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New insights into underwater adhesives
Photograph of the fabricated flexible interlocking adhesive (left) and a SEM image (center) of the PEGDMA microhook arrays of the adhesive. Shown on right is the conceptual illustration of the reversible interlocking of the PEGDMA microhook arrays via the hydration-induced shape reconfiguration of the array for high adhesion under wet conditions.
18-Jan-2018: A Korean research team, affiliated with UNIST has presented a new type of underwater adhesives that are tougher than the natural biological glues that mussels normally use to adhere to rocks, ships, and larger sea critters. This has attracted much attention as a technology that surpass the limits of conventional chemical-based adhesives that significantly lose adhesion capability when exposed to moisture or when reused.
This breakthrough has been led by Professor Hoon-Eui Jeong in the School of Mechanical Aerospace and Nuclear Engineering and his research team at UNIST.
Wet adhesives are substances that are applied to the joining surfaces in the fluid state. According to the research team, stable adhesion between surfaces under wet conditions is highly desirable for many practical applications, particularly in the bioengineering and medical fields, where most surfaces are wet. However, limitations in complicated surface treatment and expensive protocols restrain the extensive use of these natural protein adhesives. Furthermore, they are typically permanent adhesives, and therefore, have limitations for application as a reversible and reusable adhesive.
Professor Jeong solved such issues using the simple hydrogel microstructures alone. In the study, the research team presented a wet-responsive, shape-reconfigurable, and flexible hydrogel adhesives that exhibit strong adhesion under wet environments based on reversible interlocking between reconfigurable microhook arrays.
The microhooks of the adhesive were designed to exhibit a unique structural configuration with protruding heads. The adhesion between the interlocked microhook arrays is greatly enhanced under wet conditions because of the hydration-triggered shape reconfiguration of the hydrogel microstructures. Furthermore, this water-responsive shape change was reversible and the microstructure can recover its original shape and size upon water removal by drying.
"These adhesives take the form of thin flexible films with bioinspired mushroom-shaped micropillars uniformly spread on the surface of microstructure," says Hyun-Ha Park in the Ph.D. program of Mechanical Engineering, the first author of the study. "When the interlocked arrays are exposed to water, a notable volume expansion of a corresponding shape transformation of the hydrogel microhooks occurred by the swelling of the hydrogel, resulting in significantly increased wet adhesion both in the shear and normal directions."
The research team notes, "In contrast to other wet binding systems, the current interlocking mechanism does not involve any complicated surface treatment or chemical moieties, thus allowing for a simple yet efficient route to strong and reversible wet adhesion in a cost-effective manner."
"The surface of the conventional chemical adhesives softens or dissolves when exposed to moisture or water, which can lead to a significant decrease in adhesive bond strength or loss of adhesion over time," says Professor Jeong. "In contrast to other wet binding systems, the current interlocking mechanism does not involve any complicated surface treatment or chemical moieties, thus allowing for a simple yet efficient route to strong and reversible wet adhesion in a cost-effective manner."
"This wet-responsive and reversible hydrogel interlocking adhesive can serve as a robust and versatile wet adhesive for a broad range of applications which require stable and strong adhesion under diverse wet conditions," Professor Jeong adds.
Hyun-Ha Park, Minho Seong, Kahyun Sun, Hangil Ko, Sang Moon Kim, and Hoon Eui Jeong; "Flexible and Shape-Reconfigurable Hydrogel Interlocking Adhesives for High Adhesion in Wet Environments Based on Anisotropic Swelling of Hydrogel Microstructures"; ACS Macro Letters; 2017