Ultrasound monitored HIV rapid test
Ultrasound monitored HIV rapid test
批准号:
7338978
负责人:
Simon Bystryak
金额:
$49.96万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-03-01 至 2009-07-31
关键词:
Acquired Immunodeficiency SyndromeAddressAffectAgglutinationAgglutination TestsAlgorithmsAntibodiesBiologicalBiological AssayBlood ScreeningBody FluidsBusinessesCellsClinicalComplexDataDetectionDeveloped CountriesDeveloping CountriesDevicesElementsEnzyme-Linked Immunosorbent AssayEpidemicEquipmentFluorescenceGeneric DrugsGoalsHIVHuman immunodeficiency virus testImmunoassayIndividualInfectionInterventionLaboratoriesLateralLatexLicensingMeasuresMembraneMethodsMicroscopicMonitorNumbersPatientsPerformancePersonsPhasePositive Test ResultPrevention interventionPreventiveProductionPublic HealthReadingReagentReproducibilityResearchResourcesSamplingScreening procedureSensitivity and SpecificitySerologic testsSilicon DioxideSpecimenStatistically SignificantSystemTechnical ExpertiseTechnologyTest ResultTestingTimeTransfusionUltrasonicsUltrasonographyVaccinesVirus DiseasesWeekWestern Blottingbasecostdaydesignergonomicsimprovedinstrumentinstrumentationmethod developmentnew technologynovelparticleprototyperapid technique
中文摘要
描述(申请人提供):拟议研究的长期目标是开发一种新的定量颗粒凝集技术,以提高检测体液中人类免疫缺陷病毒(HIV)抗体的性能。常规的颗粒凝集试验具有灵敏度低、孵育时间长、主观性强、试剂用量大等缺点。正是在这种背景下,我们建议开发一种新的技术,它摆脱了传统的颗粒凝集试验的上述限制。所提出的免疫分析是一种使用廉价仪器的灵敏和快速的方法。值得注意的是,该方法为增强和检测不同来源的颗粒(包括胶乳、二氧化硅微粒和生物细胞)的凝集提供了一种通用的方法。这种方法的发展将使人们能够获得定量结果,提高颗粒凝集试验检测抗HIV抗体的灵敏度,并在不影响每次检测成本的情况下减少分析时间。这些研究的成功完成将为获得许可技术和制造商业产品的大量商业机会提供所需的所有技术。
英文摘要
DESCRIPTION (provided by applicant): The long-term goal of the proposed research is to develop a novel quantitative particle agglutination technology for improving the performance of detection of human immunodeficiency virus (HIV) antibody in body fluids. The conventional particle agglutination assays have serious drawbacks such as limited sensitivity, long time of incubation, subjectivity and large amount of reagents. It is in this context that we propose to develop a new technology, which is free from the aforementioned limitations of the conventional particle agglutination assays. The proposed immunoassay is a sensitive and rapid method that utilizes inexpensive instrumentation. Significantly, the method presents a general approach for enhancement and detection of agglutination of particles of different origin, including latex, silica microparticles, and biological cells. The development of this method will allow one to obtain quantitative results, increase the sensitivity of particle agglutination assays for detection of anti-HIV antibodies, and reduce time of analysis without compromising the cost per test. Successful completion of these studies will make available all of the technology needed for a substantial business opportunity to license the technology and manufacture commercial products.
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