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Titlebook: Cell and Organ Printing; Bradley R. Ringeisen,Barry J. Spargo,Peter K. Wu Book 2010 Springer Science+Business Media B.V. 2010 bacteria.bio

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书目名称Cell and Organ Printing
编辑Bradley R. Ringeisen,Barry J. Spargo,Peter K. Wu
视频video
概述This book will be the first comprehensive review of all cell-printing technologies by experts in their own discipline.Updates on the achievements, for example, resolution, throughput, speed, etc., of
图书封面Titlebook: Cell and Organ Printing;  Bradley R. Ringeisen,Barry J. Spargo,Peter K. Wu Book 2010 Springer Science+Business Media B.V. 2010 bacteria.bio
描述Cell and organ printing has become a hot topic of scientific pursuit.Since several early publications between 2000-2003 that demonstrated proof-of-concept, cell and organ printing has blossomed into a rich area for scientific exploration that is being performed by researchers across the globe. Research has thoroughly demonstrated that living cells can be printed via a number of actuations including electrospray, extrusion via micropens and ejection through photothermal, thermal or optical mechanisms. This topic has come of age and it is ripe for exploring the underpinnings of the research to date. We have included research that uses printing technology to deposit or guide cells for tissue engineering applications and for completeness, we have also included chapters describing bacteria printing, biomolecular printing that could be used to build growth factors or recruitment macromolecules into scaffolds, tissue microdissection, as well as live cell printing. The breadth of approaches includes 3D freeform fabrication, ink jet, laser guidance and modified laser direct write techniques.We hope that this book is not the final word but the first word, defining how these tools have been u
出版日期Book 2010
关键词bacteria; biology; biomaterial; biomolecule; cell; protein; tissue
版次1
doihttps://doi.org/10.1007/978-90-481-9145-1
isbn_softcover978-94-017-8517-4
isbn_ebook978-90-481-9145-1
copyrightSpringer Science+Business Media B.V. 2010
The information of publication is updating

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https://doi.org/10.1057/9780230376922vide complex scaffolds with controlled architecture and porosity however problems with incorporating cells into the scaffold structure still persist. Standard cell seeding techniques can result in a poor cell seeding density, pore occlusion and is limited with regards to cell penetration, scaffold s
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https://doi.org/10.1057/9780230376922nique allowing the deposition of tiny amounts of material from a donor thin film to a solid substrate through the action of a pulsed laser beam. Although LIFT was originally developed to operate with solid films, it has been demonstrated that deposition is also possible from liquid films. In this ca
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https://doi.org/10.1057/9780230376922om living cultures and paraffin-embedded fixed tissue sections. Detailed studies have been published that demonstrate the energy conversion layer used by BioLP to absorb incident laser energy and promote forward transfer of biological materials prevents damage to the printed cells. Additionally, thi
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https://doi.org/10.1057/9780230376922 distance and laser pulse frequency). The droplet ejection mechanism is indeed governed by vapor bubble dynamics (bubble growth and collapsing) and it is thus related to both the condition of laser irradiation and the rheological properties of the liquid film (viscosity, surface tension). We present
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Optimality Theory and Pragmaticssue. A key feature of arbitrarily engineered tissue is the ability to control the position of living cells. Maskless Mesoscale Material Deposition Technique (M3D) is a Computer Aided Design (CAD) driven Direct Write technique that has been developed for rapidly depositing a variety of materials and
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