhage

  • Daniel O. Kent  ORCID: orcid.org/0009-0006-2464-27471,2,3 na1,
  • Phoebe S. Kwon2 na1,
  • Kyle C. Wu  ORCID: orcid.org/0000-0003-0009-50494,5 na1,
  • Matthew Torre6,
  • Hamza Ijaz2,
  • Favour Omafuvwe Obuseh  ORCID: orcid.org/0009-0008-2500-41942,7,8,
  • Brittany Pattison9,
  • Arthur Nedder9,
  • Francis McGovern10,
  • Jeremy Cannon  ORCID: orcid.org/0000-0002-2969-931611,
  • David J. Mooney  ORCID: orcid.org/0000-0001-6299-11942,6 &
  • …
  • Benjamin R. Freedman  ORCID: orcid.org/0000-0001-9406-773X2,6,12 na1 

Nature Communications (2026) Cite this article

  • 4910 Accesses

  • 5 Altmetric

  • Metrics details

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Bioinspired materials
  • Biomedical engineering
  • Biomedical materials

Abstract

Hemorrhage from internal organs remains a critical challenge in both trauma care and surgical procedures, as existing hemostatic adjuncts frequently fail to provide consistent and effective bleeding control, particularly under conditions of active bleeding or impaired coagulation. Here, we develop and evaluate a Hemostatic Tough Adhesive (HTA) in controlled preclinical models of traumatic solid organ injury and compare its performance against leading commercially available hemostatic agents. The HTA consistently outperformed its counterparts, achieving 100% hemostasis in both liver and spleen injuries within an in vivo preclinical porcine model. In contrast, existing adjuncts exhibited variable and often incomplete efficacy. Beyond immediate hemostasis, the HTA demonstrated prolonged stability and biocompatibility during the postoperative wound healing phase. Notably, the HTA exhibited tissue surface adhesion energy several orders of magnitude greater than that of current hemostatic products, indicating its potential utility for surgical and trauma-related bleeding management.

Similar content being viewed by others

Quinone-mediated, tissue-adaptive double-network hydrogel for instant hemostasis and wet-tissue adhesion

Article Open access 22 April 2026

Comparison of a gelatin thrombin versus a modified absorbable polymer as a unique treatment for severe hepatic hemorrhage in swine

Article Open access 27 November 2023

The effect of different hemostatic agents following dental extraction in patients under oral antithrombotic therapy: a network meta-analysis

Article Open access 02 August 2023

Data availability

The data generated in this study are provided in the manuscript, Supplementary Information, and Source Data files.  Source data are provided with this paper.

Code availability

The custom MATLAB code for mechanical testing is available in Zenodo (https://zenodo.org/records/18827563).

References

  1. Stokes, M. E. et al. Impact of bleeding-related complications and/or blood product transfusions on hospital costs in inpatient surgical patients. BMC Health Serv. Res. 11, 135 (2011).

    Google Scholar 

  2. Baker, L. et al. Intraoperative Red Blood Cell Transfusion Decision-making: A Systematic Review of Guidelines. Ann. Surg. 274, 86–96 (2021).

    Google Scholar 

  3. Spahn, D. R. & Rossaint, R. Coagulopathy and blood component transfusion in trauma. Br. J. Anaesth. 95, 130–139 (2005).

    Google Scholar 

  4. Dyke, C. et al. Universal definition of perioperative bleeding in adult cardiac surgery. J. Thorac. Cardiovasc Surg. 147, 1458–1463 e1451 (2014).

    Google Scholar 

  5. Lewis, K. M. et al. Development and validation of an intraoperative bleeding severity scale for use in clinical studies of hemostatic agents. Surgery 161, 771–781 (2017).

    Google Scholar 

  6. Chaudhary, M. A. et al. Differences in rural and urban outcomes: a national inspection of emergency general surgery patients. J. Surg. Res. 218, 277–284 (2017).

    Google Scholar 

  7. Bhagat, V. & Becker, M. L. Degradable Adhesives for Surgery and Tissue Engineering. Biomacromolecules 18, 3009–3039 (2017).

    Google Scholar 

  8. Hong, C., Olsen, B. D. & Hammond, P. T. A review of treatments for non-compressible torso hemorrhage (NCTH) and internal bleeding. Biomaterials 283, 121432 (2022).

    Google Scholar 

  9. Haghniaz, R. et al. An All-In-One Transient Theranostic Platform for Intelligent Management of Hemorrhage. Adv. Sci. (Weinh.) 10, e2301406 (2023).

    Google Scholar 

  10. Iannitti, D. A., Kim, C., Ito, D. & Epstein, J. Impact of an active hemostatic product treatment approach on bleeding-related complications and hospital costs among inpatient surgeries in the United States. J. Med Econ. 24, 514–523 (2021).

