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紫外分光光度法测定华法林钾片的溶出度 被引量:4

Determination of Dissolution of Warfarin Potassium Tablets by UV Spectrophotometry
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摘要 目的:建立测定华法林钾片溶出度的方法。方法:采用紫外分光光度法,以0.1mol·L-1盐酸为溶媒,溶媒体积900mL,转速50r·min-1,30min取样,在283nm波长处测定其溶出度。结果:华法林钾检测浓度的线性范围为5~30μg·mL-1(r=0.9999);平均回收率为100.53%(RSD=0.69%);3批样品30min溶出度均在90%以上。结论:本方法简便、准确,结果可靠,可用于该制剂的溶出度测定。 OBJECTIVE: To establish a method for the determination of dissolution of warfarin potassium tablets. METHODS: The dissolution of warfarin potassium tablets was determined by UV spectrophotometry at a detection wavelength of 283 nm with 0.1 mol · L^- 1 hydrochloric acid as the solvent at a volume of 900 mL. The rotation speed was 50 r · min ^-1 and the sampling time was 30 min. RESULTS: The method showed a good linear relationship in the range of 5-30μg · mL ^-1( r = 0.999 9). The average recovery was 100.53% (RSD = 0.69% ). The dissolutions of 3 batches of samples were all above 90%. CONCLUSION: The method is simple, accurate and reliable, and it can be applied for the determination the dissolution of warfarin potassium tablets.
作者 金英顺
出处 《中国药房》 CAS CSCD 北大核心 2008年第13期1014-1016,共3页 China Pharmacy
关键词 华法林钾片 溶出度 紫外分光光度法 Warfarin potassium tablets Dissolution UV spectrophotometry
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参考文献2

  • 1McGilveray IJ,Midha KK, Cooper JK.Bioavailability of canadian tablet formulations of warfarin sodium and potassium[J ] . Can J Pharm Sci, 1978,13(1) :9. 被引量:1
  • 2国家药典委员会编..中华人民共和国药典 2005年版 一部[M].北京:化学工业出版社,2005:668.

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