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用于定制水凝胶热响应性和细胞粘附特性的基于普朗尼克的功能性前体的设计

Design of Functional Pluronic-Based Precursors for Tailoring Hydrogel Thermoresponsiveness and Cell-Adhesive Properties.

作者信息

Camana Giulia, Tavano Mirko, Li Min, Castiglione Franca, Rossi Filippo, Cellesi Francesco

机构信息

Dipartimento di Chimica, Materiali ed Ingegneria Chimica "G. Natta", Politecnico di Milano, Via Mancinelli 7, 20131 Milan, Italy.

Renal Research Laboratory, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Via Pace 9, 20122 Milan, Italy.

出版信息

Materials (Basel). 2023 Mar 29;16(7):2749. doi: 10.3390/ma16072749.

Abstract

In this study, functional Pluronic F127 precursors were designed and synthesized for the preparation of thermosensitive hydrogels. Using linear Pluronic thioacetate and Pluronic multi-acrylate precursors, F127-based hydrogels were prepared through thioacetate deprotection-mediated Michael-type addition. The properties of these gels were compared to those obtained through free radical crosslinking of F127 diacrylate. Temperature was found to have a clear influence on gel swelling as a result of F127 thermoresponsiveness. The macromolecular architecture and functionality of the precursors were also optimized and characterized in terms of gelation kinetics and drug diffusion. In vitro tests were conducted on fibroblasts and endothelial cells to assess their response to cellular adhesion with Pluronic gels that were functionalized with an RGD peptide or pretreated with serum proteins to promote cell adhesion. This study provides a method for creating tailored hydrogels suitable for various biomedical applications, such as soft-tissue engineering, cell encapsulation, wound healing, and sustained delivery of therapeutic molecules.

摘要

在本研究中,设计并合成了功能性普朗尼克F127前体用于制备热敏水凝胶。使用线性普朗尼克硫代乙酸酯和普朗尼克多丙烯酸酯前体,通过硫代乙酸酯脱保护介导的迈克尔型加成反应制备了基于F127的水凝胶。将这些凝胶的性能与通过F127二丙烯酸酯自由基交联获得的凝胶性能进行了比较。由于F127的热响应性,发现温度对凝胶溶胀有明显影响。还根据凝胶化动力学和药物扩散对前体的大分子结构和功能进行了优化和表征。对成纤维细胞和内皮细胞进行了体外测试,以评估它们对用RGD肽功能化或用血清蛋白预处理以促进细胞粘附的普朗尼克凝胶细胞粘附的反应。本研究提供了一种制备适合各种生物医学应用的定制水凝胶的方法,如软组织工程、细胞封装、伤口愈合和治疗分子的持续递送。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/172c/10095789/d011f00d6518/materials-16-02749-g001.jpg

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