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Fmoc-FF 和阳离子肽的多组分水凝胶基质在组织工程中的应用。

Multicomponent Hydrogel Matrices of Fmoc-FF and Cationic Peptides for Application in Tissue Engineering.

机构信息

Department of Pharmacy and Research Centre on Bioactive Peptides (CIRPeB), University of Naples "Federico II", Via Mezzocannone 16, Naples, 80134, Italy.

Department of Molecular Biotechnologies and Health Science, University of Turin, Via Nizza 52, Turin, 10125, Italy.

出版信息

Macromol Biosci. 2022 Jul;22(7):e2200128. doi: 10.1002/mabi.202200128. Epub 2022 May 18.

Abstract

In the last years, peptide-based hydrogels are being increasingly used as suitable matrices for biomedical and pharmaceutical applications, including drug delivery and tissue engineering. Recently, the synthesis and the gelation properties of a small library of cationic peptides, containing a Lys residue at the C-terminus and derivatized with an Fmoc group or with the fluorenyl methoxycarbonyl-diphenylalanine (FmocFF) at the N-terminus are derived. Here, it is demonstrated that the combination of these peptides with the well-known hydrogelator FmocFF, in different weight/weight ratios, allows the achievement of seven novel self-sorted hydrogels, which share similar peptide organization of their supramolecular matrix. Rheological and relaxometric characterization highlight a different mechanical rigidity and water mobility in the gels as demonstrated by the storage modulus values (200 Pa < G' < 35 000 Pa) and by relaxometry, respectively. In vitro studies demonstrate that most of the tested mixed hydrogels do not disturb significantly the cell viability (>95%) over 72 h of treatment. Moreover, in virtue to its capability to strongly favor adhesion, spreading and duplication of 3T3-L1 cells, one of the tested hydrogel may be eligible as synthetic extracellular matrix.

摘要

在过去几年中,基于肽的水凝胶越来越多地被用作生物医学和药物应用的合适基质,包括药物输送和组织工程。最近,合成了一小部分阳离子肽,并研究了它们的凝胶性质,这些肽在 C 末端含有赖氨酸残基,并在 N 末端衍生有 Fmoc 基团或芴甲氧羰基-二苯丙氨酸(FmocFF)。这里,我们证明了将这些肽与众所周知的水凝胶形成剂 FmocFF 以不同的重量/重量比组合,可以得到七种新的自分类水凝胶,它们具有相似的超分子基质中肽的组织。流变学和弛豫度特性分析突出了凝胶在机械硬度和水流动性方面的不同,这可以通过储能模量值(200 Pa < G' < 35,000 Pa)和弛豫度来证明。体外研究表明,在 72 小时的治疗过程中,大多数测试的混合水凝胶不会显著干扰细胞活力(>95%)。此外,由于其能够强烈促进 3T3-L1 细胞的粘附、扩散和复制,其中一种测试的水凝胶可能有资格作为合成细胞外基质。

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