journal article·2026-01-15Open access

Allomelanin: A Promising Alternative to Polydopamine for Bioapplications

Silvia Vicenzi, Agata Pane, Chiara Mattioli, Dario Mordini, Arianna Menichetti, Marco Montalti

Abstract

Allomelanin is a natural class of melanin found mainly in fungi and derived from nitrogen-free precursors such as 1,8-dihydroxynaphthalene (1,8-DHN). Despite its biological relevance, allomelanin remains significantly less explored than other synthetic melanin analogs, particularly compared to polydopamine, a synthetic analog of eumelanin. In this review, we provide a comprehensive overview of current knowledge on allomelanin, summarizing the main methods used to characterize its molecular structure, morphology, and chemical functionalities. We also present its emerging applications, ranging from human health to materials science, highlighting how its optical characteristics, ability to modulate redox processes, and antioxidant properties support its growing technological interest. Finally, we describe the natural presence and biological role of allomelanin, highlighting how knowledge of its biosynthetic processes and functions in nature can guide more effective strategies for the design and optimization of new allomelanin materials.
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Research context

OpenAlex topics: melanin and skin pigmentation · Silk-based biomaterials and applications · Mast cells and histamine

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry “Giacomo Ciamician”, University of Bologna, Via Selmi 2, 40126 Bologna, Italy

Tecnopolo di Rimini, Via Campana 71, 47921 Rimini, Italy

Funding

PRIN 2022 PNRR, Nanotherm

References (71)

