促进糖尿病创面愈合的生物材料

Juan Liu, Huaiyuan Zheng, Xinyi Dai, Shi-qiang Sun, H. Machens, A. Schilling
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引用次数: 16

摘要

伤口愈合受损是糖尿病患者非创伤性下肢截肢的主要原因。目前,由生物材料设计的皮肤替代品在糖尿病伤口的愈合过程中发挥着重要作用,特别是那些在标准伤口护理后没有显示进展的伤口。本文综述了近年来用于促进糖尿病动物模型和糖尿病患者伤口愈合的生物材料的研究进展。这些生物材料可分为组织源性支架材料、水凝胶基生物材料和信号分子控释生物材料。组织源性支架在植入后保持了完美的细胞外基质结构,有利于三维细胞生长和支架内多层组织结构的重建。基于水凝胶的生物材料被设计成类似于细胞入侵和毛细血管生长的天然细胞外基质。细胞加工的生物材料或信号分子(生长因子、细胞因子)的控制释放可以诱导血管生成、再上皮化、细胞募集和迁移,并抑制持续的炎症,从而加速伤口愈合过程。更好地了解糖尿病伤口愈合的机制将导致更好的生物材料的发展,可能包括工程化的患者来源的细胞或因子,这将有助于体内血管化和组织诱导信号的一致释放。通过回顾最近的文献,我们展望未来的新策略,以进一步改善糖尿病伤口的个体化治疗。
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Biomaterials for Promoting Wound Healing in Diabetes
Impaired wound healing is the leading cause of non-traumatic lower limb amputation in people with diabetes mellitus. Skin substitutes engineered from biomaterials currently play an important role in the healing process of diabetic wounds, especially those wounds that fail to show progress after standard wound care. This article summarizes current developments of biomaterials used for promoting the wound healing process in either diabetic animal models or patients with diabetes mellitus. Those biomaterials can be categories into tissue-derived scaffolds, hydrogel-based biomaterials and biomaterials with controlled-release of signaling molecules. Tissue-derived scaffolds maintain perfect extracellular matrix architectures for three-dimensional cell growth and rebuilding of multi-layer tissue structures within scaffolds after implantation. Hydrogel-based biomaterials are engineered to resemble the natural extracellular matrix for cell invasion and capillary growth. Biomaterials processed with cells or controlled-release of signaling molecules (growth factors, cytokines) can induce angiogenesis, re-epithelialization, cell recruitment and migration as well as inhibit consistent inflammation, thereby accelerating the wound healing process. Better understanding of the mechanism of diabetic wound healing will lead to the development of even better biomaterials possibly with inclusion of engineered patient derived cells or factors which will aid in vivo vascularization and consistent release of tissue-inductive signals. By reviewing the recent literature, we draw future perspectives on new strategies for further improvement of the individualized therapy of diabetic wounds.
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