TY - JOUR
T1 - Rapid detection of trace bacteria in biofluids using porous monoliths in microchannels
AU - Mai, Junyu
AU - Abhyankar, Vinay V.
AU - Piccini, Matthew E.
AU - Olano, Juan P.
AU - Willson, Richard
AU - Hatch, Anson V.
N1 - Funding Information:
We thank Dr. C.Y. Koh for helpful technical assistance and discussions. This work was funded by NIH WRCE , Grant no. U54 AI057156 from NIAID/NIH , and by a joint Sandia LDRD/UTMB Strategic Partnership award . Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the RCE Programs Office, NIAID, or NIH. Sandia is a multiprogram laboratory operated by Sandia Corp., a Lockheed Martin Co., for the United States Department of Energy under Contract DE-AC0494AL85000.
PY - 2014/4/15
Y1 - 2014/4/15
N2 - We present advancements in microfluidic technology for rapid detection of as few as 10 rickettsial organisms in complex biological samples. An immuno-reactive filter, macroporous polyacrylamide monolith (PAM), fabricated within a microfluidic channel enhances solid-phase immuno-capture, staining and detection of targeted bacteria. Bacterial cells in samples flowing through the channel are forced to interact with the PAM filter surface due to size exclusion, overcoming common transport and kinetic limitations for rapid (min), high-efficiency (~100%) capture. In the process, targeted cells in sample volumes of 10. μl to >100. μl are concentrated within a sub-50. nl region at the PAM filter edge in the microchannel, thus concentrating them over 1000-fold. This significantly increases sensitivity, as the hydrophilic PAM also yields low non-specific immuno-fluorescence backgrounds with samples including serum, blood and non-targeted bacteria. The concentrated target cells are detected using fluorescently-labeled antibodies. With a single 2.0×2.0×0.3. mm PAM filter, as few as 10 rickettsial organisms per 100. μl of lysed blood sample can be analyzed within 60. min, as compared to hours or even days needed for conventional detection methods. This method is highly relevant to rapid, multiplexed, low-cost point of care diagnostics at early stages of infection where diagnostics providing more immediate and actionable test results are needed to improve patient outcomes and mitigate potential natural and non-natural outbreaks or epidemics of rickettsial diseases.
AB - We present advancements in microfluidic technology for rapid detection of as few as 10 rickettsial organisms in complex biological samples. An immuno-reactive filter, macroporous polyacrylamide monolith (PAM), fabricated within a microfluidic channel enhances solid-phase immuno-capture, staining and detection of targeted bacteria. Bacterial cells in samples flowing through the channel are forced to interact with the PAM filter surface due to size exclusion, overcoming common transport and kinetic limitations for rapid (min), high-efficiency (~100%) capture. In the process, targeted cells in sample volumes of 10. μl to >100. μl are concentrated within a sub-50. nl region at the PAM filter edge in the microchannel, thus concentrating them over 1000-fold. This significantly increases sensitivity, as the hydrophilic PAM also yields low non-specific immuno-fluorescence backgrounds with samples including serum, blood and non-targeted bacteria. The concentrated target cells are detected using fluorescently-labeled antibodies. With a single 2.0×2.0×0.3. mm PAM filter, as few as 10 rickettsial organisms per 100. μl of lysed blood sample can be analyzed within 60. min, as compared to hours or even days needed for conventional detection methods. This method is highly relevant to rapid, multiplexed, low-cost point of care diagnostics at early stages of infection where diagnostics providing more immediate and actionable test results are needed to improve patient outcomes and mitigate potential natural and non-natural outbreaks or epidemics of rickettsial diseases.
KW - Blood borne bacteria detection
KW - Macroporous monolith filter
KW - Microfluidic device
KW - Point-of-care diagnostic assay
KW - Polyacrylamide monolith
KW - Rickettsia detection
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U2 - 10.1016/j.bios.2013.11.012
DO - 10.1016/j.bios.2013.11.012
M3 - Article
C2 - 24316449
AN - SCOPUS:84889593894
SN - 0956-5663
VL - 54
SP - 435
EP - 441
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
ER -