中国医药工业杂志
中國醫藥工業雜誌
중국의약공업잡지
CHINESE JOURNAL OF PHARMACEUTICALS
2010年
2期
126-128
,共3页
李娴%王本杰%袁桂艳%魏春敏%郭瑞臣
李嫻%王本傑%袁桂豔%魏春敏%郭瑞臣
리한%왕본걸%원계염%위춘민%곽서신
六味地黄丸%丹皮酚%马钱苷%莫诺苷%芍药苷%高效液相色谱%测定
六味地黃汍%丹皮酚%馬錢苷%莫諾苷%芍藥苷%高效液相色譜%測定
륙미지황환%단피분%마전감%막낙감%작약감%고효액상색보%측정
Liuwei Dihuang pills%paeonol%loganin%morroniside%paeoniflorin%HPLC%determination
建立了HPLC法同时测定六味地黄丸中的丹皮酚、马钱苷、莫诺苷和芍药苷.采用C_(18)色谱柱,以乙腈-0.1%磷酸溶液梯度洗脱,检测波长238 nm,丹皮酚、马钱苷、莫诺苷和芍药苷分别在0.5~20、0.25~10、0.5~20和0.15~6μg/ml浓度范围内线性关系良好,回收率分别为98.10%~105.44%.
建立瞭HPLC法同時測定六味地黃汍中的丹皮酚、馬錢苷、莫諾苷和芍藥苷.採用C_(18)色譜柱,以乙腈-0.1%燐痠溶液梯度洗脫,檢測波長238 nm,丹皮酚、馬錢苷、莫諾苷和芍藥苷分彆在0.5~20、0.25~10、0.5~20和0.15~6μg/ml濃度範圍內線性關繫良好,迴收率分彆為98.10%~105.44%.
건립료HPLC법동시측정륙미지황환중적단피분、마전감、막낙감화작약감.채용C_(18)색보주,이을정-0.1%린산용액제도세탈,검측파장238 nm,단피분、마전감、막낙감화작약감분별재0.5~20、0.25~10、0.5~20화0.15~6μg/ml농도범위내선성관계량호,회수솔분별위98.10%~105.44%.
An HPLC method was established for the simultaneous determination of paeonol,loganin, morroniside and paeoniflorin in Liuwei Dihuang pills.A C_(18) column was used with the mobile phase of acetonitrile-0.1% phosphoric acid for gradient elution at the detection wavelength of 238 nm.The calibration curves of the four constituents were linear in the concentration ranges of 0.5-20,0.25-10,0.5-20 and 0.15-6 μg/ml,respectively.The recoveries were 98.10%-105.44%.