摘要
目的 :本文采用磺化—紫外分光光度法及一阶导数紫外分光光度法 ,对青黛药材及青黛超临界提取物进行含量测定。方法 :样品经磺化反应后 ,用零阶光谱在 6 2 3nm波长处测定靛蓝的含量 ,用一阶导数紫外分光光度法在 4 82nm波长处测定靛玉红的含量。结果 :靛蓝的线性范围为 1 14~ 5 32 μg·ml- 1,r=0 9999,平均回收率为 10 1 0 6 % ,RSD为 1 2 7% ,靛玉红的线性范围为 0 5 2~ 5 2 μg·ml- 1,r =0 9999,平均回收率为 10 1 80 % ,RSD为 0 75 % ,放置 8h对含量测定无影响。结论 :测定数批青黛药材及青黛超临界提取物样品 ,其靛蓝含量测定与药典法测定结果无显著差别。
OBJECTIVE: To determine the contents of indigotin and indirubin in Indigo Naturalis and the extract of Indigo Naturalis with supercritical fluid extraction. METHODS:The indirubin content was determined with sulfonated reaction first order derivative UV spectrophotometry; the indigotin content was determined with sulfonated reaction UV spectrophotometry. RESULTS:The average recovery rate of indirubin was 101 80%, RSD =0 75%, and the average recovery rate of indigotin was 101 06%, RSD =1.27%. CONCLUSTION:This method is simple and repeatable, and can be used as the quality control method for the Indigo Naturalis and the extract of Indigo Naturalis with supercritical fluid extraction.
出处
《药学实践杂志》
CAS
2002年第5期291-293,共3页
Journal of Pharmaceutical Practice