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HPLC双波长等基线融合结合校正因子法测定虎杖中3种成分的含量
引用本文:郭茜,孟宪生,包永睿,王帅. HPLC双波长等基线融合结合校正因子法测定虎杖中3种成分的含量[J]. 中国药房, 2013, 0(47): 4461-4464
作者姓名:郭茜  孟宪生  包永睿  王帅
作者单位:辽宁中医药大学药学院,辽宁大连116600
基金项目:国家科技重大专项课题(No.2010ZX09401-304-515)
摘    要:目的:为虎杖中白藜芦醇苷、大黄素、大黄素甲醚的含量测定提供更为简便、合理、可靠的方法。方法:采用高效液相色谱法。色谱柱为AgilentTC—C18(250mm×4.6mm,5gm),柱温为25℃,流动相为0.1%甲酸水溶液.乙腈(梯度洗脱),流速为1ml/min,检测波长为254nm(大黄素、大黄素甲醚)与319nm(白藜芦醇苷)。使用Matlab 7.1编程进行谱图融合;在此基础上,以虎杖中大黄素为内参物,建立其与白藜芦醇苷、大黄素甲醚的相对校正因子,计算白藜芦醇苷和大黄素甲醚的含量,并对不同产地虎杖中3种成分含量校正因子法的计算值与外标法实测值进行比较。结果:白藜芦醇苷、大黄素与大黄素甲醚的进样量分剐在0.29~1.76、0.75~4.51、0.05~0.31μg范围内与各自峰面积积分值呈良好的线性关系(r分别为0.9990、0.9998、0.9996);精密度、重复性、稳定性试验的RSD〈3%;平均加样回收率分别为98.50%、101.68%、99.22%,RSD分别为1.81%、2.03%、2.44%(”均为6)。采用校正因子法与外标法测得不同产地虎杖中3种成分的含量差异无统计学意义。结论:该试验为虎杖的质量控制提供了一种更为简便、合理、可靠的方法。

关 键 词:高效液相色谱法  双波长等基线融合  校正因子  虎杖  白藜芦醇苷  大黄素  大黄素甲醚  含量测定

Content Determination of 3 Components of Polygonum cuspidatum by HPLC Dual Wavelength Baseline Fusion Combined with Correction Factor
GUO Qian,MENG Xian-sheng,BAO Yong-rui,WANG Shuai. Content Determination of 3 Components of Polygonum cuspidatum by HPLC Dual Wavelength Baseline Fusion Combined with Correction Factor[J]. China Pharmacy, 2013, 0(47): 4461-4464
Authors:GUO Qian  MENG Xian-sheng  BAO Yong-rui  WANG Shuai
Affiliation:(College of Pharmacy, Liaoning University of Traditional Chinese Medicine, Liaoning Dalian 116600, China)
Abstract:OBJECTIVE: To establish a simple, reasonable and reliable method for the content determination of polydatin, emodin and physcion in Polygonum cuspidatum. METHODS:HPLC method was adopted The determination was performed on Agilent TC-C18(250 mm×4.6 mm, 5μm) column with mobile phase consisted of 0.1% formic acid-acetonitrile (gradient elution) at flow rate of 1 ml/min. The column temperature was 25℃ and the detection wavelengths were set at 254 nm (emodin, physcion) and 319 nm (polydatin). Maflab 7.1 programming was used for chromatogram fusion; using emodin as internal standard, the relative correction factors of polydatin and physcion were established to calculate the contents of polydatin and physcion. The contents of 3 components from different producing areas calculated by correction factor method were compared with the measured values of external standard method. RESULTS: The linear ranges of polydatin, emodin and physcion were 0.29-1.76 μg(r=0.999 0), 0.75-4.51μg (r=0.999 8) and 0.05-0.31μg(r=0.999 6). RSDs of precision, reproducibility and stability tests were all lower than 3%. Average recovery rates were 98.50% (RSD= 1.81%, n=6), 101.68% (RSD=2.03%, n=6) and 99.22% (RSD=2.44%, n=6). The contents of 3 components in P. cuspidatum by above 2 methods had no significant difference. CONCLUSIONS: The method is simple, reasonable and reliable for quality control of P. cuspidatum.
Keywords:HPLC  Dual wavelength baseline fusion  Correction factor  Polygonum cuspidatum  Polydatin  Emodin  Physcion  Content determination
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