    Google Scholar 

  11. Orsini, S. et al. Bleeding risk of surgery and its prevention in patients with inherited platelet disorders. Haematologica 102, 1192–1203 (2017).

    Google Scholar 

  12. Bao, G. et al. Liquid-infused microstructured bioadhesives halt non-compressible hemorrhage. Nat. Commun. 13, 5035 (2022).

    Google Scholar 

  13. Bures, M. et al. Albumin-glutaraldehyde glue for repair of superficial lung defect: an in vitro experiment. J. Cardiothorac. Surg. 11, 63 (2016).

    Google Scholar 

  14. Furst, W. & Banerjee, A. Release of glutaraldehyde from an albumin-glutaraldehyde tissue adhesive causes significant in vitro and in vivo toxicity. Ann. Thorac. Surg. 79, 1522–1528 (2005). discussion 1529.

    Google Scholar 

  15. Gaizo, D. J. D. et al. SPOT GRADE II: Clinical Validation of a New Method for Reproducibly Quantifying Surgical Wound Bleeding: Prospective, Multicenter, Multispecialty, Single-Arm Study. Clin. Appl Thromb. Hemost. 26, 1076029620936340 (2020).

    Google Scholar 

  16. Kerris, E. W. J., Hoptay, C., Calderon, T. & Freishtat, R. J. Platelets and platelet extracellular vesicles in hemostasis and sepsis. J. Investig. Med. 68, 813–820 (2020).

    Google Scholar 

  17. Allotey, J. K. et al. Systematic review of hemostatic agents used in vascular surgery. J. Vasc. Surg. 73, 2189–2197 (2021).

    Google Scholar 

  18. Luk, A., David, T. E. & Butany, J. Complications of Bioglue postsurgery for aortic dissections and aortic valve replacement. J. Clin. Pathol. 65, 1008–1012 (2012).

    Google Scholar 

  19. Liu, C. et al. Mechanically Active and Antimicrobial Wound Closure Using an Adhesive Hydrogel-Elastomer. ACS Pharm. Transl. Sci. 8, 2795–2803 (2025).

    Google Scholar 

  20. Freedman, B. R. et al. Enhanced tendon healing by a tough hydrogel with an adhesive side and high drug-loading capacity. Nat. Biomed. Eng. 6, 1167–1179 (2021).

  21. Freedman, B. R. et al. Degradable and Removable Tough Adhesive Hydrogels. Adv. Mater. 33, e2008553 (2021).

    Google Scholar 

  22. Freedman, B. R. et al. Instant tough adhesion of polymer networks. Proc. Natl. Acad. Sci. USA 121, e2304643121 (2024).

    Google Scholar 

  23. Cruz, J. A. C. et al. Rapid Ultra-Tough Topological Tissue Adhesives. Adv. Mater. e2205567 https://doi.org/10.1002/adma.202205567 (2022).

  24. Yuk, H. et al. Rapid and coagulation-independent haemostatic sealing by a paste inspired by barnacle glue. Nat. Biomed. Eng. 5, 1131–1142 (2021).

    Google Scholar 

  25. Munoz Taboada, G., Dahis, D., Dosta, P., Edelman, E. & Artzi, N. Sprayable Hydrogel Sealant for Gastrointestinal Wound Shielding. Adv. Mater. 36, e2311798 (2024).

    Google Scholar 

  26. Naar, L. et al. Chitosan-based lifefoam improves survival in lethal noncompressible abdominal bleeding in swine. Surgery 172, 421–426 (2022).

    Google Scholar 

  27. Ma, G. W. et al. The role of sealants for achieving anastomotic hemostasis in vascular surgery. Cochrane Database Syst. Rev. 5, CD013421 (2024).

    Google Scholar 

  28. Liu, A. et al. Ionically assembled hemostatic powders with rapid self-gelation, strong acid resistance, and on-demand removability for upper gastrointestinal bleeding. Mater. Horiz. 11, 5983–5996 (2024).

    Google Scholar 

  29. Wang, J. et al. A contact-polymerizable hemostatic powder for rapid hemostasis. Biomater. Sci. 11, 3616–3628 (2023).

    Google Scholar 

  30. Lee, J. et al. Actively cross-linking hemostatic sealant enables rapid hemostasis and wound closure. Biotechnol. J. 18, e2200517 (2023).

    Google Scholar 

  31. Levy, J. H. et al. Consensus Statement: Hemostasis Trial Outcomes in Cardiac Surgery and Mechanical Support. Ann. Thorac. Surg. 113, 1026–1035 (2022).

