在全层皮肤缺损模型中,铜和钴掺杂的生物活性玻璃鱼真皮胶原电纺垫触发糖尿病伤口愈合的关键事件。

S. Jana, P. Datta, Himanka Das, S. Jaiswal, P. R. Ghosh, D. Lahiri, B. Kundu, S. Nandi
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引用次数: 6

摘要

由于愈合机制的一些缺陷,由潜在的高血糖状况引起的伤口,如糖尿病足溃疡,需要多功能的组织再生方法。本研究将罗湖鱼皮源性胶原蛋白(Fcol)与生物活性玻璃(BAG)/离子注入生物活性玻璃结合,开发了四种不同类型的电纺丝微纤维,即Fcol/BAG、Fcol/CuBAG、Fcol/CoBAG和Fcol/CuCoBAG,通过刺激糖尿病患者血管生成和ECM重建等关键事件来加速伤口愈合。SEM分析显示了多孔和微纤维结构,而EDX图谱提供了掺杂剂掺入各种无机-有机复合材料垫中的证据。纳米dma测试表明,微纤维毡具有较高的阻尼系数和非均匀的tan-delta值。掺入铜的生物活性玻璃微纤维的鱼胶原蛋白的极限拉伸强度和韧性最大,而掺入钴的微纤维的极限拉伸强度和韧性最小。当人真皮成纤维细胞(HDFs)在微纤维上培养48小时时,体外结果显示出良好的细胞-细胞和细胞-材料相互作用。当这些垫子应用于兔模型的全层糖尿病伤口时,Fcol/CuBAG, Fcol/CoBAG和Fcol/CuCoBAG微纤维可实现早期伤口愈合。值得注意的是,CD-31免疫染色显示,这些微纤维处理的伤口血管密度显著高于对照组、十二指肠和Fcol/BAG处理的伤口(p < 0.01)。在鱼胶原/离子掺杂生物活性玻璃微纤维治疗的伤口中,成熟的胶原沉积和良好的ECM重塑也很明显,这表明它们在糖尿病伤口愈合中的积极作用。
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Copper and cobalt doped bioactive glass-fish dermal collagen electrospun mat triggers key events of diabetic wound healing in full-thickness skin defect model.
The wounds arising out of underlying hyperglycemic conditions such as diabetic foot ulcers demand a multifunctional tissue regeneration approach owing to several deficiencies in the healing mechanisms. Herein, four different types of electrospun microfibers by combining Rohu fish skin-derived collagen (Fcol) with a bioactive glass (BAG)/ion-doped bioactive glass, namely, Fcol/BAG, Fcol/CuBAG, Fcol/CoBAG, and Fcol/CuCoBAG was developed to accelerate wound healing through stimulation of key events such as angiogenesis and ECM re-construction under diabetic conditions. SEM analysis shows the porous and microfibrous architecture, while the EDX mapping provides evidence of the incorporation of dopants inside various inorganic-organic composite mats. The viscoelastic properties of the microfibrous mats as measured by a nano-DMA test show a higher damping factor non-uniform tan-delta value. The maximum ultimate tensile strength and toughness are recorded for fish collagen with copper doped bioactive glass microfibers while the least values are demonstrated by microfibers with cobalt dopant. In vitro results demonstrate excellent cell-cell and cell-material interactions when human dermal fibroblasts (HDFs) were cultured over the microfibers for 48 h. When these mats were applied over full-thickness diabetic wounds in the rabbit model, early wound healing is attained with Fcol/CuBAG, Fcol/CoBAG, and Fcol/CuCoBAG microfibers. Notably, these microfibers-treated wounds demonstrate a significantly (p < 0.01) higher density of blood vessels by CD-31 immunostaining than control, Duoderm, and Fcol/BAG treated wounds. Mature collagen deposition and excellent ECM remodeling are also evident in wounds treated with fish collagen/ion-doped bioactive glass microfibers suggesting their positive role in diabetic wound healing.
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