Core E Animal Infection Models
Core E Animal Infection Models
批准号:
10394989
负责人:
David S Perlin
金额:
$118.1万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-05-01 至 2024-04-30
关键词:
AcuteAerosolsAnimal ModelAnimalsBacteremiaBacteriaBiological AssayBiological MarkersBiotechnologyChronicClinicalCommunicationCutaneousDataDevelopmentDiseaseDisease MarkerDisease modelESKAPE pathogensEnsureHistopathologyHuman ResourcesImmune responseInfectionInflammationLeadLungLung infectionsMass Spectrum AnalysisMeasurementMethodsModelingMolecularMorbidity - disease rateMucous MembraneMulti-Drug ResistanceMultidrug-Resistant TuberculosisMultiple Bacterial Drug ResistanceMusMycobacterium tuberculosisOralPenetrationPharmaceutical PreparationsPneumoniaReproducibilityRodentRouteSepsisServicesSiteSkin TissueSoft Tissue InfectionsSpatial DistributionSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationSystemic infectionTherapeuticThigh structureTissuesTreatment EfficacyTuberculosisWorkWound Infectionacute infectionanalytical methodbiodefensechronic infectiondesigndrug developmentdrug resistant bacteriadrug resistant pathogenexperiencefluorescence imagingin vivoin vivo imaginginnovationinstrumentationlaser capture microdissectionliquid chromatography mass spectrometrylung lesionmicrobialmortalitymulti-drug resistant pathogennew technologynext generationnovelpathogenpathogenic bacteriapre-clinicalpreclinical developmentsoft tissuespecific biomarkersspectroscopic imagingsubcutaneoustreatment response
中文摘要
摘要
用动物模型评价新型先导化合物对耐药细菌的治疗效果
对于将化合物推进到临床前开发阶段至关重要。目前,有一个
缺乏可复制的疾病模型,缺乏可靠的指标来评估先导化合物,甚至
更少的设施和具有专业知识的人员来进行如此重要的研究。为了满足这一点
重大挑战,拟议的CETR的动物模型核心已开发出可重复性
啮齿动物全身、肺、软组织、创伤、感染模型的临床意义
耐多药细菌。该中心的目标是:1)提供小动物感染模型
为ESKAPE、TB和NTM病原体评估先导化合物,以及2)提供最新技术
对宿主反应和细菌生物负荷分布的分析服务,以评估和量化
含铅化合物的治疗效果。动物核心已经在这方面发挥了作用超过
15年在学术、制药和生物技术领域支持药物开发的经验
扇区。在大卫·佩林博士的指导下,它成为了一个多机构的地区性动物
为第二区域RCE(东北生物防御中心)工作了11年(2003-2013),并
在过去4年多的时间里(2013年至今)支持目前的《经济、社会和文化权利国际公约》。动物核心运作
在非常高的产能下,已经记录了180多万个动物日的高威胁细菌
自2003年起代理。一支经验丰富且敬业的动物模型团队进行了广泛的
具有多种感染途径(静脉、口服、气雾剂、皮下、粘膜)和
疾病标记物(发病率/死亡率、微生物负担、组织病理学等)。这个
动物核心的管理人员与项目负责人和其他核心密切合作
董事,以确保所有新的线索在开发管道中迅速推进。
这条紧密而持续的沟通渠道允许在设计和设计方面进行必要的调整
进行研究,并在罗格斯大学取得了7项有希望的领先优势
经济、社会和文化权利国际组织2014年至2018年的项目。动物核心拥有尖端的仪器设备
感染和治疗反应的分析。纳入可复制的动物模型
由经验丰富的员工运营,并利用新技术将推动和加速
抗多重耐药细菌的有前景的先导化合物的开发。所有服务
可以在监管批准的高水平生物遏制下进行。
好了!
英文摘要
Abstract
Assessing the treatment efficacy of novel leads against drug resistant bacteria in animal models
is crucial for advancing compounds to the preclinical stage of development. Currently, there is a
paucity of reproducible disease models with reliable metrics to assess lead compounds and even
less facilities and personnel with the expertise to perform such important studies. To meet this
important challenge, the Animal Model Core for this proposed CETR has developed reproducible
systemic, pulmonary, soft tissue, wound, infection models in rodents for clinically important
multidrug resistant bacteria. The Aims of the core are to: 1) provide small animal infection models
for ESKAPE, TB and NTM pathogens to evaluate lead compounds, and 2) provide state of the art
analytical services on host response and bacterial bio-burden distribution to assess and quantify
lead compound treatment efficacy. The Animal core has functioned in this capacity for more than
15 years with experience supporting drug development for the academic, pharma and biotech
sectors. Under the direction of Dr. David Perlin, it served as a multi-institutional regional animal
core for the Region II RCE (Northeast Biodefense Center) for 11 years (2003-2013) and has
supported the current CETR for the past 4+ years (2013 to present). The Animal Core operates
at a very high capacity, having logged more than 1.8 million animal days of high threat bacterial
agents since 2003. An experienced and dedicated animal model team performs a wide range of
infection models with multiple routes of infections (iv, oral, aerosol, subcutaneous, mucosal) and
markers for disease (morbidity/mortality, microbial burden, histopathology, etc.). The
management staff of the Animal core works closely with both Project Leaders and other Core
Directors to ensure that all novel leads are rapidly advanced through the development pipeline.
