A Visible Light Cross-Linked Underwater Hydrogel Adhesive with Biodegradation and Hemostatic Ability.
Min LiangDandan WeiPengfei RenLi XuYinghua TaoLiuxin YangGuanhua JiaoTianzhu ZhangTakeshi SerizawaPublished in: Advanced healthcare materials (2024)
Hydrogel adhesives with integrated functionalities are still required to match their ever-expanding practical applications in the field of tissue repair and regeneration. A simple and effective safety strategy is reported, involving an in situ injectable polymer precursor and visible light-induced cross-linking. This strategy enables the preparation of a hydrogel adhesive in a physiological environment, offering wet adhesion to tissue surfaces, molecular flexibility, biodegradability, biocompatibility, efficient hemostatic performance, and the ability to facilitate liver injury repair. The proposed one-step preparation process of this polymer precursor involves the mixing of gelatin methacryloyl (GelMA), poly(thioctic acid) [P(TA)], poly(acrylic acid)/amorphous calcium phosphate (PAAc/ACP, PA) and FDA-approved photoinitiator solution, and a subsequent visible light irradiation after in situ injection into target tissues that resulted in a chemically-physically cross-linked hybrid hydrogel adhesive. Such a combined strategy shows promise for medical scenarios, such as uncontrollable post-traumatic bleeding.
Keyphrases
- visible light
- tissue engineering
- hyaluronic acid
- liver injury
- drug delivery
- wound healing
- drug induced
- stem cells
- climate change
- biofilm formation
- molecularly imprinted
- gene expression
- escherichia coli
- radiation therapy
- staphylococcus aureus
- machine learning
- radiation induced
- ultrasound guided
- solid state
- cell adhesion
- liquid chromatography
- deep learning
- solid phase extraction