%0 Journal Article %1 citeulike:5015896 %A Sauer-Budge, Alexis F. %A Mirer, Paul %A Chatterjee, Anirban %A Klapperich, Catherine M. %A Chargin, David %A Sharon, Andre %D 2009 %I The Royal Society of Chemistry %J Lab Chip %K 92c50-medical-applications-general 92c40-biochemistry-molecular-biology %N 19 %P 2803--2810 %R 10.1039/b904854e %T Low cost and manufacturable complete microTAS for detecting bacteria %U http://dx.doi.org/10.1039/b904854e %V 9 %X In this paper, we present a fully integrated lab-on-a-chip and associated instrument for the detection of bacteria from liquid samples. The system conducts bacterial lysis, nucleic acid isolation and concentration, polymerase chain reaction (PCR), and end-point fluorescent detection. To enable truly low-cost manufacture of the single-use disposable chip, we designed the plastic chip in a planar format without any active components to be amenable to injection molding and utilized a novel porous polymer monolith (PPM) embedded with silica that has been shown to lyse bacteria and isolate the nucleic acids from clinical samples (M. D. Kulinski, M. Mahalanabis, S. Gillers, J. Y. Zhang, S. Singh and C. M. Klapperich, Biomed. Microdevices, 2009, 11, 671-678).1 The chip is made of Zeonexregistered sign, a thermoplastic with a high melting temperature to allow PCR, good UV transmissibility for UV-curing of the PPM, and low auto-fluorescence for fluorescence detection of the amplicon. We have built a prototype instrument to automate control of the fluids, temperature cycling, and optical detection with the capability of accommodating various chip designs. To enable fluid control without including valves or pumps on the chip, we utilized a remote valve switching technique. To allow fluid flow rate changes on the valveless chip, we incorporated speed changing fluid reservoirs. The PCR thermal cycling was achieved with a ceramic heater and air cooling, while end-point fluorescence detection was accomplished with an optical spectrometer; all integrated in the instrument. The chip seamlessly and automatically is mated to the instrument through an interface block that presses against the chip. The interface block aligns and ensures good contact of the chip to the temperature controlled region and the optics. The integrated functionality of the chip was demonstrated using Bacillus subtilis as a model bacterial target. A Taqman assay was employed on-chip to detect the isolated bacterial DNA.

@article{citeulike:5015896, abstract = {{In this paper, we present a fully integrated lab-on-a-chip and associated instrument for the detection of bacteria from liquid samples. The system conducts bacterial lysis, nucleic acid isolation and concentration, polymerase chain reaction (PCR), and end-point fluorescent detection. To enable truly low-cost manufacture of the single-use disposable chip, we designed the plastic chip in a planar format without any active components to be amenable to injection molding and utilized a novel porous polymer monolith (PPM) embedded with silica that has been shown to lyse bacteria and isolate the nucleic acids from clinical samples (M. D. Kulinski, M. Mahalanabis, S. Gillers, J. Y. Zhang, S. Singh and C. M. Klapperich, Biomed. Microdevices, 2009, 11, 671-678).1 The chip is made of Zeonex[registered sign], a thermoplastic with a high melting temperature to allow PCR, good UV transmissibility for UV-curing of the PPM, and low auto-fluorescence for fluorescence detection of the amplicon. We have built a prototype instrument to automate control of the fluids, temperature cycling, and optical detection with the capability of accommodating various chip designs. To enable fluid control without including valves or pumps on the chip, we utilized a remote valve switching technique. To allow fluid flow rate changes on the valveless chip, we incorporated speed changing fluid reservoirs. The PCR thermal cycling was achieved with a ceramic heater and air cooling, while end-point fluorescence detection was accomplished with an optical spectrometer; all integrated in the instrument. The chip seamlessly and automatically is mated to the instrument through an interface block that presses against the chip. The interface block aligns and ensures good contact of the chip to the temperature controlled region and the optics. The integrated functionality of the chip was demonstrated using Bacillus subtilis as a model bacterial target. A Taqman assay was employed on-chip to detect the isolated bacterial DNA.}}, added-at = {2017-06-29T07:13:07.000+0200}, author = {Sauer-Budge, Alexis F. and Mirer, Paul and Chatterjee, Anirban and Klapperich, Catherine M. and Chargin, David and Sharon, Andre}, biburl = {https://www.bibsonomy.org/bibtex/2e7af5d064edabb7c6f56764e02164441/gdmcbain}, citeulike-article-id = {5015896}, citeulike-attachment-1 = {sauer-budge_09_low.pdf; /pdf/user/gdmcbain/article/5015896/859172/sauer-budge_09_low.pdf; 9dfc3800802b75c19e73dc0ca4e3f08a2bd1b9e4}, citeulike-linkout-0 = {http://dx.doi.org/10.1039/b904854e}, citeulike-linkout-1 = {http://www.rsc.org/Publishing/Journals/article.asp?doi=b904854e}, comment = {(private-note)listed at http://www.fhcmi.org/Publications}, doi = {10.1039/b904854e}, file = {sauer-budge_09_low.pdf}, interhash = {6789e7370254b0551839d705e247585f}, intrahash = {e7af5d064edabb7c6f56764e02164441}, journal = {Lab Chip}, keywords = {92c50-medical-applications-general 92c40-biochemistry-molecular-biology}, number = 19, pages = {2803--2810}, posted-at = {2012-12-11 09:46:32}, priority = {2}, publisher = {The Royal Society of Chemistry}, timestamp = {2019-06-03T01:03:22.000+0200}, title = {{Low cost and manufacturable complete microTAS for detecting bacteria}}, url = {http://dx.doi.org/10.1039/b904854e}, volume = 9, year = 2009 }