Show source-provided references
1. Mavridi-Printezi, A., Menichetti, A., Mordini, D., Amorati, R., and Montalti, M. (2023). Recent Applications of Melanin-like Nanoparticles as Antioxidant Agents. Antioxidants, 12.10.3390/antiox12040863 ↗
2. From melanogenesis to melanin technologies10.1038/s42004-025-01731-8 ↗
3. Unraveling the Structure and Function of Melanin through Synthesis10.1021/jacs.0c12322 ↗
4. Superior photoprotective motifs and mechanisms in eumelanins uncovered10.1021/ja501499q ↗
5. Menichetti, A., Mordini, D., Vicenzi, S., Pane, A., and Montalti, M. (2025). Unexplored Mechanisms of Photoprotection: Synergistic Light Absorption and Antioxidant Activity of Melanin. Antioxidants, 14.10.3390/antiox14040376 ↗
6. Melanin and Light10.1002/chem.202400461 ↗
7. Polydopamine and Its Derivative Materials: Synthesis and Promising Applications in Energy, Environmental, and Biomedical Fields10.1021/cr400407a ↗
8. Polydopamine and Its Derivative Surface Chemistry in Material Science: A Focused Review for Studies at KAIST10.1002/adma.201907505 ↗
9. Polydopamine Surface Chemistry: A Decade of Discovery10.1021/acsami.7b19865 ↗
10. Menichetti, A., Vicenzi, S., Pane, A., Mordini, D., Mancin, F., and Montalti, M. (2025). Photothermal Release by Melanin-like Nanoparticles: Biomedical Applications. J. Funct. Biomater., 16.10.3390/jfb16070243 ↗
11. Menichetti, A., Mordini, D., and Montalti, M. (2024). Melanin as a Photothermal Agent in Antimicrobial Systems. Int. J. Mol. Sci., 25.10.3390/ijms25168975 ↗
12. Mimicking Melanosomes: Polydopamine Nanoparticles as Artificial Microparasols10.1021/acscentsci.6b00230 ↗
13. Topical application of synthetic melanin promotes tissue repair10.1038/s41536-023-00331-1 ↗
14. Menichetti, A., Mordini, D., Vicenzi, S., and Montalti, M. (2024). Melanin for Photoprotection and Hair Coloration in the Emerging Era of Nanocosmetics. Int. J. Mol. Sci., 25.10.3390/ijms25115862 ↗
15. Polydopamine-inspired nanomaterials for energy conversion and storage10.1039/C8TA05245J ↗
16. Melanin: A Greener Route To Enhance Energy Storage under Solar Light10.1021/acsomega.9b01039 ↗
17. Omidian, H., and Wilson, R.L. (2024). Polydopamine Applications in Biomedicine and Environmental Science. Materials, 17.10.3390/ma17163916 ↗
18. Nanofibrous Photothermal Materials from Natural Resources: A Green Approach for Artwork Restoration10.1021/acsami.4c14532 ↗
19. The dual nature of biomimetic melanin
20. Bio-Inspired Structural Colors Produced via Self-Assembly of Synthetic Melanin Nanoparticles10.1021/acsnano.5b01298 ↗
21. Pralea, I.E., Moldovan, R.C., Petrache, A.M., Ilieș, M., Hegheș, S.C., Ielciu, I., Nicoară, R., Moldovan, M., Ene, M., and Radu, M. (2019). From Extraction to Advanced Analytical Methods: The Challenges of Melanin Analysis. Int. J. Mol. Sci., 20.10.3390/ijms20163943 ↗
22. Allomelanin: A Biopolymer of Intrinsic Microporosity10.1021/jacs.1c00748 ↗
23. Artificial Allomelanin Nanoparticles10.1021/acsnano.9b02160 ↗
24. Natural Eumelanin and Its Derivatives as Multifunctional Materials for Bioinspired Applications: A Review10.1021/acs.biomac.9b01413 ↗
25. Photochemical Pathways and Light-Enhanced Radical Scavenging Activity of 1,8-Dihydroxynaphthalene Allomelanin10.1021/jacs.5c01855 ↗
26. Anisotropic Synthetic Allomelanin Materials via Solid-State Polymerization of Self-Assembled 1,8-Dihydroxynaphthalene Dimers10.1002/anie.202103447 ↗
27. Synthesis and characterization of allomelanin model from 1,8-dihydroxynaphthalene autooxidation10.1038/s41598-024-84405-0 ↗
28. Synthetic fungal melanin UV absorbers10.1007/s11426-024-2034-x ↗
29. Mavridi-Printezi, A., Mollica, F., Lucernati, R., Montalti, M., and Amorati, R. (2023). Insight into the Antioxidant Activity of 1,8-Dihydroxynaphthalene Allomelanin Nanoparticles. Antioxidants, 12.10.3390/antiox12081511 ↗
30. Regulating the absorption spectrum of polydopamine10.1126/sciadv.abb4696 ↗
31. Ultrafast spectral hole burning reveals the distinct chromophores in eumelanin and their common photoresponse10.1039/C9SC04527A ↗
32. Probing the heterogeneous structure of eumelanin using ultrafast vibrational fingerprinting10.1038/s41467-020-18393-w ↗
33. Sub-50 fs Formation of Charge Transfer States Rules the Fate of Photoexcitations in Eumelanin-Like Materials10.1021/acs.jpclett.4c00170 ↗
34. Photothermal motion: Effect of low-intensity irradiation on the thermal motion of organic nanoparticles10.1039/D2NR01041K ↗
35. Applications and challenges of thermoplasmonics10.1038/s41563-020-0740-6 ↗
36. Photodynamic and Photothermal Therapies: Synergy Opportunities for Nanomedicine10.1021/acsnano.3c00891 ↗
37. Polydopamine-based nanoplatform for photothermal ablation with long-term immune activation against melanoma and its recurrence10.1016/j.actbio.2021.09.014 ↗
38. Drug-Loaded Polydopamine Nanoparticles for Chemo/Photothermal Therapy against Colorectal Cancer Cells10.1021/acsabm.3c01203 ↗
