Laboratory of Advanced Biomaterials, Research School of Engineering, The Australian National University, Canberra, ACT 2601, Australia.
Nanoscale. 2017 Sep 21;9(36):13661-13669. doi: 10.1039/c7nr05004f.
Tissue-specific self-assembling peptide (SAP) hydrogels designed based on biologically relevant peptide sequences have great potential in regenerative medicine. These materials spontaneously form 3D networks of physically assembled nanofibres utilising non-covalent interactions. The nanofibrous structure of SAPs is often compared to that of electrospun scaffolds. These electrospun nanofibers are produced as sheets that can be engineered from a variety of polymers that can be chemically modified to incorporate many molecules including drugs and growth factors. However, their macroscale morphology limits them to wrapping and bandaging applications. Here, for the first time, we combine the benefits of these systems to describe a two-component composite scaffold from these biomaterials, with the design goal of providing a hydrogel scaffold that presents 3D structures, and also has temporal control over drug delivery. Short fibres, cut from electrospun scaffolds, were mixed with our tissue-specific SAP hydrogel to provide a range of nanofibre sizes found in the extracellular matrix (10-300 nm in diameter). The composite material maintained the shear-thinning and void-filling properties of SAP hydrogels that have previously been shown to be effective for minimally invasive material injection, cell delivery and subsequent in vivo integration. Both scaffold components were separately loaded with growth factors, important signaling molecules in tissue regeneration whose rapid degradation limits their clinical efficacy. The two biomaterials provided sequential growth factor delivery profiles: the SAP hydrogel provided a burst release, with the release rate decreasing over 12 hours, while the electrospun nanofibres provided a more constant, sustained delivery. Importantly, this second release commenced 6 days later. The design rules established here to provide temporally distinct release profiles can enable researchers to target specific stages in regeneration, such as the acute immune response versus sustained protection and survival of cells following injury. In summary, this novel composite material combines the physical advantages of SAP hydrogels and electrospun nanofibres, while additionally providing a superior vehicle for the stabilisation and controlled delivery of growth factors necessary for optimal tissue repair.
基于生物相关肽序列设计的组织特异性自组装肽 (SAP) 水凝胶在再生医学中有很大的潜力。这些材料利用非共价相互作用自发形成物理组装纳米纤维的 3D 网络。SAP 的纳米纤维结构通常与静电纺丝支架的结构进行比较。这些静电纺纳米纤维被制成可以由多种聚合物制成的薄片,这些聚合物可以进行化学修饰以包含许多分子,包括药物和生长因子。然而,它们的宏观形态限制了它们只能用于包裹和包扎应用。在这里,我们首次将这些系统的优点结合起来,描述了由这些生物材料组成的两成分复合支架,其设计目标是提供具有 3D 结构的水凝胶支架,并且还可以对药物输送进行时间控制。从静电纺丝支架上切下的短纤维与我们的组织特异性 SAP 水凝胶混合,提供了在细胞外基质中发现的一系列纳米纤维尺寸(直径为 10-300nm)。复合材料保持了 SAP 水凝胶的剪切变稀和空隙填充特性,先前的研究表明,这些特性对于微创材料注射、细胞输送和随后的体内整合非常有效。两种支架成分分别负载生长因子,生长因子是组织再生中的重要信号分子,但其快速降解限制了它们的临床疗效。两种生物材料提供了顺序释放生长因子的特征:SAP 水凝胶提供了一个爆发式释放,释放速率在 12 小时内降低,而静电纺纳米纤维提供了更稳定、持续的释放。重要的是,第二个释放开始于 6 天后。这里建立的设计规则提供了时间上明显不同的释放特征,可以使研究人员针对再生的特定阶段,如急性免疫反应与受伤后细胞的持续保护和存活。总之,这种新型复合材料结合了 SAP 水凝胶和静电纺纳米纤维的物理优势,同时还为稳定和控制生长因子的输送提供了更好的载体,这对于最佳的组织修复是必要的。