摘要
目的:测定板蓝根药材中尿苷、鸟苷、腺苷的含量。方法:采用Prevail C18(4.6 mm×250 mm,5μm)色谱柱;流动相:A(水)-B(乙腈);梯度洗脱:0~34 min(2%B^20%B);柱温:25℃;流速为:0.5 mL/min;检测波长:254 nm。结果:尿苷、鸟苷、腺苷分别在1.92~38.4μg/mL,1.75~35μg/mL,2.12~42.4μg/mL范围内线性关系良好,相关系数均为0.999 9。药材提取方法的平均回收率分别为99.64%,98.98%,98.85%,精密度、稳定性及重现性均良好。结论:所建立的方法灵敏快速,操作简便,重现性好,可用于板蓝根药材的质量控制。
AIM: To establish a method for determining guanosine, ufidine, and andadenosine for Radix Isatid/s. METHODS: The Prevail C18 analytical column(4.6 mm× 250 mm,5 um)was used . The mobile phases con- sisted of water and acetonitrile with gradient. The flow rate was 0.5 mL/min and column temperature was at 25 ℃. The detection wavelength was at 254 nm. RESULTS: The method had good linear relationship within the range 1.92 - 38.4 ug/mL; 1.75 - 35ug/mL ; 2.12 - 42.4 ug/mL of guanosine, uridine and andadenosine, respectively, with the correlation coefficients of 0.999 9. The average recoveries of the three nucleosides were 99.64% (RSD =0.38% ), 98.94% (RSD =0.32% ) and 98.85% (RSD =0.48% ), correspondingly. CONCLUSION: The method is fast, rapid, convenient, accurate and can be used for quality control of Radix isatidis.
出处
《中成药》
CAS
CSCD
北大核心
2008年第11期1654-1657,共4页
Chinese Traditional Patent Medicine
关键词
板蓝根
核苷
HPLC
含量测定
Radix isatidis
nucleosides
HPLC
determination