Zhang Xiaolong, Zhang Haitao, Ji Lanju
Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining 810008, China.
Zhongguo Zhong Yao Za Zhi. 2009 Nov;34(22):2884-6.
To establish a RP-HPLC method for simultaneously determination of swertiamarin, gentiopicroside, sweroside, isoorientin in Gentiana lawrencei from Qinghai province.
The RP-HPLC method was used. Chromatographic column was the Kromasil C18 column (4.6 mm x 250 mm, 5 microm). The gradient elution solvent system was composed of acetonitrile (A) and (0.1% H3PO4) water (B). The ratio of acetonitrile was as follows: 0.00-27.00 min, 10% -17% (A); 27.00-45.00 min, 17% -33% (A); 45.01-55.00 min, 100%-100% (A). The detective wavelength was 240 nm; the flow rate was 1 mL x min(-1); column temperature was set at 25 degrees C.
Swertiamarin, gentiopicroside, sweroside and isoorientin were base-isolated. The method had good linearity within the ranges of 2.12-10.6 mg x mL(-1) for swertiamarin (r = 0.999 4), 2.46-12.3 g x L(-1) for gentiopicroside (r = 0.999 7), 2.47-12.4 g x L(-1) for sweroside (r = 0.999 2) and 0.309-1.54 mg x mL(-1) for isoorientin (r = 0.999 5).
The method is rapid, precise and repeatable, can be applied to control the quality of G. lawrencei.
建立一种同时测定青海产川西獐牙菜中獐牙菜苦苷、龙胆苦苷、獐牙菜苷、异荭草苷含量的反相高效液相色谱法。
采用反相高效液相色谱法。色谱柱为Kromasil C18柱(4.6 mm×250 mm,5μm)。梯度洗脱溶剂系统由乙腈(A)和(0.1%磷酸)水(B)组成。乙腈比例如下:0.00 - 27.00分钟,10% - 17%(A);27.00 - 45.00分钟,17% - 33%(A);45.01 - 55.00分钟,100% - 100%(A)。检测波长为240 nm;流速为1 mL·min⁻¹;柱温设定为25℃。
獐牙菜苦苷、龙胆苦苷、獐牙菜苷和异荭草苷得到基线分离。该方法在獐牙菜苦苷2.12 - 10.6 mg·mL⁻¹范围内线性良好(r = 0.999 4),龙胆苦苷2.46 - 12.3 g·L⁻¹范围内线性良好(r = 0.999 7),獐牙菜苷2.47 - 12.4 g·L⁻¹范围内线性良好(r = 0.999 2),异荭草苷0.309 - 1.54 mg·mL⁻¹范围内线性良好(r = 0.999 5)。
该方法快速、准确、重复性好,可用于控制川西獐牙菜的质量。