Al Musaimi Othman, Ng Keng Wooi, Gavva Varshitha, Mercado-Valenzo Oscar M, Haroon Hajira Banu, Williams Daryl R
School of Pharmacy, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.
Department of Chemical Engineering, Imperial College London, London SW7 2AZ, UK.
Gels. 2024 Aug 12;10(8):531. doi: 10.3390/gels10080531.
A peptide-based hydrogel sequence was computationally predicted from the Ala-rich cross-linked domains of elastin. Three candidate peptides were subsequently synthesised and characterised as potential drug delivery vehicles. The elastin-derived peptides are Fmoc-FFAAAAKAA-NH, Fmoc-FFAAAKAA-NH, and Fmoc-FFAAAKAAA-NH. All three peptide sequences were able to self-assemble into nanofibers. However, only the first two could form hydrogels, which are preferred as delivery systems compared to solutions. Both of these peptides also exhibited favourable nanofiber lengths of at least 1.86 and 4.57 µm, respectively, which are beneficial for the successful delivery and stability of drugs. The shorter fibre lengths of the third peptide (maximum 0.649 µm) could have inhibited their self-assembly into the three-dimensional networks crucial to hydrogel formation.
基于弹性蛋白富含丙氨酸的交联结构域,通过计算预测了一种基于肽的水凝胶序列。随后合成了三种候选肽,并将其表征为潜在的药物递送载体。源自弹性蛋白的肽分别为Fmoc-FFAAAAKAA-NH、Fmoc-FFAAAKAA-NH和Fmoc-FFAAAKAAA-NH。所有这三种肽序列都能够自组装成纳米纤维。然而,只有前两种能够形成水凝胶,与溶液相比,水凝胶更适合作为递送系统。这两种肽还分别呈现出至少1.86微米和4.57微米的有利纳米纤维长度,这有利于药物的成功递送和稳定性。第三种肽较短的纤维长度(最大0.649微米)可能抑制了它们自组装成水凝胶形成所必需的三维网络。