Department of Radiology, Molecular Imaging Program at Stanford, Stanford University School of Medicine, Stanford, CA 94305-5424, USA.
Clin Radiol. 2010 Jul;65(7):500-16. doi: 10.1016/j.crad.2010.03.011.
In vivo molecular imaging has a great potential to impact medicine by detecting diseases in early stages (screening), identifying extent of disease, selecting disease- and patient-specific treatment (personalized medicine), applying a directed or targeted therapy, and measuring molecular-specific effects of treatment. Current clinical molecular imaging approaches primarily use positron-emission tomography (PET) or single photon-emission computed tomography (SPECT)-based techniques. In ongoing preclinical research, novel molecular targets of different diseases are identified and, sophisticated and multifunctional contrast agents for imaging these molecular targets are developed along with new technologies and instrumentation for multi-modality molecular imaging. Contrast-enhanced molecular ultrasound (US) with molecularly-targeted contrast microbubbles is explored as a clinically translatable molecular imaging strategy for screening, diagnosing, and monitoring diseases at the molecular level. Optical imaging with fluorescent molecular probes and US imaging with molecularly-targeted microbubbles are attractive strategies as they provide real-time imaging, are relatively inexpensive, produce images with high spatial resolution, and do not involve exposure to ionizing irradiation. Raman spectroscopy/microscopy has emerged as a molecular optical imaging strategy for ultrasensitive detection of multiple biomolecules/biochemicals with both in vivo and ex vivo versatility. Photoacoustic imaging is a hybrid of optical and US techniques involving optically-excitable molecularly-targeted contrast agents and quantitative detection of resulting oscillatory contrast agent movement with US. Current preclinical findings and advances in instrumentation, such as endoscopes and microcatheters, suggest that these molecular imaging methods have numerous potential clinical applications and will be translated into clinical use in the near future.
体内分子成像具有通过早期检测疾病(筛查)、识别疾病程度、选择针对疾病和患者的治疗方法(个体化医学)、应用定向或靶向治疗以及测量治疗的分子特异性效果来影响医学的巨大潜力。目前的临床分子成像方法主要使用正电子发射断层扫描(PET)或单光子发射计算机断层扫描(SPECT)技术。在正在进行的临床前研究中,确定了不同疾病的新的分子靶标,并开发了用于这些分子靶标的复杂和多功能对比剂,以及用于多模态分子成像的新技术和仪器。对比增强的分子超声(US)与靶向分子的对比微泡一起被探索作为一种可临床转化的分子成像策略,用于在分子水平上筛查、诊断和监测疾病。光学成像用荧光分子探针和超声成像用靶向分子微泡是很有吸引力的策略,因为它们提供实时成像,相对便宜,产生具有高空间分辨率的图像,并且不涉及电离辐射。拉曼光谱/显微镜已成为一种分子光学成像策略,用于超灵敏地检测多种具有体内和体外多功能性的生物分子/生化物质。光声成像是光学和超声技术的混合体,涉及光激发的靶向分子对比剂和通过超声对产生的振荡对比剂运动的定量检测。目前的临床前研究结果和仪器的进步,如内窥镜和微导管,表明这些分子成像方法具有许多潜在的临床应用,并将在不久的将来转化为临床应用。