Corot C, Idée J-M, Raynaud J-S, Salazar J-F, Catoen S
Recherche Guerbet, Roissy CDG, France.
Ann Pharm Fr. 2012 Jan;70(1):26-34. doi: 10.1016/j.pharma.2011.11.002. Epub 2011 Dec 16.
Due to numerous technical developments, in vivo imaging is suitable for pharmacokinetic and metabolism studies of new chemical entities as well as for evaluating their pharmacological or biological effects. MRI, nuclear medicine, X-Ray, ultrasound and optical imaging are available for both clinical and experimental imaging with even higher performance. For all these imaging modalities, diagnostic agents are useful to improve contrast and specificity. Specific targeting of biological events is addressed by molecular imaging. From a pharmacodynamic perspective, radiolabeling of a new chemical entity allows in vivo visualization quantitative measure of its biodistribution, its elimination and its specific molecular binding. Non-invasive imaging methods are useful for longitudinal investigations of biological changes. Based on nanotechnologies, specificity of drug delivery can be monitored by imaging. New developments in hybrid imaging technologies as well as multimodal contrast agents reinforce in vivo experimental and clinical proof of mechanism of new chemical entities.
由于众多技术的发展,体内成像适用于新化学实体的药代动力学和代谢研究,以及评估它们的药理或生物学效应。磁共振成像(MRI)、核医学、X射线、超声和光学成像可用于临床和实验成像,且性能更高。对于所有这些成像方式,诊断剂有助于提高对比度和特异性。分子成像解决了生物事件的特异性靶向问题。从药效学角度来看,新化学实体的放射性标记可实现其体内分布、消除及其特异性分子结合的可视化定量测量。非侵入性成像方法对于生物变化的纵向研究很有用。基于纳米技术,药物递送的特异性可通过成像进行监测。混合成像技术以及多模态造影剂的新发展加强了新化学实体体内实验和临床机制证据。