Development of A 3d Cryoprinter For Printing Soft Biomaterials

Cryobiology ◽  
2021 ◽  
Vol 103 ◽  
pp. 180
Author(s):  
Linnea Warburton ◽  
Tao Lou ◽  
Boris Rubinsky
Keyword(s):  
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Guanlin Wu ◽  
Michael Gotthardt ◽  
Maik Gollasch

An amendment to this paper has been published and can be accessed via a link at the top of the paper.


Kobunshi ◽  
2004 ◽  
Vol 53 (11) ◽  
pp. 881-885
Author(s):  
Tatsuro OUCHI ◽  
Hidetoshi ARIMURA
Keyword(s):  

2018 ◽  
Vol 132 ◽  
pp. 214-234 ◽  
Author(s):  
Onur Bas ◽  
Isabelle Catelas ◽  
Elena M. De-Juan-Pardo ◽  
Dietmar W. Hutmacher
Keyword(s):  

2017 ◽  
Vol 7 (6) ◽  
pp. 20160116 ◽  
Author(s):  
Xuewen Du ◽  
Jie Zhou ◽  
Xinming Li ◽  
Bing Xu

As a novel class of biomaterials, nucleopeptides, via the conjugation of nucleobases and peptides, usually self-assemble to form nanofibres driven mainly by hydrogen bonds. Containing nucleobase(s), nucleopeptides have a unique property—interacting with nucleic acids. Here we report the design and characterization of nucleopeptides that self-assemble in water and are able to interact with single-stranded DNAs (ssDNAs). Containing nucleobases on their side chains, these nucleopeptides bind with the ssDNAs, and the ssDNAs reciprocally affect the self-assembly of nucleopeptides. In addition, the interactions between nucleopeptides and ssDNAs also decrease their proteolytic resistance against proteinase K, which further demonstrates the binding with ssDNAs. The nucleopeptides also interact with plasmid DNA and deliver hairpin DNA into cells. This work illustrates a new and rational approach to create soft biomaterials by the integration of nucleobases and peptides to bind with DNA, which may lead to the development of nucleopeptides for controlling DNA in cells.


2015 ◽  
Vol 112 (47) ◽  
pp. 14444-14451 ◽  
Author(s):  
Mark W. Tibbitt ◽  
Christopher B. Rodell ◽  
Jason A. Burdick ◽  
Kristi S. Anseth

Biomaterials that interface with biological systems are used to deliver drugs safely and efficiently; to prevent, detect, and treat disease; to assist the body as it heals; and to engineer functional tissues outside of the body for organ replacement. The field has evolved beyond selecting materials that were originally designed for other applications with a primary focus on properties that enabled restoration of function and mitigation of acute pathology. Biomaterials are now designed rationally with controlled structure and dynamic functionality to integrate with biological complexity and perform tailored, high-level functions in the body. The transition has been from permissive to promoting biomaterials that are no longer bioinert but bioactive. This perspective surveys recent developments in the field of polymeric and soft biomaterials with a specific emphasis on advances in nano- to macroscale control, static to dynamic functionality, and biocomplex materials.


Author(s):  
Wilson Eng ◽  
Max Kim ◽  
Anand Ramasubramanian ◽  
Sang-Joon John Lee

Mechanical properties of biomaterials are difficult to characterize experimentally because many relevant biomaterials such as hydrogels are very pliable and viscoelastic. Furthermore, test specimens such as blood clots retrieved from patients tend to be small in size, requiring fine positioning and sensitive force measurement. Mechanobiological studies require fast data recording, preferably under simultaneous microscope imaging, in order to monitor events such as structural remodeling or localized rupture while strain is being applied. A low-profile tensile tester that applies prescribed displacement up to several millimeters and measures forces with resolution on the order of micronewtons has been designed and tested, using alginate as a representative soft biomaterial. 1.5% alginate (cross-linked with 0.1 M and 0.2 M calcium chloride) has been chosen as a reference material because of its extensive use in tissue engineering and other biomedical applications. Prescribed displacement control with rates between 20 μm/s and 60 μm/s were applied using a commercial low-noise nanopositioner. Force data were recorded using data acquisition and signal conditioning hardware with sampling rates as high as 1 kHz. Elongation up to approximately 10 mm and force in the range of 250 mN were measured. The data were used to extract elastic and viscoelastic parameters for alginate specimens. Another biomaterial, 2% agarose, was also tested to show versatility of the apparatus for slightly stiffer materials. The apparatus is modular such that different load cells ranging in capacity from hundreds of millinewtons to tens of newtons can be used. The apparatus furthermore is compatible with real-time microscope imaging, particle tracing, and programmable positioning sequences.


2020 ◽  
Vol 28 (8) ◽  
pp. 689-702
Author(s):  
Kangseok Lee ◽  
Chaenyung Cha
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document