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机构地区:[1]西华大学生物工程学院,四川成都610039 [2]四川大学华西公共卫生学院,四川成都610041
出 处:《时珍国医国药》2009年第1期207-209,共3页Lishizhen Medicine and Materia Medica Research
基 金:四川省教育厅自然重点项目资助(No.07ZA117)
摘 要:目的建立了枳实中柚皮苷、橙皮苷、新橙皮苷、芦丁、槲皮素含量的测定方法,同时测定了枳实提取物的抗氧化作用。方法采用HPLC法,色谱柱:Phenomenex GeminiC18柱(150mm×4.6mm,5μm),柱温37℃,流动相为乙腈-磷酸溶液,检测波长280,365nm,流速1.0m1/min。采用DPPH·测定枳实提取物的自由基清除能力。结果进样量范围:柚皮苷为1.143~5.717μg,橙皮苷为0.092~0.459μg,新橙皮苷为1.179~5.895μg,芦丁为0.024~0.118μg,槲皮素为0.079~0.395μg。柚皮苷、橙皮苷、新橙皮苷的平均回收率分别为99.604%,100.150%,100.249%。RSD分别为0.515%,4.390%,0.774%。枳实提取物对DPPH·清除作用是柚皮苷的17.6倍。结论HPLC测定法简便、准确,可用于测定枳实类黄酮含量,同时枳实提取物具有较强的自由基清除作用。Objective To establish an HPLC method for determination of naringin, hesperidin, neohesperidin, rutin and quercetin in Citrus aurantium L. , and to study antioxidant activity. Methods The samples were extracted with ethanol. The chromatographic conditions were as follows: Phenomenex Gemini C lS column (150 mm × 4.6 mm, 5 μm) , column temperature at 37℃, mobile phase of acetonitrile - phosphate solution, detection wavelength at 280nm or 365nm, flow rate 1.0ml/min. In addition, DPPH radical - scavenging was employed to measure antioxidant activities. Results The calibration curves were linear in the range of 1. 143 -5. 717 μg for naringin, 0. 092 ~ 0. 459μg for hesperidin, 1. 179~ 5. 895 μg for neohesperidin, 0. 024 -0.118μg for rutin and 0. 079~ 0. 395μg for quercetin. The average recoveries of naringin, hesperidin, neohesperidin were 99. 604% , 100. 150% and i00.249% respectively. RSD were 0. 515% , 4. 390% and 0.774% respectively. The DPPH radical scavenging activity of C. aurantium L. flavoniods was 17.6 times of naringin. Conclusion The method is simple, accurate for detecting flavoniods in C. aurantium L. , and the C. aurantium L . extract has antioxidant activities.
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