目的:建立测定莪术中羟基异吉马呋内酯含量的方法,并比较不同产地莪术中羟基异吉马呋内酯的含量差异。方法:采用高效液相色谱法。色谱柱为KromasilC18(250mm×4.6mm,5μm),流动相为乙腈.水(梯度洗脱),流速为1.0ml/min,检测波长为214nm,柱温为25℃。结果:羟基异吉马呋内酯的质量浓度在1.47~14.68μg/ml范围内与其峰面积积分值呈良好线性关系(n=0.9997);精密度、稳定性、重复性试验的RSD〈3%;平均加样回收率为95.31%~95.80%,RSD为0.07%~1.36%(n=3)。不同产地同品种、同产地不同时期莪术中羟基异吉马呋内酯的含量存在差异。结论:该方法分离度好、专属性强、重复性好、简便易行。可用于莪术中羟基异吉马呋内酯的含量测定,并能完善现行莪术药材的质量标准。
OBJECTIVE: To establish the method for the content determination of hydroxyisogermafurenolide in Curcumae Rhi- zoma, and to compare the content difference of hydroxyisogermafurenolide in Curcumae Rhizoma from different habitats. METH- ODS: HPLC method was adopted. The separation was performed on Kromasil C18(250 mm×4.6 mm, 5 μm) column with mobile phase consisted of aeetonitrile-water(gradient elution) at the flow rate of 1.0 ml/min. The detection wavelength was set at 214 nm and column temperature was 25 ℃. RESULTS: The linear range of hydroxyisogermafurenolide were 1.47-14.68 μg/ml(r=0.999 7). RSDs of precision, stability and reproducibility tests were all lower than 3%. The average recovery were 95.31%-95.80% (RSD were 0.07%-1.36%, n=3). The contents of hydroxyisogermafurenolide in same types of Curcumae Rhizoma from different habitats were different from that of Curcumae Rhizoma from same habitats at different periods. CONCLUSIONS: The method is well-sepa- rated, specific, reproducible, simple and feasible. It can be used for the content determination of hydroxyisogermafurenolide in Curcumae Rhizoma and improve the present quality standard of Curcumae Rhizoma.