scholarly journals Enhancing Peptide Biomaterials for Biofabrication

Polymers ◽  
2021 ◽  
Vol 13 (16) ◽  
pp. 2590
Author(s):  
Kate Firipis ◽  
David R. Nisbet ◽  
Stephanie J. Franks ◽  
Robert M. I. Kapsa ◽  
Elena Pirogova ◽  
...  

Biofabrication using well-matched cell/materials systems provides unprecedented opportunities for dealing with human health issues where disease or injury overtake the body’s native regenerative abilities. Such opportunities can be enhanced through the development of biomaterials with cues that appropriately influence embedded cells into forming functional tissues and organs. In this context, biomaterials’ reliance on rigid biofabrication techniques needs to support the incorporation of a hierarchical mimicry of local and bulk biological cues that mimic the key functional components of native extracellular matrix. Advances in synthetic self-assembling peptide biomaterials promise to produce reproducible mimics of tissue-specific structures and may go some way in overcoming batch inconsistency issues of naturally sourced materials. Recent work in this area has demonstrated biofabrication with self-assembling peptide biomaterials with unique biofabrication technologies to support structural fidelity upon 3D patterning. The use of synthetic self-assembling peptide biomaterials is a growing field that has demonstrated applicability in dermal, intestinal, muscle, cancer and stem cell tissue engineering.

2018 ◽  
Vol 6 (6) ◽  
pp. 979-990 ◽  
Author(s):  
Batzaya Nyambat ◽  
Chih-Hwa Chen ◽  
Pei-Chun Wong ◽  
Chih-Wei Chiang ◽  
Mantosh Kumar Satapathy ◽  
...  

3D Bioscaffold with relative high mechanical property was developed using rabbit ADSCs.


2008 ◽  
Vol 83 (4) ◽  
pp. 408-420 ◽  
Author(s):  
Pankaj Godara ◽  
Clive D McFarland ◽  
Robert E Nordon

2006 ◽  
Vol 183 (4) ◽  
pp. 169-179 ◽  
Author(s):  
Ulrich Reinhart Goessler ◽  
Katrin Riedel ◽  
Karl Hörmann ◽  
Frank Riedel

Author(s):  
Young L. Kim ◽  
Zhengbin Xu ◽  
Altug Ozcelikkale ◽  
Bumsoo Han

Successful cryopreservation of engineered tissues (ETs) can greatly advance the access and availability of cell/tissue engineering products for clinical use. One of the key challenges in cryopreserving ETs is that the functionality of ETs should be maintained throughout the preservation process. Many of the functionalities are associated with the extracellular matrix (ECM) microstructure, which in turn can be a crucial marker for the post-thaw functionality. Recent studies also reported that the ECM microstructure can be affected by freezing-induced cell-fluid-matrix interactions.1–3 Thus, it is critical to assess three-dimensional (3-D) matrix structure of cryopreserved ETs in a non-destructive, non-invasive, and rapid manner.


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