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作 者:于延豹[1] 汪勇先[1] 董墨[1] 于俊峰[1] 胡伟青 周伟[1] 杨学忠 尹端氵止
机构地区:[1]中国科学院上海应用物理研究所放药中心,上海201800 [2]安盛科兴药业有限公司,上海201800
出 处:《同位素》2004年第2期99-103,共5页Journal of Isotopes
基 金:中国科学院创新工程重大项目(KJCXI-SW-08)资助
摘 要:以两种分散方法制备不同粒径分布的188Re-硫化铼混悬液,采用涡旋法制得的大颗粒混悬液,粒径大于5μm的颗粒占55%,大于10μm的占19%;超声法所得混悬液粒径小于5μm颗粒占93%,大于10μm的只占0.3%。两种方法所得混悬液粒径分布有显著差异(P<0.01)。稳定性测试结果表明,涡旋法所得混悬液在6min内稳定可靠,超声法所得混悬液在15min内能均匀分散,此后取药需重新分散,且药物仍然均匀可用,颗粒度和放化纯度无明显变化。采用涡旋分散装置制备大颗粒混悬液时,操作简便,结果重现性良好,并同时避免了涡旋分散过程中因手动操作对人体造成的辐射损伤,减少了人为因素对颗粒度的影响。Two different dispersing methods are used to prepare ^(188)Re-rhenium sulfide suspension, with obviously different particle-size distribution. Swirling device, offersus large-sized particles, 55% of which are larger than 5 μm, 19% are larger than 10 μm. However, ultrasonic dispersion can only produce suspension with large quantities of smaller particles, only 0.3% of which are larger than 10 μm and almost 93% are within 5 μm. The former suspension made by swirling device appears deposition within 6 minutes, and the other is not uniform after 15 minutes, which radiochemistry purity and particle-size distribution do not change distinctively within 24 hours. The conclusion is that both of the suspension should be regarded as radiopharmaceuticals for testing the optimal particle-size ranges for intra-articular injection.
分 类 号:R817.9[医药卫生—影像医学与核医学]
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