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引用本文:王彦,张利利.复方奥硝唑中空栓的制备及质量控制[J].中国现代应用药学,2009,(3):224-226.
WANG Yan1,ZHANG Lili2.Preparation and Quality Control of Compound Ornidazole Hollow Type Suppository[J].Chin J Mod Appl Pharm(中国现代应用药学),2009,(3):224-226.
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复方奥硝唑中空栓的制备及质量控制
王彦,张利利
作者单位
王彦,张利利  
摘要:
目的制备复方奥硝唑中空栓剂,并建立质量控制方法。方法以混合脂肪酸甘油酯为基质制备中空栓剂;采用等吸收-双波长法同时测定其主药奥硝唑和左氧氟沙星的含量;对制剂进行卫生学、刺激性及稳定性等试验。结果奥硝唑和左氧氟沙星的平均回收率(n=9)分别为99.7%,100.2%,其他各项检查均符合栓剂的有关规定。结论本制剂制备工艺简单,性质稳定,质量可控。
关键词:  奥硝唑  左氧氟沙星  中空栓  质量控制
DOI:
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基金项目:
Preparation and Quality Control of Compound Ornidazole Hollow Type Suppository
WANG Yan1,ZHANG Lili2
Abstract:
OBJECTIVE To prepare and establish quality control for the compound ornidazole hollow type suppository.METHODSThe compound ornidazole hollow type suppository was prepared with mixable fatty acid glyceride as basic;The contents of ornidazole and levofloxacin were determined by equivalent absorption dual-wavelength method;The tests of hygienic, stimulation and stability were carried out. RESULTSThe average recovery of ornidazole and levofloxacin were 99.7%(n=9),100.2%(n=9),other tests accord with the standard of suppository. CONCLUSIONThe preparation of the Hollow Suppository is simple. And its quality can be well controlled.
Key words:  ornidazole  levofloxacin  hollow suppository  quality control
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