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格替沙星片溶出度测定条件的优选实验 被引量:2

Study of Selecting an Ideal Dissolution Determining Condition of Gatifloxacin Tablet
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摘要 目的 优化格替沙星片的溶出度测定条件。方法 采用正交实验对该药片溶出度测定的基本条件 (转速、取样时间、溶出介质 )进行筛选 ,采用紫外分光光度法测定含量。结果 筛选出 80r/min ,45min取样 ,0 .1mol·L-1的盐酸作溶出介质为该药溶出度的最佳测定条件。结论 采用正交实验法筛选出的最佳溶出条件 ,快速、准确。 Aim To select an ideal dissolution determining condition of drug tablets.Methods An orthogonal design was used to select the conditions (rotational speed, sampling time and releasing media), determined by UV spectrophotometry.Results By using the orthogonal design we have got an ideal determining condition of the dissolution.Rotational speed is 80rpm,sampling time is 45min and releasing media is 0.1mol·L -1 hydrochloride.Conclusion The orthogonal design is an ideal tool in the selection of the conditions of the drug dissolution.it is rapid and accurate.
出处 《解放军药学学报》 CAS 2001年第5期278-279,共2页 Pharmaceutical Journal of Chinese People's Liberation Army
关键词 正交实验法 溶出度 紫外分光光度法 格替沙星片 Orthogonal design Dissolution UV spectrophotometry
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  • 1国家药典委员会.中国药典[s].二部.北京:中国医药科技出版社,2010.
  • 2国家食品药品监督管理局.国家药品标准新药转正标准[M].北京:人民卫生出版社,2008,72:180-181.
  • 3Clough GF, Boutsiouki P, Church MK. Comparison of the effects of lev- ocetirizine and loratadine on histamine-induced wheal, flare, and itch in human skin [J]. Allergy,2001,56(10):985-988.
  • 4Devalia JL, De Vos C, Hanotte F, et al. A randomized , double-blind, crossover comparison among eetirizine, levocetirizine, and ueb28557 on histamine-induced cutaneous responses in healthy adult volunteers [J]. Allergy,2001,56(1):50-57.
  • 5俞慧群,卓开华.6厂家多潘立酮片的溶出度考察[J].中国药师,2010,13(1):74-76. 被引量:9
  • 6田勇,唐素芳.培哚普利片的溶出度研究[J].药物分析杂志,2011,31(2):360-362. 被引量:6

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