Targeted combinatiorial therapy for treatment of periodontal disease
Targeted combinatiorial therapy for treatment of periodontal disease
批准号:
7660001
负责人:
MARK j YOUNG
金额:
$21.38万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-07-20 至 2011-06-30
关键词:
AcidsAddressAnimal ModelAntibodiesAreaBacteriaCanis familiarisChlorhexidineCollaborationsCommunitiesComplexConsultationsCoupledDevelopmentEngineeringEnhancersEquilibriumFamilyGeneticGingivaImmuneImmune systemIn VitroLifeMethodsMicrobial BiofilmsModalityModelingPeriodontal DiseasesPeriodontal InfectionPharmaceutical PreparationsPhotosensitizing AgentsProteinsResearchSchool DentistryStructureSurfaceSystemTestingTetracyclinesTissuesantimicrobialantimicrobial peptidebasebone losschemical geneticscombinatorialdesigneffective therapykillingsmembermicrobial communitynanonanomaterialsoxidationpathogenpublic health relevanceresearch studyresponsetool
中文摘要
描述(由申请人提供):一个新兴的概念是,组成牙周聚生体的复杂微生物群落由有益和致病物种组成。这意味着牙周病可以通过选择性地消除假定的病原体来治疗,同时最大限度地减少对社区成员的破坏。我们建议设计一系列纳米平台,以将光敏剂(PS)和PS/药物或抗菌肽对靶向牙周病原体。我们将检验这样的假设,即通过适当的PS/药物或PS/抗微生物肽组合可以显著增强靶向PS的选择性杀伤。我们将设计被称为蛋白质笼的纳米平台来实施我们的设计策略。在初步研究中,我们已经开发出了用光敏剂(PS)功能化的蛋白质笼靶向和杀死生物膜形成病原体的方法。与此同时,我们开发了一种用于触发释放与蛋白质笼偶联的药物的方法。我们将建立在这方面的专业知识,以制造多功能的纳米平台,有针对性的组合治疗。我们的工程纳米平台选择性杀死牙周病原体的能力将在体外系统中以牙周炎和已建立的生物膜为特征。我们将确定PS和增强剂的哪种组合在保持选择性的同时最有效地产生病原体的相加或协同杀灭。具体目标(SA)按照三种治疗方式的组合进行组织:SA 1)靶向PS与非靶向广谱抗菌剂组合; SA 2)靶向PS与两种类型广谱抗菌剂的靶向触发释放组合; SA 3)靶向PS与抗菌肽组合。我们研究团队的优势在于两个中心的专业知识:生物启发纳米材料中心和生物膜工程中心。我们专门设计了实验,以便最有前途的系统可以在牙周病的动物模型中进行测试。
公共卫生相关性:牙周病是一种常见的牙周病,是由牙周病引起的牙周病。然而,我们知道免疫系统可以与许多类型的细菌和谐相处。我们的研究将提供一种工具,选择性地消除被怀疑导致免疫功能障碍的细菌,同时保留被认为有益的细菌。
英文摘要
DESCRIPTION (provided by applicant): An emerging concept is that the complex microbial communities that comprise periodontal consortia consist of both beneficial and pathogenic species. The implication is that periodontal disease can be treated by selectively eliminating putative pathogens, while minimizing the destruction of the commensal members of the community. We propose to engineer a family of nanoplatforms to target photosensitizers (PS) and PS/drug or antimicrobial peptide pairs to periodontal pathogens. We will test the hypothesis that the selective killing of targeted PS can be significantly enhanced by appropriate PS/drug or PS/antimicrobial peptide combinations. We will engineer nanoplatforms known as protein cages to implement our design strategy. In preliminary studies we have developed methods to target and kill biofilm-forming pathogens with protein cages functionalized with a photosensitizer (PS). In parallel, we developed a method for triggered release of a drug coupled to a protein cage. We will build upon this expertise to fabricate multifunctional nanoplatforms for targeted combinatorial therapy. The ability of our engineered nanoplatforms to selectively kill periodontal pathogens will be characterized in planktonic and established biofilm in vitro systems. We will determine which combinations of PS and enhancer are most effective in producing additive or synergistic killing of pathogens while maintaining selectivity. The specific aims (SA) are organized in terms of three combinations of treatment modalities: SA1) Targeted PS combined with non-targeted broad spectrum antimicrobials; SA2) Targeted PS combined with targeted triggered release of two types of broad spectrum antimicrobials and SA3) Targeted PS combined with an antimicrobial peptide. The strength of our research team lies in the combined expertise of two centers: the Center for BioInspired Nanomaterials and the Center for Biofilm Engineering. We have specifically designed the experiments so that the most promising systems can be tested in an animal model of periodontal disease.
