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首页> 外文期刊>Biomaterials Research >Development of Stabilized Growth Factor-Loaded Hyaluronate– Collagen Dressing (HCD) matrix for impaired wound healing
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Development of Stabilized Growth Factor-Loaded Hyaluronate– Collagen Dressing (HCD) matrix for impaired wound healing

机译:稳定生长因子负载的透明质酸-胶原蛋白敷料(HCD)基质可用于伤口愈合不良

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BackgroundDiabetes mellitus is a disease lack of insulin, which has severely delayed and impaired wound healing capacity. In the previous studies, various types of scaffolds and growth factors were used in impaired wound healing. However, there were several limitations to use them such as short half-life of growth factors in vivo and inadequate experimental conditions of wound-dressing material. Thus, our study aimed to determine the biocompatibility and stability of the matrix containing structurally stabilized epidermal growth factor (S-EGF) and basic fibroblast growth factor (S-bFGF). Results and DiscussionWe stabilized EGF and bFGF that are structurally more stable than existing EGF and bFGF. We developed biocompatible matrix using S-EGF, S-bFGF, and hyaluronate– collagen dressing (HCD) matrix. The developed matrix, S-EGF and S-bFGF loaded on HCD matrix, had no cytotoxicity, in vitro . Also, these matrixes had longer releasing period that result in enhancement of half-life. Finally, when these matrixes were applied on the wound of diabetic mice, there were no inflammatory responses, in vivo . Thus, our results demonstrate that these matrixes are biologically safe and biocompatible as wound-dressing material. ConclusionsOur stabilized EGF and bFGF was more stable than existing EGF and bFGF and the HCD matrix had the capacity to efficiently deliver growth factors. Thus, the S-EGF and S-bFGF loaded on HCD matrix had improved stability. Therefore, these matrixes may be suitable for impaired wound healing, resulting in application of clinical treatment.
机译:背景技术糖尿病是缺乏胰岛素的疾病,其严重延迟和损害了伤口的愈合能力。在先前的研究中,各种类型的支架和生长因子被用于伤口愈合不良。但是,使用它们存在一些局限性,例如生长因子在体内的半衰期短以及伤口敷料的实验条件不足。因此,我们的研究旨在确定包含结构稳定的表皮生长因子(S-EGF)和碱性成纤维细胞生长因子(S-bFGF)的基质的生物相容性和稳定性。结果与讨论我们稳定了EGF和bFGF,它们在结构上比现有的EGF和bFGF更稳定。我们使用S-EGF,S-bFGF和透明质酸-胶原蛋白敷料(HCD)基质开发了生物相容性基质。加载到HCD基质上的发达基质S-EGF和S-bFGF在体外没有细胞毒性。而且,这些基质的释放时间更长,导致半衰期延长。最后,当将这些基质应用于糖尿病小鼠的伤口时,在体内没有炎症反应。因此,我们的结果表明,这些基质作为伤口敷料具有生物学安全性和生物相容性。结论我们稳定的EGF和bFGF比现有的EGF和bFGF更稳定,并且HCD基质具有有效递送生长因子的能力。因此,负载在HCD基质上的S-EGF和S-bFGF具有改善的稳定性。因此,这些基质可能适合受损的伤口愈合,从而导致临床治疗的应用。

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