Nontoxic Si Nanoprobes for Mulitple Biomarker Imaging

用于多种生物标志物成像的无毒硅纳米探针

• 批准号: 7844444
• 负责人: ANGELIQUE Y LOUIE
• 金额: $ 3.68万
• 依托单位: UNIVERSITY OF CALIFORNIA AT DAVIS
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-07-01 至 2011-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7844444
• 关键词: Acids; Acute; Affect; Animal Model; Animals; Arterial Fatty Streak; Biodistribution; Biological; Biological Markers; Blood Clot; Blood Vessels; Blood coagulation; Cadmium; Cardiovascular system; Cell Adhesion; Cell Adhesion Molecules; Cell Culture Techniques; Clinical; Clinical assessments; Color; Connective Tissue; Contrast Media; Coronary; Coronary Arteriosclerosis; Cultured Cells; Detection; Drug Kinetics; Evaluation; Event; Fibrin; Film; Fluorescence Microscopy; Goals; Health; Homeostasis; Human; Image; In Vitro; Inflammation; Injury; Ions; Label; Laboratory Research; Lead; Life; Magnetic Resonance; Magnetic Resonance Imaging; Methods; Modeling; Monitor; Morbidity - disease rate; Optical Methods; Optics; Oryctolagus cuniculus; Patients; Physicians; Positron-Emission Tomography; Prevention; Preventive Medicine; Probability; Procedures; Property; Quantum Dots; Radiolabeled; Rattus; Reporting; Resolution; Risk; Route; Rupture; Semiconductors; Silicon; Solubility; Surface; System; Thrombosis; Time; Tissues; Toxic effect; Transition Elements; Vascular Diseases; Water; Work; acute coronary syndrome; base; biological systems; bone; cell type; clinical application; cytokine; experience; imaging modality; imaging probe; in vivo; inflammatory marker; injured; interest; luminescence; macrophage scavenger receptors; mortality; nanoparticle; nanoprobe; optical imaging; quantum; radiotracer; restenosis; surface coating; tool; toxic metal; treatment planning; uptake

DESCRIPTION (provided by applicant): Plaque composition is an important assessment point in the prevention of acute coronary syndrome. More so than plaque size, the composition of a plaque and presence of specific markers indicate if a plaque is at risk for rupture. Rupture can lead to thrombotic events that cause mortality or morbidity. A number of plaque components have been identified that correlate with plaque stability, including cell types and cytokines associated with inflammation, but these are difficult to study in vivo. In addition, no single marker is an absolute predictor for plaque risk to rupture clinicians are increasingly interested in multiple marker assessment. Therefore a need exists for imaging methods that will allow for clinical assessment of many plaque components. Noninvasive methods such as magnetic resonance imaging (MRI) and positron emission tomography (PET) are capable of imaging marker expression using targeted contrast agents, but multiple markers cannot be assessed simultaneously. If a clinician is interested to examine more than one marker, studies must be done serially, with a wait time in between for the previous targeted contrast agent to clear (for MRI), or decay (for PET). The overall goal of this proposal is to develop synthetic methods and conduct imaging studies leading toward the use of nontoxic, semiconductor, nanoparticle, imaging probes (quantum dots, QDs) in the management of human coronary artery disease. We propose to develop silicon QDs that are luminescent and also paramagnetic to allow both optical and MR imaging. Unlike traditional cadmium based QDs, silicon nanoparticles have the promise to be nontoxic as even free silicon relatively nontoxic. The QDs can be targeted to identify specific biomarkers important in cardiovascular preventative medicine and both magnetic resonance and optical imaging are then employed to assess plaque composition--MRI is used to detect regions where biomarkers are expressed, while optical methods are employed to interrogate these regions to identify the types of biomarkers present. In this proposal we describe methods to synthesize Si QDs of specific size and imaging properties, characterize the toxicity and uptake of these nanoparticles in cell cultures, and demonstrate the utility for these QDs to label multiple biomarkers of plaque stability in an animal model. The proposed work develops a new imaging material that would allow physicians to assess whether an arterial plaque was at risk to rupture. Plaque rupture is a graver threat to health than the size of the plaque. The physician can use this information to decide on treatment plans for the patient and to identify plaques that need to be more carefully monitored. The proposed work develops a new imaging material that would allow physicians to assess whether an arterial plaque was at risk to rupture. Plaque rupture is a graver threat to health than the size of the plaque. The physician can use this information to decide on treatment plans for the patient and to identify plaques that need to be more carefully monitored.

描述(申请人提供)：斑块成分是预防急性冠脉综合征的一个重要评估点。斑块的组成和特定标志物的存在比斑块的大小更能表明斑块是否有破裂的风险。破裂可导致血栓事件，导致死亡或发病。已经确定了许多与斑块稳定性相关的斑块成分，包括与炎症相关的细胞类型和细胞因子，但这些很难在体内进行研究。此外，没有单一标记物是斑块破裂风险的绝对预测因子，临床医生对多标记物评估越来越感兴趣。因此，需要能够对许多斑块成分进行临床评估的成像方法。磁共振成像(MRI)和正电子发射断层扫描(PET)等非侵入性方法可以利用靶向造影剂对标记物的表达进行成像，但不能同时评估多个标记物。如果临床医生有兴趣检查不止一个标志物，研究必须按顺序进行，中间要有一段时间等待先前的靶向造影剂清除(对于MRI)或衰变(对于PET)。这项提议的总体目标是开发合成方法并进行成像研究，从而使无毒、半导体、纳米颗粒、成像探针(量子点、量子点)在人类冠状动脉疾病的治疗中得到使用。我们建议开发发光和顺磁性的硅量子点，以允许光学和磁共振成像。与传统的基于镉的量子点不同，硅纳米颗粒有望是无毒的，因为即使是游离的硅也相对无毒。量子点可以被用来识别心血管预防医学中重要的特定生物标记物，然后使用磁共振和光学成像来评估斑块的组成--核磁共振被用来检测表达生物标记物的区域，而光学方法被用来询问这些区域以识别存在的生物标记物的类型。在这项建议中，我们描述了合成特定尺寸和成像特性的硅量子点的方法，表征了这些纳米颗粒在细胞培养中的毒性和摄取，并在动物模型中展示了这些量子点用于标记斑块稳定性的多个生物标记物的效用。这项拟议的工作开发了一种新的成像材料，可以让医生评估动脉斑块是否有破裂的风险。斑块破裂对健康的威胁比斑块的大小更严重。医生可以使用这些信息来决定患者的治疗计划，并识别需要更仔细监控的斑块。这项拟议的工作开发了一种新的成像材料，使医生能够评估动脉 斑块有破裂的危险。斑块破裂对健康的威胁比斑块的大小更严重。这个 医生可以使用这些信息来决定患者的治疗计划，并识别需要的斑块 需要更仔细地监控。