Light-activated Electronic p-Chips for Tagging Samples in Biorepositories and Cry
Light-activated Electronic p-Chips for Tagging Samples in Biorepositories and Cry
批准号:
8719366
负责人:
WLODEK MANDECKI
金额:
$51.38万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-20 至 2015-08-31
关键词:
AdhesionsAdhesivesBar CodesBiologicalBiomedical ResearchCellsCommunitiesComputer softwareContractsCryingDatabasesDevicesElectronicsEvaluationFailureFeedbackFreezingGoalsHuman ResourcesIceInstitutionLabelLaboratoriesLasersLightLinkLiquid substanceManufacturer NameMedical ResearchMethodologyMethodsNitrogenOpticsPerformancePhasePlayPositioning AttributeProceduresProcessProtocols documentationReaderReadingResearch PersonnelRoleSamplingSiliconSilicon DioxideSiteSolutionsSurfaceSystemTechniquesTechnologyTemperatureTestingTimeTissuesTubeValidationVial deviceWorkWritingbasebiobankbiological researchcold temperaturecomparativecostcost effectivedesigndesign and constructiondigitalextreme temperatureimprovedoperationprototypesoftware developmentvalidation studies
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The purpose of the present project is to implement a new RFID tagging system for rapid identification of vials in biorepositories. It is based on the PharmaSeq laser light- activated microtransponder, which is also known as a p-Chip. Its main advantages are its small size, low cost, inertness (silica-based), and durability under extremes of temperature. P-Chips have been shown to be viable and easy to read under conditions, such as the presence of frost, where traditional bar code labels fail due to problems related to interference or adhesive failure. Determining the serial ID numbers of p-Chips imbedded in the walls of vials is done with a dedicated reader that can be configured in several ways. The software associates a particular vial ID with a database to determine the provenance of the sample. Reading is extremely rapid giving the opportunity to maintain (or be close to) the storage temperature during polling. The main goals of this project are to: (1) design and optimize the process for embedding p-Chips in one or more types of sample vials for use at varying storage temperatures; (2) modify the existing p-Chip/reader system for use with vials, including designing and implementing bench-top readers that can either poll single vials or entire racks of vials; (3) improve key features of the p-Chips themselves for very low temperature conditions; (4) provide software routines that are compatible with existing enterprise systems for biorepositories; and (5) to validate the system with several collaborators. Successful completion of this work will result in a method and standard operating procedures that will improve sample storage techniques and provide more reliable samples to the biomedical research community.
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海外基金