摘要
目的 建立莲草口服液的质量标准。方法采用高效液相色谱法对莲草口服液中的主要成分野黄芩苷、对香豆酸进行含量测定。结果野黄芩苷进样量在0.208~1.042μg范围内与峰面积线性关系良好,(r=09999)(n=5),平均回收率为100.3%,RSD=081%(n=6);对香豆酸进样量在0.079-0.394μg范围内与峰面积线性关系良好,(r=0.9994)(n=5),平均回收率为99.6%,RSD=0.94%(n=6)。结论建立了莲草口服液的含量测定方法。该方法精确,重现性好,操作简便,可作为莲草口服液质最控制标准。
Objective To establish the quality standard of Liancao Oral Liquid. Methods The content of scutellarin and p-Coumaric acid in Liancao Oral Liquid was determined by HPLC. Results There was a good linearity for scutellarin in the range of0.208-1.042μg (r=0.9999) (n=5) , The average recovery rate was 100.3%, RSD:0.81% (n = 6 ) ; There was a good linearity for p-Coumaric acid in the range of 0.079-0.394 μg (r=0.9994 ) (n= 5 ) , The average recovery rate was 99.6%, RSD: 0.94% (n= 6) . Conclusion To develop a method of determining the content of Liancao Oral Liquid. The methods are simple, effective with good reproducibility, which can be used for the quality control of Liancao Oral Liquid.
出处
《国际中医中药杂志》
2010年第2期171-172,共2页
International Journal of Traditional Chinese Medicine