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Editorial ARTICLE

Front. Chem., 20 December 2019 | https://doi.org/10.3389/fchem.2019.00883

Editorial: Catechol and Polyphenol Chemistry for Smart Polymers

  • 1Department of Biomedical Engineering, Michigan Technological University, Houghton, MI, United States
  • 2Department of Chemistry, Aarhus University, Aarhus, Denmark
  • 3Department of Chemistry, Korea Advanced Institute of Science and Technology, Daejeon, South Korea

This special issue of Frontiers in Chemistry features papers that utilize phenolic compounds such as catechols for designing functional coatings and materials. Recently, scientists worldwide have incorporated catechols and various phenolic compounds in designing advanced and multifunctional materials with unique properties (e.g., self-healing, underwater adhesion, stimuli responsive properties, etc.) (Forooshani and Lee, 2017; Andersen et al., 2019). These materials have potential in a wide range of applications in the biomedical, energy, industrial, and possibly other fields. The reasons for the wide adoption of phenolic compounds in material design is due to the unique ability of these compounds to participate in both irreversible and reversible interactions. This diversity in chemistry enable these phenolic compounds to function as adhesive primer to wide ranges of surfaces. Most importantly, by simply functionalizing polymeric materials with phenolic compounds, these initially inert materials are imparted with the unique properties (e.g., adhesive property, redox active, etc.) of these phenolic compounds.

Jalaber et al. employed atmospheric aerosol assisted pulsed plasma process to directly polymerize a catechol-modified monomer, dopamine acrylamide, and directly deposit catechol-containing thin films on to a surface. This process occurred in a dry and catalyst-free condition, and overcame limitations associated with polymerization in a solution that often resulted in poor wetting and the formation of inhomogeneous coatings. The plasma discharge rate and timing were used to tune the morphology, deposition rate and catechol content for creating homogeneous catechol-bearing polymer thin films.

The formation of polydopamine coatings involves the autoxidation and crosslinking of dopamine to form an adhesive primer for additional surface functionalization (Ryu et al., 2018). Alfieri et al. reported the effect of aliphaticdiamine, hexamethylenediamine (HMDA), on the polymerization process of dopamine to form a polydopamine coating. HMDA promoted intermolecular crosslinking between the oxidized form of catechol and subsequently promoted film deposition. This article further confirmed the use of resorcinol as an inhibitor to polydopamine formation.

Forooshani et al. utilized polydopamine to design antimicrobial coatings that releases the disinfectant, hydrogen peroxide (H2O2) when the coating was hydrated in an aqueous solution. H2O2 is generated as a byproduct during catechol autoxidation (Meng et al., 2015). Polydopamine was coated onto inert polypropylene mesh, which is often used in soft tissue reconstruction surgery. A two-step coating approach was used to optimize the coating for H2O2 generation and the generated H2O2 was effective against both gram positive and negative bacteria.

Tyo et al. investigated the effect of H2O2 generated from polydopamine coating on Psychrobacter cryohalolentis, the most common bacteria found on the surface of humpback whale skin. The generated H2O2 was found to be biostatic against P. cryohalolentis and reduced its attachment. Polydopamine coating can potentially be used to impart antimicrobial properties to satellite telemetry tags used for tracking the migration patterns of large cetaceans, which is a critical first step in the conservation of these animals.

Kim et al. provided a mini-review that discussed the pro- and antioxidant properties of catechol containing chitosan films. This review describe the methods of fabrication and characterization of the film. Conditions that promoted either the antioxidant or pro-oxidant behavior of the redox active catechol film were also reviewed, which can potentially be useful for designing functional materials aimed at radical scavenging activities or antimicrobial functions.

Yang and Lee utilize the adhesive property of catechol to create a lubricious, antifouling hydrogel coating to prevent the binding of bacteria to urethral catheter. Catechol was chemically linked to three types of biopolymers (chitosan, hyaluronic acid, and human serum albumin) and coated onto various elastomers commonly used to fabricate urethral catheters. The coating significantly lowered the friction coefficient of the elastomers. Additionally, incorporation of silver nanoparticles into the coating enhanced the antimicrobial property of the coating.

Author Contributions

All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

Andersen, A., Chen, Y. Q., and Birkedal, H. (2019). Bioinspired metal-polyphenol materials: self-healing and beyond. Biomimetics 4:30. doi: 10.3390/biomimetics4020030

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Forooshani, P. K., and Lee, B. P. (2017). Recent approaches in designing bioadhesive materials inspired by mussel adhesive protein. J. Polym. Sci. Part A Polym. Chem. 55, 9–33. doi: 10.1002/pola.28368

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Meng, H., Li, Y., Faust, M., Konst, S., and Lee, B. P. (2015). Hydrogen peroxide generation and biocompatibility of hydrogel-bound mussel adhesive moiety. Acta Biomater. 17, 160–169. doi: 10.1016/j.actbio.2015.02.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Ryu, J. H., Messersmith, P. B., and Lee, H. (2018). Polydopamine surface chemistry: a decade of discovery. ACS Appl. Mater. Interfaces 10, 7523–7540. doi: 10.1021/acsami.7b19865

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Keywords: catechol, polymer, smart materials, polyphenol, interface

Citation: Lee BP, Birkedal H and Lee H (2019) Editorial: Catechol and Polyphenol Chemistry for Smart Polymers. Front. Chem. 7:883. doi: 10.3389/fchem.2019.00883

Received: 20 November 2019; Accepted: 06 December 2019;
Published: 20 December 2019.

Edited and reviewed by: Pellegrino Musto, Italian National Research Council (CNR), Italy

Copyright © 2019 Lee, Birkedal and Lee. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Bruce P. Lee, bplee@mtu.edu