目的探索建立陈皮饮片的质量控制方法。方法采用Agilent TC-C18(2)(4.6 mm×250 mm,5μm),以乙腈-水为流动相,梯度洗脱,体积流量1.0 mL/min,波长范围220~375 nm,柱温30℃。结果陈皮饮片中的芸香柚皮苷、橙皮苷、甜橙黄酮、川陈皮素、橘皮素等的线性范围和相关系数分别为29.98~479.68μg/mL(r=0.999 8),198.88~3 182.08μg/mL(r=0.999 8),0.158~2.528μg/mL(r=0.999 8),1.008~16.128μg/mL(r=0.999 9),0.398~6.368μg/mL(r=0.999 8);加样回收率分别为99.91%(RSD=1.3%),99.59%(RSD=1.2%),100.22%(RSD=1.3%),99.85%(RSD=1.3%)和99.71%(RSD=1.5%);方法精密度、重复性良好,RSD均小于2.0%。结论本法操作简便,结果可靠,重复性好,检测快速,定量准确,可作为陈皮饮片质量控制的方法。
AIM To establish a method for the quality control for decoction pieces of Citri reticulatae Pericapium. METHODS The RP-HPLC method was used for methanolic extract of Citri reticulatae Pericapium,which chromatographic conditions were C18column and photodiode-array-detector. The mobile phase was acetonitrile-water in gradient elution manner,the flow rate was 1. 0 mL /min,wavelength detection was set between 220 nm and 375 nm,the column temperature was maintained at 30 ℃. RESULTS The linear ranges of narirutin,hesperidin,sinensetin,nobiletin,and tangeretin fell within 29. 98- 479. 68 μg /mL( r = 0. 999 8),198. 88- 3 182. 08 μg / mL( r =0. 9998),0. 158- 2. 528 μg /mL( r = 0. 999 8),1. 008- 16. 128 μg /mL( r = 0. 999 9) and 0. 398- 6. 368 μg /mL( r =0.999 8),respectively. The average recoveries were 99.91%,99.59%,100.22%,99.85% and 99.71%with corresponding RSDs of 1. 3%,1. 2%,1. 3%,1. 3% and 1. 5%,respectively. The RSDs of precision and accuracy of the assay were not more than 2. 0%( n = 6). CONCLUSION The method is rapid,accurate,reliable and can be used for quality control of the decoction pieces of Citri reticulatae Pericapium.