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高效液相色谱法测定缓解视疲劳片中原花青素的含量
引用本文:刘荣丽,;钟碧萍,;黄宏南,;周芬霞,;刘怀勇.高效液相色谱法测定缓解视疲劳片中原花青素的含量[J].食品与药品,2014(3):193-195.
作者姓名:刘荣丽  ;钟碧萍  ;黄宏南  ;周芬霞  ;刘怀勇
作者单位:[1]福建中医药大学,福建福州350122; [2]福建医科大学,福建福州350122; [3]福建省疾病预防控制中心,福建福州350001
摘    要:目的建立缓解视疲劳片中原花青素的含量测定方法。方法原花青素经铁盐催化降解为花青素离子后进行HPLC分析。通过正交试验优化降解条件为:1.0 mL供试品溶液加10 mg/mL硫酸高铁铵溶液0.2 mL和正丁醇-盐酸混合液(97:3,v/v)8.8 mL,100℃水浴加热1 h。色谱条件:Ultimate XB-C18色谱柱(4.6 mm×150 mm,5μm),流动相为甲醇-0.1%磷酸(45:55),流速0.5 mL/min,柱温30℃,检测波长530 nm。结果原花青素在考察的浓度范围内线性良好(r=0.9994),检出限9.33μg/mL,定量限31.12μg/mL,平均回收率95.56%。结论此方法操作简单,重现性好,可为该产品的质量控制提供参考。

关 键 词:原花青素  高效液相色谱法  降解  花青素离子

Determination of Proanthocyanidins in Asthenopia-relieving Tablets by HPLC
Affiliation:LIU Rong-li,ZHONG Bi-ping,HUANG Hong-nan,ZHOU Fen-xia,LIU Huai-yong(Fujian University of Traditional Chinese Medicine, Fuzhou 350122, China;Fujian Medical University, Fuzhou 350122, China;Fujian Center for Disease Control and Prevention, Fuzhou 350001, China)
Abstract:Objective To establish a method for the determination ofproanthocyanidins in Asthenopia-relieving Tablets by HPLC.Methods The content of proanthocyanidins was determined after degradation in n-butanol-HC1 reaction medium using iron salt as catalyst.The degradation condition was optimized through single factor and orthogonal experiments,which was that taking 0.2 mL 10 g/L ferric ammoniun sulfate solution and 8.8 mL n-butanol-HCl(93∶7,v/v) mixture into 1 mL sample solution and reacting at 100 ℃ for 1 h.The analysis was achieved on the Ultimate XB-C18 (4.6 mm× 150 mm,5 μm) column,with mobile phase consisted of methanol and 0.1% phosphoric acid(45∶55,v/v) at a flow-rate of 0,5 mL/min.The column temperature was set at 30 ℃ and wavelength of detector was 530nm.Results The calibration curve showed good linear regression,the detection limit was 9.33 μg/mL and the limit of quantitation was 31.12 μg/mL.The average recovery of assay was 95.56 %.Conclusion The method is full of simplicity,reproducibility and accuracy.It can offer a reference for the quality evaluation and control of this product.
Keywords:proanthocyanidin  high performance liquid chromatography  degradation  anthocyanin ion
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