Mechanical stiffness-defined matrices for stem cell research and drug screening
Thesis (M. Eng.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2008. === MIT Science Library copy: printed in leaves. === Also issued printed in leaves. === Includes bibliographical references (p. 74-78). === Synthetic polymer matrices or subtrata with tailored...
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ndltd-MIT-oai-dspace.mit.edu-1721.1-453912019-05-02T16:21:37Z Mechanical stiffness-defined matrices for stem cell research and drug screening Ha, Vu Nguyen Tuan Krystyn J. Van Vliet. Massachusetts Institute of Technology. Dept. of Materials Science and Engineering. Massachusetts Institute of Technology. Dept. of Materials Science and Engineering. Materials Science and Engineering. Thesis (M. Eng.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2008. MIT Science Library copy: printed in leaves. Also issued printed in leaves. Includes bibliographical references (p. 74-78). Synthetic polymer matrices or subtrata with tailored elastic properties provide a powerful method to direct biological cell' differentiation and foster cell multiplication. By changing the stiffness of the substrate, human mesenchymal stem cell (MSCs) could be directed along neuronal, muscle, or bone lineages. Matrix elastic modulus can also control anchorage dependent cell's motility, localization, tissue formation and organization. Besides that, synthetic materials such as biodegradable polymers offer a versatile alternative to naturally derived biopolymers. Their mechanical properties can be highly tailored and they are easy to synthesize and shape. Moreover, these platforms can be readily "biologically" fine-tuned toward a particular cell linage by incorporating well-documented parameters, which play crucial roles in cell-extra cellular matrix (ECM) signaling pathway, such as growth factor, surface topology and stimulation signal. Hence, these materials are suitable candidates to develop engineered matrices for stem cell culture, cell manipulating platforms in biological research and drug development. In this thesis, commercialization aspects of these engineered matrices for stem cell research, cell culture and drug development markets are evaluated both in USA and in Singapore markets. Technological barriers, intellectual property and a preliminary cost model are analyzed. A business plan is presented and discussed for applications in both the stem cell research and the drug screening markets. Although these two markets are ill-defined, both of them are growing rapidly and appear to be very promising. A review of the technology itself led to the conclusion that the matrix is capable of induce anchorage dependent cell into specific lineage but the success rate is not yet quantified and further research need to be done to achieve good reproducibility and to meet the required efficacy of the industry. by Vu Nguyen Tuan Ha. M.Eng. 2009-04-29T17:34:52Z 2009-04-29T17:34:52Z 2008 2008 Thesis http://hdl.handle.net/1721.1/45391 317402676 eng M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 79, [2] p. application/pdf Massachusetts Institute of Technology |
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Materials Science and Engineering. Ha, Vu Nguyen Tuan Mechanical stiffness-defined matrices for stem cell research and drug screening |
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Thesis (M. Eng.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2008. === MIT Science Library copy: printed in leaves. === Also issued printed in leaves. === Includes bibliographical references (p. 74-78). === Synthetic polymer matrices or subtrata with tailored elastic properties provide a powerful method to direct biological cell' differentiation and foster cell multiplication. By changing the stiffness of the substrate, human mesenchymal stem cell (MSCs) could be directed along neuronal, muscle, or bone lineages. Matrix elastic modulus can also control anchorage dependent cell's motility, localization, tissue formation and organization. Besides that, synthetic materials such as biodegradable polymers offer a versatile alternative to naturally derived biopolymers. Their mechanical properties can be highly tailored and they are easy to synthesize and shape. Moreover, these platforms can be readily "biologically" fine-tuned toward a particular cell linage by incorporating well-documented parameters, which play crucial roles in cell-extra cellular matrix (ECM) signaling pathway, such as growth factor, surface topology and stimulation signal. Hence, these materials are suitable candidates to develop engineered matrices for stem cell culture, cell manipulating platforms in biological research and drug development. In this thesis, commercialization aspects of these engineered matrices for stem cell research, cell culture and drug development markets are evaluated both in USA and in Singapore markets. Technological barriers, intellectual property and a preliminary cost model are analyzed. A business plan is presented and discussed for applications in both the stem cell research and the drug screening markets. Although these two markets are ill-defined, both of them are growing rapidly and appear to be very promising. A review of the technology itself led to the conclusion that the matrix is capable of induce anchorage dependent cell into specific lineage but the success rate is not yet quantified and further research need to be done to achieve good reproducibility and to meet the required efficacy of the industry. === by Vu Nguyen Tuan Ha. === M.Eng. |
author2 |
Krystyn J. Van Vliet. |
author_facet |
Krystyn J. Van Vliet. Ha, Vu Nguyen Tuan |
author |
Ha, Vu Nguyen Tuan |
author_sort |
Ha, Vu Nguyen Tuan |
title |
Mechanical stiffness-defined matrices for stem cell research and drug screening |
title_short |
Mechanical stiffness-defined matrices for stem cell research and drug screening |
title_full |
Mechanical stiffness-defined matrices for stem cell research and drug screening |
title_fullStr |
Mechanical stiffness-defined matrices for stem cell research and drug screening |
title_full_unstemmed |
Mechanical stiffness-defined matrices for stem cell research and drug screening |
title_sort |
mechanical stiffness-defined matrices for stem cell research and drug screening |
publisher |
Massachusetts Institute of Technology |
publishDate |
2009 |
url |
http://hdl.handle.net/1721.1/45391 |
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AT havunguyentuan mechanicalstiffnessdefinedmatricesforstemcellresearchanddrugscreening |
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