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临床分子成像

Clinical molecular imaging.

作者信息

Miller Janet C, Thrall James H

机构信息

Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.

出版信息

J Am Coll Radiol. 2004 Jan;1(1 Suppl):4-23. doi: 10.1016/S1546-1440(03)00025-5.

Abstract

This review summarizes the rapidly growing field of molecular imaging, the spatially localized and/or temporally resolved sensing of molecular and cellular processes in vivo. Molecular imaging is used to map the anatomic locations of specific molecules of interest within living tissue and has enormous potential as a powerful means to diagnose and monitor disease. Molecular imaging agents comprise a targeting component that confers localization and a component that enables external detectability with an imaging modality, such as PET, SPECT, MRI, optical, and ultrasound. The advantages and disadvantages of each of these modalities are discussed in regard to spatial resolution, temporal resolution, sensitivity, and cost. Molecular imaging agents can be divided into three categories, Type A, which bind directly to a target molecule, Type B, which are accumulated by molecular or cellular activity by the target, and Type C, which are undetectable when injected but can be imaged after they are activated by the target. The current status of clinical molecular imaging agents is presented as well as examples of some preclinical applications. The value of molecular imaging is illustrated by some examples for diseases such as cancer, neurological and psychiatric disorders, cardiovascular disease, infection and inflammation, and the monitoring of gene therapy and stem cell therapy.

摘要

本综述总结了快速发展的分子成像领域,即对体内分子和细胞过程进行空间定位和/或时间分辨的传感。分子成像用于绘制活组织内特定感兴趣分子的解剖位置,作为诊断和监测疾病的有力手段具有巨大潜力。分子成像剂包括赋予定位功能的靶向成分和能够通过PET、SPECT、MRI、光学和超声等成像方式进行外部检测的成分。针对空间分辨率、时间分辨率、灵敏度和成本等方面讨论了每种成像方式的优缺点。分子成像剂可分为三类:A类直接与靶分子结合;B类通过靶标的分子或细胞活性积累;C类注射时不可检测,但在被靶标激活后可成像。文中介绍了临床分子成像剂的现状以及一些临床前应用实例。通过癌症、神经和精神疾病、心血管疾病、感染和炎症等疾病的一些实例以及基因治疗和干细胞治疗监测的实例,说明了分子成像的价值。

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