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氯诺昔康片溶出度测定方法的研究

Study on Test Method of Dissolution for Lornoxicam Tablets
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摘要 目的 建立氯诺昔康片溶出度测定方法。方法 选用中国药典 2 0 0 0年版溶出度测定第二法 ,紫外分光光度法检测。结果 测定波长为 376nm ,浓度在 0 .5~ 1 0 μg·ml-1 范围内 ,与吸收度呈良好的线性关系 (r =0 .9999) ,平均回收率为 1 0 0 .1 3% ,RSD 为 0 .6 8% ,每片溶出量应为标示量的 80 %以上。结论 本法适合于氯诺昔康片的溶出度测定。 Aim To develop a method of dissolution test for lornoxicam tablets.Methods Dissolution method Ⅱ of the Chinese Pharmacopoeia 2000 was used.UV spectrophotometry was adopted for the determination.Results Detection wave length was 376nm,the average recovery was 100.13%,RSD=0.68%.It had good linearity in the concentration range of 0.5~10μg·ml -1 ,r=0.999 9,the percentage of dissolution of lornoxicam in 45min were more than 80%.Conclusion This method could be applied to the determination of dissolution of lornoxicam tablets.
出处 《解放军药学学报》 CAS 2003年第5期382-383,共2页 Pharmaceutical Journal of Chinese People's Liberation Army
关键词 氯诺昔康片 非甾体抗炎药 溶出度 紫外分光光度法 Lornoxicam tablets Dissolution UV spectrophotometry method
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参考文献2

  • 1Press - T - P, Stroissing - H, Radhofer - Wehe - S, et al . Overview of the pharmacologied properties, pharmacokinetics and animal safety assessment of lornoxicam[ J]. Postgrad Med J , 1990,66:Suppl. 4,18.
  • 2Penkler, Lawrence J, Glintenkamp, et al . 1998 United States Patent 5,854,226[ P] December 29.

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