Administration and management
Administration and management
批准号:
7557500
负责人:
DAVID E LENZ
金额:
$15.47万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
Academic Medical CentersAcetylcholinesteraseAddressAdoptionAdvanced DevelopmentAgreementAlgaeAntidotesAreaArizonaBackBaltimoreBiochemicalBiologicalBloodBlood CirculationButyrylcholinesteraseCapitalChemical AgentsChemical WarfareChemical Warfare AgentsChemical WeaponsChemicalsChemistryChinaCholinesterase InhibitorsClassClinical TrialsCollectionComplexConflict (Psychology)Costs and BenefitsCoupledDatabasesDrug Metabolic DetoxicationEnsureEnzymesEthiopiaEvaluationExposure toGeneral PopulationGenesGenetic EngineeringGermanyGoalsHumanHuman ActivitiesHuman ResourcesHydrolaseHydrolysisIn VitroInsecticidesInstitutesInstitutionInternationalIranIraqIsraelJapanKineticsLaboratoriesLeadMammalian CellMarylandMedicalMedical ResearchMilitary PersonnelModelingModificationMolecularMolecular BiologyMolecular EvolutionMolecular and Cellular BiologyMutateNatureOffice of Administrative ManagementOhioOrganismParaoxonPathway interactionsPesticidesPharmaceutical PreparationsPlantsPlasmaPoisonPoisoningPopulationProcessProductionProteinsRecombinantsResearchResearch InfrastructureResearch InstituteResearch Project GrantsResourcesSarinSeriesSiteSourceStreamStructural ProteinSynapsesSystemTechniquesTechnologyTestingTherapeuticTimeToxic effectTranslationsUnited States National Institutes of HealthUniversitiesVertebratesVulnerable PopulationsWorkWorld War IIX-Ray Crystallographyanimal resourcearyldialkylphosphatasebasebioscavengercombinatorial chemistrycomputational chemistryconceptcostdesigndrug developmentdrug discoverydrug productionefficacy evaluationemergency service responderfeedingimprovedin vivomutantnerve agentnovelprogramsprophylacticprotein expressionresearch clinical testingresponseskillssuccesstooltoxicanttransmission process
中文摘要
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英文摘要
Two proteins, human plasma BuChE, and a recombinant human BuChE are both in advanced development
as potential prophylacitcs for protecting against chemical warfare agents. These proteins react rapidly and
stoiciometrically to effectively scavenge the poisons in the blood stream but they require relatively large
amounts of protein to provide protection. The challenge of identifying a protein based drug that would
require less material while providing improved protection with the advantage of enhanced user acceptance
cannot be ignored. Recent efforts the laboratories alinged with the Center have identified several human
enzymes, paraoxonase (PON) and a mutant of butyrylcholinesterase that can catalyze the hydrolysis of all
nerve agents. As such these are excellent candidate for prophylactic administration to provide protection for
first responders to a terrorist attack or military forces in a civilian peacekeeping setting subject to an
asymmetric threat. If it were administered intravenously it could also serve as a rapid-onset therapeutic
antidote to a segment of the civilian popuation exposed to nerve agents. Preliminary studies have shown
that these objectives are both feasible and obtainable. The cost/benefit ratio of such a drug is such that it is
an excellent candidate for success and has the potential to be the first in a series of a novel class of drugs.
The center will coordinate the overall effort directed toward the enhancement of the the native catalytic
activity of these human enzymes to create a viable candidate for transition to advancement to clinical trials
within a five year period. This will address a critical gap in the national goal of protecting the civilian
population against a terrorist-initiated chemical weapons attack.
Current medical protection against chemical nerve agent exposure by terrorists is limited to post exposure
treatment. We will identify and develop for clinical testing a human protein capable of providing rapid and
long lasting prophylactic protection against exposure to chemical warfare nerve agents. Such a drug will
address the critical national goal of providing improved protection to the general population against a
terrorist-initiated chemical weapons attack.
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Center for Catalytic Bioscavenger Medical Defense Research - U54
-
批准号:7920104
-
项目类别:
-
资助金额:$220.63万
-
财政年份:2006
-
负责人:DAVID E LENZ
-
依托单位:
Rational design of human paraoxonase to design enhanced catalytic efficiency
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批准号:7235226
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项目类别:
-
资助金额:$10.7万
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财政年份:2006
-
负责人:DAVID E LENZ
-
依托单位:
Center for Catalytic Bioscavenger Medical Defense Research - U54
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批准号:7224613
-
项目类别:
-
资助金额:$306.18万
-
财政年份:2006
-
负责人:DAVID E LENZ
-
依托单位:
Center for Catalytic Bioscavenger Medical Defense Research - U54
-
批准号:7692000
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项目类别:
-
资助金额:$5.0万
-
财政年份:2006
-
负责人:DAVID E LENZ
-
依托单位:
Center for Catalytic Bioscavenger Medical Defense Research - U54
-
批准号:7689889
-
项目类别:
-
资助金额:$212.8万
-
财政年份:2006
-
负责人:DAVID E LENZ
-
依托单位:
Center for Catalytic Bioscavenger Medical Defense Research - U54
-
批准号:7295925
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项目类别:
-
资助金额:$280.55万
-
财政年份:2006
-
负责人:DAVID E LENZ
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依托单位:
Administration and management
-
批准号:7235235
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项目类别:
-
资助金额:$15.16万
-
财政年份:2006
-
负责人:DAVID E LENZ
-
依托单位:
Center for Catalytic Bioscavenger Medical Defense Research - U54
-
批准号:7487885
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项目类别:
-
资助金额:$278.07万
-
财政年份:2006
-
负责人:DAVID E LENZ
-
依托单位:
Rational design of human paraoxonase to design enhanced catalytic efficiency
-
批准号:7487878
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项目类别:
-
资助金额:$11.31万
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财政年份:--
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负责人:DAVID E LENZ
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依托单位:
Rational design of human paraoxonase to design enhanced catalytic efficiency
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批准号:8117141
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项目类别:
-
资助金额:$8.83万
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财政年份:--
-
负责人:DAVID E LENZ
-
依托单位:
Rational design of human paraoxonase to design enhanced catalytic efficiency
-
批准号:7689881
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项目类别:
-
资助金额:$11.3万
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财政年份:--
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负责人:DAVID E LENZ
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依托单位:
Administration and management
-
批准号:7920103
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项目类别:
-
资助金额:$11.71万
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财政年份:--
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负责人:DAVID E LENZ
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依托单位:
Rational design of human paraoxonase to design enhanced catalytic efficiency
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批准号:7920096
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项目类别:
-
资助金额:$8.58万
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财政年份:--
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负责人:DAVID E LENZ
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依托单位:
Administration and management
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批准号:8117148
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项目类别:
-
资助金额:$12.06万
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财政年份:--
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负责人:DAVID E LENZ
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依托单位:
Administration and management
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批准号:7689888
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项目类别:
-
资助金额:$15.45万
-
财政年份:--
-
负责人:DAVID E LENZ
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依托单位:
海外基金