Hydroxypyridonate Gd Complexes: MRI Agents

羟基吡啶酮酸钆复合物：MRI 试剂

• 批准号: 7885681
• 负责人: KENNETH N RAYMOND
• 金额: $ 35.63万
• 依托单位: UNIVERSITY OF CALIFORNIA BERKELEY
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-04-01 至 2014-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7885681
• 关键词: Address; Adverse effects; Architecture; Area; Atherosclerosis; Biological Markers; Capsid; Chemistry; Clinical; Complex; Contrast Media; Cyclodextrins; Dendrimers; Detection; Development; Diagnosis; Diagnostic; Disease; Disease Marker; Dissociation; Dose; Electronics; Electrons; Ensure; Europium; Exhibits; Family; Fibrosis; Gadolinium; Goals; Hospitals; Image; Image Enhancement Agent; Impairment; Injury; Ions; Iron; Kidney; Kidney Diseases; Kinetics; Ligands; Light; Magnetic Resonance Imaging; Malignant Neoplasms; Manganese; Measurement; Measures; Medical; Medicine; Metals; Methods; Multimodal Imaging; Patients; Pentetic Acid; Performance; Price; Proteins; Protons; Relaxation; Renal clearance function; Research; Research Personnel; Resolution; S-1 Antimetabolite agent; Safety; Signal Transduction; Soft Tissue Injuries; Staging; Structure; Thermodynamics; Time; Tissues; Virus; Water; Work; analog; base; carboxylate; design; disease diagnosis; dosage; flexibility; imaging modality; improved; in vivo; instrument; interest; macromolecule; metal complex; optical imaging; patient safety; prevent; public health relevance; scaffold; small molecule; tool

DESCRIPTION (provided by applicant): Magnetic resonance imaging (MRI) has provided dramatic new capabilities for diagnostic medicine. MRI enables the acquisition of high resolution three-dimensional images, aiding detection of a wide variety of physical abnormalities, and recent advances in dynamic MRI are providing real-time imaging. Over 30% of MRI scans are now acquired using a paramagnetic contrast agent, which enhances the proton relaxation and hence image quality. Gadolinium complexes are most widely used, and these complexes currently are all based on a poly(amino-carboxylate) ligand scaffold . Although the use of contrast agents has become routine, agents in clinical use are sub optimal in several important areas. Current imaging agents show relaxivities of less than 5% of the theoretical maximum. This low performance means that grams of gadolinium must be administered for a full-body MRI scan. This low sensitivity also precludes targeted imaging. The large amounts of agent used are particularly problematic in light of the recent research suggesting that nephrogenic systemic fibrosis (NSF, alternately NFD) is caused by release of Gd from the contrast agent before it clears through the kidneys. Improving performance, and thereby reducing dosage, would significantly improve patient safety. This project has developed gadolinium complexes based on a hexadentate hydroxypyridonate ligand scaffold that are stable and have substantially higher relaxivity due to a higher number of coordinated water molecules (2-3) and a water exchange rate at least two orders of magnitude higher than commercial agents. Having developed the agents and demonstrated their thermodynamic stability, we intend to continue their development, to enable new kinds of MR imaging. Relaxivities of more than 300mM-1s-1 are the target, to be achieved through the development of macromolecular contrast agents that are also highly stable. The use of macromolecular conjugation to improve relaxivity increases the need for high contrast agent kinetic stability. While long renal clearance times of most macromolecules allows for greater flexibility in image acquisition time, Gd dissociation will become an issue even in patients with healthy kidneys. There is therefore a need for agents with extremely high kinetic stability. If these agents also have higher performance compared to current agents, much less Gd will be needed to obtain an image. This will also enable new types of imaging with MRI. Thus the goals of this project are to improve contrast agent performance--both to lower administered doses and to enable target-selective imaging-and to develop agents with extremely high kinetic stability, to ensure patient safety. PUBLIC HEALTH RELEVANCE: Magnetic resonance imaging (MRI) has provided dramatic new capabilities for diagnostic medicine, with over 30% of MRI scans now acquired using a contrast agent, usually containing gadolinium, which enhances image quality. However, due to the low performance of current agents, gram quantities of gadolinium have to be injected into a patient, which has recently led to Nephrogenic Systemic Fibrosis in patients with kidney disorders. In order to prevent this toxic side effect of MRI contrast agents, we propose to improve the performance of MRI contrast agents up to two orders of magnitude over current agents and maximize in vivo stability to ensure patient safety.

描述（由申请人提供）：磁共振成像（MRI）为诊断医学提供了戏剧性的新能力。MRI能够获得高分辨率的三维图像，帮助检测各种身体异常，动态MRI的最新进展正在提供实时成像。现在，超过30%的MRI扫描是使用顺磁造影剂进行的，这可以增强质子弛豫，从而提高图像质量。钆配合物是应用最广泛的配合物，目前这些配合物都是基于聚氨基羧酸酯配体支架。虽然造影剂的使用已成为常规，但临床使用的造影剂在几个重要领域并不理想。目前显像剂显示的弛豫率小于理论最大值的5%。这种低性能意味着必须使用数克钆进行全身核磁共振扫描。这种低灵敏度也妨碍了靶向成像。鉴于最近的研究表明肾源性系统性纤维化（NSF，或NFD）是由造影剂在通过肾脏清除之前释放Gd引起的，因此大量使用造影剂尤其成问题。提高性能，从而减少剂量，将显著提高患者的安全性。该项目开发了基于六齿羟基嘧啶配体支架的钆配合物，由于具有更多的配位水分子（2-3）和至少比商业试剂高两个数量级的水交换率，该配合物稳定且具有更高的弛性。在开发了这些试剂并证明了它们的热力学稳定性之后，我们打算继续开发它们，以实现新型的磁共振成像。松弛度超过300mM-1s-1是目标，要通过开发高度稳定的大分子造影剂来实现。使用大分子偶联来提高弛豫度增加了对高造影剂动力学稳定性的需求。虽然大多数大分子的肾脏清除时间较长，可以在图像采集时间上有更大的灵活性，但Gd解离即使在肾脏健康的患者中也会成为一个问题。因此，需要具有极高动力学稳定性的药剂。如果这些代理与当前代理相比也具有更高的性能，那么获得图像所需的Gd就会少得多。这也将使新型的核磁共振成像成为可能。因此，该项目的目标是提高造影剂的性能——既降低给药剂量，又使目标选择性成像成为可能——并开发具有极高动力学稳定性的造影剂，以确保患者安全。