This close and constant line of communication permits the necessary adjustments in design and
execution of studies, and has resulted in the advancement of 7 promising leads in the Rutgers
CETR projects from 2014 to 2018. the Animal core possesses cutting edge instrumentation for
analysis of infections and therapeutic responses. The incorporation of reproducible animal models
operated by highly experienced staff and utilizing novel technologies will advance and accelerate
the development of promising Lead compounds against multidrug resistant bacteria. All services
can be performed under high-level biocontainment with regulatory approval.
!
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Accelerated development of advanced leads against SARS-CoV-2 and other pandemic viruses
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批准号:10513922
-
项目类别:
-
资助金额:$388.58万
-
财政年份:2022
-
负责人:David S Perlin
-
依托单位:
Metropolitan AntiViral Drug Accelerator
-
批准号:10513913
-
项目类别:
-
资助金额:$6514.17万
-
财政年份:2022
-
负责人:David S Perlin
-
依托单位:
Administrative Core
-
批准号:10513914
-
项目类别:
-
资助金额:$755.88万
-
财政年份:2022
-
负责人:David S Perlin
-
依托单位:
Animal Model Core
-
批准号:10513920
-
项目类别:
-
资助金额:$558.04万
-
财政年份:2022
-
负责人:David S Perlin
-
依托单位:
A CETR-based partnership accelerator for rapid drug development targeting SARS-CoV-2 and pan-CoVs
-
批准号:10187269
-
项目类别:
-
资助金额:$61.99万
-
财政年份:2020
-
负责人:David S Perlin
-
依托单位:
Center to develop innovative therapeutics to multidrug resistant high-threat bacterial agents
-
批准号:10394984
-
项目类别:
-
资助金额:$663.83万
-
财政年份:2019
-
负责人:David S Perlin
-
依托单位:
Critical Factors Influencing Echinocandin Resistance in Candidaglabrata
-
批准号:10451830
-
项目类别:
-
资助金额:$71.06万
-
财政年份:2019
-
负责人:David S Perlin
-
依托单位:
Novel bi-specific immunoprophylactics against multi-drug resistant Gram-negativebacterial infections
-
批准号:10380759
-
项目类别:
-
资助金额:$107.68万
-
财政年份:2019
-
负责人:David S Perlin
-
依托单位:
Novel bi-specific immunoprophylactics against multi-drug resistant Gram-negative bacterial infections
-
批准号:9898899
-
项目类别:
-
资助金额:$107.06万
-
财政年份:2019
-
负责人:David S Perlin
-
依托单位:
Critical Factors Influencing Echinocandin Resistance in Candidaglabrata
-
批准号:10215271
-
项目类别:
-
资助金额:$71.06万
-
财政年份:2019
-
负责人:David S Perlin
-
依托单位:
Novel bi-specific immunotherapeutic against high-threat Gram-negative pathogens
-
批准号:10337197
-
项目类别:
-
资助金额:$114.2万
-
财政年份:2019
-
负责人:David S Perlin
-
依托单位:
Center to develop innovative therapeutics to multidrug resistant high-threat bacterial agents
-
批准号:9923564
-
项目类别:
-
资助金额:$663.81万
-
财政年份:2019
-
负责人:David S Perlin
-
依托单位:
Core E Animal Infection Models
-
批准号:10613892
-
项目类别:
-
资助金额:$144.96万
-
财政年份:2019
-
负责人:David S Perlin
-
依托单位:
Administrative Core
-
批准号:10613884
-
项目类别:
-
资助金额:$73.49万
-
财政年份:2019
-
负责人:David S Perlin
-
依托单位:
Administrative Core
-
批准号:10394985
-
项目类别:
-
资助金额:$54.33万
-
财政年份:2019
-
负责人:David S Perlin
-
依托单位:
Novel bi-specific immunotherapeutic against high-threat Gram-negative pathogens
-
批准号:10551227
-
项目类别:
-
资助金额:$114.2万
-
财政年份:2019
-
负责人:David S Perlin
-
依托单位:
Center to develop innovative therapeutics to multidrug resistant high-threat bacterial agents
-
批准号:10613883
-
项目类别:
-
资助金额:$652.13万
-
财政年份:2019
-
负责人:David S Perlin
-
依托单位:
Novel bi-specific immunoprophylactics against multi-drug resistant Gram-negative bacterial infections
-
批准号:9926819
-
项目类别:
-
资助金额:$105.13万
-
财政年份:2019
-
负责人:David S Perlin
-
依托单位:
Critical Factors Influencing Echinocandin Resistance in Candida glabrata
-
批准号:8614663
-
项目类别:
-
资助金额:$48.77万
-
财政年份:2014
-
负责人:David S Perlin
-
依托单位:
Critical Factors Influencing Echinocandin Resistance in Candida glabrata
-
批准号:8897999
-
项目类别:
-
资助金额:$52.5万
-
财政年份:2014
-
负责人:David S Perlin
-
依托单位:
海外基金