Catalytic Bioscavengers with Broad Specificity Against OP Nerve Agents
Catalytic Bioscavengers with Broad Specificity Against OP Nerve Agents
批准号:
7915498
负责人:
James Robert Wild
金额:
$33.89万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-09-29 至 2011-05-31
关键词:
AcidsAddressAdverse effectsAnimal ModelAnimalsAntidotesBlood CirculationCaviaChemical WarfareChemical Warfare AgentsChemicalsConsultationsDataData AnalysesDendrimersDevelopmentDisadvantagedDoseDrug KineticsEncapsulatedEngineeringEnzymesEventExperimental DesignsExposure toGoalsHistopathologyHumanHuman ResourcesHydrolaseHydrolysisIn VitroInjection of therapeutic agentInterventionIntoxicationIntramuscularLeadLethal Dose 50MammalsMedicalMilitary PersonnelMissionMusOrganismOrganophosphorus CompoundsPathologyPesticidesPoisonPoisoningPopulationPositioning AttributePreparationProductionProteinsPublic HealthResearchResearch PersonnelRouteSafetySarinSoldierSomanSpecificitySterically Stabilized LiposomeStructureSubstrate SpecificitySurvivorsTechniquesTechnologyTestingTherapeuticTimeToxic effectTreatment ProtocolsVeterinary MedicineWorkantinerve agentaryldialkylphosphatasebasebioscavengercollegecyclosarindesignefficacy evaluationexperiencegraduate studentimprovedin vivomembernerve agentneurotoxicnovel strategiespharmacokinetic modelpre-clinicalprogramsprophylacticprotective efficacyresearch studyresidencetabun
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): The central hypothesis of this project is that catalytic bioscavengers with broad substrate specificity can be developed as safe and effective medical countermeasures against the high priority organophosphorus (OP) nerve agents. There currently exist a panel of well-characterized enzymes, both native and engineered, which have been evaluated as therapeutic or prophylactic agents against OP nerve agents. Preliminary studies have demonstrated that some of these enzymes can protect mice against the toxic effects of exposures up to 800 x LD50 for some OP pesticides. The current major obstacle to the development of these enzymes as effective bioscavengers is their presumed rapid clearance from the circulation of mammals resulting in short in vivo residence times. Preliminary studies indicate that encapsulation of these enzymes has the potential to provide the required extended residence times. The long term objective of this research is to produce catalytic bioscavengers of OP nerve agents that protect against a minimum of 5 x LD50 exposure; the protection should itself be safe, long lasting (> 3 weeks duration), and broad spectrum. The specific aims for this project are to produce, encapsulate and provide the essential pharmacokinetic efficacy evaluation for the selected catalytic bioscavengers: Specific Aim 1. Produce and test encapsulated enzymes for their capacity to hydrolyze OP nerve agents in vitro; Specific Aim 2. Generate and compare the pharmacokinetic profiles of the selected bioscavengers following IM delivery to guinea pigs; Specific Aim 3. Determine protective ratios provided by the catalytic bioscavengers with OP nerve agents. The stated mission of the CounterAct U01 program is "to develop new and improved medical countermeasures against chemical threats"; the studies proposed here will address this mission by providing new, effective and safe medical countermeasures against OP neurotoxic agents. The research is designed to provide pre-clinical pharmacokinetic and efficacy data suitable for submission to the FDA in support of an IND application. The relevance to public health lies in the recognition that the civilian chemical threat spectrum now includes nerve agents and other chemicals, including OP pesticides. The catalytic bioscavengers that will be characterized in these studies will have dual-use application for both military and civilian personnel in mass casualty scenarios involving either nerve agents or OP pesticides.
期刊论文(9)
专著(0)
科研奖励(0)
会议论文
Nanoencapsulated and microencapsulated enzymes in drug antidotal therapy.
药物解毒治疗中的纳米胶囊和微胶囊酶。
DOI:
10.1177/0748233711416946
发表时间:
2012
期刊:
Toxicology and industrial health
影响因子:
1.9
作者:
[Szilasi,Maria, Budai,Marianna, Budai,Livia, Petrikovics,Ilona]
通讯作者:
Petrikovics,Ilona
Allosteric signal transmission involves synergy between discrete structural units of the regulatory subunit of aspartate transcarbamoylase.
变构信号传递涉及天冬氨酸转氨甲酰酶调节亚基的离散结构单元之间的协同作用。
DOI:
10.1006/abbi.1999.1570
发表时间:
2000
期刊:
Archives of biochemistry and biophysics
影响因子:
3.9
作者:
[Liu,L, Wales,ME, Wild,JR]
通讯作者:
Wild,JR
Orientation specific positioning of organophosphorus hydrolase on solid interfaces for biosensor applications.
