增强全层皮肤伤口愈合的仿生纳米工程支架

Nooshin Zandi, Banafsheh Dolatyar, Roya Lotfi, Yousef Shallageh, M. Shokrgozar, E. Tamjid, N. Annabi, A. Simchi
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引用次数: 52

摘要

创面愈合是一个复杂的过程,基于信号分子的协调和工程支架与新形成的组织之间的动态相互作用。到目前为止,大多数用于全层皮肤伤口愈合的工程支架不能模拟天然细胞外基质(ECM)的复杂性,因此不能为内源性组织再生提供合适的生态位[1]。为了解决这一问题并加速伤口愈合过程,我们提出了由明胶纳米纤维(GFS)和负载表皮生长因子(EGF)的光交联复合水凝胶组成的仿生双层支架。纳米纤维作为真皮层,负载表皮生长因子的复合水凝胶作为表皮基质,用于全层伤口愈合。该水凝胶由明胶甲基丙烯酰(GelMA)和硅酸盐纳米薄片(Laponite)修饰而成。为了克服表皮生长因子经皮给药的挑战,包括半衰期短和缺乏有效的配方,通过将表皮生长因子固定在拉波石上实现了精确、可控的给药。结果表明,添加1wt%硅酸盐纳米板可使水凝胶的压缩模量提高170%。体外伤口闭合分析也表明,支架与原生组织的粘附性提高了3.5倍。此外,由于带负电荷的纳米血小板,支架具有可调节的止血能力。在建立的切除全层创面模型中,与对照组(GFS组和盐水处理组)相比,14天后创面愈合增强(高达93.1±1.5%)。具有持续释放生长因子的工程粘合剂和止血支架具有刺激皮肤完全再生以实现全层伤口愈合的潜力。
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Biomimetic Nanoengineered Scaffold for Enhanced Full-Thickness Cutaneous Wound Healing
Wound healing is a complex process based on the coordinated signaling molecules and dynamic interactions between the engineered scaffold and newly formed tissue. So far, most of the engineered scaffolds used for the healing of full-thickness skin wounds do not mimic the natural extracellular matrix (ECM) complexity and therefore are not able to provide an appropriate niche for endogenous tissue regeneration [1]. To address this gap and to accelerate the wound healing process, we present biomimetic bilayer scaffolds compositing of gelatin nanofibers (GFS) and photocrosslinkable composite hydrogels loaded with epidermal growth factors (EGF). The nanofibers operate as the dermis layer, and EGF-loaded composite hydrogels acted as the epidermis matrix for the full-thickness wound healing application. The hydrogels are composed of gelatin metacryloyl (GelMA) modified with silicate nanoplatelets (Laponite). To overcome the challenges of transdermal delivery of EGF, including short half-life and lack of efficient formulation precise, controlled delivery was attained by immobilization of EGF on Laponite. It is shown that the addition of 1wt% silicate nanoplatelet increases the compressive modulus of the hydrogels by 170%. In vitro wound closure analysis also demonstrated improved adhesion of the scaffolds to the native tissue by 3.5 folds. Moreover, the tunable hemostatic ability of the scaffolds due to the negatively charged nanoplatelets is shown. In an established excisional full-thickness wound model, an enhanced wound closure (up to 93.1 ± 1.5%) after 14 days relative to controls (GFS and saline-treated groups) is demonstrated. The engineered adhesive and hemostatic scaffolds with sustained release of the growth factors have the potential to stimulate complete skin regeneration for full-thickness wound healing.
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