Chitosan-Based Microneedle Patch with Multi-Anchoring and Integrated Hemostatic Mechanisms for Highly Efficient Bleeding Control in Dynamic, Wet Intestinal Conditions
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引用次数: 0
Abstract
Severe intestinal bleeding poses life-threatening risks, including hemorrhagic shock, organ damage, infection, and death. Current hemostatic materials struggle to adhere to wet, dynamic intestinal tissues, hindering effective hemostasis. Inspired by the hookworm’s rigid mouthpart and flexible body, which enable robust anchoring in the intestine, we developed a hydrogel microneedle patch (40K@P/G MNs) integrating multianchoring and hemostatic mechanisms. The patch leverages microneedle topology and gallic acid-grafted chitosan for enhanced mucosal adhesion, coupled with an extensible backing layer of optimized elasticity, achieving robust tissue adhesion (86.17 ± 26.19 mm Hg) in porcine intestinal models. The patch enhances clotting through a synergistic mechanism involving both chitosan and kaolin, which collectively promote platelet adhesion and activate the coagulation cascade, yielding a low blood coagulation index (4.92 ± 0.68%). It demonstrated excellent hemostatic performance in a rat liver hemorrhage model, achieving hemostasis within 35 s and preventing rebleeding. Its backing layer matches the intestine’s mechanical stress, providing elasticity to withstand peristaltic forces. This multianchoring microneedle patch offers a carbohydrate-based solution for rapid, localized hemostasis in challenging intestinal environments.
严重的肠道出血会危及生命,包括出血性休克、器官损伤、感染和死亡。目前的止血材料很难粘附在潮湿的、动态的肠道组织上,阻碍了有效的止血。受钩虫坚硬的口器和灵活的身体的启发,我们开发了一种集多重锚定和止血机制于一体的水凝胶微针贴片(40K@P/G MNs)。该贴片利用微针拓扑结构和没食子酸移植的壳聚糖增强粘膜黏附,再加上可扩展的优化弹性背衬层,在猪肠道模型中实现了良好的组织黏附(86.17±26.19 mm Hg)。该贴片通过壳聚糖和高岭土的协同机制促进凝血,共同促进血小板粘附,激活凝血级联,使凝血指数降低(4.92±0.68%)。在大鼠肝出血模型中表现出优异的止血效果,可在35s内止血并防止再出血。它的衬底层与肠道的机械应力相匹配,提供弹性以承受蠕动力。这种多锚定微针贴片提供了一种基于碳水化合物的解决方案,可在具有挑战性的肠道环境中快速、局部止血。
期刊介绍:
Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine.
Topics covered by Biomacromolecules include, but are not exclusively limited to: sustainable polymers, polymers based on natural and renewable resources, degradable polymers, polymer conjugates, polymeric drugs, polymers in biocatalysis, biomacromolecular assembly, biomimetic polymers, polymer-biomineral hybrids, biomimetic-polymer processing, polymer recycling, bioactive polymer surfaces, original polymer design for biomedical applications such as immunotherapy, drug delivery, gene delivery, antimicrobial applications, diagnostic imaging and biosensing, polymers in tissue engineering and regenerative medicine, polymeric scaffolds and hydrogels for cell culture and delivery.