TY - JOUR
T1 - Bio-inspired Incrustation Interfacial Polymerization of Dopamine and Cross-linking with Gelatin toward Robust, Biodegradable Three-Dimensional Hydrogels
AU - Abe, Hiroya
AU - Yabu, Hiroshi
N1 - Funding Information:
H.A. thanks Dr. Yuta Nakayasu, Tohoku University for helping with XPS measurements. H.A. wishes to acknowledge funding from KAKENHI, JSPS (grant no. 19K15598), a Research Institutes Ensemble Grant for Young Researchers, a Sasakawa Scientific Research Grant from the Japan Science Society, and the FRIS Creative Interdisciplinary Collaboration Program at Tohoku University. H.Y. wishes to acknowledge funding from KAKENHI, JSPS (grant nos. 18H05482 and 19KK0357).
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/5/25
Y1 - 2021/5/25
N2 - In nature, laccase enzymatically catalyzes the reaction of phenolic compounds with oxygen to produce hardened surfaces known as cuticles on insects and plants. Inspired by this natural process, the present work investigated a robust, biodegradable hydrogel synthesized from dopamine and gelatin. This gel is obtained by the oxidation of dopamine dissolved in water, after which the resulting quinone compound automatically undergoes self-polymerization. The oxidized dopamine subsequently undergoes Schiff base and Michael addition reactions with gelatin, such that the exposed gelatin surface cross-links to generate a continuous hardened hydrogel film. Because gelatin transitions between sol and gel states with changes in temperature, two- and three-dimensional structures could be obtained from the gel state. This bio-inspired interfacial cross-linking reaction provides a simple means of forming complex morphologies and represents a promising technique for bio-applications.
AB - In nature, laccase enzymatically catalyzes the reaction of phenolic compounds with oxygen to produce hardened surfaces known as cuticles on insects and plants. Inspired by this natural process, the present work investigated a robust, biodegradable hydrogel synthesized from dopamine and gelatin. This gel is obtained by the oxidation of dopamine dissolved in water, after which the resulting quinone compound automatically undergoes self-polymerization. The oxidized dopamine subsequently undergoes Schiff base and Michael addition reactions with gelatin, such that the exposed gelatin surface cross-links to generate a continuous hardened hydrogel film. Because gelatin transitions between sol and gel states with changes in temperature, two- and three-dimensional structures could be obtained from the gel state. This bio-inspired interfacial cross-linking reaction provides a simple means of forming complex morphologies and represents a promising technique for bio-applications.
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U2 - 10.1021/acs.langmuir.1c00364
DO - 10.1021/acs.langmuir.1c00364
M3 - Article
C2 - 33949870
AN - SCOPUS:85106536393
SN - 0743-7463
VL - 37
SP - 6201
EP - 6207
JO - Langmuir
JF - Langmuir
IS - 20
ER -