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本文主要就~(131)I胶丸研制进行了一系列的工艺条件的可行性试验。例如,对不同产家的胶丸溶胀、液体固化剂配方、固化时间、在固化期内~(131)I在空气中排放、~(131)I浓度对葡萄糖(或维生素)加入量影响、不同条件下制备的固化剂吸附性能试验、~(131)I胶丸产品核纯分析、放化纯分析以及其粒间均匀性测量等。采纳本工艺研制的~(131)I胶丸符合国际药典的规定指标,使用安全、简单方便。
This paper mainly on the ~ (131) I capsules developed a series of feasibility studies of the conditions. For example, different manufacturers of plastic swollen, liquid curing agent formulations, curing time, during the curing period of ~ (131) I in the air emissions, ~ (131) I concentration of glucose (or vitamin) Conditions of the curing agent prepared by the adsorption performance test, ~ (131) I pellet product nuclear pure analysis, pure chemical analysis and the uniformity of the intergranular measurement. The ~ (131) I capsule developed by adopting this technology complies with the stipulations of the International Pharmacopoeia and is safe and easy to use.