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机构地区:[1]广东食品药品职业学院实验中心,广州510520 [2]广东药科大学附属第一医院药学部,广州510080
出 处:《中国药房》2016年第21期2972-2975,共4页China Pharmacy
基 金:广东省中医药局项目(No.20141199)
摘 要:目的:建立同时测定野老鹳草中没食子酸、原儿茶酸、儿茶素、柯里拉京、短叶苏木酚含量的方法。方法:采用高效液相色谱法。色谱柱为Wonda Sil C18WR,流动相为乙腈-0.1%磷酸溶液(梯度洗脱),流速为1.0 ml/min,检测波长为280 nm,柱温为40℃,进样量为20μl。结果:没食子酸、原儿茶酸、儿茶素、柯里拉京、短叶苏木酚的检测质量浓度线性范围分别为0.02~20.02、0.01~20.10、0.02~19.78、0.02~20.02、0.02~20.10(r=0.999 9、0.999 7、0.999 6、0.999 9、0.999 5);精密度、稳定性、重复性试验的RSD〈3.0%;加样回收率分别为95.1%~100.6%(RSD=2.20%,n=6)、95.8%~100.6%(RSD=1.74%,n=6)、95.1%~101.9%(RSD=2.71%,n=6)、97.7%~103.1%(RSD=2.04%,n=6)、95.3%~99.0%(RSD=1.46%,n=6)。结论:该方法操作简便、结果准确、重复性好,可用于同时测定野老鹳草中没食子酸、原儿茶酸、儿茶素、柯里拉京、短叶苏木酚的含量。OBJECTIVE:To establish a method for simultaneous determination of gallic acid,protocatechuic acid,catechuic acid,corilagin and brevifolincarboxylic acid in Geranium carolinianum. METHODS:HPLC was performed on the column of Wonda Sil C18 WR with mobile phase of acetonitrile-0.1% Phosphoric acid(gradient elution)at a flow rate of 1.0 ml/min,the detection wavelength was 280 nm,the column temperature was 40 ℃,and the volume injection was 20 μl. RESULTS:The linear range was0.02-20.02 for gallic acid(r=0.999 9),0.01-20.10 for protocatechuic acid(r=0.999 7),0.02-19.78 for catechuic acid(r=0.999 6),0.02-20.02 for corilagin(r=0.999 9)and 0.02-20.10 for brevifolincarboxylic acid(r=0.999 5);RSDs of precision,stability and reproducibility tests were lower than〈 3.0%;recoveries were 95.1%-100.6%(RSD=2.20%,n=6),95.8%-100.6%(RSD=1.74%,n=6),95.1%-101.9%(RSD=2.71%,n=6),97.7%-103.1%(RSD=2.04%,n=6)and 95.3%-99.0%(RSD=1.46%,n=6). CONCLUSIONS:The method is simple,accurate and reproducible,and can be used for the contents determination of gallic acid,protocatechuic acid,catechuic acid,corilagin and brevifolincarboxylic acid in G. carolinianum.
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