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具有快速溶胶-凝胶转变和增强机械性能的物理交联丝素蛋白水凝胶

Physically Cross-Linked Silk Fibroin Hydrogel with Rapid Sol-Gel Transition and Enhanced Mechanical Performance.

作者信息

Niu Longxing, Chen Shengjia, Guo Xiangshu, Feng Yanfei, Wang Rong

机构信息

Laboratory of Advanced Theranostic Materials and Technology, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, 315201, P. R. China.

Zhejiang International Scientific and Technological Cooperative Base of Biomedical Materials and Technology, Ningbo Cixi Institute of Biomedical Engineering, Ningbo, 315300, P. R. China.

出版信息

Macromol Rapid Commun. 2025 Jul;46(14):e2401016. doi: 10.1002/marc.202401016. Epub 2025 May 14.

Abstract

It remains a great challenge to fabricate physically cross-linked silk fibroin (SF) hydrogels with rapid gelation and robust mechanical properties. In this study, a novel SF hydrogel is obtained by synergistically modulating the SF molecular weight (MW) and the freeze-inducing process, avoiding the use of any exterior additives. First, the effects of MW on the self-assembly behaviors of SF are investigated under physiological temperature. The results demonstrate that high MW SF derived from papain degumming (PSF) facilitates the sol-gel transition with increasing β-sheet content, and contributed to the construction of the hierarchical micro-nanofiber structure. Subsequently, cryo-concentration treatment is applied to further accelerate the gelation process. The resultant PSF (F-PSF) exhibits rapid sol-gel transition (within 1 h), a high compressive modulus (54.2 ± 3.7 kPa), and a high storage modulus (up to 247.9 kPa), which are superior to traditional physically cross-linked SF hydrogels. The relatively low β-sheet content and dense structure endow the F-PSF hydrogels with excellent mechanical flexibility, physiological environmental stability, and long-term mechanical stability. In vitro cellular experiments show that F-PSF hydrogels are beneficial to cell proliferation and spreading. These attractive features enable the physically cross-linked SF hydrogels to be promising for tissue engineering and regenerative medicine.

摘要

制备具有快速凝胶化和强大机械性能的物理交联丝素蛋白(SF)水凝胶仍然是一个巨大的挑战。在本研究中,通过协同调节SF分子量(MW)和冷冻诱导过程,获得了一种新型的SF水凝胶,避免了使用任何外部添加剂。首先,在生理温度下研究了MW对SF自组装行为的影响。结果表明,木瓜蛋白酶脱胶得到的高MW SF(PSF)随着β-折叠含量的增加促进了溶胶-凝胶转变,并有助于构建分级微纳米纤维结构。随后,采用冷冻浓缩处理进一步加速凝胶化过程。所得的PSF(F-PSF)表现出快速的溶胶-凝胶转变(在1小时内)、高压缩模量(54.2±3.7 kPa)和高储能模量(高达247.9 kPa),优于传统的物理交联SF水凝胶。相对较低的β-折叠含量和致密结构赋予F-PSF水凝胶优异的机械柔韧性、生理环境稳定性和长期机械稳定性。体外细胞实验表明,F-PSF水凝胶有利于细胞增殖和铺展。这些吸引人的特性使物理交联的SF水凝胶在组织工程和再生医学方面具有广阔的应用前景。

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