Durr Hannah A, Abri Shahrzad, Salinas Samuel D, Adkins-Travis Kayla, Amini Rouzbeh, Shriver Leah P, Leipzig Nic D
Integrated Biosciences Program, Department of Biology, University of Akron, Akron, OH, USA.
Department of Chemical, Biomolecular, and Corrosion Engineering, University of Akron, Akron, OH, USA.
Acta Biomater. 2025 Jun 1;199:166-177. doi: 10.1016/j.actbio.2025.04.062. Epub 2025 May 1.
Diabetic foot ulcers (DFUs) are a multifactorial medical problem that require multifaceted approaches for effective healing. Most research on DFU healing has concentrated on promoting wound closure, with less emphasis on the quality of repaired tissue. This is problematic, however, since quality of the repaired tissues can have potential to improve wound healing outcomes and limit re-ulceration. If more functionally active dermis replaces the lost tissue, this can effectively maximize strength, organization, and overall structure of the plantar surface. Additionally, DFUs commonly show multi-strain infection, which further exacerbates the non-healing status of these wounds. Treatment of chronic wounds can be benefitted by application of oxygen and localized infection treatment, both can be achieved via our methacrylated chitosan-based (MACF) hydrogel. A non-healing diabetic infected wound model was used to explore extracellular matrix (ECM) organization, tensile strength, and metabolomic profiles at a 21-day endpoint as a marker for maturation and improved functionality of repaired tissues over normal scar formation. Effective remediation of infection was achieved with 14 days of polyhexamethylene biguanide (PHMB) application with improved wound repair compared to continuous treatment. Prolonged (21 day) application of PHMB showed resulting necrosis, although standard application times for patients with infected wounds can reach up to 28 continuous days. Biaxial mechanical analysis showed improved isotropic strength of infected tissues treated with MACF with PHMB stopped on D14, supported by collagen fiber orientation in second harmonics generation (SHG) imaging. Oxygenating MACF treatments also improved collagen deposition through the enhancement of the hydroxyproline fibrillary collagen synthesis pathway. These structural and mechanical results demonstrate a promising potential treatment for infected diabetic foot ulcers which shows improved dermal functionality. STATEMENT OF SIGNIFICANCE: Diabetic foot ulcers are a multifaceted problem in the medical field exacerbated by infection, with potential for gangrene, lower limb amputation, sepsis, or death. Current treatment regimens include oxygen therapy, physical debridement, and strong antibacterials. However, there is a lack of multi-faceted approaches, which we have designed in our oxygenating chitosan-based hydrogels capable of delivering antibiotics. Treatments currently focus on closure of wounds; however, functionality of regenerated tissues are limited due to fibrotic scar formation. Therefore, we have chosen to focus not only on closure, but also quality of regenerated tissues through mechanical testing and analysis of extracellular matrix composition and organization, with a goal of improving functionality of regenerated tissues.
糖尿病足溃疡(DFUs)是一个多因素的医学问题,需要多方面的方法才能有效愈合。大多数关于DFU愈合的研究都集中在促进伤口闭合上,而对修复组织的质量关注较少。然而,这是有问题的,因为修复组织的质量有可能改善伤口愈合结果并限制再次溃疡。如果更多功能活跃的真皮替代丢失的组织,这可以有效地最大化足底表面的强度、组织结构和整体结构。此外,DFUs通常表现为多菌株感染,这进一步加剧了这些伤口的不愈合状态。慢性伤口的治疗可以通过应用氧气和局部感染治疗而受益,这两者都可以通过我们的甲基丙烯酸化壳聚糖基(MACF)水凝胶来实现。使用一个不愈合的糖尿病感染伤口模型,在21天的终点探索细胞外基质(ECM)组织、拉伸强度和代谢组学谱,作为修复组织成熟和功能改善的标志,与正常瘢痕形成相比。通过应用聚六亚甲基双胍(PHMB)14天实现了有效的感染治疗,与持续治疗相比,伤口修复得到改善。虽然感染伤口患者的标准应用时间可达连续28天,但延长(21天)应用PHMB会导致坏死。双轴力学分析表明,在第14天停止使用PHMB并用MACF处理的感染组织的各向同性强度有所改善,二次谐波产生(SHG)成像中的胶原纤维取向支持了这一点。充氧MACF处理还通过增强羟脯氨酸纤维状胶原合成途径改善了胶原沉积。这些结构和力学结果表明,一种有前景的潜在治疗方法可用于感染性糖尿病足溃疡,显示出改善的真皮功能。重要性声明:糖尿病足溃疡是医学领域中一个因感染而加剧的多方面问题,有发生坏疽、下肢截肢、败血症或死亡的可能性。当前的治疗方案包括氧疗、物理清创和强效抗菌药物。然而,缺乏多方面的方法,我们在能够递送抗生素的充氧壳聚糖基水凝胶中进行了设计。目前的治疗主要集中在伤口闭合上;然而,由于纤维化瘢痕形成,再生组织的功能受到限制。因此,我们不仅选择关注闭合,还通过力学测试以及对细胞外基质组成和组织的分析来关注再生组织的质量,目标是改善再生组织的功能。