A micro Hall chip for circulating microvesicle based cancer monitoring
A micro Hall chip for circulating microvesicle based cancer monitoring
批准号:
8733954
负责人:
David Aaron Issadore
金额:
$23.07万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-09-01 至 2017-07-31
关键词:
AddressAntibodiesBenchmarkingBiological AssayBiological MarkersBiological ModelsBloodBlood TestsBlood specimenCA-15-3 AntigenCancer CenterCellsCentrifugationClinicalDetectionDevelopmentDevicesDiagnosisDisease ProgressionDisease modelERBB2 geneEpidermal Growth Factor ReceptorEquipmentFutureGeneticGoldHalf-LifeHarvestHeterogeneityHourHumanIn VitroLabelLettersMagnetismMalignant NeoplasmsMeasurementMeasuresMethodsMicrofluidicsMicrospheresMolecularMolecular TargetMonitorNeoplasm MetastasisOncogenicPTPRC genePatient CarePatientsPreparationProceduresProteomicsSamplingStructure of thyroid parafollicular cellSurfaceSystemTACSTD2 geneTechniquesTimeTranslationsWestern BlottingWhole BloodWorkassay developmentbasebiomaterial compatibilitycell typedrug efficacygallium arsenidehuman ITGB3 proteinimprovedin vitro Modelinnovationmicrochipmultidisciplinarynanomaterialsnanoparticlenanoscaleneoplastic cellprotein expressionpublic health relevancesensorstemtumor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Tumor cells are known to shed nano-scale objects called circulating microvesicles (C¿Vs) into patients' blood. These C¿Vs have been shown to carry molecular information from the tumor, which can potentially be used to diagnose and monitor cancer using only a blood test. However, due to their extremely small size (d ~ 50 nm), there has not been a clinically viable method to detect and profile these C¿Vs. To address these challenges, we propose a microchip-based platform that can quantitatively profile C¿Vs directly in unprocessed whole blood. On this chip, we harness the small feature size of microelectronics and combine it with the biocompatibility of microfluidics and magnetic nanoparticles (MNPs) to measure these nano-scale objects. Our proposed device is handheld and aims to reduce measurement times from several hours using conventional equipment to less than thirty minutes. Moreover, due to the high sensitivity of our micro-magnetic sensing method, the biomarker specific limit of detection (100 C¿V/mL) will exceed that of conventional techniques. This innovative, clinically practical approach to C¿V detection has great potential for non-invasive, routine monitoring of disease progression, drug efficacy, and metastasis, offering tremendous benefits for patients.
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依托单位:
海外基金