NONINVASIVE MEASUREMENT OF BLOOD ANALYTES

血液分析物的无创测量

• 批准号: 8364132
• 负责人: ISHAN BARMAN
• 金额: $ 2.97万
• 依托单位: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-06-01 至 2012-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8364132
• 关键词: Algorithms; Biomedical Research; Blood; Calibration; Detection; Development; Forearm; Funding; Glucose; Goals; Grant; Healthcare; Human; Individual; Intercellular Fluid; Lasers; Measurement; Methods; National Center for Research Resources; Photobleaching; Photons; Physiological; Population; Principal Investigator; Procedures; Prospective Studies; Raman Spectrum Analysis; Randomized; Research; Research Infrastructure; Resources; Sampling; Source; Technology; Tissue Model; Tissues; United States National Institutes of Health; clinically relevant; cost; diabetic patient; human subject; in vivo; migration; tissue phantom

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. The goal of this project is the measurement of clinically-relevant analytes in the blood tissue matrix of human subjects using near-infrared Raman spectroscopy. Such a technology could have great impact on the healthcare practices for the entire population, with the shorter term research directed towards glucose measurements for diabetic patients. We have recently demonstrated detection feasibility of glucose concentrations in vivo from transcutaneous measurements of the forearm by performing individual calibration. From these measurements we have identified the following sources of prediction error when a calibration algorithm is applied on a larger human population: (A) variability in sample turbidity, (B) presence of tissue autofluorescence and photobleaching and (C) physiological lag between blood and interstitial fluid (ISF) glucose. We have previously completed the development of a method (called turbidity corrected Raman spectroscopy, TCRS) for the correction of turbidity-induced distortions in Raman spectra utilizing the photon migration approach. We have demonstrated that, upon application of TCRS, the widely varying Raman spectra observed from a set of tissue phantoms having the same concentration of Raman scatterers but different turbidities tend to show near perfect coalescence onto a single spectral profile. Furthermore, in a prospective study that employs physical tissue models with varying turbidities and randomized concentrations of Raman scatterers and interfering agents, a 20% reduction in prediction error is obtained by applying the turbidity correction procedure to the acquired Raman spectra.

该子项目是利用资源的众多研究子项目之一 由 NIH/NCRR 资助的中心拨款提供。子项目的主要支持 并且子项目的主要研究者可能是由其他来源提供的， 包括其他 NIH 来源。 子项目可能列出的总成本 代表子项目使用的中心基础设施的估计数量， NCRR 赠款不直接向子项目或子项目工作人员提供资金。 该项目的目标是使用近红外拉曼光谱测量人类受试者血液组织基质中的临床相关分析物。这种技术可能会对整个人群的医疗保健实践产生巨大影响，短期研究将针对糖尿病患者的血糖测量。我们最近证明了通过进行个体校准，通过前臂的经皮测量来检测体内葡萄糖浓度的可行性。通过这些测量，我们确定了将校准算法应用于较大人群时的以下预测误差来源：(A) 样品浊度的变异性，(B) 组织自发荧光和光漂白的存在，以及 (C) 血液和血液之间的生理滞后。间质液（ISF）葡萄糖。我们之前已经完成了一种方法（称为浊度校正拉曼光谱，TCRS）的开发，用于利用光子迁移方法校正拉曼光谱中浊度引起的畸变。我们已经证明，在应用 TCRS 后，从具有相同拉曼散射体浓度但不同浊度的一组组织模型中观察到的广泛变化的拉曼光谱往往会显示出近乎完美的聚结到单个光谱轮廓上。此外，在一项采用具有不同浊度以及随机浓度的拉曼散射体和干扰剂的物理组织模型的前瞻性研究中，通过对采集的拉曼光谱应用浊度校正程序，可以将预测误差降低 20%。