A new experimental platform to study biofilms: Microfluidic-DHM
A new experimental platform to study biofilms: Microfluidic-DHM
批准号:
7512736
负责人:
Roman Stocker
金额:
$23.07万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-07-01 至 2010-06-30
关键词:
AdoptedAntibiotic ResistanceAntibioticsArtsBacteriaBacterial InfectionsBehaviorBiocompatible MaterialsCell-Matrix JunctionCellsChemicalsClinicalCommunicable DiseasesComputer softwareConditionCoupledDataDependenceDimensionsEngineeringEnvironmentFigs - dietaryFoundationsGlassGoalsHealthHeterogeneityHolographyHost DefenseHumanImageImageryImplantIn VitroIndividualInfectionInjection of therapeutic agentInvestigationLasersLeadLifeLife StyleLinkLiquid substanceMicrobial BiofilmsMicrofluidicsMicroscopeMicroscopyMolecular GeneticsMotionNutrientOpticsOutcomePathogenesisPerformancePliabilityPositioning AttributeProcessProsthesisProtocols documentationPumpRangeRationalizationResearchResolutionResortRight-OnSlideSurfaceSwimmingSyringesSystemTechniquesTechnologyTestingTherapeuticThree-Dimensional ImageThree-Dimensional ImagingTimebasecharge coupled device cameraclinical applicationcostdesigndigitalfluid flowimage processingimprovedinstrumentlensparticlepreventspatiotemporalsuccesswastingwater channel
中文摘要
描述(申请人提供):我们建议开发一个新的研究生物膜的实验平台。生物膜是由生活在表面的细菌组成的。它们对宿主防御的固有耐受性和对抗生素日益增加的耐药性在许多临床应用中引起了越来越多的关注,包括传染病的发病机制以及假体和生物材料的临床感染。到目前为止,小空间尺度、异质性和时间依赖性已经击败了生物膜过程在一般机械原理方面的合理化,迫使治疗学主要求助于有限成功的经验策略。目前的实验技术只提供了控制生物膜微环境的粗略手段,在以适当的时空分辨率在单细胞水平上量化微尺度过程方面受到严重限制。我们的方法是整合微流控和数字全息显微镜这两项最先进的实验技术,为生物膜研究创造一个强大的新平台。我们称其为5Fluidic-DHM。5流体-DHM将利用微流体在精确操纵微环境条件方面的多功能性,包括几何、化学和流体动力学参数,以及数字全息技术捕捉单细胞水平和高时间分辨率的三维动力学的能力。我们这个R21项目的目标是开发、验证和优化5Fluidic-DHM平台。我们将通过在两个重要的生物膜过程中进行测试来展示这种方法的优势:细胞附着到表面和通过生物膜水通道流动。该项目与人类健康直接相关,因为它将通过使用一种具有前所未有的准确性、分辨率和灵活性的仪器来推进生物膜实验的最先进水平,从而提高我们治疗生物膜起源感染的能力。这最终将导致在广泛的临床应用中加强治疗策略。
英文摘要
DESCRIPTION (provided by applicant): We propose to develop a new experimental platform for the study of biofilms. Biofilms consist of bacterial consortia living on surfaces. Their inherent tolerance to host defenses and increasing resistance to antibiotics cause growing concern in many clinical applications, including pathogenesis of infectious diseases and clinical infection of prosthetic implants and biomaterials. To date, the small spatial scales, heterogeneity and time-dependence have defeated the rationalization of biofilm processes in terms of general mechanistic principles, forcing therapeutics to resort primarily to empirical strategies of limited success. Current experimental techniques provide only crude means of controlling a biofilm's microenvironment and are severely limited in quantifying microscale processes at the single-cell level with appropriate spatiotemporal resolution. Our approach is to integrate two state-of-the-art experimental techniques, microfluidics and digital holographic microscopy, to create a powerful new platform for biofilm studies. We call this 5Fluidic-DHM. 5Fluidic-DHM will exploit the versatility of microfluidics in accurately manipulating microenvironmental conditions, including geometrical, chemical and fluid dynamical parameters, coupled with the ability of digital holography to capture three-dimensional dynamics at single-cell level and high temporal resolution. Our goal for this R21 project is to develop, validate and optimize a 5Fluidic-DHM platform. We will showcase the advantages of this approach by testing it on two important biofilm processes: cell attachment to surfaces and flow through biofilm water channels. This project is directly relevant to human health, as it will improve our ability to treat biofilm- originated infection by advancing the state-of-the-art in biofilm experimentation with an instrument of unprecedented accuracy, resolution and flexibility. This will ultimately lead to enhanced therapeutic strategies in a wide range of clinical applications.
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A new experimental platform to study biofilms: Microfluidic-DHM
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批准号:7628032
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项目类别:
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资助金额:$19.35万
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财政年份:2008
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负责人:Roman Stocker
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依托单位:
海外基金