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Published on: January 17, 2019
Dual-Wavelength Responsive Hydrogel Glue with Visible-Light Bonding and UV-Triggered Debonding via Ortho-Nitrobenzyl
Huaming Wang1, Xianyan Shen1, Changling Du1
1Department of Pharmaceutical Science, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Abstract:
Removable adhesives with controllable bonding and debonding capabilities are essential for biomedical devices, temporary fixation, and recyclable materials. Here, a dual-wavelength hydrogel glue is presented that integrates visible-light polymerization (470 nm) for strong adhesion and UV-induced degradation (365 nm) for rapid debonding. The system leverages camphorquinone as a visible-light photoinitiator and ortho-nitrobenzyl poly(ethylene glycol) dimethacrylate (ONB-PEGDMA) as a UV-cleavable crosslinker, ensuring independent control over adhesion and detachment with orthogonal polymerization and degradation. The degradation rate of ONB-PEGDMA increases proportionally with light intensity, providing precise control over cleavage kinetics, with first-order rate constants of 0.155, 0.278, and 0.669 min-1 for 20, 50, and 100 mW cm- 2, respectively. The hydrogel exhibits strong adhesion (≈200 kPa) and undergoes a fourfold reduction in adhesion strength within 90 s of 365 nm irradiation at 100 mW cm- 2 under a constant tensile load of 10 N, enabling efficient removal. Rheological analysis confirms a significant decrease in storage modulus and crosslinking density after UV exposure, leading to network softening and structural failure. This work pioneers a phototunable hydrogel glue that bridges photopolymerization and photodegradation, offering a promising platform for next-generation adhesives with precise spatiotemporal control and with easy application, good bonding, and rapid UV-triggered debonding.
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Nucleotide Excision Repair
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...

