摘要
目的 :考察不同厂家双氯芬酸钠 ( DS)缓释制剂的含量及溶出度 ,评价其内在质量。方法 :紫外分光光度法测定含量及溶出度 ,检测波长 :2 76 nm。结果 :不同厂家的 DS缓释制剂的体外溶出度有显著性差异。结论 :为了确保 DS缓释制剂的临床疗效 。
AIM:To determine content and dissolution of diclofenac sodium sustained release medication. METHODS: The content and dissolution were determined by UV at 276 nm. RESULTS: There were significant differences in dissolution between the products from different factories. CONCLUSION: It is necessary to control the dissolution of diclofenac sodium sustained release medication before clinical use.
出处
《中国临床药学杂志》
CAS
2001年第2期105-106,共2页
Chinese Journal of Clinical Pharmacy
