Point-of-care HIV viral load system using RPA and MXR
Point-of-care HIV viral load system using RPA and MXR
批准号:
10665089
负责人:
Jay Kenneth Fisher
金额:
$95.04万
依托单位:
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:
2019-08-01 至 2024-07-31
关键词:
AddressAgitationAgreementAreaBiological AssayBullaCaringClinicalCold ChainsCollaborationsCountryCoupledDetectionDevelopmentDevicesDiagnosticDiagnostic SensitivityDiagnostic SpecificityDrynessEquipmentFiltrationGenomicsGoalsHIVHIV-1HourHuman ResourcesHuman immunodeficiency virus testIncomeIndividualInfrastructureLaboratoriesLeftLifeLiquid substanceMagnetismMeasuresMethodsMicrofluidic MicrochipsMicrofluidicsMolecularMonitorNucleic Acid Amplification TestsNucleic AcidsPerformancePersonsPhasePlasmaPolymeraseQuantitative Reverse Transcriptase PCRRNAReactionReagentResolutionRodSamplingSensitivity and SpecificitySmall Business Innovation Research GrantSpecific qualifier valueSpecificitySpeedSurfaceSystemTechnologyTemperatureTestingTimeTrainingTransportationValidationViral Load resultVirionantiretroviral therapyclinical research sitecostdetection limitflexibilityimprovedinstrumentlaboratory equipmentmagnetic beadsoperationpoint of carepoint of care testingportabilityprogramsrecombinaserural areasuccess
中文摘要
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英文摘要
ABSTRACT
The most accurate way to monitor the efficacy of antiretroviral therapy is through nucleic acid
amplification tests (NAATs) that directly measure HIV RNA (viral load). In the developing and
developed world these tests are primarily conducted in centralized laboratories in urban centers.
However, a significant number of persons living with HIV reside in rural locations, and due
tolack of transportation, financial constraints, or a combination of these factors, would be better
served by a test closer to the point-of-care (POC). Despite advancements in portable nucleic
acid amplification technology there remains significant opportunity to improve affordability, time-
to-result, and ease-of-use of POC HIV viral load (VL) testing. To this end we will complete
development of our rapid, sample-to-answer HIV VL test that achieves better metrics in these
areas than today’s commercial platforms.
In this Phase II project, we will continue our collaboration with the Diagnostics Program at PATH
(Seattle, WA) to finalize and test the completed device. In Aim 1 Redbud Labs will finalize and
integrate the test cartridge and device into a compact, robust instrument. In Aim 2 Redbud Labs
will verify quantitation and genomic coverage of the automated assay. In Aim 3 PATH will
perform analytic validation of the system using clinical samples, comparing those results against
a gold standard. At this project’s completion we will have a platform ready for multi-site clinical
validation.
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海外基金