Cited by 378Polymer Surface Interaction StudiesConducting polymers and applicationsmelanin and skin pigmentation

Perspectives on poly(dopamine)

Dreyer, Daniel R., Miller, Daniel J., Freeman, Benny D., Paul, Donald R., Bielawski, Christopher W.·2013·Chemical Science

Abstract

Poly(dopamine) has emerged in recent years as a readily accessible synthetic analogue of the naturally occurring melanins. However, the polymer's structure has proved difficult to unambiguously elucidate and a variety of models have been proposed. Despite these challenges, poly(dopamine) has found extraordinary utility in a range of applications including surface coatings, biotechnology and biomedicine, and water purification membranes. Most of these applications take advantage of the robust polymer films that deposit onto a wide range of surfaces, as well as its inertness to harsh chemical environments. In view of the expansion of interest in poly(dopamine), we provide perspective on this material, focusing on its history, chemical relationship to melanins, recent applications, and potential areas for future study.

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Crossref · 10.1039/c3sc51501j

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1 of 1 references verified0 citation errors · 0 not checkable

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  • The adhesive mechanism of PDA on the interface of various substrates still remains debating due to the complexities of structural analysis of PDA and its analogous molecules such as eumelanin.

    “However, the adhesive mechanism of PDA on the interface of various substrates still remains debating due to the complexities of structural analysis of PDA and its analogous molecules such as eumelanin [32–35].”
  • The second model is the "noncovalent bonding (quinhydrones)" polymerization fashion where DA monomers are linked together by noncovalent interaction including hydrogen bonding, charge transfer, ionic interaction, and π-stacking to aggregate into a structural macroassembly.

    “The second model is the “noncovalent bonding (quinhydrones)” polymerization fashion where DA monomers are linked together by noncovalent interaction including hydrogen bonding, charge transfer, ionic interaction, and π-stacking to aggregate into a structural macroassembly [35, 45–47].”

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Authors
Dreyer, D. R., Miller, D. J., Freeman, B. D., Paul, D. R., & Bielawski, C. W.
Affiliations
  • The University of Texas at Austin (US)
  • Seoul National University (KR)
Corresponding author
  • Freeman, Benny D.
  • Paul, Donald R.
  • Bielawski, Christopher W.
Venue
Chemical Science
Published
2013
Volume
4
Issue
10
Pages
3796
ISSN
  • 2041-6520 (ISSN-L)
  • 2041-6539
OpenAlex
W2087581197
Cited by
378
References
1
Citations by year
2026: 7 · 2025: 16 · 2024: 14 · 2023: 26 · 2022: 38 · 2021: 20 · 2020: 32 · 2019: 40 · 2018: 36 · 2017: 37 · 2016: 37 · 2015: 37 · 2014: 33 · 2013: 5
FWCI
14.77
Type
journal article
Language
en
Open access
closed
Locations
  • Chemical Science (publishedVersion)
  • Scholarworks@UNIST (Ulsan National Institute of Science and Technology) (submittedVersion)
Funders
  • National Science Foundation
  • Welch Foundation
Topics
  • Physical Sciences › Materials Science › Surfaces, Coatings and Films › Polymer Surface Interaction Studies
  • Physical Sciences › Materials Science › Polymers and Plastics › Conducting polymers and applications
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › melanin and skin pigmentation
Keywords
polydopamine, melanin, polymer films, surface coating, biotechnology applications, biomedical applications, water purification membranes, chemical inertness

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