39. Polydopamine-based nanostructures: A new generation of versatile, multi-tasking, and smart theranostic tools10.1016/j.nantod.2024.102151 ↗
40. Hydrophobic Melanin via Post-Synthetic Modification for Controlled Self-Assembly10.1021/acsnano.2c08114 ↗
41. Munteanu, I.G., and Apetrei, C. (2021). Analytical Methods Used in Determining Antioxidant Activity: A Review. Int. J. Mol. Sci., 22.10.3390/ijms22073380 ↗
42. Relationships between Free Radical Scavenging and Antioxidant Activity in Foods10.1021/jf803436c ↗
43. Polydopamine Nanoparticles as a Potential Non-Pharmaceutical Antioxidant Tool against Mitochondrial Disorders10.1021/acsanm.5c03169 ↗
44. Gulcin, İ., and Alwasel, S.H. (2023). DPPH Radical Scavenging Assay. Processes, 11.10.3390/pr11082248 ↗
45. Hydrogen Atom Transfer from HOO to ortho-Quinones Explains the Antioxidant Activity of Polydopamine10.1002/anie.202101033 ↗
46. Allomelanin-based biomimetic nanotherapeutics for orthotopic glioblastoma targeted photothermal immunotherapy10.1016/j.actbio.2023.05.037 ↗
47. Nanomodulators Capable of Timely Scavenging ROS for Inflammation and Prognosis Control Following Photothermal Tumor Therapy10.1002/adfm.202213151 ↗
48. A hyaluronic acid hydrogel as a mild photothermal antibacterial, antioxidant, and nitric oxide release platform for diabetic wound healing10.1016/j.jconrel.2024.05.011 ↗
49. Versatile conductive hydrogel orchestrating neuro–immune microenvironment for rapid diabetic wound healing through peripheral nerve regeneration10.1016/j.biomaterials.2024.122841 ↗
50. Zhang, Y.G., Malo, M.E., Tschirhart, T., Xia, Y., Wang, Z., Dadachova, E., and Sun, J. (2023). Effects of Melanized Bacteria and Soluble Melanin on the Intestinal Homeostasis and Microbiome In Vivo. Toxics, 11.10.3390/toxics11010013 ↗
51. Ototoxicity-Alleviating and Cytoprotective Allomelanin Nanomedicine for Efficient Sensorineural Hearing Loss Treatment
52. Porous polymer-modified metal–organic framework (AM@UIO-66-NH2) for electrochemical detection of dopamine in human serum10.1016/j.micromeso.2025.113726 ↗
53. Reusable melanin-based biosorbents for efficient methylene blue removal: The new frontier of fungi-inspired allomelanin coatings for sustainable water remediation processes
54. Silver Nanocatalysts Supported by Multiple Melanin Carriers with a Photothermal Effect for Reduction of Methylene Blue and 4-Nitrophenol10.1021/acsanm.3c04882 ↗
55. Metal-Organic Frameworks with a Bioinspired Porous Polymer Coating for Sieving Separation10.1021/jacs.3c02195 ↗
56. Li, Q., Guo, Y., Wu, M., Deng, F., Feng, J., Liu, J., Liu, S., Ouyang, C., Duan, W., and Yi, S. (2023). Fluorinated Polyimide/Allomelanin Nanocomposites for UV-Shielding Applications. Molecules, 28.10.3390/molecules28145523 ↗
57. Allomelanin-Inspired Polyurethane Nanocomposites with Multi-Radiation Resistance and Enhanced Mechanical Properties10.1021/acsami.5c05674 ↗
58. Isolation and Characterization of Allomelanin from Pathogenic Black Knot Fungus─A Sustainable Source of Melanin10.1021/acsomega.1c05030 ↗
59. Qiu, Z., Wang, S., Zhao, J., Cui, L., Wang, X., Cai, N., Li, H., Ren, S., Li, T., and Shu, L. (2023). Synthesis and structural characteristics analysis of melanin pigments induced by blue light in Morchella sextelata. Front. Microbiol., 14.10.3389/fmicb.2023.1276457 ↗
60. Ahn, S.Y., Jang, S., Sudheer, P.D.V.N., and Choi, K.Y. (2021). Microbial production of melanin pigments from caffeic acid and l-tyrosine using streptomyces glaucescens and fcs-ech-expressing escherichia coli. Int. J. Mol. Sci., 22.10.3390/ijms22052413 ↗
61. Alfieri, M.L., Panzella, L., Oscurato, S.L., Salvatore, M., Avolio, R., Errico, M.E., Maddalena, P., Napolitano, A., and D’Ischia, M. (2018). The Chemistry of Polydopamine Film Formation: The Amine-Quinone Interplay. Biomimetics, 3.10.3390/biomimetics3030026 ↗
62. Direct Evidence for the Polymeric Nature of Polydopamine10.1002/anie.201811763 ↗
63. Mussel-inspired surface chemistry for multifunctional coatings10.1126/science.1147241 ↗
64. Polydopamine films: Electrochemical growth and sensing applications10.1016/j.eurpolymj.2022.111346 ↗
65. Polydopamine-based functional materials and their applications in energy, environmental, and catalytic fields: State-of-the-art review10.1016/j.cej.2020.124019 ↗
66. Mavridi-Printezi, A., Menichetti, A., Mordini, D., and Montalti, M. (2023). Functionalization of and through Melanin: Strategies and Bio-Applications. Int. J. Mol. Sci., 24.10.3390/ijms24119689 ↗
67. New insights in polydopamine formation via surface adsorption10.1038/s41467-023-36303-8 ↗
68. Chemistry of Polydopamine—Scope, Variation, and Limitation10.1002/ejoc.201900445 ↗
69. Laser-induced graphitization of polydopamine leads to enhanced mechanical performance while preserving multifunctionality10.1038/s41467-020-18654-8 ↗
70. Laser-Induced Graphitization of Polydopamine on Titania Nanotubes
71. Dihydroxynaphthalene-Based Allomelanins: A Source of Inspiration for Innovative Technological Materials10.1021/acsomega.2c00641 ↗