首页> 外文期刊>Research Journal of Phytochemistry >Analysis of Curcumin in Ethanolic Extract of Curcuma longa Linn. and Curcuma xanthorriza Roxb. Using High Performance Liquid Chromatography with UV-Detection
【24h】

Analysis of Curcumin in Ethanolic Extract of Curcuma longa Linn. and Curcuma xanthorriza Roxb. Using High Performance Liquid Chromatography with UV-Detection

机译:姜黄乙醇提取物中姜黄素的分析。和姜黄xorhorriza Roxb。结合高效液相色谱和紫外检测

获取原文
       

摘要

A simple and isocratic liquid chromatographic using UV detection at wavelength of 425 nm have been validated and used for quantitative analysis of curcumin in ethanolic extract of turmeric ( Curcuma longa Linn.) and Curcuma xanthorriza (Zingiberaceae), indigenous to Java region, Indonesia. The method was optimized for separation of three curcuminoids namely curcumin, demethoxycurcumin and bisdemethoxycurcumin using Waters Xterra MS C18 column (4.6×250 mm, 5 μm). The mobile phase used consisted of aquabidestilata and acetonitrile (65:35 v/v) containing 1% acetic acid. The analytical method was validated in terms of linearity, sensitivity, precision and accuracy. The developed method was linear over the curcumin concentration range of 10-60 μg mL?1 with correlation coefficient value of 0.999. The precision of the developed method expressed as Relative Standard Deviation (RSD) value was in the range of 0.17-1.17% for three different levels of sample. The recoveries obtained for the accuracy assessment were 8.50-101.23%. The sensitivity of analytical method was expressed with Limit of Detection (LoD) and Limit of Quantification (LoQ). The values of LoD and LoQ were 1.13 and 3.34 μg mL?1, respectively. The method was successfully used for quantitative analysis of curcumin in the rhizomes of Curcuma longa and Curcuma xanthorriza . The levels of curcumin found in those rhizomes are in the range of 3.03±0.01-7.31±0.02 ( C. longa ) and in the range of 1.69±0.02-4.92±0.01 ( C. xanthorriza ).
机译:已验证了使用紫外线检测器在425 nm波长处进行的简单且等度的液相色谱,并将其用于定量分析印度尼西亚爪哇地区的姜黄(Curcuma longa Linn。)和姜黄(Zinghorriza)(Zingiberaceae)乙醇提取物中的姜黄素。该方法针对使用Waters Xterra MS C18色谱柱(4.6×250 mm,5μm)分离三种姜黄素(姜黄素,去甲氧基姜黄素和双去甲氧基姜黄素)进行了优化。所用的流动相包括水合杀虫剂和含1%乙酸的乙腈(65:35 v / v)。该分析方法在线性,灵敏度,精密度和准确性方面得到了验证。该方法在姜黄素浓度范围为10-60μgmL ?1 时呈线性,相关系数值为0.999。对于三种不同水平的样品,用相对标准偏差(RSD)值表示的方法的精密度在0.17-1.17%的范围内。准确性评估获得的回收率为8.50-101.23%。分析方法的灵敏度用检测限(LoD)和定量限(LoQ)表示。 LoD和LoQ的值分别为1.13和3.34μgmL ?1 。该方法成功地用于姜黄和姜黄根茎中姜黄素的定量分析。在那些根茎中发现的姜黄素水平在3.03±0.01-7.31±0.02(长角衣原体)的范围内,并且在1.69±0.02-4.92±0.01(长角衣原体)的范围内。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号