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Positron Emission Tomography for Future Drug Development
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pp.137-151 (15) Authors: Ryogo Minamimoto, Chumpol Theeraladanon, Akiko Suzuki, Tomio Inoue doi: 10.2174/1877613211101020137
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| Abstract |
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Productivity in the drug discovery and development process has seen a drastic decline over the last few years. Clearly, traditional approaches to drug development are not working. The new concept called “microdosing studies” was recently announced as a promising methodology for accreting drug development. The microdosing studies is a concept by administrating a low dose (microdose) of a candidate compound to human volunteers to obtain in vivo human pharmacokinetic (PK) data at an early stage of drug development. As a result unpromising candidate drugs can be eliminated at an earlier stage of drug development. A key component for this concept is highly sensitive analytical methods such as positron emission tomography (PET), accelerator mass spectrometry (AMS) and liquid chromatography-mass spectrometry (LC/MS/MS). This issue focuses on PET methodology from basic to future prospects for drug development and patents related to it.
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Keywords:
Positron emission tomography (PET), PET/CT, drug development, microdosing, imaging, microdosing approach, primary pharmacodynamics, conventional clinical trials, accelerator mass spectrometry, liquid chromatography-mass spectrometry, non-invasive imaging, in vivo human pharmacokinetic, proton-rich isotopes, line of response, radiopharmaceutical sciences
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Affiliation:
Division of Nuclear Medicine, Department of Radiology, National Center for Global Health and Medicine, 1-21-1, Toyama, Shinjyuku-ku, Tokyo, 162-8655, Japan.
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