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作 者:田雁钰
机构地区:[1]河南省南阳市食品药品检验所,南阳473008
出 处:《海峡药学》2013年第10期41-43,共3页Strait Pharmaceutical Journal
摘 要:目的 建立同时测定清热灵颗粒中黄芩苷、连翘苷和靛玉红含量的HPLC双波长梯度洗脱法.方法 色谱柱:Kromasil C18(250mm×4.6mm,5μm).以乙腈(A)-0.5%三乙胺水溶液(磷酸调pH至3.05)(B)为流动相梯度洗脱.检测波长λ1=277nm,λ2=289nm,流速:1.0mL·min-1;柱温:25℃.结果 黄芩苷线性范围为1.64~104.96μg·mL-1(r=0.9999),平均回收率为98.98%,RSD为0.37%(n=6);连翘苷线性范围为1.62~103.63μg·mL-1(r=0.9999),平均回收率为98.84%,RSD为0.23%(n=6);靛玉红线性范围为0.75~48.03μg·mL-1(r=0.9999),平均回收率为98.34%,RSD为0.68%(n=6).结论 方法简便可靠,结果重现性好,为控制清热灵颗粒的内在质量提供了科学依据.OBJECTIVE To establish a method for determination the content of baicalin and forsythin and In- dirubin in Qingreling Keli by HPLC. METHODS The Kromasil C is column (250mm×4.6mm,5μm) was used, The mobile phase was acetonitrile (A)-0. 5% triethylamine( adjust pH to 3.05 with phosphoric acid) (B). The de- tection wavelength was at λ1= 277nm, k2 = 289nm, the flow rate was 1.0mL·min - 1. The temperatu re of the column at 25℃. RESULTS The linear range for baicalin and forythin and Indirubin was 1.64 - 104. 96μg·mL-1 ( r = 0. 9999) andl. 62 -103.63μg·mL-1(r =0. 9999) and 0. 75 -48. 03μg·mL-1( r =0. 9999) ,the average recov- ery was 98.98% ( RSD 0. 37%, n = 6) and 98.84% ( RSD 0. 23%, n = 6) and 98.34% ( RSD 0. 68%, n = 6) o CONCLUSION The method is simple, accurate, reliable and can be applied to the quality control of Qingreling Keli.
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