Dhyani Abhishek, Repetto Taylor, VanAken Shannon, Nemzek Jean, VanEpps J Scott, Mehta Geeta, Tuteja Anish
Department of Emergency Medicine, University of Michigan, Ann Arbor, Michigan.
Unit for Laboratory Animal Medicine, University of Michigan, Ann Arbor, Michigan.
Shock. 2024 Oct 1;62(4):588-595. doi: 10.1097/SHK.0000000000002426. Epub 2024 Aug 8.
Infection of wounds delays healing, increases treatment costs, and leads to major complications. Current methods to manage such infections include antibiotic ointments and antimicrobial wound dressings, both of which have significant drawbacks, including frequent reapplication and contribution to antimicrobial resistance. In this work, we developed wound dressings fabricated with a medical-grade polyurethane coating composed of natural plant secondary metabolites, cinnamaldehyde, and alpha-terpineol. Our wound dressings are easy to change and do not adhere to the wound bed. They kill gram-positive and -negative microbes in infected wounds due to the Food and Drug Administration-approved for human consumption components. The wound dressings were fabricated by dip coating. Antimicrobial efficacy was determined by quantifying the bacteria colonies after a 24 h of immersion. Wound healing and bacterial reduction were assessed in an in vivo full-thickness porcine burn model. Our antimicrobial wound dressings showed a > 5-log reduction (99.999%) of different gram-positive and gram-negative bacteria, while maintaining absorbency. In the in vivo porcine burn model, our wound dressings were superior to bacitracin in decreasing bacterial burden during daily changes, without interfering with wound healing. Additionally, the dressings had a significantly lower adhesion to the wound bed. Our antimicrobial wound dressings reduced the burden of clinically relevant bacteria more than commercial antimicrobial wound dressings. In an in vivo infected burn wound model, our coatings performed as well or better than bacitracin. We anticipate that our wound dressings would be useful for the treatment of various types of acute and chronic wounds.
伤口感染会延迟愈合、增加治疗成本并导致严重并发症。目前处理此类感染的方法包括抗生素软膏和抗菌伤口敷料,但这两种方法都有显著缺点,包括需要频繁重新涂抹以及会导致抗菌耐药性。在这项研究中,我们开发了一种伤口敷料,其采用由天然植物次生代谢产物肉桂醛和α-萜品醇组成的医用级聚氨酯涂层制成。我们的伤口敷料易于更换,且不会粘连在伤口床上。由于其成分经美国食品药品监督管理局批准可用于人类消费,因此能杀死感染伤口中的革兰氏阳性和阴性微生物。这些伤口敷料通过浸涂法制备。抗菌效果通过在浸泡24小时后对细菌菌落进行定量来确定。在体内全层猪烧伤模型中评估伤口愈合和细菌减少情况。我们的抗菌伤口敷料对不同的革兰氏阳性和阴性细菌显示出大于5个对数的减少(99.999%),同时保持吸水性。在体内猪烧伤模型中,我们的伤口敷料在每日更换时降低细菌负荷方面优于杆菌肽,且不干扰伤口愈合。此外,该敷料与伤口床的粘连性显著更低。我们的抗菌伤口敷料比商用抗菌伤口敷料更能减轻临床相关细菌的负担。在体内感染烧伤伤口模型中,我们的涂层表现与杆菌肽相当或更好。我们预计我们的伤口敷料将对各种类型的急性和慢性伤口的治疗有用。