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作 者:车爽[1] 李清[2] 霍艳双[2] 陈晓辉[2] 毕开顺[2]
机构地区:[1]沈阳药科大学中药学院,辽宁沈阳110016 [2]沈阳药科大学药学院,辽宁沈阳110016
出 处:《药学学报》2010年第4期494-497,共4页Acta Pharmaceutica Sinica
摘 要:建立同时测定茯苓不同部位中去氢土莫酸、猪苓酸C、3-表去氢土莫酸、去氢茯苓酸和茯苓酸含量的方法。采用紫外-波长转换检测的RP-HPLC法:色谱柱为KromasilC18柱(250mm×4.6mm,5μm);流动相为乙腈(A)-0.05%磷酸水溶液(B)系统,梯度洗脱(0~5min,60%A~64%A;5~35min,64%A~65%A;35~35.01min,65%A~73%A;35.01~53min,73%A);流速为1.0mL.min-1;检测波长为0~48min,241nm(去氢土莫酸、猪苓酸C、3-表去氢土莫酸、去氢茯苓酸),48~55min,210nm(茯苓酸)。去氢土莫酸、猪苓酸C、3-表去氢土莫酸、去氢茯苓酸和茯苓酸分别在30.5~610.0μg·mL-1(r=0.9996)、12.66~253.2μg·mL-1(r=0.9995)、2.99~59.7μg·mL-1(r=0.9997)、6.13~122.5μg·mL-1(r=0.9995)、11.3~226.0μg·mL-1(r=0.9995)内浓度与峰面积呈良好的线性关系;方法回收率分别为98.5%(RSD=1.9%)、99.4%(RSD=1.7%)、97.9%(RSD=1.2%)、96.7%(RSD=2.5%)和97.9%(RSD=2.3%)。结果表明,本方法简便、准确、重现性好,为茯苓药材的质量控制提供了依据。To establish a method for simultaneous determination of dehydrotumulosic acid,polyporenic acid C,3-epi-dehydrotumulosic acid,dehydropachymic acid and pachymic acid in Poria,a RP-HPLC method detected by UV wavelengths switch had been developed,including 210 nm (48-55 min) for pachymic acid and 241 nm (0-48 min) for dehydrotumulosic acid,polyporenic acid C,3-epi-dehydrotumulosic acid,dehydropachymic acid,separately. The system consisting of a Kromasil C18 column (250 mm × 4.6 mm,5 μm) and a mixture of acetonitrile and 0.05% phosphate acid as the mobile phase was adopted; The flow rate was 1.0 mL.min-1. The linear response range was 30.5-610.0 μg·mL^-1 (r = 0.999 6) for dehydrotumulosic acid,12.66-253.2 μg·mL^-1 (r = 0.999 5) for polyporenic acid C,2.99-59.7 μg·mL^-1 (r = 0.999 7) for 3-epi-dehydrotumulosic acid,6.13-122.5 μg·mL^-1 (r = 0.999 5) for dehydropachymic acid and 11.3-226.0 μg·mL^-1 (r = 0.999 5) for pachymic acid. The average recoveries of these compounds were 98.5% (RSD = 1.9%),99.4% (RSD = 1.7%),97.9% (RSD = 1.2%),96.7% (RSD = 2.5%) and 97.9% (RSD = 2.3%),respectively. The method is simple,accurate and reproducible for quality control of Poria.
分 类 号:R917[医药卫生—药物分析学]
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