摘要
目的 :探讨疏肝舒乳颗粒的制备及质量控制标准。方法 :采用紫外分光光度法检测制剂中延胡索乙素的含量。结果 :处方设计合理 ,制备方法简便 ,平均回收率 99.2 0 %。结论 :用该方法作为检测手段 ,简单、灵敏、快速 ,可作为疏肝舒乳颗粒的质量控制方法。
Objective: To establish the preparation process and the quality control standards for SGSR Granules. Methods:Tetrahydropalmatine in SGSR Granules was determined by UV. Results: Tetrahydropalmatine showed a good linearity in the range of 7.84～39.20 μg·ml -1 ; r =0.999 8. Conclusion: This method is simple, accurate and specific. It can be used for the quality control of SGSR.
出处
《时珍国医国药》
CAS
CSCD
2004年第5期269-270,共2页
Lishizhen Medicine and Materia Medica Research
