Multifunctional hydrogel–acellular dermal matrix composite patch: an anticalcification barrier with antibacterial and anti-inflammatory properties for abdominal wall repair
Xin Zheng, Ying Zhang, Nianhua Dan, Yining Chen, Zhengjun Li, Yunbing Wang
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引用次数: 0
Abstract
Calcification, infection, and inflammation are common complications associated with the in vivo application of biological patches. Porcine acellular dermal matrix (pADM), composed mainly of collagen with excellent bioactivity, is widely utilized as a substrate for such patches. However, integrating multiple therapeutic functions into pADM remains a significant challenge. To overcome this limitation, a hydrogel-encapsulated pADM patch (H-Cur-pADM) was developed, aiming to provide barrier protection and multifunctional enhancement. This design involves the in situ formation of a curcumin-loaded hydrogel (GelMA-DTT-Cur) on the surface of pADM via a thiol–ene click reaction. The resulting hybrid not only reinforces the anticalcification capacity of the patch but also imparts anti-infective and anti-inflammatory properties. By combining the mechanical support of pADM with the functional versatility of the hydrogel, this innovative approach enhances the overall performance of the biological patch. The GelMA-DTT-Cur hydrogel layer demonstrated robust structural integrity, interconnected porosity, and sustained release of curcumin micelles following a Fickian diffusion mechanism. In vitro, the hydrogel-encapsulated pADM displayed significant antibacterial activity against Escherichia coli and Staphylococcus aureus, good cytocompatibility, and pronounced anticalcification properties. In vivo studies showed that calcium deposition in the H-Cur-pADM group was only 5.2% of that observed in glutaraldehyde-cross-linked pADM after 21 days of implantation. The H-Cur-pADM patch also displayed strong anti-inflammatory effects and effectively promoted healing in an abdominal wall defect model. This work presents a novel strategy for improving the therapeutic performance of biological patches by integrating drug-loaded hydrogel encapsulation with pADM, offering promising potential for clinical applications in abdominal wall repair.
钙化、感染和炎症是与生物贴片在体内应用相关的常见并发症。猪脱细胞真皮基质(pADM)主要由胶原蛋白组成,具有良好的生物活性,被广泛用作这种贴片的底物。然而,将多种治疗功能整合到pADM中仍然是一个重大挑战。为了克服这一限制,开发了一种水凝胶封装的pADM贴片(H-Cur-pADM),旨在提供屏障保护和多功能增强。该设计涉及通过巯基点击反应在pADM表面原位形成装载姜黄素的水凝胶(GelMA-DTT-Cur)。由此产生的混合物不仅加强了贴片的抗钙化能力,而且还赋予抗感染和抗炎特性。通过将pADM的机械支持与水凝胶的功能通用性相结合,这种创新的方法增强了生物贴片的整体性能。GelMA-DTT-Cur水凝胶层表现出坚固的结构完整性,相互连接的孔隙,以及在菲克扩散机制下姜黄素胶束的持续释放。在体外,水凝胶包封的pADM对大肠杆菌和金黄色葡萄球菌具有明显的抗菌活性,具有良好的细胞相容性和明显的抗钙化性能。体内研究表明,植入21天后,h - cu -pADM组的钙沉积仅为戊二醛交联pADM组的5.2%。h - cu - padm贴片也显示出很强的抗炎作用,并有效促进腹壁缺损模型的愈合。本研究提出了一种通过将载药水凝胶包封与pADM结合来提高生物贴片治疗性能的新策略,为腹壁修复的临床应用提供了广阔的前景。图形抽象