Gluing blood into gel by electrostatic interaction using a water-soluble polymer as an embolic agent
Open accessAbstract
Liquid embolic agents are widely used for the endovascular embolization of vascular conditions. However, embolization based on phase transition is limited by the adhesion of the microcatheter to the embolic agent, use of an organic solvent, unintentional catheter retention, and other complications. By mimicking thrombus formation, a water-soluble polymer that rapidly glues blood into a gel without triggering coagulation was developed. The polymer, which consists of cationic and aromatic residues with adjacent sequences, shows electrostatic adhesion with negatively charged blood substances in a physiological environment, while common polycations cannot. Aqueous polymer solutions are injectable through clinical microcatheters and needles. The formed blood gel neither adhered to the catheter nor blocked the port. Postoperative computed tomography imaging showed that the polymer can block the rat femoral artery in vivo and remain at the injection site without nontarget embolization. This study provides an alternative for the development of waterborne embolic agents.
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BA and PEA effectively expel water from the contact interface, and when neighbouring with ATAC, they could enhance electrostatic interactions with the negatively charged glass surface.
“This is because BA and PEA effectively expel water from the contact interface, and, when neighbouring with ATAC (Supplementary Fig. 11), they could enhance electrostatic interactions with the negatively charged glass surface27,40–43 (Supplementary Fig. 12).”
From Data-driven de novo design of super-adhesive hydrogels (2025) · cites this paper as [41]
The Conclusions (page unavailable) state that polymers with adjacent cationic and aromatic groups interact electrostatically with negatively charged blood substances in saline water; the Formation of Blood Gel section contrasts this with ATAC alone. Our copy does not establish that BA and PEA expel interfacial water or that they enhance interaction specifically with a negatively charged glass surface. (LLM, conf=0.85)
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- Authors
- Jin, Z., Fan, H., Osanai, T., Nonoyama, T., Kurokawa, T., Hyodoh, H., Matoba, K., Takeuchi, A., Gong, J. P., & Fujimura, M.
- Affiliations
- Hokkaido University (JP)
- Corresponding author
- Fan, Hailong
- Osanai, Toshiya
- ORCID
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2022-10-10
- Volume
- 119
- Issue
- 42
- Pages
- e2206685119-e2206685119
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC9586266
- OpenAlex
- W4304098326
- Cited by
- 16
- References
- 33
- Citations by year
- 2026: 2 · 2025: 6 · 2024: 6 · 2023: 2
- FWCI
- 1.15
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Hokkaido University Collection of Scholarly and Academic Papers (Hokkaido University) (submittedVersion)
- Institutional Repositories DataBase (IRDB) (submittedVersion)
- Funders
- Japan Society for the Promotion of Science (23K21134, 20K10287, 21K14676, 22H04968)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Hydrogels: synthesis, properties, applications
- Health Sciences › Medicine › Genetics › Vascular Anomalies and Treatments
- Health Sciences › Medicine › Hematology › Hemostasis and retained surgical items
- Keywords
- water-soluble polymers, liquid embolic agents, endovascular embolization, electrostatic interactions, cationic polymers, femoral artery occlusion, nontarget embolization, injectable polymers
- MeSH terms
- Animals, Embolization, Therapeutic, Polymers, Solvents, Water, Rats, Static Electricity
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