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Central Nervous System Drug Evaluation Using Positron Emission Tomography
Clinical Psychopharmacology and Neuroscience ; : 9-16, 2011.
Article in English | WPRIM | ID: wpr-201613
ABSTRACT
In conventional pharmacological research in the field of mental disorders, pharmacological effect and dose have been estimated by ethological approach and in vitro data of affinity to the site of action. In addition, the frequency of administration has been estimated from drug kinetics in blood. However, there is a problem regarding an objective index of drug effects in the living body. Furthermore, the possibility that the concentration of drug in blood does not necessarily reflect the drug kinetics in target organs has been pointed out. Positron emission tomography (PET) techniques have made progress for more than 20 years, and made it possible to measure the distribution and kinetics of small molecule components in living brain. In this article, we focused on rational drug dosing using receptor occupancy and proof-of-concept of drugs in the drug development process using PET.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Brain / Kinetics / Central Nervous System / Receptors, Dopamine D2 / Positron-Emission Tomography / Drug Evaluation / Electrons / Norepinephrine Plasma Membrane Transport Proteins / Serotonin Plasma Membrane Transport Proteins / Mental Disorders Type of study: Diagnostic study Language: English Journal: Clinical Psychopharmacology and Neuroscience Year: 2011 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Brain / Kinetics / Central Nervous System / Receptors, Dopamine D2 / Positron-Emission Tomography / Drug Evaluation / Electrons / Norepinephrine Plasma Membrane Transport Proteins / Serotonin Plasma Membrane Transport Proteins / Mental Disorders Type of study: Diagnostic study Language: English Journal: Clinical Psychopharmacology and Neuroscience Year: 2011 Type: Article