用于生物传感器应用的有机磷水解酶在固体界面上的方向特异性定位。
DOI:
10.1021/la9007526
发表时间:
2009
期刊:
Langmuir : the ACS journal of surfaces and colloids
影响因子:
--
作者:
[Reeves,TonyE, Paliwal,Sheetal, Wales,MelindaE, Wild,JamesR, Simonian,AleksandrL]
通讯作者:
Simonian,AleksandrL
Catalytic Bioscavengers with Broad Specificity Against OP Nerve Agents
-
批准号:7225011
-
项目类别:
-
资助金额:$29.58万
-
财政年份:2006
-
负责人:James Robert Wild
-
依托单位:
Catalytic Bioscavengers with Broad Specificity Against OP Nerve Agents
-
批准号:7294970
-
项目类别:
-
资助金额:$36.69万
-
财政年份:2006
-
负责人:James Robert Wild
-
依托单位:
Catalytic Bioscavengers with Broad Specificity Against OP Nerve Agents
-
批准号:7470594
-
项目类别:
-
资助金额:$37.15万
-
财政年份:2006
-
负责人:James Robert Wild
-
依托单位:
Catalytic Bioscavengers with Broad Specificity Against OP Nerve Agents
-
批准号:7667270
-
项目类别:
-
资助金额:$35.23万
-
财政年份:2006
-
负责人:James Robert Wild
-
依托单位:
SMALL INSTRUMENTATION GRANT
-
批准号:3524206
-
项目类别:
-
资助金额:$2.71万
-
财政年份:1991
-
负责人:James Robert Wild
-
依托单位:
SMALL INSTRUMENTATION PROGRAM
-
批准号:3524778
-
项目类别:
-
资助金额:$2.77万
-
财政年份:1989
-
负责人:James Robert Wild
-
依托单位:
BIOMEDICAL RESEARCH SUPPORT
-
批准号:3518271
-
项目类别:
-
资助金额:$9.18万
-
财政年份:1987
-
负责人:James Robert Wild
-
依托单位:
MINORITY HIGH SCHOOL STUDENT RESEARCH APPRENTICE PROGRAM
-
批准号:3512762
-
项目类别:
-
资助金额:$0.45万
-
财政年份:1987
-
负责人:James Robert Wild
-
依托单位:
BIOMEDICAL RESEARCH SUPPORT
-
批准号:3518270
-
项目类别:
-
资助金额:$10.13万
-
财政年份:1986
-
负责人:James Robert Wild
-
依托单位:
BIOMEDICAL RESEARCH SUPPORT
-
批准号:3518269
-
项目类别:
-
资助金额:$9.31万
-
财政年份:1985
-
负责人:James Robert Wild
-
依托单位:
ORGANIZATION AND REGULATION OF THE ATCASE CISTRONS
-
批准号:3282590
-
项目类别:
-
资助金额:$16.42万
-
财政年份:1984
-
负责人:James Robert Wild
-
依托单位:
ORGANIZATION AND REGULATION OF THE ATCASE CISTRONS
-
批准号:2176897
-
项目类别:
-
资助金额:$18.6万
-
财政年份:1984
-
负责人:James Robert Wild
-
依托单位:
ORGANIZATION AND REGULATION OF THE ATCASE CISTRONS
-
批准号:3282588
-
项目类别:
-
资助金额:$9.53万
-
财政年份:1984
-
负责人:James Robert Wild
-
依托单位:
ORGANIZATION AND REGULATION OF THE ATCASE CISTRONS
-
批准号:3282587
-
项目类别:
-
资助金额:$10.37万
-
财政年份:1984
-
负责人:James Robert Wild
-
依托单位:
ORGANIZATION AND REGULATION OF THE ATCASE CISTRONS
-
批准号:3282589
-
项目类别:
-
资助金额:$10.66万
-
财政年份:1984
-
负责人:James Robert Wild
-
依托单位:
ORGANIZATION AND REGULATION OF THE ATCASE CISTRONS
-
批准号:3282591
-
项目类别:
-
资助金额:$17.04万
-
财政年份:1984
-
负责人:James Robert Wild
-
依托单位:
ORGANIZATION AND REGULATION OF THE ATCASE CISTRONS
-
批准号:3282592
-
项目类别:
-
资助金额:$17.69万
-
财政年份:1984
-
负责人:James Robert Wild
-
依托单位:
ORGANIZATION AND REGULATION OF THE ATCASE CISTRONS
-
批准号:3282585
-
项目类别:
-
资助金额:$16.89万
-
财政年份:1984
-
负责人:James Robert Wild
-
依托单位:
BIOMEDICAL RESEARCH SUPPORT
-
批准号:3518272
-
项目类别:
-
资助金额:$9.22万
-
财政年份:1979
-
负责人:James Robert Wild
-
依托单位:
BIOMEDICAL RESEARCH SUPPORT
-
批准号:3518274
-
项目类别:
-
资助金额:$7.21万
-
财政年份:1979
-
负责人:James Robert Wild
-
依托单位:
海外基金