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正电子发射断层扫描成像在抗癌药物研发中的小动物应用

Positron emission tomography imaging of small animals in anticancer drug development.

作者信息

Aboagye Eric O

机构信息

Molecular Therapy and PET Oncology Research group, The Clinical Sciences Centre, Faculty of Medicine, Hammersmith Hospital Campus, Imperial College London, Rm. 242 MRC Cyclotron Building, London, W12 0NN, UK.

出版信息

Mol Imaging Biol. 2005 Jan-Feb;7(1):53-8. doi: 10.1007/s11307-005-0886-2.

Abstract

Positron emission tomography (PET) imaging of small animals enables researchers to bridge the gap between in vitro science and in vivo human studies. The imaging paradigm can be established and refined in animals before implementation in humans and image data related to ex vivo assays of biological activity. Small animal PET (saPET) imaging enables assessment of baseline focal pathophysiology, pharmacokinetics, biological target modulation and the efficacy of novel drugs. The potential and challenge of this technology as applied to anticancer drug development is discussed here.

摘要

小动物正电子发射断层扫描(PET)成像使研究人员能够弥合体外科学与体内人体研究之间的差距。在应用于人体之前,可以在动物身上建立和完善成像模式,并获取与生物活性体外测定相关的图像数据。小动物PET(saPET)成像能够评估基线局灶性病理生理学、药代动力学、生物靶点调节以及新药的疗效。本文将讨论该技术在抗癌药物研发中的潜力和挑战。

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