    Google Scholar 

  32. Wells, C. I. et al. Haemostatic Efficacy of Topical Agents During Liver Resection: A Network Meta-Analysis of Randomised Trials. World J. Surg. 44, 3461–3469 (2020).

    Google Scholar 

  33. Matonick, J. P. & Hammond, J. Hemostatic efficacy of EVARREST, Fibrin Sealant Patch vs. TachoSil(R) in a heparinized swine spleen incision model. J. Invest Surg. 27, 360–365 (2014).

    Google Scholar 

  34. Amit, M., Binenbaum, Y., Cohen, J. T. & Gil, Z. Effectiveness of an oxidized cellulose patch hemostatic agent in thyroid surgery: a prospective, randomized, controlled study. J. Am. Coll. Surg. 217, 221–225 (2013).

    Google Scholar 

  35. Kessler, U. et al. Comparison of porcine and human coagulation by thrombelastometry. Thromb. Res. 128, 477–482 (2011).

    Google Scholar 

  36. Stettler, G. R. et al. Thrombelastography indicates limitations of animal models of trauma-induced coagulopathy. J. Surg. Res. 217, 207–212 (2017).

    Google Scholar 

  37. Wu, K. C. et al. A tough bioadhesive hydrogel supports sutureless sealing of the dural membrane in porcine and ex vivo human tissue. Sci. Transl. Med. 16, eadj0616 (2024).

    Google Scholar 

  38. Wu, D. T. et al. Tough Adhesive Hydrogel for Intraoral Adhesion and Drug Delivery. J. Dent. Res. 102, 497–504 (2023).

    Google Scholar 

  39. Lazow, S. P. et al. A novel two-component, expandable bioadhesive for exposed defect coverage: Applicability to prenatal procedures. J. Pediatr. Surg. https://doi.org/10.1016/j.jpedsurg.2020.09.030 (2020).

    Google Scholar 

  40. Li, J. et al. Tough adhesives for diverse wet surfaces. Science 357, 378–381 (2017).

    Google Scholar 

  41. Mondal, P., Chakraborty, I. & Chatterjee, K. Injectable Adhesive Hydrogels for Soft tissue Reconstruction: A Materials Chemistry Perspective. Chem. Rec. 22, e202200155 (2022).

    Google Scholar 

  42. Chaudhuri, O., Cooper-White, J., Janmey, P. A., Mooney, D. J. & Shenoy, V. B. Effects of extracellular matrix viscoelasticity on cellular behaviour. Nature 584, 535–546 (2020).

    Google Scholar 

Download references

Acknowledgements

This work was supported by the Wyss Institute for Biologically Inspired Engineering at Harvard (DJM) and the National Institute on Aging of the NIH (K99/R00AG065495) (BRF). We thank Des White for assistance in the peristaltic pump setup. We thank Katarina Richter and Emmanuel Osorno for support in illustrations.

Author information

Author notes
  1. These authors contributed equally: Daniel O. Kent, Phoebe S. Kwon, Kyle C. Wu, Benjamin R. Freedman.

Authors and Affiliations

  1. Department of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA

    Daniel O. Kent

  2. Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA

    Daniel O. Kent, Phoebe S. Kwon, Hamza Ijaz, Favour Omafuvwe Obuseh, David J. Mooney & Benjamin R. Freedman

