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Effect of Composite Biodegradable Biomaterials on Wound Healing in Diabetes

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Date 2022 Dec 12
PMID 36507270
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Abstract

The repair of diabetic wounds has always been a job that doctors could not tackle quickly in plastic surgery. To solve this problem, it has become an important direction to use biocompatible biodegradable biomaterials as scaffolds or dressing loaded with a variety of active substances or cells, to construct a wound repair system integrating materials, cells, and growth factors. In terms of wound healing, composite biodegradable biomaterials show strong biocompatibility and the ability to promote wound healing. This review describes the multifaceted integration of biomaterials with drugs, stem cells, and active agents. In wounds, stem cells and their secreted exosomes regulate immune responses and inflammation. They promote angiogenesis, accelerate skin cell proliferation and re-epithelialization, and regulate collagen remodeling that inhibits scar hyperplasia. In the process of continuous combination with new materials, a series of materials that can be well matched with active ingredients such as cells or drugs are derived for precise delivery and controlled release of drugs. The ultimate goal of material development is clinical transformation. At present, the types of materials for clinical application are still relatively single, and the bottleneck is that the functions of emerging materials have not yet reached a stable and effective degree. The development of biomaterials that can be further translated into clinical practice will become the focus of research.

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References
1.
Kondo S, Niiyama H, Yu A, Kuroyanagi Y . Evaluation of a wound dressing composed of hyaluronic acid and collagen sponge containing epidermal growth factor in diabetic mice. J Biomater Sci Polym Ed. 2011; 23(13):1729-40. DOI: 10.1163/092050611X597799. View

2.
Hu M, Borrelli M, Lorenz H, Longaker M, Wan D . Mesenchymal Stromal Cells and Cutaneous Wound Healing: A Comprehensive Review of the Background, Role, and Therapeutic Potential. Stem Cells Int. 2018; 2018:6901983. PMC: 5985130. DOI: 10.1155/2018/6901983. View

3.
Chu Y, Yu D, Wang P, Xu J, Li D, Ding M . Nanotechnology promotes the full-thickness diabetic wound healing effect of recombinant human epidermal growth factor in diabetic rats. Wound Repair Regen. 2010; 18(5):499-505. DOI: 10.1111/j.1524-475X.2010.00612.x. View

4.
Griffin D, Weaver W, Scumpia P, Di Carlo D, Segura T . Accelerated wound healing by injectable microporous gel scaffolds assembled from annealed building blocks. Nat Mater. 2015; 14(7):737-44. PMC: 4615579. DOI: 10.1038/nmat4294. View

5.
Fromer M, Chang S, Hagaman A, Koko K, Nolan R, Zhang P . The endothelial cell secretome as a novel treatment to prime adipose-derived stem cells for improved wound healing in diabetes. J Vasc Surg. 2017; 68(1):234-244. DOI: 10.1016/j.jvs.2017.05.094. View