Zhao Lian-Hua, Zhao Hong-Zheng, Zhao Xue, Kong Wei-Jun, Hu Yi-Chen, Yang Shi-Hai, Yang Mei-Hua
Jilin Agricultural University, Changchun, 130118, China.
Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100193, China.
Phytochem Anal. 2016 May;27(3-4):168-73. doi: 10.1002/pca.2612.
Citri Reticulatae Pericarpium (CRP) is a commonly-used traditional Chinese medicine with flavonoids as the major bioactive components. Nevertheless, the contents of the flavonoids in CRP of different sources may significantly vary affecting their therapeutic effects. Thus, the setting up of a reliable and comprehensive quality assessment method for flavonoids in CRP is necessary.
To set up a rapid and sensitive ultra-fast liquid chromatography coupled with tandem mass spectrometry (UFLC-MS/MS) method for simultaneous quantification of seven bioactive flavonoids in CRP.
A UFLC-MS/MS method coupled to ultrasound-assisted extraction was developed for simultaneous separation and quantification of seven flavonoids including hesperidin, neohesperidin, naringin, narirutin, tangeretin, nobiletin and sinensetin in 16 batches of CRP samples from different sources in China.
The established method showed good linearity for all analytes with correlation coefficient (R) over 0.9980, together with satisfactory accuracy, precision and reproducibility. Furthermore, the recoveries at the three spiked levels were higher than 89.71% with relative standard deviations (RSDs) lower than 5.19%. The results indicated that the contents of seven bioactive flavonoids in CRP varied significantly among different sources. Among the samples under study, hesperidin showed the highest contents in 16 samples ranged from 27.50 to 86.30 mg/g, the contents of hesperidin in CRP-15 and CRP-9 were 27.50 and 86.30 mg/g, respectively, while, the amount of narirutin was too low to be measured in some samples.
This study revealed that the developed UFLC-MS/MS method was simple, sensitive and reliable for simultaneous quantification of multi-components in CRP with potential perspective for quality control of complex matrices. Copyright © 2016 John Wiley & Sons, Ltd.
陈皮是一种常用的传统中药,其主要生物活性成分是黄酮类化合物。然而,不同来源陈皮中黄酮类化合物的含量可能存在显著差异,从而影响其治疗效果。因此,建立一种可靠且全面的陈皮中黄酮类化合物质量评估方法很有必要。
建立一种快速、灵敏的超快速液相色谱-串联质谱(UFLC-MS/MS)方法,用于同时定量陈皮中的七种生物活性黄酮类化合物。
建立了一种结合超声辅助提取的UFLC-MS/MS方法,用于同时分离和定量来自中国不同来源的16批陈皮样品中的七种黄酮类化合物,包括橙皮苷、新橙皮苷、柚皮苷、橙皮芸香苷、橘皮素、诺米林和川陈皮素。
所建立的方法对所有分析物均显示出良好的线性,相关系数(R)超过0.9980,同时具有令人满意的准确度、精密度和重现性。此外,三个加标水平的回收率均高于89.71%,相对标准偏差(RSD)低于5.19%。结果表明,不同来源的陈皮中七种生物活性黄酮类化合物的含量存在显著差异。在所研究的样品中,橙皮苷在16个样品中的含量最高,范围为27.5至86.30 mg/g,陈皮-15和陈皮-9中橙皮苷的含量分别为27.50和86.30 mg/g,而在一些样品中橙皮芸香苷的含量过低无法测定。
本研究表明,所建立的UFLC-MS/MS方法用于同时定量陈皮中的多成分简单、灵敏且可靠,对复杂基质的质量控制具有潜在的应用前景。版权所有© 2016约翰威立父子有限公司。