A Guanosine-Quadruplex Hydrogel as Cascade Reaction Container Consuming Endogenous Glucose for Infected Wound Treatment-A Study in Diabetic Mice.
Yuanfeng LiLinzhu SuYongxin ZhangYong LiuFan HuangYijin RenYingli AnLinqi ShiHenny C van der MeiHenk J BusscherPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2022)
Diabetic foot ulcers infected with antibiotic-resistant bacteria form a severe complication of diabetes. Antimicrobial-loaded hydrogels are used as a dressing for infected wounds, but the ongoing rise in the number of antimicrobial-resistant infections necessitates new, nonantibiotic based designs. Here, a guanosine-quadruplex (G 4 )-hydrogel composed of guanosine, 2-formylphenylboronic acid, and putrescine is designed and used as a cascade-reaction container. The G 4 -hydrogel is loaded with glucose-oxidase and hemin. The first cascade-reaction, initiated by glucose-oxidase, transforms glucose and O 2 into gluconic acid and H 2 O 2 . In vitro, this reaction is most influential on killing Staphylococcus aureus or Pseudomonas aeruginosa in suspension, but showed limited killing of bacteria in biofilm-modes of growth. The second cascade-reaction, however, transforming H 2 O 2 into reactive-oxygen-species (ROS), also enhances killing of biofilm bacteria due to hemin penetration into biofilms and interaction with eDNA G-quadruplexes in the biofilm matrix. Therewith, the second cascade-reaction generates ROS close to the target bacteria, facilitating killing despite the short life-time of ROS. Healing of infected wounds in diabetic mice proceeds faster upon coverage by these G 4 -hydrogels than by clinically common ciprofloxacin irrigation. Moreover, local glucose concentrations around infected wounds decrease. Concluding, a G 4 -hydrogel loaded with glucose-oxidase and hemin is a good candidate for infected wound dressings, particularly in diabetic patients.
Keyphrases
- wound healing
- staphylococcus aureus
- drug delivery
- pseudomonas aeruginosa
- reactive oxygen species
- blood glucose
- biofilm formation
- hyaluronic acid
- candida albicans
- cystic fibrosis
- dna damage
- cell death
- type diabetes
- tissue engineering
- cardiovascular disease
- cancer therapy
- drug release
- healthcare
- metabolic syndrome
- electron transfer
- early onset
- multidrug resistant
- drug induced
- oxidative stress
- insulin resistance
- skeletal muscle