A sparse reconstruction algorithm for superparamagnetic relaxometry
A sparse reconstruction algorithm for superparamagnetic relaxometry
批准号:
9319535
负责人:
Sara Lynn Loupot Thrower
金额:
$2.8万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-08-01 至 2018-07-31
关键词:
3-DimensionalABCG2 geneAlgorithmsBiologicalBiomedical TechnologyCellsCharacteristicsClinicCollectionComputer SimulationDataDevelopmentDevicesDiseaseEarly DiagnosisElectromagneticsEnvironmentFutureGeometryGoalsImaging TechniquesKnowledgeLawsLearning SkillLiteratureLocationMagnetismMalignant NeoplasmsMeasurementMeasuresMethodsModelingNoiseOne-Step dentin bonding systemOutcomePerformancePhysicsPropertyResearchResearch PersonnelResolutionSensitivity and SpecificitySignal TransductionSiteSourceSystemTechniquesTechnologyTestingTrainingTranslatingTranslationsUncertaintyWorkbasecancer cellcancer sitecareerclinical applicationdesigndetectorexperimental studyhigh riskimage guidedimprovedmagnetic dipolemouse modelnanoparticlenew technologynovelparticlepre-clinical trialpreclinical studyreconstructionresponsesource localizationsuperconducting quantum interference devicetreatment responsetumor
中文摘要
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英文摘要
Project Summary
Superparamagnetic relaxometry (SPMR) is a novel nanoparticle imaging technique that utilizes the
magnetic properties of biologically targeted superparamagnetic nanoparticles to potentially detect as few as
15,000 cancer cells. Source reconstruction in SPMR requires solving the ill-posed magnetic inverse problem.
There is currently a gap in knowledge about how to solve this inverse problem in order to determine which of
the many possible solutions represents the true location of bound particles. The long-term goal of this project
is to translate SPMR into the clinic as an early detection technique for cancer. The objective for this project is
to develop an algorithm that can reconstruct the location of cancer-bound nanoparticles in 3 dimensions
without any prior knowledge of the number of sites with bound particles. The hypothesis of the work is that a
sparse reconstruction algorithm based on physics models and tuned to the SPMR environment will reliably
reconstruct the 3-dimensional distribution of cancer-bound nanoparticles. We plan to test this hypothesis with
these specific aims: Specific Aim 1: Develop an experimentally informed forward model. The forward
model for the sparse reconstruction algorithm will be based on the application of the Biot-Savart law to the
physical conditions of the MRX device. The model will then be adjusted to best simulate data collected from
the device. Specific Aim 2: Apply and characterize the performance of the inverse algorithm. A sparse
reconstruction algorithm will be implemented to reconstruct the distribution of particles from the signal returned
by the detectors. The sensitivity, resolution and accuracy of the algorithm across a range of environmental and
user-defined variables will then be characterized and optimized. The expected outcome of these aims is a
novel reconstruction algorithm that will significantly improve source localization and quantification in magnetic
relaxometry. The development of a robust and well characterized reconstruction method will positively impact
the field of SPMR by opening it up to possible applications in image guidance and novel early detection
techniques. The knowledge that gained of the minimum detectability of the algorithm and the characterization
of its response with respect to environmental noise and optimization parameters will inform the design of future
experiments towards preclinical studies. The robust reconstruction algorithm developed by this project will
bring this novel technology one step closer to realizing its potential to detect early disease with unparalleled
sensitivity and specificity.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
A compressed sensing approach to immobilized nanoparticle localization for superparamagnetic relaxometry.
用于超顺磁弛豫测量的固定纳米粒子定位的压缩传感方法。
DOI:
10.1088/1361-6560/ab3c06
发表时间:
2019
期刊:
Physics in medicine and biology
影响因子:
3.5
作者:
[Thrower,SL, Kandala,SK, Fuentes,D, Stefan,W, Sowko,N, Huang,M, Mathieu,K, Hazle,JD]
通讯作者:
Hazle,JD