Design of Stretchable and Conductive Self-Adhesive Hydrogels as Flexible Sensors by Guar-Gum-Enabled Dynamic Interactions.
Yali LiYanru LiuHui LiuShengsheng YuZhaowen BaMingming LiuShuanhong MaLing-Bao XingPublished in: Langmuir : the ACS journal of surfaces and colloids (2024)
The limited elasticity and inadequate bonding of hydrogels made from guar gum (GG) significantly hinder their widespread implementation in personalized wearable flexible electronics. In this study, we devise GG-based self-adhesive hydrogels by creating an interpenetrating network of GG cross-linked with acrylic, 4-vinylphenylboronic acid, and Ca 2+ . With the leverage of the dynamic interactions (hydrogen bonds, borate ester bonds, and coordination bonds) between -OH in GG and monomers, the hydrogel exhibits a high stretchability of 700%, superior mechanical stress of 110 kPa, and robust adherence to several substrates. The adhesion strength of 54 kPa on porcine skin is obtained. Furthermore, the self-adhesive hydrogel possesses stable conductivity, an elevated gauge factor (GF), and commendable durability. It can be affixed to the human body as a strain sensor to obtain precise monitoring of human movement behavior. Our research offers possibilities for the development of GG-based hydrogels and applications in wearable electronics and medical monitoring.
Keyphrases
- hyaluronic acid
- drug delivery
- tissue engineering
- wound healing
- endothelial cells
- drug release
- extracellular matrix
- healthcare
- induced pluripotent stem cells
- primary care
- heart rate
- pluripotent stem cells
- insulin resistance
- skeletal muscle
- escherichia coli
- stress induced
- adipose tissue
- blood pressure
- gold nanoparticles
- soft tissue
- cystic fibrosis