Cited by 428Polymer Surface Interaction StudiesSurgical Sutures and AdhesivesHydrogels: synthesis, properties, applications

Bio-inspired adhesive catechol-conjugated chitosan for biomedical applications: A mini review

Ryu, Ji Hyun, Hong, Seonki, Lee, Haeshin·2015·Acta Biomaterialia

Abstract

The development of adhesive materials, such as cyanoacrylate derivatives, fibrin glues, and gelatin-based adhesives, has been an emerging topic in biomaterial science because of the many uses of these materials, including in wound healing patches, tissue sealants, and hemostatic materials. However, most bio-adhesives exhibit poor adhesion to tissue and related surfaces due to the presence of body fluid. For a decade, studies have aimed at addressing this issue by developing wet-resistant adhesives. Mussels demonstrate robust wet-resistant adhesion despite the ceaseless waves at seashores, and mussel adhesive proteins play a key role in this adhesion. Adhesive proteins located at the distal end (i.e., those that directly contact surfaces) are composed of nearly 60% of amino acids called 3,4-dihydroxy-l-phenylalanine (DOPA), lysine, and histidine, which contain side chains of catechol, primary amines, and secondary amines, respectively. Inspired by the abundant catecholamine in mussel adhesive proteins, researchers have developed various types of polymeric mimics, such as polyethylenimine-catechol, chitosan-catechol, and other related catecholic polymers. Among them, chitosan-catechol is a promising adhesive polymer for biomedical applications. The conjugation of catechol onto chitosan dramatically increases its solubility from zero to nearly 60mg/mL (i.e., 6% w/v) in pH 7 aqueous solutions. The enhanced solubility maximizes the ability of catecholamine to behave similar to mus…

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Crossref · 10.1016/j.actbio.2015.08.043

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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].”

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Authors
Ryu, J. H., Hong, S., & Lee, H.
Affiliations
  • Korea Advanced Institute of Science and Technology (KR)
  • Massachusetts General Hospital (US)
Corresponding author
Lee, Haeshin
Venue
Acta Biomaterialia
Publisher
Elsevier BV
Published
2015-11
Volume
27
Pages
101-115
ISSN
1742-7061 (ISSN-L)
OpenAlex
W1189346619
Cited by
428
References
1
Citations by year
2026: 18 · 2025: 39 · 2024: 40 · 2023: 44 · 2022: 50 · 2021: 73 · 2020: 50 · 2019: 42 · 2018: 32 · 2017: 25 · 2016: 13
FWCI
1.49
Type
journal article
Language
en
Open access
closed
Locations
  • Acta Biomaterialia (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Research Foundation of South Korea (2015021564, 20090083525)
  • Ministry of Industry, Trade, and Natural Resources
Topics
  • Physical Sciences › Materials Science › Surfaces, Coatings and Films › Polymer Surface Interaction Studies
  • Health Sciences › Medicine › Surgery › Surgical Sutures and Adhesives
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Hydrogels: synthesis, properties, applications
Keywords
catechol, mussel adhesive proteins, bioinspired adhesives, wet adhesion, hemostatic materials, tissue adhesion, wound healing, chitosan solubility, tissue sealants
MeSH terms
Adhesiveness, Animals, Biocompatible Materials, Catechols, Hardness, Tensile Strength, Tissue Adhesives, Biomimetic Materials, Chitosan, Bivalvia, Nanoconjugates

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