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Shuichi Takayama
Researcher at Georgia Institute of Technology
Publications - 394
Citations - 26258
Shuichi Takayama is an academic researcher from Georgia Institute of Technology. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 77, co-authored 361 publications receiving 23775 citations. Previous affiliations of Shuichi Takayama include Parker H. Petit Institute for Bioengineering & Bioscience & Ulsan National Institute of Science and Technology.
Papers
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Soft Lithography in Biology and Biochemistry
TL;DR: Soft lithography offers the ability to control the molecular structure of surfaces and to pattern the complex molecules relevant to biology, to fabricate channel structures appropriate for microfluidics, and topattern and manipulate cells.
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Patterning proteins and cells using soft lithography
TL;DR: This review describes the pattering of proteins and cells using a non-photolithographic microfabrication technology, which consists of a set of related techniques, each of which uses stamps or channels fabricated in an elastomeric ('soft') material for pattern transfer.
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Opportunities and challenges for use of tumor spheroids as models to test drug delivery and efficacy.
TL;DR: The suitability of spheroids as an in vitro platform for testing drug delivery systems is examined and the assay techniques required for the characterization of drug delivery and efficacy in sp Heroids are discussed.
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High-throughput 3D spheroid culture and drug testing using a 384 hanging drop array
Yi-Chung Tung,Yi-Chung Tung,Amy Y. Hsiao,Steven G. Allen,Yu Suke Torisawa,Mitchell Ho,Shuichi Takayama,Shuichi Takayama +7 more
TL;DR: A 384-well format hanging drop culture plate is described that makes spheroid formation, culture, and subsequent drug testing on the obtained 3D cellular constructs as straightforward to perform and adapt to existing high-throughput screening (HTS) instruments as conventional 2D cultures.
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Zwitterionic SAMs that Resist Nonspecific Adsorption of Protein from Aqueous Buffer
TL;DR: This paper describes the use of surface plasmon resonance spectroscopy and self-assembled monolayers (SAMs) of alkanethiols on gold to evaluate the ability of surfaces terminating in different combinations of charged groups to resist the nonspecific adsorption of proteins from aqueous buffer.