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KMID : 0364920100350040151
Journal of Radiation Protection and Research
2010 Volume.35 No. 4 p.151 ~ p.156
A Study on the Quality Control of 18F-FDG Radiopharmaceutical
Kim Ssang-Tae

Yong Chul-Soon
Han Eun-Ok
Abstract
The types of test items which were recorded in this test report of quality control domestic 18F-FDG radiopharmaceutical which consisted of 13 different types: appearance, half-life, radioactive heterokaryosis, radiochemical Confirmation (measure of Rf value), radiochemical Purity, Ethanol, Acetonitrile, Kryptofix, Aluminium, pH, Endotoxin, aseptic test, and radioactivity¡¤ml-1. The record was fully recorded in ¡®appearance¡¯, ¡®radioactive heterokaryosis¡¯, ¡®pH¡¯, ¡®Endotoxin¡¯, and ¡®aseptic test¡¯. In ¡®half-life¡¯, ¡®radiochemical Confirmation (measure of Rf value), ¡®radiochemical Purity¡¯, ¡®Ethanol¡¯, ¡®Acetonitrile¡¯, ¡®Kryptofix¡¯, ¡®Aluminium¡¯, ¡®radioactivity¡¤ml-1¡¯, there were differences in records of each manufacturing business on radioactive medicine and medical supplies. The result of the test showed all 13 items of quality control test were 100% suitable on the basis of recorded data. There were more radiopharmaceutical made in the laboratory than in hospitals and businesses and in for result of suitability test, the laboratory showed higher suitability than did the hospitals or businesses. Domestically, there are differences of the test report items in the safety of radiopharmaceutical of each facility, and since it is not standardized, supplements are needed. To submit standardized test reports of quality guarantee in radiopharmaceutical, GMP of U.S. and CE Mark of Europe should be referred as well as receiving advice from professionals to standardize as suitable domestic standard.
KEYWORD
Quality Control, 18F-FDG, Radiopharmaceutical
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