课题基金 / 基金详情

Non-invasive beta-cell imaging using a Ga-68-labeled glucagone-like peptide-1 ana

Non-invasive beta-cell imaging using a Ga-68-labeled glucagone-like peptide-1 ana
使用 Ga-68 标记的胰高血糖素样肽 1 ana 进行非侵入性 β 细胞成像
批准号:
7224577
负责人:
Martin Gotthardt
金额:
$15.0万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-09-30 至 2009-08-31

项目摘要

项目成果

Martin Gotthardt的其他基金

相似基金

相关文献

中文摘要
翻译
描述(由申请人提供): 胰腺β细胞的功能是糖尿病的关键问题,但只能间接评估。目前,关于β细胞质量的几个方面仍有待阐明,例如:(1)2型糖尿病发作时总β细胞质量是否减少,(2)β细胞质量在疾病过程中如何发展,(3)哪些因素影响β细胞质量,以及(4)β细胞质量如何与对治疗的反应相关。因此,在胰岛移植后测量β细胞质量将是非常有趣的。由于没有可靠的方法来评估和量化体内人β细胞质量,研究受到阻碍。如果β细胞质量可以通过非侵入性方法确定,这将是推进这一研究领域的巨大资产。 我们已经开发了一种放射性标记剂(DOTA-Lys 40-Exendin 4),可以进行特异性β细胞成像。在小鼠中,示踪剂显示每克胰腺组织摄取约9%的注射活性。因此,这种特定的示踪剂是一个有前途的工具,在体内β细胞imaging在human.Under这个补助金的建议,我们将开发一个Ga-68标记DOTA-Exendin化合物的体内β细胞成像与正电子发射断层扫描(PET)。使用诸如Ga-68的正电子发射体将提供优于常规核医学成像的许多优点:1.高空间分辨率,2.准确定量,3.通过使用集成PET/CT扫描仪(CT=计算机断层扫描)精确定位胰腺/β细胞区域,即使β细胞丢失后胰腺示踪剂摄取减少。与磁共振成像(MRI)相比,该方法非常敏感,并且不需要直接标记β细胞用于成像目的。直接标记(例如用铁)只能在β细胞移植中进行(在胰岛移植之前),但不适合于胰腺β细胞的体内成像。 在这个项目中,我们将研究在不同的糖尿病动物模型中Ga-68标记的DOTA-Exendin的摄取和β细胞质量的相关性。在示踪剂的临床前开发成功后,将在人体中进行初步研究。除了在健康志愿者和I型和II型糖尿病患者中进行的原理验证研究外,还将建立一种剂量测定方法,通过PET成像简单可靠地定量β细胞质量。
英文摘要
DESCRIPTION (provided by applicant): The function of pancreatic beta-cell cells is a key issue in diabetes mellitus, but can only be assessed indirectly. Currently, several aspects regarding beta-cell mass remain to be elucidated, for example: (1) Is the total beta-cell mass at the onset of type 2 diabetes diminished or not, (2) how does the beta-cell mass develop during the course of the disease, (3) which factors affect beta-cell mass, and (4) how does beta-cell mass relate to the response to therapy. Futhermore, it would be of great interest to measure beta-cell mass after islet-transplantation. Research is hampered by the fact that no reliable methods exist to assess and quantify human beta-cell mass in vivo. If beta-cell mass could be determined by a non-invasive method, this would be of a tremendous asset in advancing this field of research. We have developed a radiolabeled agent (DOTA-Lys40-Exendin 4) that allows specific beta-cell imaging. In mice the tracer shows uptake of approximately 9% of the injected activity per gram of pancreas tissue. This specific tracer is therefore a promising tool for in vivo beta-cell imaging in humans.Under this grant proposal, we will develop a Ga-68 labeled DOTA-Exendin compound for imaging of beta-cells in vivo with positron emission tomography (PET). The use of a positron emitter such as Ga-68 will offer a number of advantages over conventional nuclear medicine imaging: 1. high spatial resolution, 2. accurate quantification, 3. exact localization of the pancreas / the beta-cell areas by use of an integrated PET/CT scanner (CT=computed tomography), even if pancreatic tracer uptake is decreased after beta-cell loss. In comparison to Magnetic Resonance Imaging (MRI), the approach is very sensitive and will not require direct labeling of beta-cells for imaging purposes. Direct labeling (for example with iron) can only be done in beta-cell transplantation (prior to islet transplantation) but is not suitable for imaging of pancreatic beta-cells in vivo. In this project, we will investigate the correlation of uptake of the Ga-68-labeled DOTA-Exendin and beta-cell mass in different animal models of diabetes. Upon succesful pre-clinical development of the tracer, pilot studies in humans will be conducted. Apart from proof-of-principle studies in healthy volunteers and diabetes type I and II patients, a dosimetric method will be established to simply and reliably quantify beta-cell mass by PET imaging.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Non-invasive beta-cell imaging using a Ga-68-labeled glucagone-like peptide-1 ana
Non-invasive beta-cell imaging using a Ga-68-labeled glucagone-like peptide-1 ana
海外基金