Cited by 668melanin and skin pigmentationPolymer Surface Interaction StudiesConducting polymers and applications

Polydopamine and Eumelanin: From Structure–Property Relationships to a Unified Tailoring Strategy

d’Ischia, Marco, Napolitano, Alessandra, Ball, Vincent, Chen, Chun-Teh, Buehler, Markus J.·2014·Accounts of Chemical Research

Abstract

CONSPECTUS: Polydopamine (PDA), a black insoluble biopolymer produced by autoxidation of the catecholamine neurotransmitter dopamine (DA), and synthetic eumelanin polymers modeled to the black functional pigments of human skin, hair, and eyes have burst into the scene of materials science as versatile bioinspired functional systems for a very broad range of applications. PDA is characterized by extraordinary adhesion properties providing efficient and universal surface coating for diverse settings that include drug delivery, microfluidic systems, and water-treatment devices. Synthetic eumelanins from dopa or 5,6-dihydroxyindoles are the focus of increasing interest as UV-absorbing agents, antioxidants, free radical scavengers, and water-dependent hybrid electronic-ionic semiconductors. Because of their peculiar physicochemical properties, eumelanins and PDA hold considerable promise in nanomedicine and bioelectronics, as they are biocompatible, biodegradable, and exhibit suitable mechanical properties for integration with biological tissues. Despite considerable similarities, very few attempts have so far been made to provide an integrated unifying perspective of these two fields of technology-oriented chemical research, and progress toward application has been based more on empirical approaches than on a solid conceptual framework of structure-property relationships. The present Account is an attempt to fill this gap. Following a vis-à-vis of PDA and eumelanin chemistries, i…

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Crossref · 10.1021/ar500273y

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  • The analogy of PDA to eumelanin is a useful approach to understand the chemical formation of PDA layer.

    “The analogy of PDA to eumelanin is a useful approach to understand the chemical formation of PDA layer [36].”

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Authors
d’Ischia, M., Napolitano, A., Ball, V., Chen, C.-T., & Buehler, M. J.
Affiliations
  • University of Naples Federico II (IT)
  • Inserm (FR)
  • Massachusetts Institute of Technology (US)
Corresponding author
  • d’Ischia, Marco
  • Ball, Vincent
  • Buehler, Markus J.
Venue
Accounts of Chemical Research
Published
2014-10-23
Volume
47
Issue
12
Pages
3541-3550
ISSN
  • 0001-4842 (ISSN-L)
  • 1520-4898
OpenAlex
W2071058847
Cited by
668
References
5
Citations by year
2026: 48 · 2025: 52 · 2024: 44 · 2023: 57 · 2022: 77 · 2021: 74 · 2020: 58 · 2019: 62 · 2018: 63 · 2017: 58 · 2016: 39 · 2015: 36
FWCI
22.09
Type
journal article
Language
en
Open access
closed
Locations
  • Accounts of Chemical Research (publishedVersion)
  • PubMed (publishedVersion)
  • Scuola Normale Superiore di Pisa (submittedVersion)
Funders
Ministero dell'Istruzione, dell'Università e della Ricerca
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › melanin and skin pigmentation
  • Physical Sciences › Materials Science › Surfaces, Coatings and Films › Polymer Surface Interaction Studies
  • Physical Sciences › Materials Science › Polymers and Plastics › Conducting polymers and applications
Keywords
polydopamine, structure-property relationships, dopaquinone, dopachrome, biomimetic materials, molecular disorder, hierarchy, molecular dynamics simulation, surface coating, UV absorption, antioxidants, radical scavengers
MeSH terms
Computer Simulation, Indoles, Melanins, Polymers, Drug Design, Molecular Structure

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