John W. Pettit - Derwood MD, US James P. Landers - Charlottesville VA, US Joan M. Bienvenue - Fredericksburg VA, US Daniel J. Marchiarullo - North Haledon NJ, US Brian E. Root - Charlottesville VA, US Orion N. Scott - Charlottesville VA, US
Assignee:
LOCKHEED MARTIN CORPORATION - BETHESDA MD
International Classification:
C12Q 1/68 C12M 1/34
US Classification:
435 612, 4352872
Abstract:
Aspects of the disclosure provides a DNA analyzer to facilitate an integrated single-chip DNA analysis. The DNA analyzer includes an interface for coupling a microfluidic chip to the DNA analyzer. The microfluidic chip includes a first domain configured for polymerase chain reaction (PCR) amplification of DNA fragments, and a second domain fluidically coupled to the first domain to receive the DNA fragments and perform electrophoretic separation of the DNA fragments. The DNA fragments are tagged with fluorescent labels. The DNA analyzer includes a detection module to excite the fluorescent labels to emit fluorescence and detect the emitted fluorescence. The detection module includes a laser source, a set of optical elements, a filter module and a photo-detector.
Method And System For Sample Collection, Storage, Preparation And Detection
- Southampton, GB Christopher Birch - Charlottesville VA, US Daniel Mills - Charlottesville VA, US Brian Root - Charlottesville VA, US James Landers - Charlottesville VA, US Jingyi Li - Charlottesville VA, US Matthew Yeung - Mount Waverley, AU David Saul - Dunedin, AU David Vigil - Mount Waverley, AU Andrew Guy - Mount Waverley, AU Stan Wada - Mount Waverley, AU Betina De Gorordo - Mount Waverley, AU Steward Dodman - Mount Waverley, AU Tom Moran - Southampton, GB Stuart Knowles - Mount Waverley, AU Fernando Dias - Mount Waverley, AU Rick Gardner - Mount Waverley, AU
A collection device for a biological sample to capture target compounds such as viruses or other pathogens or particles for testing from within the sample and move the captured target compound to a separate chamber for subsequent processing. The collection device can include an openable substance blister including capture particles located in a cup interior. Capture particles can attract and bind the target compounds from the sample. An extraction tube extracts any nucleic acid from the target compound for storage or subsequent amplification and testing to confirm presence of known microorganisms. The extraction tube can comprise a heat-deformable material and can be connected to a microfluidic cartridge for further processing of nucleic acid including, amplification and detection. The microfluidic cartridge includes valves and a plurality of chambers for amplification.
- Bethesda MD, US - Hamilton, NZ James LANDERS - Charlottesville VA, US Douglas J. SOUTH - Rockville MD, US Brian E. ROOT - Charlottesville VA, US
Assignee:
LOCKHEED MARTIN CORPORATION - Bethesda MD ZYGEM CORPORATION LTD. - Hamilton
International Classification:
C12Q 1/686
Abstract:
A cartridge interface module (CIM), configured to engage with a removable microfluidic cartridge in a nucleic acid analyzer system can include a fluidics component, which is configured to initiate and support a liquid extraction of nucleic acids from a biological sample contained in the removable microfluidic cartridge. The CIM also includes a polymerase chain reaction (PCR) assembly component which can be configured to initiate and support amplification of the extracted nucleic acids. The CIM may also include a high voltage electrodes component that is configured to initiate and support separation of the amplified nucleic acids into nucleic acid fragments in a separation channel of the removable microfluidic cartridge. The CIM also includes a detection optics component that can be configured to collect, detect, and direct label nucleic acid fragments. The CIM is configured to integrate with a microfluidic chip architecture of an inserted removable microfluidic cartridge.
Devices And Methods For Extraction, Separation And Thermocycling
- Charlottesville VA, US Jacquelyn A. DuVall - Raleigh NC, US Delphine Le Roux - Barboursville VA, US Brian Root - Charlottesville VA, US Daniel MIlls - Charlottesville VA, US Daniel A. Nelson - Charlottesville VA, US An-chi Tsuei - Charlottesville VA, US Brandon L. Thompson - Charlottesville VA, US Jingyi Li - Charlottesville VA, US Christopher Birch - Charlottesville VA, US
International Classification:
B01L 3/00 B01L 7/00 G01N 27/447
Abstract:
A method to extract, amplify and separate nucleic acid in a microfluidic device having a plurality of chambers and channels can include a) introducing cells having nucleic acid to a first chamber of the microfluidic device and subjecting the cells in the first chamber to conditions that lyse the cells. The method can further include b) subjecting the first chamber to centrifugal force, thereby allowing the lysate or a portion thereof having nucleic acid to be distributed to a second chamber through a first channel in the microfluidic device. The method can also include c) combining the lysate or the portion thereof and reagents for amplification of the nucleic acid, thereby providing a second mixture. The method can also include d) subjecting the second chamber to centrifugal force, thereby allowing gas to be expelled from the second mixture.
- Charlottesville VA, US - Bethesda MD, US James Landers - Charlottesville VA, US Brian Root - Charlottesville VA, US Orion Scott - Charlottesville VA, US
Assignee:
ZyGEM CORPORATION LTD. - Charlottesville VA LOCKHEED MARTIN CORPORATION - Bethesda MD
International Classification:
B01L 7/00 C12Q 1/68
Abstract:
A microfluidic chip includes one or more reaction chambers to hold fluids for chemical or biochemical reactions, such as PCR. A non-contact heat source heats the reaction chamber and the fluid, such that the heat source does not contact the reaction chamber or the fluid. The heat source can heat the reaction chamber and the fluid separately, where the reaction chamber and the fluid separately absorb heat radiation from the heat source. A temperature sensor acquires a temperature of the reaction chamber and/or the fluid. Control circuitry controls the heat source according to a cycling profile for the reaction in the fluid to cycle the heat source between heating and not heating the reaction chamber and the fluid based on the temperature acquired by the temperature sensor. Cooling can be provided passively or actively.
- Hamilton, NZ - Bethesda MD, US James Landers - Charlottesville VA, US Douglas J. South - Rockville MD, US Brian E. Root - Charlottesville VA, US
Assignee:
ZYGEM CORPORATION LTD. - Hamilton LOCKHEED MARTIN CORPORATION - Bethesda MD
International Classification:
C12Q 1/68
US Classification:
435 612, 4352872
Abstract:
A cartridge interface module (CIM), configured to engage with a removable microfluidic cartridge in a nucleic acid analyzer system can include a fluidics component, which is configured to initiate and support a liquid extraction of nucleic acids from a biological sample contained in the removable microfluidic cartridge. The CIM also includes a polymerase chain reaction (PCR) assembly component which can be configured to initiate and support amplification of the extracted nucleic acids. The CIM may also include a high voltage electrodes component that is configured to initiate and support separation of the amplified nucleic acids into nucleic acid fragments in a separation channel of the removable microfluidic cartridge. The CIM also includes a detection optics component that can be configured to collect, detect, and direct label nucleic acid fragments. The CIM is configured to integrate with a microfluidic chip architecture of an inserted removable microfluidic cartridge.
Name / Title
Company / Classification
Phones & Addresses
Brian Root
ROOT'S PLASTERING LLC
Brian Root
SYMMES VALLEY BIDDY LEAGUE BB, INC
Resumes
Director Of Project Management And Capture Services
University of Virginia
Director of Project Management and Capture Services
Microlab Diagnostics Subsidiary of Zygem Corp Oct 2011 - Sep 2014
Director of Systems Integration
Microlab Diagnostics Mar 2009 - Sep 2011
Scientist
Education:
Northwestern University 2004 - 2009
Doctorates, Doctor of Philosophy, Materials Science, Engineering
Lafayette College 2000 - 2004
Bachelors, Bachelor of Science, Chemical Engineering
Skills:
Biotechnology Microfluidics Chemistry R&D Purification Commercialization Polymers Dna Assay Development Nanotechnology Microscopy Protein Chemistry Technology Transfer Science Lifesciences Life Sciences Biochemistry Molecular Biology Research and Development
Brian Kattle (1986-1987), Ronald Zahn (1953-1957), Brian Root (1971-1975), Jacki Rohac (1999-2003), Matthew Lamrouex (1979-1983), Esther Strunk (1950-1954)