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Pre-clinical evaluation of soybean-based wound dressings and dermal substitute formulations in pig healing and non-healing in vivo models

机译:基于大豆的伤口敷料和皮肤替代制剂在猪愈合和不愈合体内模型中的临床前评估

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摘要

In the last decade, a new class of natural biomaterials derived from de-fatted soybean flour processed by either thermoset or extraction procedures has been developed. These biomaterials uniquely combine adaptability to various clinical applications to proven tissue regeneration properties. In the present work, the biomaterials were formulated either as hydrogel or as paste formulation and their potential as wound dressing material or as dermal substitute was assessed by two in vivo models in pig skin: The healing full-thickness punch biopsy model and the non-healing full-thickness polytetrafluoroethylene (PTFE) chamber model. The results clearly show that collagen deposition is induced by the presence of these biomaterials. A unique pattern of early inflammatory response, eliciting neutrophils and controlling macrophage infiltration, is followed by tissue cell colonization of the wound bed with a significant deposition of collagen fibers. The study also highlighted the importance in the use of optimal formulations and appropriate handling upon implantation. In large size, non-healing wounds, wound dermis was best obtained with the paste formulation as hydrogels appeared to be too loose to ensure lasting scaffolding properties. On the contrary, packing of the granules during the application of paste reduced biomaterial degradation rate and prevent the penetration of newly vascularized tissue, thus impeding grafting of split-thickness autologous skin grafts on the dermal substitute base.
机译:在过去的十年中,已经开发出了一类新的天然生物材料,这些材料是通过热固性或提取程序加工的脱脂大豆粉制成的。这些生物材料独特地结合了对各种临床应用的适应性和经证明的组织再生特性。在目前的工作中,将生物材料配制成水凝胶或糊剂制剂,并通过两种猪皮体内模型评估了其作为伤口包扎材料或真皮替代物的潜力:愈合性全厚度打孔活检模型和非皮肤修复全厚度聚四氟乙烯(PTFE)腔室模型。结果清楚地表明,胶原蛋白的沉积是由这些生物材料的存在诱导的。早期炎症反应的独特模式,引起嗜中性粒细胞并控制巨噬细胞浸润,然后组织细胞在伤口床上定植,胶原纤维明显沉积。该研究还强调了在植入时使用最佳制剂和适当处理的重要性。在大的,不愈合的伤口中,最好使用糊状制剂获得伤口真皮,因为水凝胶似乎太松散而无法确保持久的脚手架性能。相反,在糊剂施用过程中颗粒的堆积降低了生物材料的降解速率并防止了新血管化组织的渗透,从而阻碍了在皮肤替代物基体上嫁接了厚皮自体皮肤移植物。

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