为建立一种灵芝子实体中灵芝酸A的高效液相色谱(HPLC)定量测定方法,通过对灵芝子实体萃取物分离效果的影响因素进行对比试验,确定了灵芝中灵芝酸A的分离条件:色谱柱为ZORBAX SB-C18(4.6 mm×150 mm,5μm);流动相组成(A:1.0%醋酸水溶液,B:甲醇),A∶B比例为40%∶60%,流速0.5 mL/min,柱温25℃,进样量5μL;在此条件下,灵芝子实体萃取物中灵芝酸A的HPLC保留时间13.619 min,分离度1.5;绘制的标准曲线为y=8.802 1x-1.45,r2=0.990 2;其测定结果的重现性、精密度和加标回收率(99.58%)均较佳,RSD均小于2%。因此,该方法可作为灵芝子实体中灵芝酸A的HPLC定量测定方法。
In order to establish a quantitative measurement method to dertermine the ganoderic acid A from Ganoderma lucidum by HPLC, the comparative experiments were used to study the effects of several influencing factors on separation of ganoderic acid A and the separation condition was determined. The results showed that, the optimum HPLC separation was accomplished through ZORBAX SB-C18 column (4.6 mm×150 mm, 5μm), taking 1.0%acetate buffer and methanol (40%:60%) as mobile phase, 0.5 mL/min as flow rate, 25℃as column temperature and 5μL as injection volume. Under the HPLC separation condition, the retention time of the ganoderic acid A was 13.619 min and the resolution was larger than 1.5. The standard curve was y=8.802 1x-1.45 (r2=0.990 2). The repeatability, precision and recovery(99.58%) of the quantitative measurement method were all good, and relative standard deviation(RSD) of all results were less than 2%. Therefore, the obtained HPLC method could be used as the quantita