Low cost and manufacturable complete microTAS for detecting bacteria.

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(R), 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.

[1]  Samuel K Sia,et al.  Lab-on-a-chip devices for global health: past studies and future opportunities. , 2007, Lab on a chip.

[2]  G. Procop Molecular diagnostics for the detection and characterization of microbial pathogens. , 2007, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[3]  Dmitri Ivnitski,et al.  Nucleic acid approaches for detection and identification of biological warfare and infectious disease agents. , 2003, BioTechniques.

[4]  C. Klapperich,et al.  Thermoplastic microfluidic device for on-chip purification of nucleic acids for disposable diagnostics. , 2006, Analytical chemistry.

[5]  P. Paul,et al.  Imaging of Pressure- and Electrokinetically Driven Flows through Open Capillaries. , 1998, Analytical chemistry.

[6]  A Manz,et al.  Miniaturised nucleic acid analysis. , 2004, Lab on a chip.

[7]  Stephen S Morse,et al.  Immunoassay of infectious agents. , 2003, BioTechniques.

[8]  C. Klapperich,et al.  Sample preparation module for bacterial lysis and isolation of DNA from human urine , 2009, Biomedical microdevices.

[9]  J. Henry Clinical diagnosis and management by laboratory methods , 1979 .

[10]  Andreas Manz,et al.  Total nucleic acid analysis integrated on microfluidic devices. , 2007, Lab on a chip.

[11]  C. Klapperich,et al.  Cell lysis and DNA extraction of gram-positive and gram-negative bacteria from whole blood in a disposable microfluidic chip. , 2009, Lab on a chip.

[12]  Catherine M. Klapperich,et al.  Microfluidics-based extraction of viral RNA from infected mammalian cells for disposable molecular diagnostics , 2008 .

[13]  J. Josserand,et al.  Mixing processes in a zigzag microchannel: finite element simulations and optical study. , 2002, Analytical chemistry.

[14]  C. Chin,et al.  Lab-ona-chip devices for global health : Past studies and future opportunities , 2006 .

[15]  Robin H. Liu,et al.  Self-contained, fully integrated biochip for sample preparation, polymerase chain reaction amplification, and DNA microarray detection. , 2004, Analytical chemistry.

[16]  Michael G. Roper,et al.  A fully integrated microfluidic genetic analysis system with sample-in–answer-out capability , 2006, Proceedings of the National Academy of Sciences.

[17]  S. Sickafoose,et al.  Low-distortion, high-strength bonding of thermoplastic microfluidic devices employing case-II diffusion-mediated permeant activation. , 2007, Lab on a chip.