  3. Department of Surgery, University of California, San Francisco, San Francisco, CA, USA

    Daniel O. Kent

  4. Department of Neurosurgery, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA

    Kyle C. Wu

  5. Department of Neurosurgery, The Ohio State University and James Cancer Hospital, Columbus, OH, USA

    Kyle C. Wu

  6. Department of Pathology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA

    Matthew Torre, David J. Mooney & Benjamin R. Freedman

  7. John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA

    Favour Omafuvwe Obuseh

  8. Harvard-MIT Health Science and Technology, Massachusetts Institute of Technology, Cambridge, MA, USA

    Favour Omafuvwe Obuseh

  9. Boston Children’s Hospital, Boston, MA, USA

    Brittany Pattison & Arthur Nedder

  10. Department of Urologic Surgery, Massachusetts General Hospital, Boston, MA, USA

    Francis McGovern

  11. Department of Surgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA

    Jeremy Cannon

  12. Department of Orthopaedic Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA

    Benjamin R. Freedman

Authors
  1. Daniel O. Kent
    View author publications

    Search author on:PubMed Google Scholar

  2. Phoebe S. Kwon
    View author publications

    Search author on:PubMed Google Scholar

  3. Kyle C. Wu
    View author publications

    Search author on:PubMed Google Scholar

  4. Matthew Torre
    View author publications

    Search author on:PubMed Google Scholar

  5. Hamza Ijaz
    View author publications

    Search author on:PubMed Google Scholar

  6. Favour Omafuvwe Obuseh
    View author publications

    Search author on:PubMed Google Scholar

  7. Brittany Pattison
    View author publications

    Search author on:PubMed Google Scholar

  8. Arthur Nedder
    View author publications

    Search author on:PubMed Google Scholar

  9. Francis McGovern
    View author publications

    Search author on:PubMed Google Scholar

  10. Jeremy Cannon
    View author publications

    Search author on:PubMed Google Scholar

  11. David J. Mooney
    View author publications

    Search author on:PubMed Google Scholar

  12. Benjamin R. Freedman
    View author publications

    Search author on:PubMed Google Scholar

Contributions

D.O.K., P.S.K., K.C.W., D.J.M., and B.R.F. conceived the study and designed the experiments. D.O.K., P.S.K., K.C.W., H.I., F.O.O., and B.R.F. performed the experiments and collected data. D.O.K., P.S.K., K.C.W., F.O.O., B.P., A.N., and B.R.F. contributed to animal procedures and data acquisition. M.T. performed histological analysis. D.O.K., K.C.W., F.M., and J.C. provided clinical input and assisted with study design and interpretation. P.S.K. and B.R.F. analyzed the data. D.O.K., P.S.K., K.C.W., and B.R.F. wrote the manuscript. D.J.M. and B.R.F. supervised the project. All authors reviewed and approved the final manuscript.

Corresponding authors

Correspondence to David J. Mooney or Benjamin R. Freedman.

Ethics declarations

Competing interests

B.R.F. has the following interests: Amend Surgical, licensed IP; Limax Biosciences, equity. D.J.M. has the following interests: Lyell, equity; Attivare, equity; IVIVA Medical, consulting and equity; J&J, consulting; Boston Scientific, consulting; Limax Biosciences, equity; Epoulosis, equity; Revela, equity; Amend Surgical and Sirenex, licensed IP. P.K. has the following interests: Limax Biosciences, equity. H.I. has the following interests: Limax Biosciences, equity. All other authors declare no competing interests.

Peer review

Peer review information

Nature Communications thanks Yaobin Wu, Haiqing Liu, and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. A peer review file is available.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Supplementary Information (download PDF )

Description of Additional Supplementary Files (download PDF )

Supplementary Movie 1 (download MOV )

Transparent Peer Review file (download PDF )

Source data

Source Data (download XLSX )

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kent, D.O., Kwon, P.S., Wu, K.C. et al. Hemostatic Tough Adhesives seal tissue and control hemorrhage. Nat Commun (2026). https://doi.org/10.1038/s41467-026-71235-z

Download citation

  • Received: 24 June 2025

  • Accepted: 12 March 2026

  • Published: 08 April 2026

  • DOI: https://doi.org/10.1038/s41467-026-71235-z

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

Download PDF

Advertisement

Explore content

  • Research articles
  • Reviews & Analysis
  • News & Comment
  • Videos
  • Collections
  • Subjects
  • Follow us on Facebook
  • Follow us on X
  • Sign up for alerts
  • RSS feed

About the journal

  • Aims & Scope
  • Editors
  • Journal Information
  • Open Access Fees and Funding
  • Calls for Papers
  • Editorial Values Statement
  • Journal Metrics
  • Editors' Highlights
  • Contact
  • Editorial policies
  • Top Articles

Publish with us

  • For authors
  • For Reviewers
  • Language editing services
  • Open access funding
  • Submit manuscript

Search

Advanced search

Quick links

  • Explore articles by subject
  • Find a job
  • Guide to authors
  • Editorial policies

Nature Communications (Nat Commun)

ISSN 2041-1723 (online)

nature.com footer links

About Nature Portfolio

  • About us
  • Press releases
  • Press office
  • Contact us

Discover content

  • Journals A-Z
  • Articles by subject
  • protocols.io
  • Nature Index

Publishing policies

  • Nature portfolio policies
  • Open access

Author & Researcher services

  • Reprints & permissions
  • Research data
  • Language editing
  • Scientific editing
  • Nature Masterclasses
  • Research Solutions

Libraries & institutions

  • Librarian service & tools
  • Librarian portal
  • Open research
  • Recommend to library

Advertising & partnerships

  • Advertising
  • Partnerships & Services
  • Media kits
  • Branded content

Professional development

  • Nature Awards
  • Nature Careers
  • Nature Conferences

Regional websites

  • Nature Africa
  • Nature China
  • Nature India
  • Nature Japan
  • Nature Middle East
  • Privacy Policy
  • Use of cookies
  • Legal notice
  • Accessibility statement
  • Terms & Conditions
  • Your US state privacy rights
Springer Nature

© 2026 Springer Nature Limited

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing