Awardee OrganizationHUMAN BIOMOLECULAR RESEARCH INSTITUTE
Description
Abstract Text
DESCRIPTION (provided by applicant): Changes in the security situation facing citizens in the United States and military personnel abroad have greatly increased the threat that chemical weapons will be used against American forces and American civilians in the field as well as at home. In addition, hundreds of thousands of Americans are exposed to significant levels of pesticide organophosphates (OP) every year. These situations point to an urgent need for an efficient, fieldable and inexpensive way to detect OP. Detection instrumentation is an essential component of any protection paradigm, and thus a challenge is to develop sensitive and inexpensive detection methodology for various OP agents. The goal of our work is to be able to detect biomarkers of OP nerve agent exposure that can be readily and inexpensively deployed using a portable automated multianalyte biosensor. Our long-term goals are to develop a sensitive biosensor to detect biomarkers of OP exposure to provide information to protect populations at risk for exposure to chemical warfare agents or OP pesticides. The Aims for this research include: Aim 1) Design and synthesize biomarker reagents for a system to detect nerve agents including tabun, sarin, soman, VX, GF and tabun; Aim 2) Prepare and test antibodies to biomarkers of nerve agent exposure; Aim 3) Obtain biological samples from animals exposed to nerve agents or their surrogates; Aim 4) Develop the biosensor for nerve agent exposure and Aim 5) Build and test the final biosensor. Biochemical validation and development of a robust, portable Array Biosensor employing the optimized reagents and using currently available technology will be done in collaboration with the Naval Research Laboratory. With the success of the proposed work, we will obtain: 1) new reagents and technology for identifying OP-biomolecule conjugates of relevance to nerve agent and pesticide OP exposure, 2) verification of the robustness of the technology with biological samples, 3) development of an array-based methodology to selectively detect OP and 4) elaboration and testing of an Array Biosensor in the field with biological samples taken from animals exposed to low doses of nerve agents or nerve agent analogs. The final sensitive and selective product will be of use in a rapid screening format of physiological fluids for OP exposure.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
Active SitesAgricultureAmericanAnimalsAntibodiesBiochemicalBiochemistryBiologicalBiological AssayBiological MarkersBiosensorBloodBuffersChemical WarfareChemical Warfare AgentsChemical WeaponsChemicalsCollaborationsComputer softwareConditionDetectionDevelopmentDoseExposure toFood SafetyGoalsHome environmentHumanImmunochemistryLaboratory ResearchLiquid substanceMedicalMethodologyMethodsMicrofluidic MicrochipsMilitary PersonnelMolecularMolecular BiologyMonitorOrganophosphatesPeptidesPesticidesPhasePhysiologicalPopulations at RiskPurposeReagentResearchSamplingSarinScreening procedureSecuritySiteSomanStandards of Weights and MeasuresSurfaceSynthesis ChemistrySystemTechnologyTestingTimeTissuesUnited StatesValidationWorkanalogbasebrain tissuedesigndetectorgallium alloy GFimprovedinstrumentationnerve agentprototyperapid detectionsensorsuccesstabuntoxic organophosphate insecticide exposure
National Institute of Neurological Disorders and Stroke
CFDA Code
853
DUNS Number
030864867
UEI
NABAZEM87R81
Project Start Date
30-September-2006
Project End Date
31-May-2011
Budget Start Date
01-June-2007
Budget End Date
31-May-2008
Project Funding Information for 2007
Total Funding
$871,044
Direct Costs
$645,339
Indirect Costs
$389,673
Year
Funding IC
FY Total Cost by IC
2007
NIH Office of the Director
$871,044
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5U01NS058038-02
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 5U01NS058038-02
Patents
No Patents information available for 5U01NS058038-02
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 5U01NS058038-02
Clinical Studies
No Clinical Studies information available for 5U01NS058038-02
News and More
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History
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Similar Projects
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