Cited by 44Hemostasis and retained surgical itemsHydrogels: synthesis, properties, applicationsSurgical Sutures and Adhesives

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An in situ catechol functionalized ε-polylysine/polyacrylamide hydrogel formed by hydrogen bonding recombination with high mechanical property for hemostasis

Man, Zhang, Sidi, Li, Xubo, Yuan, Jin, Zhao, Xin, Hou·2021·International Journal of Biological Macromolecules

Abstract

In situ hydrogel has attracted widely attention in hemostasis due to its ability to match irregular defects, but its application is limited by insufficient mechanical strength and long gelation time. Although some specifical in situ chemically cross-linked hydrogels could be fast formed and exhibit high mechanical strength, they unable to absorb blood. Hence their applications were further limited in emergency hemostasis usage. In this study, a robust hydrogel formed by hydration of powders was developed using multiple hydrogen bonds crosslinking. Here, catechol groups modified ε-polylysine (PL-CAT) and polyacrylamide (PAAM) were used to construct the PL-CAT/PAAM hydrogel. This hydrogel could be formed within 7 s to adhere and seal bleeding sites. The catechol groups endowed the hydrogel outstanding adhesive strength, which was 3.5 times of fibrin glue. Besides, the mechanical performance of in-situ PL-CAT/PAAM hydrogel was explored and the results showed that the hydrogel exhibited high compressive strength (0.47 MPa at 85% strain). Most importantly, the blood loss of wound treated with PL-CAT/PAAM hydrogel powders was 1/7 of untreated group, indicating the hydrogel's excellent hemostatic effect. And the cytotoxicity studies indicated that the PL-CAT/PAAM hydrogel had low toxicity. To summarize, this hydrogel could be a potential hemostatic material in emergency situations.

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Crossref · 10.1016/j.ijbiomac.2021.09.100

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  • Using classic organic reactions, the catechol group has been successfully incorporated into a series of natural polymers, such as PL, HA, chitosan, SA, and gelatin, and synthetic polymers, such as PEG-based polymers.

    “Using these classic organic reactions, the catechol group has been successfully incorporated into a series of natural polymers, such as PL, HA, chitosan, SA, and gelatin (GT), and synthetic polymers, such as polyethylene glycol (PEG)-based polymers [45,47,51,52,53,54,55].”
  • Interactions including hydrogen bonding, π-π stacking, cation-π interactions, electrostatic forces, and hydrophobic effects are frequently employed to create self-healable hydrogel networks.

    “Interactions, including hydrogen bonding, π-π stacking, cation-π interactions, electrostatic forces, and hydrophobic effects, are frequently employed to create self-healable hydrogel networks [3,51].”

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Metadata

Authors
Man, Z., Sidi, L., Xubo, Y., Jin, Z., & Xin, H.
Affiliations
Tianjin University (CN)
Corresponding author
  • Jin, Zhao
  • Xin, Hou
Venue
International Journal of Biological Macromolecules
Publisher
Elsevier BV
Published
2021-11
Volume
191
Pages
714-726
ISSN
0141-8130 (ISSN-L)
OpenAlex
W3203050421
Cited by
44
References
0
Citations by year
2026: 5 · 2025: 7 · 2024: 11 · 2023: 9 · 2022: 12
FWCI
5.24
Type
journal article
Language
en
Open access
closed
Locations
  • International Journal of Biological Macromolecules (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Natural Science Foundation of China (51673144, 51673146, 51773151)
Topics
  • Health Sciences › Medicine › Hematology › Hemostasis and retained surgical items
  • Physical Sciences › Materials Science › Biomaterials › Hydrogels: synthesis, properties, applications
  • Health Sciences › Medicine › Surgery › Surgical Sutures and Adhesives
Keywords
in situ forming hydrogels, hemostasis, catechol functionalization, ε-polylysine, polyacrylamide, hydrogen bonding crosslinking, wound dressings, adhesion strength, compressive strength, blood loss reduction, emergency hemostasis, cytotoxicity
MeSH terms
Polyacrylamides, Acrylic Resins, Adhesives, Animals, Blood Cells, Catechols, Cell Line, Cells, Cultured, Fibroblasts, Hemostatics, Hydrogen Bonding, Polylysine, Tensile Strength, Hydrogels, Mice, Rats

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