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.
引用
收藏
页数:14
相关论文
共 75 条
  • [21] Photolithographic patterning of polyethylene glycol hydrogels
    Hahn, MS
    Taite, LJ
    Moon, JJ
    Rowland, MC
    Ruffino, KA
    West, JL
    [J]. BIOMATERIALS, 2006, 27 (12) : 2519 - 2524
  • [22] Study on bioactive PEGDA/ECM hybrid bi-layered hydrogel scaffolds fabricated by electro-writing for cartilage regeneration
    Han, Yu
    Lian, Meifei
    Zhang, Chenyu
    Jia, Bo
    Wu, Qiang
    Sun, Benlin
    Qiao, Zhiguang
    Sun, Binbin
    Dai, Kerong
    [J]. APPLIED MATERIALS TODAY, 2022, 28
  • [23] Thermo-Responsive Polyurethane Hydrogels Based on Poly(ε-caprolactone) Diol and Amphiphilic Polylactide-Poly(Ethylene Glycol) Block Copolymers
    Hsu, Shan-Hui
    Chen, Cheng-Wei
    Hung, Kun-Che
    Tsai, Yi-Chun
    Li, Suming
    [J]. POLYMERS, 2016, 8 (07):
  • [24] Engineering three-dimensional cell mechanical microenvironment with hydrogels
    Huang, Guoyou
    Wang, Lin
    Wang, ShuQi
    Han, Yulong
    Wu, Jinhui
    Zhang, Qiancheng
    Xu, Feng
    Lu, Tian Jian
    [J]. BIOFABRICATION, 2012, 4 (04)
  • [25] Bioactive biomaterials
    Hubbell, JA
    [J]. CURRENT OPINION IN BIOTECHNOLOGY, 1999, 10 (02) : 123 - 129
  • [26] Physics and Physiology of Cell Spreading in Two and Three Dimensions
    Janmey, Paul A.
    Hinz, Boris
    McCllioch, Christopher A.
    [J]. PHYSIOLOGY, 2021, 36 (06) : 382 - 391
  • [27] Endothelialization of microporous YIGSR/PEG-modified polyurethaneurea
    Jun, HW
    West, JL
    [J]. TISSUE ENGINEERING, 2005, 11 (7-8): : 1133 - 1140
  • [28] Nitric oxide-producing polyurethanes
    Jun, HW
    Taite, LJ
    West, JL
    [J]. BIOMACROMOLECULES, 2005, 6 (02) : 838 - 844
  • [29] Modification of polyurethaneurea with PEG and YIGSR peptide to enhance endothelialization without platelet adhesion
    Jun, HW
    West, JL
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS, 2005, 72B (01) : 131 - 139
  • [30] Development of a YIGSR-peptide-modified polyurethaneurea to enhance endothelialization
    Jun, HW
    West, J
    [J]. JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2004, 15 (01) : 73 - 94