Cited by 726Polymer composites and self-healingHydrogels: synthesis, properties, applicationsSupramolecular Self-Assembly in Materials

Rapid self-healing hydrogels

Open access
Phadke, Ameya, Zhang, Chao, Arman, Bedri, Hsu, Cheng-Chih, Mashelkar, Raghunath A., Lele, Ashish K., Tauber, Michael J., Arya, Gaurav +1 more·2012·Proceedings of the National Academy of Sciences

Abstract

Synthetic materials that are capable of autonomous healing upon damage are being developed at a rapid pace because of their many potential applications. Despite these advancements, achieving self-healing in permanently cross-linked hydrogels has remained elusive because of the presence of water and irreversible cross-links. Here, we demonstrate that permanently cross-linked hydrogels can be engineered to exhibit self-healing in an aqueous environment. We achieve this feature by arming the hydrogel network with flexible-pendant side chains carrying an optimal balance of hydrophilic and hydrophobic moieties that allows the side chains to mediate hydrogen bonds across the hydrogel interfaces with minimal steric hindrance and hydrophobic collapse. The self-healing reported here is rapid, occurring within seconds of the insertion of a crack into the hydrogel or juxtaposition of two separate hydrogel pieces. The healing is reversible and can be switched on and off via changes in pH, allowing external control over the healing process. Moreover, the hydrogels can sustain multiple cycles of healing and separation without compromising their mechanical properties and healing kinetics. Beyond revealing how secondary interactions could be harnessed to introduce new functions to chemically cross-linked polymeric systems, we also demonstrate various potential applications of such easy-to-synthesize, smart, self-healing hydrogels.

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Crossref · 10.1073/pnas.1201122109

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  • Chemically crosslinked hydrogels are crosslinked by covalent bonding, resulting in superior mechanical deformability.

    “chemically crosslinked hydrogels are crosslinked by covalent bonding between polymer chains, resulting in superior mechanical deformability”

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Authors
Phadke, A., Zhang, C., Arman, B., Hsu, C.-C., Mashelkar, R. A., Lele, A. K., Tauber, M. J., Arya, G., & Varghese, S.
Affiliations
  • Departments of Bioengineering,
  • NanoEngineering, and
  • University of California San Diego (US)
  • National Chemical Laboratory (IN)
Venue
Proceedings of the National Academy of Sciences
Published
2012-03-05
Volume
109
Issue
12
Pages
4383-4388
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2008346231
Cited by
726
References
0
Citations by year
2026: 33 · 2025: 25 · 2024: 40 · 2023: 36 · 2022: 52 · 2021: 62 · 2020: 66 · 2019: 81 · 2018: 76 · 2017: 67 · 2016: 56 · 2015: 41 · 2014: 40 · 2013: 36 · 2012: 14
FWCI
32.96
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • California Institute of Regenerative Medicine (RN2-00945)
  • University of California, San Diego
Topics
  • Physical Sciences › Materials Science › Polymers and Plastics › Polymer composites and self-healing
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Hydrogels: synthesis, properties, applications
  • Physical Sciences › Materials Science › Biomaterials › Supramolecular Self-Assembly in Materials
Keywords
self-healing hydrogels, hydrogen bonding, steric hindrance, hydrophobic collapse, secondary interactions, stimuli-responsive hydrogels, mechanical properties
MeSH terms
Amino Acids, Buffers, Cross-Linking Reagents, Hydrogen Bonding, Hydrogen-Ion Concentration, Materials Testing, Molecular Conformation, Polystyrenes, Spectrum Analysis, Raman, Stress, Mechanical, Temperature, Urea, Water, Spectroscopy, Fourier Transform Infrared, Hydrogels, Hydrogel, Polyethylene Glycol Dimethacrylate, Biomimetics

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