Building‐Block Diversity in Polydopamine Underpins a Multifunctional Eumelanin‐Type Platform Tunable Through a Quinone Control Point
Abstract
Rational approaches to engineering polydopamine films with tailored properties for surface coating and functionalization are currently challenged by the lack of detailed information about the polymer structure and the mechanism of buildup. Using an integrated chemical and spectroscopic approach enables the demonstration of: a) a three‐component structure of polydopamine, comprising uncyclized (catecholamine) and cyclized (indole) units, as well as novel pyrrolecarboxylic acid moieties; b) remarkable variations in the relative proportions of the cyclized and uncyclized units with starting dopamine concentration; c) the occurrence of oligomer components up to the tetramer level; d) the covalent incorporation of Tris buffer; and e) the role of dopamine quinone as a crucial control point for directing the buildup pathways and tuning the properties. The importance of the uncyclized amine‐containing units in polydopamine adhesion is also highlighted. The proper selection of substrate concentration and buffer is thus proposed as a practical means of tailoring polydopamine functionality via control of competing pathways downstream of dopamine quinone.
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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].”
From Polydopamine-Assisted Surface Modification for Bone Biosubstitutes (2016) · cites this paper as [45]
Cites
5,6-Dihydroxyindoles and indole-5,6-diones
d’Ischia, M., Napolitano, A., Pezzella, A., Land, E. J., Ramsden, C. A., & Riley, P. A. (2005) · Advances in Heterocyclic Chemistry · doi:10.1016/s0065-2725(05)89001-4 · Cited by 86 · see citing works
Self-citation5,6‐Dihydroxyindole Chemistry: Unexplored Opportunities Beyond Eumelanin
d'Ischia, M., Napolitano, A., & Pezzella, A. (2011) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201100796 · Cited by 62 · see citing works
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Melanins and melanogenesis: Methods, standards, protocols
d'Ischia, M., Wakamatsu, K., Napolitano, A., Briganti, S., Garcia‐Borron, J., Kovacs, D., Meredith, P., Pezzella, A., Picardo, M., Sarna, T., et al. (2013) · Pigment Cell & Melanoma Research · doi:10.1111/pcmr.12121 · Cited by 484 · see citing works
Self-citationAdvances in functionalized polymer coatings on biodegradable magnesium alloys–A review
Li, L.-Y., Cui, L.-Y., Zeng, R.-C., Li, S.-Q., Chen, X.-B., Zheng, Y., & Kannan, M. B. (2018) · Acta Biomaterialia · doi:10.1016/j.actbio.2018.08.030 · Cited by 466 · see citing works
Polydopamine-Assisted Surface Modification for Bone Biosubstitutes
Huang, S., Liang, N., Hu, Y., Zhou, X., & Abidi, N. (2016) · BioMed Research International · doi:10.1155/2016/2389895 · Cited by 97 · see citing works
- Authors
- Della Vecchia, N. F., Avolio, R., Alfè, M., Errico, M. E., Napolitano, A., & d'Ischia, M.
- Affiliations
- National Research Council (IT)
- University of Naples Federico II (IT)
- Venue
- Advanced Functional Materials
- Publisher
- Wiley
- Published
- 2012-10-09
- Volume
- 23
- Issue
- 10
- Pages
- 1331-1340
- ISSN
- 1616-301X (ISSN-L)
- 1616-3028
- OpenAlex
- W1970209371
- Cited by
- 582
- References
- 2
- Citations by year
- 2026: 25 · 2025: 29 · 2024: 47 · 2023: 40 · 2022: 43 · 2021: 47 · 2020: 54 · 2019: 61 · 2018: 50 · 2017: 41 · 2016: 44 · 2015: 35 · 2014: 44 · 2013: 20 · 2012: 2
- FWCI
- 14.27
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Advanced Functional Materials (publishedVersion)
- Scuola Normale Superiore di Pisa (submittedVersion)
- Topics
- Physical Sciences › Materials Science › Surfaces, Coatings and Films › Polymer Surface Interaction Studies
- Physical Sciences › Materials Science › Polymers and Plastics › Conducting polymers and applications
- Physical Sciences › Engineering › Ocean Engineering › Marine Biology and Environmental Chemistry
- Keywords
- polydopamine, dopamine quinone, catecholamines, indole, oligomerization, polymer film structure, surface coating, surface functionalization, adhesion, polymerization pathways
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