Feasibility study of a biochip for mumps virus enzyme-linked immunosorbent assay (ELISA)
Plastic chips were fabricated for the purpose of creating a lab-on-a-chip to miniaturise the Mumps virus enzyme-linked immunosorbent assay (ELISA). The pattern of microfluidic channels was first transferred from a glass master template possessing an inverse image of the channels to polystyrene chips...
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sg-ntu-dr.10356-53992023-03-11T17:05:42Z Feasibility study of a biochip for mumps virus enzyme-linked immunosorbent assay (ELISA) Woon, Fung Peng. Gong, Thomas Haiqing School of Mechanical and Production Engineering DRNTU::Engineering::Mechanical engineering::Bio-mechatronics Plastic chips were fabricated for the purpose of creating a lab-on-a-chip to miniaturise the Mumps virus enzyme-linked immunosorbent assay (ELISA). The pattern of microfluidic channels was first transferred from a glass master template possessing an inverse image of the channels to polystyrene chips which were then bonded to polycarbonate covers. A good imprint of the channels and wells could be obtained at a hot embossing temperature of 110°C and by holding the press for 3 minutes. The chip could be tightly bonded to its cover at 110 °C while maintaining the press for 3 minutes. Results showed that it was possible to reduce the volume of reagents used and the time taken to perform the immunoassay on the biochip as compared with performing it on microtiter wells supplied in commercial test kits. Master of Science (Biomedical Engineering) 2008-09-17T10:49:39Z 2008-09-17T10:49:39Z 2003 2003 Thesis http://hdl.handle.net/10356/5399 Nanyang Technological University application/pdf |
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DRNTU::Engineering::Mechanical engineering::Bio-mechatronics Woon, Fung Peng. Feasibility study of a biochip for mumps virus enzyme-linked immunosorbent assay (ELISA) |
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Plastic chips were fabricated for the purpose of creating a lab-on-a-chip to miniaturise the Mumps virus enzyme-linked immunosorbent assay (ELISA). The pattern of microfluidic channels was first transferred from a glass master template possessing an inverse image of the channels to polystyrene chips which were then bonded to polycarbonate covers. A good imprint of the channels and wells could be obtained at a hot embossing temperature of 110°C and by holding the press for 3 minutes. The chip could be tightly bonded to its cover at 110 °C while maintaining the press for 3 minutes. Results showed that it was possible to reduce the volume of reagents used and the time taken to perform the immunoassay on the biochip as compared with performing it on microtiter wells supplied in commercial test kits. |
author2 |
Gong, Thomas Haiqing |
author_facet |
Gong, Thomas Haiqing Woon, Fung Peng. |
format |
Theses and Dissertations |
author |
Woon, Fung Peng. |
author_sort |
Woon, Fung Peng. |
title |
Feasibility study of a biochip for mumps virus enzyme-linked immunosorbent assay (ELISA) |
title_short |
Feasibility study of a biochip for mumps virus enzyme-linked immunosorbent assay (ELISA) |
title_full |
Feasibility study of a biochip for mumps virus enzyme-linked immunosorbent assay (ELISA) |
title_fullStr |
Feasibility study of a biochip for mumps virus enzyme-linked immunosorbent assay (ELISA) |
title_full_unstemmed |
Feasibility study of a biochip for mumps virus enzyme-linked immunosorbent assay (ELISA) |
title_sort |
feasibility study of a biochip for mumps virus enzyme-linked immunosorbent assay (elisa) |
publishDate |
2008 |
url |
http://hdl.handle.net/10356/5399 |
_version_ |
1761781742323105792 |