PUBLIC HEALTH RELEVANCE: The bone loss and tissue destruction that accompany periodontal disease are caused by the response of the immune system to bacteria. However, we know that the immune system can live in harmony with many types of bacteria. Our research will provide a tool to selectively eliminate bacteria suspected of causing immune malfunction while sparing bacteria thought to be beneficial.
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Small molecular weight targeted killing agents against a periodontal pathogen
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批准号:8583754
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项目类别:
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资助金额:$18.0万
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财政年份:2013
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负责人:MARK j YOUNG
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依托单位:
Small molecular weight targeted killing agents against a periodontal pathogen
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批准号:8740477
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项目类别:
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资助金额:$21.6万
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财政年份:2013
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负责人:MARK j YOUNG
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依托单位:
VIRUS BASED BIO-IMAGING & THERAPEUTIC DELIVERY SYSTEMS
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批准号:6520256
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项目类别:
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资助金额:$21.56万
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财政年份:2000
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负责人:MARK j YOUNG
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依托单位:
VIRUS BASED BIO-IMAGING & THERAPEUTIC DELIVERY SYSTEMS
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批准号:6094647
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项目类别:
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资助金额:$22.57万
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财政年份:2000
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负责人:MARK j YOUNG
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依托单位:
SHARED ELECTRON MICROSCOPE WITH CRYO-CAPACITY
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批准号:6051614
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项目类别:
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资助金额:$32.16万
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财政年份:2000
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负责人:MARK j YOUNG
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依托单位:
VIRUS BASED BIO-IMAGING & THERAPEUTIC DELIVERY SYSTEMS
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批准号:6387166
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项目类别:
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资助金额:$21.56万
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财政年份:2000
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负责人:MARK j YOUNG
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依托单位:
ANALYSIS OF SPHERICAL VIRUS ASSEMBLY
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批准号:6099745
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项目类别:
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资助金额:$0.0万
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财政年份:1997
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负责人:MARK j YOUNG
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依托单位:
CONTROL OF ILIAC ARTERY VASOACTIVITY
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批准号:3471178
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项目类别:
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资助金额:$8.46万
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财政年份:1987
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负责人:MARK j YOUNG
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依托单位:
CONTROL OF ILIAC ARTERY VASOACTIVITY
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批准号:3471177
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项目类别:
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资助金额:$7.37万
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财政年份:1987
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负责人:MARK j YOUNG
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依托单位:
ENDOTHELIAL CONTROL OF LARGE CORONARY ARTERY VASOACTIVI
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批准号:3448920
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项目类别:
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资助金额:$5.5万
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财政年份:1985
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负责人:MARK j YOUNG
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依托单位:
ENDOTHELIAL CONTROL OF LARGE ILIAC ARTERY VASOACTIVITY
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批准号:3448921
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项目类别:
-
资助金额:$4.69万
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财政年份:1985
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负责人:MARK j YOUNG
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依托单位:
RESIDENCY TRAINING IN GIM AND/OR GP
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批准号:3015260
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项目类别:
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资助金额:$0.0万
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财政年份:1985
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负责人:MARK j YOUNG
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依托单位:
海外基金