In Situ Growth of Zeolitic Imidazolate Framework-L in Macroporous PVA/CMC/PEG Composite Hydrogels with Synergistic Antibacterial and Rapid Hemostatic Functions for Wound Dressing.
Hang YangXianyu LanYuzhu XiongPublished in: Gels (Basel, Switzerland) (2022)
Although many advances have been made in medicine, traumatic bleeding and wound infection are two of the most serious threats to human health. To achieve rapid hemostasis and prevent infection by pathogenic microbes, the development of new hemostatic and antibacterial materials has recently gained significant attention. In this paper, safe, non-toxic, and biocompatible polyvinyl alcohol (PVA); carboxymethyl cellulose (CMC), which contains several carboxyl and hydroxyl groups; and polyethylene glycol (PEG), which functions as a pore-forming agent, were used to prepare a novel PVA/CMC/PEG-based composite hydrogel with a macroporous structure by the freeze-thaw method and the phase separation technique. In addition, a PVA/CMC/PEG@ZIF-L composite hydrogel was prepared by the in situ growth of zeolitic imidazolate framework-L (ZIF-L). ZIF-L grown in situ on hydrogels released Zn 2+ and imidazolyl groups. They elicited a synergistic antibacterial effect in hemostasis with PVA and CMC, rendering the PVA/CMC/PEG@ZIF-L hydrogel with a good antibacterial effect against Staphylococcus aureus . At the same time, the macroporous structure enabled the rapid release of Zn 2+ and imidazolyl groups in ZIF-L and promoted cell proliferation at an early stage, enhancing the coagulation efficiency. A rat liver injury model was used to confirm its rapid hemostasis capacity.
Keyphrases
- drug delivery
- wound healing
- cancer therapy
- liver injury
- drug release
- silver nanoparticles
- human health
- early stage
- staphylococcus aureus
- drug induced
- hyaluronic acid
- cell proliferation
- risk assessment
- tissue engineering
- heavy metals
- spinal cord injury
- ionic liquid
- oxidative stress
- anti inflammatory
- climate change
- escherichia coli
- essential oil
- atrial fibrillation
- cystic fibrosis
- biofilm formation
- pseudomonas aeruginosa
- surgical site infection
- candida albicans