Bioactive Polyurethane-Poly(ethylene Glycol) Diacrylate Hydrogels for Applications in Tissue Engineering

被引:3
作者
Yuan, Yixuan [1 ]
Tyson, Caleb [2 ]
Szyniec, Annika [1 ]
Agro, Samuel [1 ]
Tavakol, Tara N. [3 ]
Harmon, Alexander [2 ]
Lampkins, Dessarae [2 ]
Pearson, Lauran [2 ]
Dumas, Jerald E. [4 ]
Taite, Lakeshia J. [1 ]
机构
[1] Univ Virginia, Dept Chem Engn, Charlottesville, VA 22903 USA
[2] Hampton Univ, Dept Chem Engn, Hampton, VA 23668 USA
[3] Univ Virginia, Dept Biomed Engn, Charlottesville, VA 22908 USA
[4] North Carolina Agr & Tech State Univ, Joint Sch Nanosci & Nanoengn, Greensboro, NC 27401 USA
基金
美国国家科学基金会;
关键词
polyurethane; poly(ethylene glycol) diacrylate; hydrogels; photocrosslinking; cell adhesion; tissue engineering; scaffolds; YIGSR-PEPTIDE; MATRIX; ENDOTHELIALIZATION; POLYURETHANES; PEG; IMMOBILIZATION; COATINGS;
D O I
10.3390/gels10020108
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polyurethanes (PUs) are a highly adaptable class of biomaterials that are among some of the most researched materials for various biomedical applications. However, engineered tissue scaffolds composed of PU have not found their way into clinical application, mainly due to the difficulty of balancing the control of material properties with the desired cellular response. A simple method for the synthesis of tunable bioactive poly(ethylene glycol) diacrylate (PEGDA) hydrogels containing photocurable PU is described. These hydrogels may be modified with PEGylated peptides or proteins to impart variable biological functions, and the mechanical properties of the hydrogels can be tuned based on the ratios of PU and PEGDA. Studies with human cells revealed that PU-PEG blended hydrogels support cell adhesion and viability when cell adhesion peptides are crosslinked within the hydrogel matrix. These hydrogels represent a unique and highly tailorable system for synthesizing PU-based synthetic extracellular matrices for tissue engineering applications.
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页数:14
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