A micro Hall chip for circulating microvesicle based cancer monitoring
A micro Hall chip for circulating microvesicle based cancer monitoring
批准号:
8890809
负责人:
David Aaron Issadore
金额:
$23.41万
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 specimenCancer CenterCellsClinicalDetectionDevicesDiagnosisDisease ProgressionDisease modelERBB2 geneEpidermal Growth Factor ReceptorEquipmentFutureHarvestHealthHeterogeneityHourHumanLabelLettersMagnetic nanoparticlesMagnetismMalignant NeoplasmsMeasurementMeasuresMethodsMicrofluidicsMicrospheresModelingMolecularMolecular TargetMonitorMucin-1 Staining MethodNeoplasm MetastasisOncogenicPTPRC genePatient CarePatientsPreparationProceduresProteomicsSamplingSystemTACSTD2 geneTechniquesTimeTranslationsUltracentrifugationWestern BlottingWhole BloodWorkbasebiomaterial compatibilitycell typedrug efficacygallium arsenidegenetic informationhuman ITGB3 proteinimprovedinnovationmicrochipmultidisciplinarynanomaterialsnanoparticlenanoscaleneoplastic cellprotein expressionsensorstemtemporal measurementtumor
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 (CμVs) into patients' blood. These CμVs 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 CμVs. To address these challenges, we propose a microchip-based platform that can quantitatively profile CμVs 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 CμV/mL) will exceed that of conventional techniques. This innovative, clinically practical approach to CμV 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