On-chip irreversible electroporation for bacterial cell membrane rupture
In this work, the DNA preparation process for genetic analysis was developed. To rupture the cell membrane of Salmonella on a microfluidic chip, high electric field pulses were applied through gold electrode. The applied voltage was less than 10V DC voltage. Electric field pulses were short-duration...
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th-mahidol.141282018-06-11T11:47:29Z On-chip irreversible electroporation for bacterial cell membrane rupture S. Jaikla T. Maturos T. Pogfay C. Neatpisarnvanit P. Sritongkham A. Tuantranont Mahidol University Thailand National Electronics and Computer Technology Center Engineering In this work, the DNA preparation process for genetic analysis was developed. To rupture the cell membrane of Salmonella on a microfluidic chip, high electric field pulses were applied through gold electrode. The applied voltage was less than 10V DC voltage. Electric field pulses were short-duration in microsecond. Fluorescent spectrophotometer was employed for live/dead bacterial cells detection. The live bacterial cells were tagged by SYTO 9 green fluorescent stain. The red-fluorescent nucleic acid stain, propidium iodide was used to tag the dead cells. The highest percentage of 95% dead cells was at 7V applied voltage and 90 μs pulse duration. This result was confirmed by plate count with completely dead cell. ©2012 IEEE. 2018-06-11T04:47:29Z 2018-06-11T04:47:29Z 2012-12-01 Conference Paper 5th 2012 Biomedical Engineering International Conference, BMEiCON 2012. (2012) 10.1109/BMEiCon.2012.6465456 2-s2.0-84875086374 https://repository.li.mahidol.ac.th/handle/123456789/14128 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84875086374&origin=inward |
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Engineering S. Jaikla T. Maturos T. Pogfay C. Neatpisarnvanit P. Sritongkham A. Tuantranont On-chip irreversible electroporation for bacterial cell membrane rupture |
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In this work, the DNA preparation process for genetic analysis was developed. To rupture the cell membrane of Salmonella on a microfluidic chip, high electric field pulses were applied through gold electrode. The applied voltage was less than 10V DC voltage. Electric field pulses were short-duration in microsecond. Fluorescent spectrophotometer was employed for live/dead bacterial cells detection. The live bacterial cells were tagged by SYTO 9 green fluorescent stain. The red-fluorescent nucleic acid stain, propidium iodide was used to tag the dead cells. The highest percentage of 95% dead cells was at 7V applied voltage and 90 μs pulse duration. This result was confirmed by plate count with completely dead cell. ©2012 IEEE. |
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Mahidol University |
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Mahidol University S. Jaikla T. Maturos T. Pogfay C. Neatpisarnvanit P. Sritongkham A. Tuantranont |
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Conference or Workshop Item |
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S. Jaikla T. Maturos T. Pogfay C. Neatpisarnvanit P. Sritongkham A. Tuantranont |
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S. Jaikla |
title |
On-chip irreversible electroporation for bacterial cell membrane rupture |
title_short |
On-chip irreversible electroporation for bacterial cell membrane rupture |
title_full |
On-chip irreversible electroporation for bacterial cell membrane rupture |
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On-chip irreversible electroporation for bacterial cell membrane rupture |
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On-chip irreversible electroporation for bacterial cell membrane rupture |
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on-chip irreversible electroporation for bacterial cell membrane rupture |
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2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/14128 |
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